Disease on EC 1.1.1.49 - glucose-6-phosphate dehydrogenase (NADP+)

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DISEASE
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5'-nucleotidase deficiency
Enzymatic diagnosis in non-spherocytic hemolytic anemia.
Hemolytic anemia in hereditary pyrimidine 5'-nucleotidase deficiency: nucleotide inhibition of G6PD and the pentose phosphate shunt.
[Hemolytic anemias caused by erythrocyte enzyme disorders]
6-phosphogluconolactonase deficiency
6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiency.
Abdominal Pain
Hemolysis caused by G-6PD deficiency after a difficult and prolonged therapeutic endoscopic retrograde cholangiopancreatography.
[Posthepatic obstructive jaundice caused by primary extragonadal germ-cell tumor in a patient with glucose-6-phosphatase dehydrogenase deficiency].
Abortion, Habitual
[Glucose-6-phosphate dehydrogenase in couples with habitual abortion]
Abortion, Septic
Pancreatitis in acute hemolysis.
Abortion, Spontaneous
Hofbauer cell activation and its increased glucose-6-phosphate dehydrogenase activity in second trimester-spontaneous abortion: an ultrastructural dual staining enzyme-cytochemical study.
Prenatal selection and fetal development disturbances occurring in carriers of G6PD deficiency.
[Role of disorders of pentosephosphate pathway of glucose oxidation in the pathogenesis of the arrest of fetal development in miscarriage]
Acatalasia
A DUAL HEREDITARY RED BLOOD CELL DEFECT IN ONE FAMILY: HYPOCATALASEMIA AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.
Activities of catalase in leucocytes and glucose-6-phosphate dehydrogenase in erythrocytes of hypocatalasemia and acatalasemia.
[Glucose-6-phosphate dehydrogenase activity in the red blood cell in hypo-catalasemia and acatalasemia]
acetylcholinesterase deficiency
Paroxysmal nocturnal hemoglobinuria (PNH) as a clonal disorder.
Acidosis
Alterations of rat kidney, liver and erythrocytes glucose 6-phosphate dehydrogenase activity by chronic acidosis.
Patients with genetic defects in the gamma-glutamyl cycle.
Predictors of Acute Bilirubin Encephalopathy Among Nigerian Term Babies with Moderate-to-severe Hyperbilirubinaemia.
Stimulation of rat-kidney hexose monophosphate shunt dehydrogenase activity by chronic metabolic acidosis.
[Biochemical markers of strophanthin arrhythmia]
[Effect of sodium oxybutyrate on metabolic indices in ischemic hypoxia of muscle tissue]
[Generalized saturnine paralysis. Discovery of a double congenital disease: glucose-6-phosphate dehydrogenase deficiency (new variant) and distal tubular acidosis]
Acne Vulgaris
Aczone, a topical gel formulation of the antibacterial, anti-inflammatory dapsone for the treatment of acne.
Diet in dermatology: revisited.
Hematologic safety of dapsone gel, 5%, for topical treatment of acne vulgaris.
Is topical dapsone safe in glucose-6-phosphate dehydrogenase-deficient and sulfonamide-allergic patients?
[Determination of glucose-6-phosphate dehydrogenase activity in acne vulgaris]
Acquired Immunodeficiency Syndrome
Purification and characterization of glucose-6-phosphate dehydrogenase from Cryptococcus neoformans: identification as "nothing dehydrogenase".
Acrocephalosyndactylia
Apert syndrome with glucose-6-phosphate dehydrogenase deficiency: a case report.
Acrodermatitis
Diet in dermatology: revisited.
Actinomycosis
[Perineogluteal actinomycosis and G6PD deficiency]
Acute Coronary Syndrome
Antiplatelet and invasive treatment in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency and acute coronary syndrome. The safety of aspirin.
Acute Kidney Injury
Acute renal failure due to intravascular hemolysis in the North Indian patients.
Acute renal failure following analgesic overdose in G6PD deficiency.
Acute renal failure in a glucose-6-phosphate dehydrogenase deficient individual with infectious mononucleosis.
Acute renal failure in favism revealing familial glucose-6-phosphate dehydrogenase deficiency.
Acute renal failure in glucose-6-phosphate dehydrogenase (G6 P.D.) deficiency.
Acute renal failure in tropical Africa.
Acute viral hepatitis E presenting with haemolytic anaemia and acute renal failure in a patient with glucose-6-phosphate dehydrogenase deficiency.
Acute viral hepatitis, glucose-6-phosphate dehydrogenase deficiency and prolonged acute renal failure: a case report.
Chloroquine induced haemolysis and acute renal failure in subjects with G-6-PD deficiency.
Detection of Occult Acute Kidney Injury in Glucose-6-Phosphate Dehydrogenase Deficiency Anemia.
Determination of erythrocyte superoxide dismutase, catalase, glucose-6-phosphate dehydrogenase, reduced glutathione and malonyldialdehyde in uremia.
Dialytic support in acute renal failure.
Glucose-6-phosphate dehydrogenase deficiency and acute renal failure.
I.V. ascorbic acid for treatment of apparent rasburicase-induced methemoglobinemia in a patient with acute kidney injury and assumed glucose-6-phosphate dehydrogenase deficiency.
N-acetylcysteine overdose after acetaminophen poisoning.
Severe hyperbilirubinemia and acute renal failure associated with hepatitis E in a patient whose glucose-6-phosphate dehydrogenase levels were normal.
The effects of erdosteine on the activities of some metabolic enzymes during cisplatin-induced nephrotoxicity in rats.
[Acute kidney failure and hemolytic anemia caused by erythrocytic G6PD dificit revealed by chloroquine administration]
[Acute renal failure manifest of glucose-6-phosphate dehydrogenase deficiency: severity of iatrogenic hemolysis. Originality of genetic distribution in a family from Sardinia]
[Recurrent acute renal failure during the course of hemolytic crisis in a patient with glucose-6-phosphate dehydrogenase deficiency]
Adenocarcinoma
Effect of actinomycin C on glucose-6-phosphate dehydrogenase activity of a human adenocarcinoma growing in a heterologous host.
Effect of estrogen on synthesis of glucose-6-phosphate dehydrogenase in R3230AC mammary tumors and uteri.
Glucose-6-phosphate dehydrogenase from lactating rat mammary gland and R3230AC adenocarcinoma.
Human colon tumors: enzymic and histological characteristics.
Inactivation of metabolic enzymes by photo-treatment with zinc meta N-methylpyridylporphyrin.
Oxygen insensitivity of the histochemical assay of glucose-6-phosphate dehydrogenase activity for the detection of (pre)neoplasm in rat liver.
Sequential histochemical and morphometric studies on preneoplastic and neoplastic lesions induced in rat colon by 1,2-dimethylhydrazine.
Targeted Proteomics for Multiplexed Verification of Markers of Colorectal Tumorigenesis.
[Histocytospectrophotometric characteristics of lung cancer]
[Oxidoreductase activity in the cells of stomach cancer]
Adenoma
A compound adrenal medullary tumor (pheochromocytoma and ganglioneuroma) and a cortical adenoma in the ipsilateral adrenal gland. A case report with enzyme histochemical and immunohistochemical studies.
Biology of hepatocellular neoplasia in the mouse. II. Sequential enzyme histochemical analysis of BALB/c mouse liver during safrole-induced carcinogenesis.
Comparison of the various forms of glutathione S-transferase with glucose-6-phosphate dehydrogenase and gamma-glutamyltranspeptidase as markers of preneoplastic and neoplastic lesions in rat kidney induced by N-ethyl-N-hydroxyethylnitrosamine.
Enzymatic characteristics of tubular adenomas and carcinomas of the large intestine.
Enzyme patterns and flow cytometric DNA measurements in colorectal hyperplastic polyps and tubular adenomas less than five millimeters.
Epidemiology of polyps in the rectum and sigmoid colon. Size, enzyme levels, DNA distributions, and nuclear diameter in polyps of the large intestine.
Hepatic preneoplasia in hepatitis B virus transgenic mice.
Histochemical and histoenzymatic action of crinofizin in cystic mastosis and prostate adenoma studied in cell and organotypic cultures.
Histochemical profile of mouse hepatocellular adenomas and carcinomas induced by a single dose of diethylnitrosamine.
Spironolactone bodies in aldosteronomas and in the attached adrenals. Enzyme histochemical study of 19 cases of primary aldosteronism and a case of aldosteronism due to bilateral diffuse hyperplasia of the zona glomerulosa.
Targeted Proteomics for Multiplexed Verification of Markers of Colorectal Tumorigenesis.
[Glucose-6-phosphate dehydrogenase and transketolase activity in the blood of neurological oncologic patients preoperatively and in the dynamics of the postoperative period]
Adenoma, Bile Duct
Enzyme histochemical and immunohistochemical characterization of oval and parenchymal cells proliferating in livers of rats fed a choline-deficient/DL-ethionine-supplemented diet.
Adenoma, Liver Cell
Enzyme histochemical and immunohistochemical characterization of oval and parenchymal cells proliferating in livers of rats fed a choline-deficient/DL-ethionine-supplemented diet.
Histogenesis of dieldrin and DDT-induced hepatocellular carcinoma in Balb/c mice.
adenylate kinase deficiency
Enzymatic diagnosis in non-spherocytic hemolytic anemia.
Adrenal Hyperplasia, Congenital
Current and future perspective of newborn screening: an Indian scenario.
Neonatal biochemical screening for disease.
Newborn screening in the Philippines.
Newborn screening: need of the hour in India.
Preliminary report on neonatal screening for congenital hypothyroidism, congenital adrenal hyperplasia and glucose-6-phosphate dehydrogenase deficiency: a Chandigarh experience.
The status of neonatal screening in China, 2013.
Adrenal Insufficiency
Is GERD a Factor in Osteonecrosis of the Jaw? Evidence of Pathology Linked to G6PD Deficiency and Sulfomucins.
Adrenocortical Adenoma
Probable clonal origin of aldosteronomas versus multicellular origin of parathyroid "adenomas".
Adrenocortical Hyperfunction
[The glucose-6-phosphate dehydrogenase isoenzyme spectrum of subcellular organ fractions from rabbits with endogenous and exogenous hypercorticism]
Agammaglobulinemia
Chronic parvovirus infection and G6PD deficiency masquerading as Diamond-Blackfan anemia.
Agranulocytosis
Genetic factors and risk of agranulocytosis from metamizol.
Albinism
Detection of inherited metabolic disorders via tandem mass spectrometry in Thai infants.
Alopecia
Activity of glucose-6-phosphate 1-dehydrogenase in hair follicles with male-pattern alopecia.
Histochemical quantification of glucose-6-phosphate dehydrogenase activity in human hair follicles.
alpha-Thalassemia
Alpha-thalassemia in Papua New Guinea.
Anemia in newborn.
Clinical and hematological phenotype of homozygous hemoglobin E: revisit of a benign condition with hidden reproductive risk.
Erythrocyte glucose-6-phosphate dehydrogenase and pyruvate kinase activities in hemoglobin H disease.
G6PD deficiency, absence of alpha-thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia.
Genetic benefits of consanguinity through selection of genotypes protective against malaria.
Genetic modifiers of sickle cell anemia in the BABY HUG cohort: influence on laboratory and clinical phenotypes.
Glucose-6-phosphate dehydrogenase and hemoglobin variants in Kel Kummer Tuareg and related groups. Indirect evidence for alpha-thalassemia trait.
Hematologic disorders and nonimmune hydrops fetalis.
Influence of hemoglobin E trait on the antimalarial effect of artemisinin derivatives.
Influence of hemoglobin E trait on the severity of Falciparum malaria.
Jordan: communities and community genetics.
Laboratory and field comparisons of adenosine influx in Plasmodium falciparum and Plasmodium vivax infected erythrocytes with genetic abnormalities from patients in Myanmar.
NADH-methemoglobin reductase (cytochrome b5 reductase) levels in two groups of American blacks and whites.
Neonatal screening for sickle cell disease, glucose-6-phosphate dehydrogenase deficiency and a-thalassemia in Qatif and Al Hasa.
Pathogenesis of anemia in malaria: a concise review.
Prevalence of hemoglobin E, alpha-thalassemia and glucose-6-phosphate dehydrogenase deficiency in 1,000 cord bloods studied in Bangkok.
Reticulocyte analysis in iron deficiency anemia and hemolytic anemia.
Risk assessment of gene variants for neonatal hyperbilirubinemia in Taiwan.
The role of red blood cell polymorphisms in resistance and susceptibility to malaria.
[Abnormal hemoglobins, alpha thalassemia and erythrocyte G6PD deficiency in newborn infants of the negroid race]
[Favism, hemoglobin H, alpha-thalassemia and hemoglobinopathy in various Sardinian families. Studies on glucose-6-phosphate dehydrogenase]
[G-6-PD deficiency with hemoglobinopathy and alpha-thalassemia]
[Neonatal screening of hemoglobinopathies and G6PD deficiency in Catalonia (Spain). Molecular study of sickle cell disease associated with alpha thalassemia and G6PD deficiency]
Alzheimer Disease
Activities of key glycolytic enzymes in the brains of patients with Alzheimer's disease.
Chromosomal fragility associated with familial Alzheimer's disease.
Evidence of an oxidative challenge in the Alzheimer's brain.
Glucose-6-phosphate dehydrogenase a novel hope on a blood-based diagnosis of Alzheimer's disease.
Glucose-6-phosphate dehydrogenase deficiency and Alzheimer's disease: Partners in crime? The hypothesis.
High-dose vitamin therapy stimulates variant enzymes with decreased coenzyme binding affinity (increased K(m)): relevance to genetic disease and polymorphisms.
Increased cerebral glucose-6-phosphate dehydrogenase activity in Alzheimer's disease may reflect oxidative stress.
Increased neuronal glucose-6-phosphate dehydrogenase and sulfhydryl levels indicate reductive compensation to oxidative stress in Alzheimer disease.
Amyotrophic Lateral Sclerosis
Enzymatic analysis of individual posterior root ganglion cells in olivopontocerebellar atrophy, amyotrophic lateral sclerosis and Duchenne muscular dystrophy.
Oxidant-antioxidant imbalance in the erythrocytes of sporadic amyotrophic lateral sclerosis patients correlates with the progression of disease.
Anaphylaxis
Ceftriaxone-related fatal hemolysis in an adolescent with perinatally acquired human immunodeficiency virus infection.
Anemia
A comparative study of acute haemolytic anaemia in patients of viral hepatitis in relation to erythrocyte glucose 6-phosphate dehydrogenase deficiency.
A hematological survey of preschool children of the United Arab Emirates.
A longitudinal study of red cell enzymes in infants of low birth weight.
A model of glucose-6-phosphate dehydrogenase deficiency in the zebrafish.
A new G-6-PD variant associated with chronic non-spherocytic haemolytic anaemia in a negro family.
A novel single-base mutation in the glucose 6-phosphate dehydrogenase gene is associated with chronic non-spherocytic haemolytic anaemia.
ABO incompatibility and glucose-6-phosphate dehydrogenase deficiency presenting as Hydrops Foetalis.
Acute haemolytic anaemia and myolysis due to G6PD deficiency.
Acute massive haemolysis in children with glucose-6-phosphate dehydrogenase deficiency.
Acute viral hepatitis E presenting with haemolytic anaemia and acute renal failure in a patient with glucose-6-phosphate dehydrogenase deficiency.
Aczone, a topical gel formulation of the antibacterial, anti-inflammatory dapsone for the treatment of acne.
Adequate hemodialysis improves anemia by enhancing glucose-6-phosphate dehydrogenase activity in patients with end-stage renal disease.
Adult-onset Still's disease associated with G6PD deficiency: a case report and literature review.
Agriculture-related anaemias.
An audit of the precipitating factors for haemolytic crisis among glucose-6-phosphate dehydrogenase-deficient paediatric patients.
An experimental study of hemolysis induced by onion (Allium cepa) poisoning in dogs.
Anaemia and antioxidant defence of the red blood cells.
Anaemia, a common but often unrecognized risk in diabetic patients: A review.
Anaemic crisis in sickle cell disease.
Anemia and the liver. Hepatobiliary manifestations of anemia.
Anemia associated with new-onset diabetes: improvement with blood glucose control.
Anemia during actue infections. Role of glucose-6-phosphate dehydrogenase deficiency in Negroes.
Anemia in Patients with Coinherited Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency.
Anemia in pregnancy.
Anemia of premature infant: the glucose-6-phosphate dehydrogenase activity in erythrocytes of cmrd blood from premature and full-term infants.
Anemia, cataracts, and seizures in patient with glucose-6-phosphate dehydrogenase deficiency.
Aspirin-induced acute haemolytic anaemia in glucose-6-phosphate dehydrogenase-deficient children with systemic arthritis.
Assessment of erythrocyte deformability with the laser-assisted optical rotational cell analyzer (LORCA).
Assessment of potential donors for living related liver transplantation.
Assessment of the red cell proteome of young patients with unexplained hemolytic anemia by two-dimensional differential in-gel electrophoresis (DIGE).
Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia.
Association of glucose-6-phosphate dehydrogenase deficiency and X-linked chronic granulomatous disease in a child with anemia and recurrent infections.
Association of homozygous sickle cell anemia and glucose-6-phosphate dehydrogenase deficiency.
Association of naphthalene with acute hemolytic anemia.
Behaviour of cell physiological and biochemical indicators of maturation and aging of red blood cells in density fractionated red blood cells during a bleeding anaemia of the rabbit.
Biochemical changes in equine erythrocytes during experimental regenerative anemia.
Blood glucose normalization-induced haemolysis in three adolescents with type 1 diabetes mellitus at onset and unknown G-6-PD deficiency.
Case report: Acute hepatitis E infection with coexistent glucose-6-phosphate dehydrogenase deficiency.
Catalase deficiency may complicate urate oxidase (rasburicase) therapy.
Ceramide in suicidal death of erythrocytes.
Changing trends in malaria--a decade's experience at a referral hospital.
Characterization of glucose-6-phosphate dehydrogenase in Sardinian children with congenital nonspherocytic haemolytic anaemia.
Chronic haemolytic anaemia and glucose-6 phosphate dehydrogenase deficiency. Case report and review of the literature.
Chronic haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency.
Chronic non-spherocytic haemolytic disorders associated with glucose-6-phosphate dehydrogenase variants.
Chronic parvovirus infection and G6PD deficiency masquerading as Diamond-Blackfan anemia.
Ciprofloxacin-induced acute haemolytic anaemia in a patient with glucose-6-phosphate dehydrogenase Mediterranean deficiency: a case report.
Clinical and biochemical interactions of glucose-6-phosphate dehydrogenase deficiency and sickle-cell anemia.
Clinical and haematological consequences of recurrent G6PD mutations and a single new mutation causing chronic nonspherocytic haemolytic anaemia.
Clinical disorders of the red cell membrane skeleton.
Combined G-6PD and 6-PGD deficiency in a Hindu boy.
Complete repair of tetralogy associated with sickle cell anemia and G-6-PD deficiency.
Congenital dyserythropoietic anaemia type II associated with a new type of G6PD deficiency (G6PD Gabrovizza).
Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child.
Congenital erythrocyte enzyme deficiencies.
Congenital haemolytic anaemia associated with adenylate kinase deficiency.
Coombs-negative severe hemolysis associated with hepatitis A.
Cost-benefit analysis of G6PD screening in Lebanese newborn males.
Dapsone therapy for malaria during pregnancy: maternal and fetal outcomes.
Deletion of leucine 61 in glucose-6-phosphate dehydrogenase leads to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections.
Dengue infection in hematologic-oncologic pediatric patients: aggravation of anemia and bleeding risk.
Depression of erythrocyte glucose-6-phosphate dehydrogenase (G6PD) activity in enteric fever.
Detection of G6PD and pyruvate kinase deficiencies in reticulocytosis by reference to erythrocyte creatine.
Detection of Occult Acute Kidney Injury in Glucose-6-Phosphate Dehydrogenase Deficiency Anemia.
Diabetic ketoacidosis does not precipitate haemolysis in patients with the Mediterranean variant of glucose-6-phosphate dehydrogenase deficiency.
Diabetic ketoacidosis revealing glucose-6-phosphate dehydrogenase deficiency: description of an adult case.
Does G gamma/A gamma ratio and Hb F level influence the severity of sickle cell anaemia.
Drug induced acute haemolytic anaemia in glucose-6-phosphate dehydrogenase deficiency subjects.
Drug-eluting stents in a patient with favism: is the aspirin administration safe?
Drug-induced anemia associated with glucose-6-phosphate dehydrogenase deficiency.
Drug-induced haemolysis in glucose-6-phosphate dehydrogenase deficiency.
DRUG-INDUCED HEMOYTIC ANEMIAS ASSOCIATED WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY: AGENETICALLY HETEROGENOUS TRAIT.
Effect of alpha thalassaemia, G-6-PD deficiency and Hb F on the nature of sickle cell anaemia in south-western Saudi Arabia.
Effect of anaemia on red cell metabolism in cattle.
Effect of desferrioxamine in acute haemolytic anaemia of glucose-6-phosphate dehydrogenase deficiency.
Effect of experimental anaemia on red cell GSH and enzyme activities in guinea-pig and rabbit.
Effects of an NADPH-generating system on primaquine degradation by hamster liver fractions.
Effects of glucose-6-phosphate dehydrogenase deficiency upon sickle cell anaemia.
Effects of glucose-6-phosphate dehydrogenase deficiency upon sickle cell anemia.
Enhanced erythrocyte apoptosis in sickle cell anemia, thalassemia and glucose-6-phosphate dehydrogenase deficiency.
EP21.21: Fetal anemia caused by the Guadalajara variant of G6PD deficiency.
Erythrocyte programmed cell death.
Erythrocyte reduced glutathione level in sickle cell anaemia and glucose-6-phosphate dehydrogenase deficient Saudi subjects.
Evaluation of the phenotypic test and genetic analysis in the detection of glucose-6-phosphate dehydrogenase deficiency.
Excessive fluoride consumption increases haematological alteration in subjects with iron deficiency, thalassaemia, and glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.
Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.
Fatal familial haemolytic anaemia.
Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community.
Favism: looking for an autosomal gene associated with glucose-6-phosphate dehydrogenase deficiency.
Fetal anemia caused by the Guadalajara variant of G6PD deficiency.
Fetal haemoglobin production and the sickle gene in the oases of Eastern Saudi Arabia.
First report of co-morbidity of pantothenate kinase-associated neurodegeneration and three types of chronic hemolytic anemias.
Frequency of glucose 6 phosphate dehydrogenase deficiency and related hemolytic anemia in Riyadh, Saudi Arabia.
Frequency of glucose-6-phosphate dehydrogenase (G6PD) mutations in Chinese, Filipinos, and Laotians from Hawaii.
Fructosamine in HbS and G6PD-deficient Saudi Arabs in the Eastern Province of Saudi Arabia.
G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia.
G6PD (Dublin): chronic non-spherocytic haemolytic anaemia resulting from glucose-6-phosphate dehydrogenase deficiency in an Irish kindred.
G6PD deficiency and absence of ?-thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia.
G6PD Deficiency in an HIV Clinic Setting in the Dominican Republic.
G6PD deficiency with hemolytic anemia due to a rare gene deletion--a report of the first case in Malaysia.
G6PD deficiency, absence of alpha-thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia.
G6PD deficiency: a classic example of pharmacogenetics with on-going clinical implications.
G6PD deficiency: global distribution, genetic variants and primaquine therapy.
G6PD gene mutations in India producing drug-induced haemolytic anaemia.
G6PD hillbrow: a new variant of glucose-6-phosphate dehydrogenase associated with drug-induced haemolytic anaemia.
G6PD sumaré: a novel mutation in the G6PD gene (1292 T-->G) associated with chronic nonspherocytic anemia.
G6PD Varadero. A new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
G6PD/PK ratio: a reliable parameter to identify glucose-6-phosphate dehydrogenase deficiency associated with microcytic anemia in heterozygous subjects.
G6PD: population genetics and clinical manifestations.
Gd (+) Laguna, a new rare glucose-6-phosphate dehydrogenase variant from Brazil.
Genetic compounds--Hb S, thalassaemias and enzymopathies: spectrum of interactions.
Glucose 6 phosphate dehydrogenase deficiency in adults.
Glucose 6-phosphate dehydrogenase and the kidney.
Glucose 6-phosphate dehydrogenase deficiency and red cell membrane defects: additive or synergistic interaction in producing chronic haemolytic anaemia.
Glucose 6-phosphate dehydrogenase deficiency and sickle cell anemia: frequency and features of the association in an African community.
Glucose 6-phosphate dehydrogenase Palermo R257M: a novel variant associated with chronic non-spherocytic haemolytic anaemia.
Glucose 6-phosphate dehydrogenase, hexokinase activities and ATP levels as a function of cell density in thalassemia and iron deficiency anemia.
Glucose-6-phosphate dehydrogenase (G-6-PD) deficiency in Switzerland. Demonstration of a new variant (G-6-PD Aarau) with chronic nonsphaerocytic haemolytic anaemia.
Glucose-6-phosphate dehydrogenase (G-6-PD) Hamburg, a new variant with chronic nonspherocytic haemolytic anaemia.
Glucose-6-phosphate dehydrogenase deficiency among Yemeni children residing in malaria-endemic areas of Hodeidah governorate and evaluation of a rapid diagnostic test for its detection.
Glucose-6-phosphate dehydrogenase deficiency and reduced haemoglobin levels in African children with severe malaria.
Glucose-6-phosphate dehydrogenase deficiency and sickle cell disease in Brazil.
Glucose-6-phosphate dehydrogenase deficiency and sickle-cell anemia.
Glucose-6-phosphate dehydrogenase deficiency in a native Danish family. A new variant.
Glucose-6-Phosphate Dehydrogenase Deficiency in Brazilian Children With Sickle Cell Anemia is not Associated With Clinical Ischemic Stroke or High-Risk Transcranial Doppler.
Glucose-6-phosphate dehydrogenase deficiency in northern Mexico and description of a novel mutation.
Glucose-6-phosphate dehydrogenase deficiency in Sickle-cell anemia. A study in adults.
Glucose-6-phosphate dehydrogenase deficiency in triplets of African-American descent.
Glucose-6-phosphate dehydrogenase deficiency, chlorproguanil-dapsone with artesunate and post-treatment haemolysis in African children treated for uncomplicated malaria.
Glucose-6-phosphate dehydrogenase deficiency.
Glucose-6-phosphate dehydrogenase deficiency: an unusual cause of acute jaundice after paracetamol overdose.
Glucose-6-phosphate dehydrogenase deficiency: correlation between the genotype, biochemistry and phenotype.
Glucose-6-phosphate dehydrogenase deficiency: the added value of cytology.
Glucose-6-phosphate dehydrogenase Guadalajara--a case of chronic non-spherocytic haemolytic anaemia responding to splenectomy and the role of splenectomy in this disorder.
Glucose-6-phosphate dehydrogenase Jackson. A new variant associated with hemolytic anemia.
Glucose-6-phosphate dehydrogenase Johannesburg: a new variant with reduced activity in a patient with congenital non-spherocytic haemolytic anaemia.
Glucose-6-phosphate dehydrogenase status and severity of malarial anaemia in Nigerian children.
Glucose-6-phosphate dehydrogenase Velletri.
Glucose-6-phosphate dehydrogenase, reduced glutathione and heinz bodies in congenital haemolytic anaemia.
Glycosylated hemoglobin in Saudi sickle cell patients with glucose-6-phosphate dehydrogenase deficiency.
Growth-and Documentation-Deficits: Where To Start in Helping Families.
Haematological parameters and altered erythrocyte metabolism in anaemic dogs.
Haemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in a Scandinavian perspective.
Haemolysis during diabetic ketoacidosis treatment in two girls with incomplete glucose-6-phosphate dehydrogenase deficiency.
Haemolytic anaemia after ingestion of Neem (Azadirachta indica) tea.
Haemolytic anaemia after nitrofurantoin treatment in a pregnant woman with G6PD deficiency.
Haemolytic anaemia due to glucose-6-phosphate dehydrogenase (G6PD) deficiency: demonstration of two new biochemical variants, G6PD Hamm and G6PD Tarsus.
Haemolytic anaemia with massive haemoglobinuria due to glucose-6-phosphate dehydrogenase deficiency in Ceylon.
Haptoglobin therapy for acute favism: a Japanese boy with glucose-6-phosphate dehydrogenase Guadalajara.
Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania.
HbE-beta-thalassemia associated with G6PD deficiency.
Hematological findings and severity of G6PD deficiency in Vataliya Prajapati subjects.
Hematological predictors of increased severe anemia in Kenyan children coinfected with Plasmodium falciparum and HIV-1.
Hematological profile in neonatal jaundice.
Hemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in hospital births in Bahrain.
Hemolytic crisis in a G6PD-deficient infant after ingestion of pumpkin.
Henna (Lawsonia inermis Linn.) induced haemolytic anaemia in siblings.
Hereditary anaemias and iron deficiency in a tribal population (the Baiga) of central India.
Hereditary anaemias in Portugal: epidemiology, public health significance, and control.
High prevalence of anaemia among African migrants in Germany persists after exclusion of iron deficiency and erythrocyte polymorphisms.
High prevalence of G6PD deficiency in Vataliya Prajapati community in western India.
High prevalence of microcytic anaemia in Omani children: a prospective study.
High risk of severe anaemia after chlorproguanil-dapsone+artesunate antimalarial treatment in patients with G6PD (A-) deficiency.
Hyperbilirubinemia following hepatitis A in a patient with G6pD deficiency.
Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA.
Identification of Inflammatory Biomarkers for Pediatric Malarial Anemia Severity using Novel Statistical Methods.
Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective study.
In Tanzania, hemolysis after a single dose of primaquine coadministered with an artemisinin is not restricted to glucose-6-phosphate dehydrogenase-deficient (G6PD A-) individuals.
Increased incidence of sepsis and altered monocyte functions in severely injured type A- glucose-6-phosphate dehydrogenase-deficient African American trauma patients.
Inherited, non-spherocytic haemolysis due to deficiency of glucose-6-phosphate dehydrogenase.
Inhibition of hexose monophosphate shunt in young erythrocytes by pyrimidine nucleotides in hereditary pyrimidine 5' nucleotidase deficiency.
Interaction between glucose-6-phosphate dehydrogenase deficiency and sickle cell gene in Saudi Arabia.
Interesting case of G6PD deficiency anemia with severe hemolysis.
Intraerythrocytic distribution of glucose-6-phosphate dehydrogenase (G-6-PD) in haemolytic anaemias.
Jordan: communities and community genetics.
Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia.
Marked decrease in specific activity contributes to disease phenotype in two human glucose 6-phosphate dehydrogenase mutants, G6PD(Union) and G6PD(Andalus).
Mass primaquine treatment to eliminate vivax malaria: lessons from the past.
Massive acute haemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient preterm triplets.
Massive acute haemolysis in neonates with glucose-6-phosphate dehydrogenase deficiency.
Mean reticulocyte volume: a specific parameter to screen for hereditary spherocytosis.
Mechanisms and pathophysiological significance of eryptosis, the suicidal erythrocyte death.
Mechanisms and Significance of Eryptosis, the Suicidal Death of Erythrocytes.
Mechanisms of smooth muscle antibody production: a clinical study in children with infections, haemolytic syndromes, and idiopathic thrombocytopenic purpura.
Medications and glucose-6-phosphate dehydrogenase deficiency: an evidence-based review.
Membrane characteristics and metabolic properties of glucose-6-phosphate dehydrogenase deficient red cells.
Metabolic findings in the erythrocytes of cardiopathic and anaemic dogs.
Modelling primaquine-induced haemolysis in G6PD deficiency.
Molecular basis and enzymatic properties of glucose 6-phosphate dehydrogenase volendam, leading to chronic nonspherocytic anemia, granulocyte dysfunction, and increased susceptibility to infections.
Molecular basis of chronic non-spherocytic haemolytic anaemia: a new G6PD variant (393 Arg----His) with abnormal KmG6P and marked in vivo instability.
Molecular characterisation of an Italian G6PD variant responsible for chronic non-spherocytic haemolytic anaemia.
Molecular variants of G6PD deficiency among certain tribal communities of Orissa, India.
National G6PD neonatal screening program in Gaza Strip of Palestine: rationale, challenges and recommendations.
Neutrophil dysfunction, chronic granulomatous disease, and non-spherocytic haemolytic anaemia caused by complete deficiency of glucose-6-phosphate dehydrogenase.
New glucose-6-phosphate dehydrogenase mutations associated with chronic anemia.
Nonimmune hydrops fetalis caused by G6PD deficiency hemolytic crisis and congenital dyserythropoietic anemia.
Nutritional Status of Young Children with Inherited Blood Disorders in Western Kenya.
Origins and implications of neglect of G6PD deficiency and primaquine toxicity in Plasmodium vivax malaria.
Oxidative Stress and Suicidal Erythrocyte Death.
Oxidative stress as a potential causal factor for autoimmune hemolytic anemia and systemic lupus erythematosus.
Pathogenesis, laboratory diagnosis, and clinical implications of erythrocyte enzyme deficiencies in dogs, cats, and horses.
PGI*3(Israel), a new, unstable allele in the phosphoglucose isomerase system.
Pharmacoanthropology: outline, problems, and the nature of case histories.
Plan and process for hematology laboratory standard in Thailand.
Population screening for glucose-6-phosphate dehydrogenase deficiencies in Isabel Province, Solomon Islands, using a modified enzyme assay on filter paper dried bloodspots.
Predictors of Acute Bilirubin Encephalopathy Among Nigerian Term Babies with Moderate-to-severe Hyperbilirubinaemia.
Prevalence and molecular characterization of G6PD deficiency in two Plasmodium vivax endemic areas in Venezuela: predominance of the African A-(202A/376G) variant.
Prevalence of anemia, iron deficiency, thalassemia and glucose-6-phosphate dehydrogenase deficiency among hill-tribe school children in Omkoi District, Chiang Mai Province, Thailand.
Prevalence of G6PD deficiency in selected populations from two previously high malaria endemic areas of Sri Lanka.
Primaquine treatment for Plasmodium vivax--an essential tool for malaria control and elimination in Papua New Guinea.
Pyruvate kinase deficiency in mice protects against malaria.
Rasburicase: a potent uricolytic agent.
Reappraisal of known malaria resistance loci in a large multicenter study.
Red blood cell-derived microparticles: An overview.
Red cell glucose-6-phosphate dehydrogenase status and pyruvate kinase activity in a Nigerian population.
Red cell membrane protein in thalassemia and glucose-6-phosphate dehydrogenase deficiency anemia.
Reduced prevalence of Plasmodium falciparum infection and of concomitant anaemia in pregnant women with heterozygous G6PD deficiency.
Reticulocyte analysis in iron deficiency anemia and hemolytic anemia.
Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia.
Screening for glucose-6-phosphate dehydrogenase deficiency can prevent severe neonatal jaundice.
Serum ferritin in patients with various haemolytic disorders.
Severe haemolysis associated with hepatitis A and normal glucose-6-phosphate dehydrogenase status.
Some observations on glutathione instability and glucose-6-phosphate dehydrogenase deficiency in infants and children having anaemia and jaundice.
SPECIFIC INHIBITION OF HEPATIC GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN IRON DEFICIENCY ANEMIA IN ALBINO RATS.
Sporadic G6PD deficiency with haemolytic anaemia in two children of West European ancestry.
Studies on dapsone induced haemolytic anaemia. I. Methaemoglobin production and G-6-PD activity in correlation with dapsone dosage.
Studies on the mechanisms of oxidation in the erythrocyte by metabolites of primaquine.
Study of red cell membrane lipids in glucose-6-phosphate dehydrogenase deficiency anemia.
Study of some erythrocytic enzymes in extracorpuscular hemolytic anemias.
Suicide for survival--death of infected erythrocytes as a host mechanism to survive malaria.
Targeted disruption of the housekeeping gene encoding glucose 6-phosphate dehydrogenase (G6PD): G6PD is dispensable for pentose synthesis but essential for defense against oxidative stress.
Thalassaemia is a tropical disease.
The distribution of the parasitic fauna dictates the distribution of the haemochromatosis genes.
The effects of glucose-6-phosphate dehydrogenase deficiency on the haematological parameters and clinical manifestations in patients with sickle cell anaemia.
The First Case of a Class I Glucose-6-phosphate Dehydrogenase Deficiency, G6PD Santiago de Cuba (1339 GA), in a Chinese Population as Found in a Survey for G6PD Deficiency in Northeastern and Central China.
The influence of oxidative bursts of phagocytes on red blood cell oxidation in anemic cattle infected with Theileria sergenti.
The investigation of plasma glucose-6-phosphate dehydrogenase, 6-phoshogluconate dehydrogenase, glutathione reductase in premenauposal patients with iron deficiency anemia.
The potential use of xylitol in glucose-6-phosphate dehydrogenase deficiency anemia.
The relationship between red cell aging and enzyme activities in experimental animals.
The role of erythrocyte enzyme glucose-6-phosphate dehydrogenase (G6PD) deficiency in the pathogenesis of anemia in patients on hemodialysis.
The role of oxidative stress in hemolytic anemia.
Therapeutic potential of manipulating suicidal erythrocyte death.
Tolerability and safety of weekly primaquine against relapse of Plasmodium vivax in Cambodians with glucose-6-phosphate dehydrogenase deficiency.
Tolerability of tiaprofenic acid in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency.
Triggers, inhibitors, mechanisms, and significance of eryptosis: the suicidal erythrocyte death.
Two new mutations of the glucose-6-phosphate dehydrogenase (G6PD) gene associated with haemolytic anaemia: clinical, biochemical and molecular relationships.
Two novel glucose-6-phosphate dehydrogenase variants found in newborn mass-screening for galactosaemia.
Typhoid fever and haemolytic anaemia in a black patient with glucose-6-phosphate dehydrogenase deficiency. A case report.
Use and safety of elevated dosages of vitamin E in adults.
Viral hepatitis with haemolytic anaemia due to glucose-6-phosphate dehydrogenase deficiency.
[A case of falciparum malaria successfully treated with intravenous artesunate]
[A search for glucose-6-phosphate dehydrogenase deficiency, among Toros Seljouck Turks, in both normal and pathological conditions. The explanation of hemolytic anemias seen, in snake bite and poisonous insect bites cases. Three cases of favism and hemolytic syndrome]
[Activities of erythrocyte glucose-6-phosphate dehydrogenase and catalase during pregnancies associated with anemia]
[Activity of glucose-6-phosphate dehydrogenase and glutathione reductase in early anemia of premature infants]
[Activity of the enzymes phosphoglyceraldehyde dehydrogenase, lactate dehydrogenase and glucose-6-phosphate dehydrogenase in the erythrocytes in deficiency anemia]
[Anemia and jaundice caused by hereditary glucose-6-phosphate dehydrogenase deficit.]
[Biology of glucose-6-phosphate dehydrogenase deficiency]
[Case of nonspherocytic anemia complicated by glucose-6-phosphate dehydrogenase deficiency of the erythrocytes]
[Chronic haemolytic anemia due to a defect of glucose-6-phosphate dehydrogenase (G6PD) in a Lorraine family. Demonstration of a new type of the enzyme: Gd(-) Nancy]
[CHRONIC HEMOLYTIC NON SPHEROCYTIC ANEMIA SECONDARY TO DEFICIENCY OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE. DESCRIPTION OF A CASE.]
[Clinical, erythrokinetic and metabolic aspects of congenital hemolytic non-spherocytic anemia due to erythrocytic glucose-6-phosphate dehydrogenase deficiency]
[Common anemias in neonatology]
[Concerning the level of erythrocytic glucose-6-phosphate dehydrogenase in patients with microdrepanocytic anemia]
[Congenital hemolytic anemias with glutatione metabolism disorders (excluding glucose-6-phosphate dehydrogenase deficiency)]
[Congenital hemolytic non-spherocytic anemia caused by glucose-6-phosphate dehydrogenase deficiency (case contribution)]
[Congenital nonspherocytic hemolytic anemias caused by glucose-6-phosphate dehydrogenase deficiency of the erythrocytes in a Japanese family]
[Consciousness disorders and severe haemolytic anaemia in a patient coming from overseas]
[Contribution to the study of hemolysis in Francoi's anemia. Intermediary deficiency of G-6-PD in a male patient]
[Deficiency of glucose-6-phosphate dehydrogenase in a family]
[Density-specific distribution of erythrocytes in different types of anemia]
[Diagnosis of hemolytic anemia with unstable hemoglobin]
[Dissimilar glucose-6-phosphate dehydrogenase (G-6-PD) deficiency in the Afars and the Somalis of Djibouti]
[Erythrocyte defects and parasitemia density in patients with Plasmodium falciparum malaria in Buenaventura, Colombia]
[Etiology of hemolytic anemia]
[Evaluation of the incidence of glucose-6-phosphate dehydrogenase deficiency in children with sickle cell anemia in Brazzaville (Congo)]
[Federal District glucose-6-phosphate dehydrogenase Gd(-). A new variant associated with moderate enzyme deficiency and occasional hemolytic anemia]
[Frequency of G6PD deficiency in a group of preschool-aged children in a centrally located area of Cambodia]
[Genetic, biochemical, pathogenetic and laboratory aspects of thalassemia. Heterozygote thalassemia in Alghero]
[Glucose-6-phosphate dehydrogenase (G6PD) deficiency--a cause of anaemia in pregnant women]
[GLUCOSE-6-PHOSPHATE DEHYDROGENASE AND SURVIVAL OF ERYTHROCYTES IN VARIOUS FORMS OF ANEMIA.]
[Glucose-6-phosphate dehydrogenase deficiency in an 81-year-old]
[Glucose-6-phosphate dehydrogenase type Schwaben. A new enzyme variant with spontaneous hemolytic anemia]
[Haemolytic anemia associated with G-6-PD deficiency]
[Hematologic characteristics in Black Africa]
[Hemolytic anemia after voluntary ingestion of henna (Lawsonia inermis) decoction by a young girl with G6PD deficiency].
[Hemolytic anemia associated with minor salmonellosis in an HIV positive, G6PD deficient Congolese woman]
[Hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency. Condition with diagnostic pitfalls].
[HEMOLYTIC ANEMIAS DUE TO GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.]
[Hemolytic congenital nonspherocytic anemia secondary to an erythrocyte glucose-6-phosphate dehydrogenase deficiency. Description of 2 new variants: Gd (-) Saint-Louis (Paris) and Gd (-) Hayem]
[Hydrops fetalis and G-6-PD deficiency]
[Importance of the determination of glucose-6-phosphate dehydrogenase in the diagnosis of congenital hemolytic anemias]
[Molecular analysis of glucose-6-dehydrogenase deficiency in Spain]
[Molecular-genetic studies of carrier stage of glucose-6-phosphate dehydrogenase deficiency]
[Non-spherocytic congenital hemolytic anemias due to G6PD deficiency. Clinical and hematologic aspects and mechanism of hyperhemolysis]
[On congenital hemolytic, nonspherocytic anemias with a deficiency of glucose-6-phosphate dehydrogenase in red blood cells.]
[ON THE SIGNIFICANCE OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE ACTIVITY IN ERYTHROCYTES FOR THE DIFFERENTIAL DIAGNOSIS OF ANEMIAS.]
[One hundred and twenty-three cases of sickle-cell trait (author's transl)]
[OPEN PROBLEMS IN THE FIELD OF ANEMIAS DUE TO DEFICIENCY OF GLUCOSE-6-PHOSPHATE DEHYDROGENASE.]
[Plasmodium vivax, a parasite coming out of the shadows].
[Recurrence problems with preventive primaquine treatment in patients with malaria]
[Review of abnormal genes. II. Hereditary enzyme defects in the erythrocytes: drug-induced hemolytic anemia indirectly caused by glucose-6-phosphate dehydrogenase deficiency]
[Screening for hemoglobinopathies and G-6-PD deficiency anemia in school children of a city in the Turin region]
[Sickle-cell anemia and glucose-6-phosphate dehydrogenase deficiency]
[The African variant of glucose-6-phosphate dehydrogenase deficiency as a factor favoring anemia: comparative study of 157 deficient adults and 300 non-deficient adults]
[The behavior of respiration and glucose-6-phosphate dehydrogenase of red blood cells of different ages during hemorrhagic anemia in rabbits.]
[The C1155G mutation of the red blood cell glucose-6-phosphate dehydrogenase gene in a subject with severe hereditary chronic nonspherocytic anaemia]
[The osmotic stability, glucose-6-phosphate dehydrogenase and glutathione reductase activity of the erythrocytes of leukemia and anemia patients]
[The role glucose-6-phosphate dehydrogenase in pathogenesis of anemia in leptospirosis]
Anemia, Aplastic
[Macrolides in the treatment of children with Mediterranean spotted fever]
Anemia, Diamond-Blackfan
Chronic parvovirus infection and G6PD deficiency masquerading as Diamond-Blackfan anemia.
Anemia, Dyserythropoietic, Congenital
Assessment of erythrocyte deformability with the laser-assisted optical rotational cell analyzer (LORCA).
Congenital dyserythropoietic anaemia type II associated with a new type of G6PD deficiency (G6PD Gabrovizza).
Congenital dyserythropoietic anemia type II associated with G6PD Seattle in a Sicilian child.
Nonimmune hydrops fetalis caused by G6PD deficiency hemolytic crisis and congenital dyserythropoietic anemia.
The role of oxidative stress in hemolytic anemia.
Anemia, Hemolytic
'Gd(-) Hôtel Dieu': a new G-6PD variant with chronic hemolysis in a Negro patient from Senegal.
6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiency.
A case of congenital dyserythropoietic anemia in a male Chinese.
A comprehensive analysis of membrane and morphology of erythrocytes from patients with glucose-6-phosphate dehydrogenase deficiency.
A glucose 6-phosphate dehydrogenase Gd (-) Castilla variant characterized by mild deficiency associated with drug-induced hemolytic anemia.
A glucose-6-phosphate dehydrogenase variant, Gd(-) Santamaria found in Costa Rica.
A hemolysis trigger in glucose-6-phosphate dehydrogenase enzyme deficiency. Vicia sativa (Vetch).
A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger.
A new exon 9 glucose-6-phosphate dehydrogenase mutation (G6PD "Rehovot") in a Jewish Ethiopian family with variable phenotypes.
A new glucose-6-phosphate dehydrogenase variant (G6PD Iwate) associated with congenital non-spherocytic hemolytic anemia.
A new glucose-6-phosphate dehydrogenase variant (G6PD Nagano) associated with congenital hemolytic anemia.
A new glucose-6-phosphate dehydrogenase variant (G6PD Tsukui) associated with congenital hemolytic anemia.
A new glucose-6-phosphate dehydrogenase variant G6PD Sugao (826C-->T) exhibiting chronic hemolytic anemia with episodes of hemolytic crisis immediately after birth.
A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova). Biochemical characterization and mosaicism expression in the heterozygote.
A new glucose-6-phosphate dehydrogenase variant, Gd(-) Tepic, characterized by moderate enzyme deficiency and mild episodes of hemolytic anemia.
A novel cytofluorometric assay for the detection and quantification of glucose-6-phosphate dehydrogenase deficiency.
A Novel de novo Mutation in the G6PD Gene in a Korean Boy with Glucose-6-phosphate Dehydrogenase Deficiency: Case Report.
A novel G6PD mutation leading to chronic hemolytic anemia.
A novel missense mutation in glucose-6-phosphate dehydrogenase gene causing chronic nonspherocytic hemolytic anemia in an Indian family.
A novel mutation in the glucose-6-phosphate dehydrogenase gene in a subject with chronic nonspherocytic hemolytic anemia--characterization of enzyme using yeast expression system and molecular modeling.
A Review of Pharmacogenetics of Antimalarials and Associated Clinical Implications.
A simple, rapid fluorometric assay for the determination of glucose 6-phosphate dehydrogenase activity in dried blood spot specimens.
A unique electrophoretic slow-moving glucose 6-phosphate dehydrogenase variant (G6PD Asahikawa) with a markedly acidic pH optimum.
A variant glucose-6-phosphate dehydrogenase Gd(-) Chiapas associated with moderate enzyme deficiency and occasional hemolytic anemia.
Activated oxygen generation by a primaquine metabolite: inhibition by antioxidants derived from Chinese herbal remedies.
Acute hemolysis in a patient with a newly diagnosed glioblastoma.
Acute hemolytic anaemia due to phenazopyridine hydrochloride in G-6-PD deficient subject.
Acute hemolytic anemia complicating viral hepatitis in patients with glucose-6-phosphate dehydrogenase deficiency.
Acute Hemolytic Anemia in Glucose-6-Phosphate Dehydrogenase Deficiency Complicated by Ginkgo biloba.
Acute hemolytic anemia induced by a pyrazolonic drug in a child with glucose-6-phosphate dehydrogenase deficiency.
Acute hemolytic anemia precipitated by myocardial infarction and pericardial tamponade in G6PD deficiency.
Age-related red cell enzymes in children with transient erythroblastopenia of childhood and with hemolytic anemia.
An In vivo Drug Screening Model Using Glucose-6-Phosphate Dehydrogenase Deficient Mice to Predict the Hemolytic Toxicity of 8-Aminoquinolines.
Anemia in Patients with Coinherited Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency.
Apparent hemolysis in an AIDS patient receiving trimethoprim/sulfamethoxazole: case report and literature review.
Aseptic meningitis, hemolytic anemia, hepatitis, and orthostatic hypotension in a patient treated with trimethoprim-sulfamethoxazole.
Assessment of Point-of-Care Diagnostics for G6PD Deficiency in Malaria Endemic Rural Eastern Indonesia.
Autoimmune hemolytic anemia.
Automated determination of glucose-6-phosphate dehydrogenase (G6PD) on a SPOTCHECK Microflow analyzer.
Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome.
Brucellosis triggering hemolytic anemia in glucose-6-phosphate dehydrogenase deficiency.
Changes in red blood cell membrane structure in G6PD deficiency: An atomic force microscopy study.
Characteristics of a new abnormal variant of G-6-PD in human red cells.
Chronic hemolytic anemia associated with glucose 6-phosphate dehydrogenase (Guadalajara)1 159 C --> T (387 Arg --> Cys) deficiency associated with Gilbert syndrome in a Turkish patient.
Chronic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency or glutathione synthetase deficiency: the role of vitamin E in its treatment.
Chronic hemolytic anemia is associated with a new glucose-6-phosphate dehydrogenase in-frame deletion in an older woman.
Chronic nonspherocytic hemolytic anemia (CNSHA) and glucose 6 phosphate dehydrogenase (G6PD) deficiency in a patient with familial amyloidotic polyneuropathy (FAP). Molecular study of a new variant (G6PD Clinic) with markedly acidic pH optimum.
Chronic nonspherocytic hemolytic anemia and G6PD deficiency.
Chronic nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency: report of two families with novel mutations causing G6PD Bangkok and G6PD Bangkok Noi.
Chronic severe hemolytic anemia due to G-6-PD Charleston: a new deficient variant.
Cimetropium bromide, a new antispasmodic agent, has no hemolytic effects in humans.
Clinical consequences of enzyme deficiencies in the erythrocyte.
Clinical Pharmacogenetics Implementation Consortium (CPIC) guidelines for rasburicase therapy in the context of G6PD deficiency genotype.
Clinical spectrum and severity of hemolytic anemia in glucose 6-phosphate dehydrogenase-deficient children receiving dapsone.
Clinical spectrum of hemolytic anemia associated with glucose-6-phosphate dehydrogenase deficiency.
Comparison of serum copper, magnesium, zinc and calcium levels between G6PD deficient and normal Chinese adults.
Complications related to dapsone use for Pneumocystis jirovecii pneumonia prophylaxis in solid organ transplant recipients.
Congenital nonspherocytic hemolytic anemia associated with erythrocyte glucose-6-phosphate dehydrogenase deficiency in a Negro family.
Congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency in a Japanese child. Clinical and metabolic studies.
Congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase East Harlem: a new deficient variant.
Cooperating G6PD mutations associated with severe neonatal hyperbilirubinemia and cholestasis.
Copper sulfate-induced hemolytic anemia. Inhibition of glucose-6-phosphate dehydrogenase and other possible etiologic mechanisms.
Cytomegalovirus infection and hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency.
Dapsone induced hemolysis in a patient with ANCA associated glomerulonephritis and normal G6PD level and implications for clinical practice: case report and review of the literature.
Dapsone-induced hemolytic anemia: role of glucose-6-phosphate dehydrogenase in the hemolytic response of rat erythrocytes to N-hydroxydapsone.
Death from drug-induced hemolytic anemia.
Definition of the mutations of G6PD Wayne, G6PD Viangchan, G6PD Jammu, and G6PD 'LeJeune'.
Dental Considerations in Children with Glucose-6-phosphate Dehydrogenase Deficiency (Favism): A Review of the Literature and Case Report.
Direct detection for G6PD Bangkok and G6PD Bangkok Noi mutations in the families with chronic nonspherocytic hemolytic anemia (CNSHA).
Discussion on Pharmacogenetic Interaction in G6PD Deficiency and Methods to Identify Potential Hemolytic Drugs.
Disorders in the metabolism of erythrocytes in a case of congenital nonspherocytic hemolytic anemia with glucose-6-phosphate dehydrogenase deficiency.
Distinct phenotypic expression of two de novo missense mutations affecting the dimer interface of glucose-6-phosphate dehydrogenase.
Diurnal fluctuation of leukocyte G6PD activity. A possible explanation for the normal neutrophil bactericidal activity and the low incidence of pyogenic infections in patients with severe G6PD deficiency in Israel.
Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.
DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants.
Effect of primaquine standard dose (15 mg/day for 14 days) in the treatment of vivax malaria patients in Thailand.
Epigenetic therapy reprograms hereditary disease.
Equine glucose-6-phosphate dehydrogenase deficiency.
Erythrocyte membrane protein changes in glucose-6-phosphate dehydrogenase mutants with chronic hemolytic disease: an example of postsynthetic modification of membrane proteins.
Evaluation of DNA damage in leukocytes of G6PD-deficient Iranian newborns (Mediterranean variant) using comet assay.
Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community.
Four new electrophoretically slow-moving glucose 6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: Gd(-) Kurume, Gd(-) Fukushima, Gd(-) Yamaguchi and Gd(-) Wakayama.
Frostbite: A Novel Presentation of Glucose-6-Phosphate Dehydrogenase Deficiency?
Functional and Biochemical Characterization of Three Recombinant Human Glucose-6-Phosphate Dehydrogenase Mutants: Zacatecas, Vanua-Lava and Viangchan.
G-6-PD Guadalajara. A new mutant associated with chronic nonspherocytic hemolytic anemia.
G-6-PD hemolytic anemia complicating diabetic ketoacidosis.
G-6-PD Long Prairie: a new glucose-6-phosphate dehydrogenase mutant exhibiting normal sensitivity to inhibition by NADPH and accompanied by nonspherocytic hemolytic anemia.
G-6-PD Manchester: a new variant associated with chronic nonspherocytic hemolytic anemia.
G-6-PD Poznań, variant with severe enzyme deficiency.
G-6-PD Walter Reed: possible insight into "structural" NADP in G-6-PD.
G6PD Deficiency at Sumba in Eastern Indonesia Is Prevalent, Diverse and Severe: Implications for Primaquine Therapy against Relapsing Vivax Malaria.
G6PD deficiency in Vataliya Prajapati community settled in Surat.
G6PD deficiency with hemolytic anemia due to a rare gene deletion--a report of the first case in Malaysia.
G6PD Heian, a glucose-6-phosphate dehydrogenase variant associated with hemolytic anemia found in Japan.
G6PD Huntsville: a new glucose-6-phosphate dehydrogenase associated with chronic hemolytic anemia.
G6Pd Kanazawa: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
G6PD San Francisco: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
G6PD Sendagi: a new glucose-6-phosphate dehydrogenase variant associated with congenital hemolytic anemia.
G6PD Varadero. A new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
G6PD-deficiency: a potential high-risk group to copper and chlorite ingestion.
G6PD-Puerto Limón: a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
Gas Chromatography/Mass Spectrometry-Based Metabolomic Profiling Reveals Alterations in Mouse Plasma and Liver in Response to Fava Beans.
Gd(-) Carapicuiba, a rare glucose-6-phosphate dehydrogenase variant associated with moderate enzyme deficiency and chronic hemolysis.
Gd(-) Rennes, a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in France.
Genetic disorders of human red blood cells.
Glucose 6 phosphate dehydrogenase deficiency unmasked by diabetic ketoacidosis: an underrated phenomenon.
Glucose 6-phosphate dehydrogenase deficiency enhances germ cell apoptosis and causes defective embryogenesis in Caenorhabditis elegans.
Glucose 6-phosphate dehydrogenase variants in Japan.
Glucose 6-phosphate dehydrogenase variants: a unique variant (G6PD Kobe) showed an extremely increased affinity for galactose 6-phosphate and a new variant (G6PD Sapporo) resembling G6PD Pea Ridge.
Glucose-6-phosphate dehydrogenase (G6PD) Iserlohn and G6PD Regensburg: two new severe enzyme defects in German families.
Glucose-6-phosphate dehydrogenase (G6PD)-deficient epithelial cells are less tolerant to infection by Staphylococcus aureus.
Glucose-6-phosphate dehydrogenase activity of erythrocytes in hemolytic anemia.
Glucose-6-Phosphate Dehydrogenase and Hemolytic Anemia.
Glucose-6-phosphate dehydrogenase and red cell pyruvate kinase deficiency in neonatal jaundice cases in egypt.
Glucose-6-phosphate dehydrogenase aveiro: a de novo mutation associated with chronic nonspherocytic hemolytic anemia.
Glucose-6-phosphate dehydrogenase Beaumont: a new variant with severe enzyme deficiency and chronic nonspherocytic hemolytic anemia.
Glucose-6-phosphate dehydrogenase deficiency A- variant in febrile patients in Haiti.
Glucose-6-phosphate dehydrogenase deficiency associated stuttering priapism: report of a case.
Glucose-6-phosphate dehydrogenase deficiency in hemolytic anemia.
Glucose-6-phosphate dehydrogenase deficiency in two returning Operation Iraqi Freedom soldiers who developed hemolytic anemia while receiving primaquine prophylaxis for malaria.
Glucose-6-phosphate dehydrogenase Durham: a de novo mutation associated with chronic hemolytic anemia.
Glucose-6-phosphate dehydrogenase dye test on patients and their family members of acute hemolytic anemia.
Glucose-6-phosphate dehydrogenase Jackson. A new variant associated with hemolytic anemia.
Glucose-6-phosphate dehydrogenase mutations and haplotypes in Mexican Mestizos.
Glucose-6-phosphate dehydrogenase variants: reexamination of G6PD Chicago and Cornell and a new variant (G6PD Pea Ridge) resembling G6PD Chicago.
Glucose-6-phosphate dehydrogenase--from oxidative stress to cellular functions and degenerative diseases.
Glucose-6-Phosphate Dehydrogenase: Update and Analysis of New Mutations around the World.
Gold nanostructures for the multiplex detection of glucose-6-phosphate dehydrogenase gene mutations.
Groups at potentially high risk from chlorine dioxide treated water.
HAART has no major impact on hematological and plasma bilirubin changes in HIV-infected patients with congenital G-6-PD deficiency.
Heinz-body anemia: "bite cell" variant--a light and electron microscopic study.
Hemolysis and Mediterranean G6PD mutation (c.563 C>T) and c.1311 C>T polymorphism among Palestinians at Gaza Strip.
Hemolysis and methemoglobinemia secondary to rasburicase administration.
Hemolytic anemia after acetaminophen overdose in patient with glucose-6-phosphate dehydrogenase deficiency.
Hemolytic anemia and erythrocyte glucose-6-phosphate dehydrogenase deficiency.
Hemolytic anemia and G-6-PD deficiency.
Hemolytic anemia and G6PD deficiency.
Hemolytic anemia caused by G-6-PD Carswell, a new variant.
Hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency.
Hemolytic anemia complicating viral hepatitis and G-6-PD deficiency.
Hemolytic anemia due to G6PD deficiency and urate oxidase in a kidney-transplant patient.
Hemolytic anemia following succimer administration in a glucose-6-phosphate dehydrogenase deficient patient.
Hemolytic anemia in hereditary pyrimidine 5'-nucleotidase deficiency: nucleotide inhibition of G6PD and the pentose phosphate shunt.
Hemolytic anemia in two patients with glioblastoma multiforme: A possible interaction between vorinostat and dapsone.
Hemolytic Anemia Induced by Pegloticase Infusion in a Patient With G6PD Deficiency.
Hemolytic crisis in a non-ketotic and euglycemic child with glucose-6-phosphate dehydrogenase deficiency and onset of type 1 diabetes mellitus.
Hereditary erythrocyte pyrimidine 5'-nucleotidase deficiency: A biochemical, genetic and clinical overview.
Heterozygous pyruvate kinase deficiency and severe hemolytic anemia in a pregnant woman with concomitant, glucose-6-phosphate dehydrogenase deficiency.
Human mutations in glucose 6-phosphate dehydrogenase reflect evolutionary history.
Humanized mouse model of glucose 6-phosphate dehydrogenase deficiency for in vivo assessment of hemolytic toxicity.
Hypohidrotic ectodermal dysplasia associated with glucose-6-phosphate dehydrogenase deficiency.
Identification of two novel deletion mutations in glucose-6-phosphate dehydrogenase gene causing hemolytic anemia.
Improved quantitative method for G6PD deficiency detection.
In vivo gene marking of rhesus macaque long-term repopulating hematopoietic cells using a VSV-G pseudotyped versus amphotropic oncoretroviral vector.
Increased basal oxidation of peroxiredoxin 2 and limited peroxiredoxin recycling in glucose-6-phosphate dehydrogenase-deficient erythrocytes from newborn infants.
Induction of hemolytic anemia by nonsteroidal antiinflammatory drugs.
Intestinal iron absorption under the influence of available storage iron and erythroblastic hyperplasia. Comparative studies in children with hereditary spherocytosis, nonspherocytic enzymopenic hemolytic anemia, acquired hemolytic anemia, vitamin B12 deficiency induced megaloblastic anemia, erythroblastic hypoplasia and aplastic anemia.
Intragenic interspecific complementation of glucose 6-phosphate dehydrogenase in human-hamster cell hybrids.
Irreversible AE1 tyrosine phosphorylation leads to membrane vesiculation in G6PD deficient red cells.
Is topical dapsone safe in glucose-6-phosphate dehydrogenase-deficient and sulfonamide-allergic patients?
Kernicterus by glucose-6-phosphate dehydrogenase deficiency: a case report and review of the literature.
Letters to the editor: Acute hemolytic anemia, G-6PD deficiency and viral hepatitis.
Markers of oxidative stress in umbilical cord blood from G6PD deficient African newborns.
Mean reticulocyte volume: a specific parameter to screen for hereditary spherocytosis.
Mechanisms of perturbation of erythrocyte calcium homeostasis in favism.
Membrane deformability of erythrocytes with glucose-6-phosphate dehydrogenase Hamburg.
Metabolism of human erythrocytes. Studies in health and disease.
Metabolism of the hexose monophosphate shunt in glucose-6-phosphate dehydrogenase deficiency and closely interrelated reactions.
Metformin-Induced Hemolytic Anemia in a Patient With Glucose-6-Phosphate Dehydrogenase Deficiency.
Mild hemolysis in a girl with G6PD Sumaré (class I variant) associated with G6PD A-.
Molecular abnormality of a Japanese glucose-6-phosphate dehydrogenase variant (G6PD Tokyo) associated with hereditary non-spherocytic hemolytic anemia.
Molecular basis of erythroenzymopathies associated with hereditary hemolytic anemia: tabulation of mutant enzymes.
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Kurdish population of Western Iran.
Molecular characterization of glucose-6-phosphate dehydrogenase variants from Brazil.
Molecular cloning and nucleotide sequence of cDNA for human glucose-6-phosphate dehydrogenase variant A(-).
Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Mexico: overall results of a 7-year project.
Multiple glucose 6-phosphate dehydrogenase-deficient variants correlate with malaria endemicity in the Vanuatu archipelago (southwestern Pacific).
Mutation analysis of glucose-6-phosphate dehydrogenase (G6PD) variants in Costa Rica.
N-acetyl cysteine, L-cysteine, and beta-mercaptoethanol augment selenium-glutathione peroxidase activity in glucose-6-phosphate dehydrogenase-deficient human erythrocytes.
Naphthalene-induced hemolytic anemia in a child with erythrocyte glucose-6-phosphate dehydrogenase deficiency.
National G6PD neonatal screening program in Gaza Strip of Palestine: rationale, challenges and recommendations.
Neonatal cholestasis and glucose-6-P-dehydrogenase deficiency.
Neonatal nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency in a Danish infant.
New glucose-6-phosphate dehydrogenase mutations associated with chronic anemia.
Nonimmune hydrops fetalis caused by G6PD deficiency hemolytic crisis and congenital dyserythropoietic anemia.
Noninferiority of glucose-6-phosphate dehydrogenase deficiency diagnosis by a point-of-care rapid test vs the laboratory fluorescent spot test demonstrated by copper inhibition in normal human red blood cells.
Oxidant damage to erythrocyte membrane in glucose-6-phosphate dehydrogenase deficiency: correlation with in vivo reduced glutathione concentration and membrane protein oxidation.
Oxidative stress, inflammation and carcinogenesis are controlled through the pentose phosphate pathway by transaldolase.
Ozone: a possible cause of hemolytic anemia in glucose-6-phosphate dehydrogenase deficient individuals.
Pancreatitis in acute hemolysis.
Perioperative management of the glucose-6-phosphate dehydrogenase deficient patient: a review of literature.
Perspectives on hydrogen peroxide and drug-induced hemolytic anemia in glucose-6-phosphate dehydrogenase deficiency.
Pharmacogenetic considerations in the treatment of gout.
Phase I study of urate oxidase in the reduction of acute graft-versus-host disease after myeloablative allogeneic stem cell transplantation.
Phenazopyridine-induced hemolytic anemia in a patient with G6PD deficiency.
Phenazopyridine-induced hemolytic anemia in G-6-PD deficiency.
Plasma and erythrocyte magnesium, manganese, zinc, and plasma calcium levels in G-6-PD-deficient and normal male children.
Point-of-care G6PD diagnostics for Plasmodium vivax malaria is a clinical and public health urgency.
Positively selected G6PD-Mahidol mutation reduces Plasmodium vivax density in Southeast Asians.
Possible potentiation of hemolytic anemia by tolbutamide. Report of a patient with erythrocyte glucose-6-phosphate dehydrogenase deficiency.
Prevalence of G6PD deficiency in a large cohort of HIV-infected patients.
Rasburicase Causing Severe Oxidative Hemolysis and Methemoglobinemia in a Patient with Previously Unrecognized Glucose-6-Phosphate Dehydrogenase Deficiency.
Rasburicase-induced methemoglobinemia: case report, literature review, and proposed treatment algorithm.
Rasburicase: an innovative new treatment for hyperuricemia associated with tumor lysis syndrome.
Reactivity of Blood Samples Spotted onto Filter Papers in the WST-8 Method for Screening of G6PD Deficiency.
Red cell enzymopathies as a model of inborn errors of metabolism.
Red cell glucose 6-phosphate dehydrogenase deficiency in the northern region of Turkey: is G6PD deficiency exclusively a male disease?
Relationship between erythrocyte glucose-6-phosphate dehydrogenase and the hemolytic anemia of infection.
Reticulocyte analysis in iron deficiency anemia and hemolytic anemia.
Rush hemolysis. A 'bite-cell' hemolytic anemia associated with volatile liquid nitrite use.
Scalable preparation and differential pharmacologic and toxicologic profiles of primaquine enantiomers.
Seven different glucose-6-phosphate dehydrogenase variants including a new variant distributed in Lam Dong Province in southern Vietnam.
Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism.
Severe glucose-6-phosphate dehydrogenase deficiency leads to susceptibility to infection and absent NETosis.
Severe hemolysis and renal failure in glucose-6-phosphate dehydrogenase deficient patients with hepatitis E.
Severe hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency and Epstein-Barr virus infection.
Severe hemolytic anemia in black children with glucose-6-phosphate dehydrogenase deficiency.
Severe jaundice in a patient with a previously undescribed glucose-6-phosphate dehydrogenase (G6PD) mutation and Gilbert syndrome.
Severe-glucose-6-phosphate dehydrogenase (G6PD) deficiency associated with chronic hemolytic anemia, granulocyte dysfunction, and increased susceptibility to infections: description of a new molecular variant (G6PD Barcelona).
Single dose primaquine in a preclinical model of G6PD deficiency: implications for use in malaria transmission blocking programs.
Somatic-cell selection is a major determinant of the blood-cell phenotype in heterozygotes for glucose-6-phosphate dehydrogenase mutations causing severe enzyme deficiency.
Structure and function of human erythrocyte pyruvate kinase. Molecular basis of nonspherocytic hemolytic anemia.
Targeting 6-phosphogluconate dehydrogenase in the oxidative PPP sensitizes leukemia cells to antimalarial agent dihydroartemisinin.
The ocular findings in glucose-6-phosphate dehydrogenase deficiency.
The value of methemoglobin reduction test as a screening test for neonatal glucose 6-phosphate dehydrogenase deficiency.
Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita.
Three new exon 10 glucose-6-phosphate dehydrogenase mutations.
Three new variants of glucose-6-phosphate dehydrogenase associated with chronic nonspherocytic hemolytic anemia: G-6-PD Lincoln Park, G-6-PD Arlington Heights, and G-6-PD West Town.
Transcriptional and epigenetic basis for restoration of G6PD enzymatic activity in human G6PD-deficient cells.
Two distinct Indian G6PD variants G6PD Jamnagar and G6PD Rohini caused by the same 949 G-->A mutation.
Two new glucose 6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: GD(-) Tokushima and GD(-) Tokyo.
Two new glucose-6 phosphate dehydrogenase (G6PD) variants associated with hemolytic anemia: G6PD Amman-1 and G6PD Amman-2.
Two new glucose-6-phosphate dehydrogenase mutations causing chronic hemolysis.
Two new variants of glucose-6-phosphate dehydrogenase associated with hereditary non-spherocytic hemolytic anemia: G6PD Wayne and G6PD Huron.
Two novel DNA variants associated with glucose-6-phosphate dehydrogenase deficiency found in Argentine pediatric patients.
Ultrasound-Guided Regional Anesthesia in a Glucose-6-Phosphate Dehydrogenase (G6PD)-Deficient Geriatric Trauma Patient.
Use of trimethoprim-sulfamethoxazole in a glucose-6-phosphate dehydrogenase-deficient population.
[A case of acute hemolytic anemia caused by deficiency of glucose-6-phosphate dehydrogenase (G-6-PD) in erythrocytes]
[A case of new glucose 6-phosphate dehydrogenase (G-6-PD) variant with chronic nonspherocytic hemolytic anemia: G-6-PD Maebashi (author's transl)]
[A family of new glucose 6-phosphate dehydrogenase (G 6 PD) variant associated with chronic nonspherocytic hemolytic anemia: G 6 PD Kurume (author's transl)]
[Acute drug-induced hemolytic anemia in persons with congenital glucose-6-phosphate dehydrogenase deficiency in the erythrocytes]
[Acute hemolysis and renal failure caused by hepatitis A infection with underlying glucose-6-phosphate dehydrogenase deficiency]
[Acute hemolytic anemia after the consumption of fava beans. Familial case study on glucose-6-phosphate dehydrogenase deficiency]
[Acute hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency]
[Acute hemolytic anemia consequent to administration of nitrofuran and novalgine, in 2 patients with erythrocytic glucose-6-phosphate dehydrogenase]
[Acute hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency (apropos of a case)]
[Acute hemolytic anemia in the course of spesis caused by Proteus morganii in a subject with erythrocytic glucose-6-phosphate dehydrogenase deficiency]
[Acute kidney failure and hemolytic anemia caused by erythrocytic G6PD dificit revealed by chloroquine administration]
[Anesthesia in patients with glucose-6-phosphate dehydrogenase deficiency: case report and perioperative anesthesiologic management]
[CHRONIC HEMOLYTIC ANEMIA WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.]
[Congenital non spherocytic hemolytic anemia due to G-6PD deficiency: physiological and biochemical study of an unusual variant. Relationship to Benevento G-6PD]
[Congenital non spherocytic hemolytic anemia due to lack of glucose-6-phosphate dehydrogenase (G-6-PD)]
[Congenital nonspherocytic hemolytic anemia resulting from G-6-PD inactivity]
[Congenital nonspherocytic hemolytic anemia with deficiency of glucose-6-phosphate dehydrogenase]
[Congenital nonspherocytic hemolytic anemia, cataract and glucose-6-phosphate dehydrogenase deficiency]
[Detection of a new anomalous variant of glucose-6-phosphate dehydrogenase in human erythrocytes]
[Early detection of color blindness from the viewpoint of occupational medicine with various references to internistic and human genetic symptom complexes]
[Electrophoretic and kinetic properties of the erythrocyte glucose-6-phosphate dehydrogenase of patients with hemolytic anemia related to a deficit in the activity of that enzyme]
[Enzyme-deficient hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency in a child of German descent]
[Erythrocytic enzymopathy in Uzbekistan].
[Familial study in a case of congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency]
[Federal District glucose-6-phosphate dehydrogenase Gd(-). A new variant associated with moderate enzyme deficiency and occasional hemolytic anemia]
[G-6-PD deficiency hemolytic anemia with abnormal BSP retention]
[Glucose-6-phosphate dehydrogenase deficiency and hemolytic anemia in a Danish boy]
[Glucose-6-phosphate dehydrogenase deficiency in children: a case report].
[Glucose-6-phosphate dehydrogenase deficiency in Japan].
[Glucose-6-phosphate dehydrogenase deficiency with recurrent infections: case report]
[Glucose-6-phosphate dehydrogenase deficiency, 1 of the forms of hemolytic anemia (review of the literature)]
[Glucose-6-phosphate dehydrogenase deficiency. Diagnosis during treatment of a mandibular fracture]
[Glucose-6-phosphate dehydrogenase type Schwaben. A new enzyme variant with spontaneous hemolytic anemia]
[Glucose-6-phosphate dehydrogenase]
[Hemolytic anemia after treatment with sulfamethoxypyridazine in a child with temporary G-6-PD deficiency and grave hypothyroidism]
[Hemolytic anemia associated with minor salmonellosis in an HIV positive, G6PD deficient Congolese woman]
[Hemolytic anemia based on congenital glucose-6-phosphate dehydrogenase deficiency in erythrocytes in the Taszhik SSR]
[Hemolytic anemia caused by association of a double anomaly: beta-thalassemia and deficiency of G6PD]
[HEMOLYTIC ANEMIA CAUSED BY GLUCOSE-6-PHOSPHATE DEHYDROGENASE (G-6-PD) DEFICIENCY.]
[Hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency during typhoid fever]
[Hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency. Aprpos of 20 cases from 1969 to 1974]
[HEMOLYTIC ANEMIA CAUSED BY GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.]
[Hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency]
[Hemolytic anemia due to congenital glucose-6-phosphate dehydrogenase deficiency.]
[Hemolytic anemia due to G6PD deficiency. Apropos of 3 cases]
[Hemolytic anemia due to the dysfunction of the protection against oxidative attack]
[Hemolytic anemia in children caused by deficiency of the enzyme glucose-6-phosphate dehydrogenase in erythrocytes]
[Hereditary non-spherocytic hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency. Formation of an enzyme protein with modified characteristics in the blood cells of a German family]
[II. Chronic hemolytic anemia caused by erythrocytic deficiency of glucose-6-phosphate dehydrogenase (G6PD)]
[Impaired glutathione metabolism in hemolytic anemia]
[Lethal acute hemolytic anemia in viral hepatitis, caused by glucose-6-phosphate dehydrogenase deficiency]
[Letter: Hemolytic anemia after antibilharzia treatment with niridazole in an Antillean with G6PD deficiency]
[Macrolides in the treatment of children with Mediterranean spotted fever]
[Neonatal hemolytic anemia due to G-6-PD deficiency in a family of the South-West. Detection of a double set of erythrocytes in heterozygotes]
[New anomalous variant of "Kremenchug" glucose-6-phosphate dehydrogenase linked to acute drug-induced hemolytic anemia]
[New variant of glucose-6-phosphate dehydrogenase (G-6-PD "Kaluga") from erythrocytes of a patient with chronic nonspherocytic hemolytic anemia]
[OBSERVATION OF A CASE OF ACUTE HEMOLYTIC ANEMIA RELATED TO A GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.]
[ON A CASE OF HEMOLYTIC ANEMIA DUE TO SULFAMETHOXYPYRIDAZINE IN A SUBJECT WITH ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.]
[On a rare form of glucose-6-phosphate dehydrogenase deficiency with congenital nonspherocytic hemolytic anemia]
[On case histories of acute hemolytic anemia in persons with glucose-6-phosphate dehydrogenase deficiency in the erythrocytes]
[Relations between chronic non-spherocytic hemolytic anemia and neonatal jaundice due to deficiency of glucose-6-phosphate dehydrogenase]
[Review of abnormal genes. II. Hereditary enzyme defects in the erythrocytes: drug-induced hemolytic anemia indirectly caused by glucose-6-phosphate dehydrogenase deficiency]
[Severe hemolytic anemia for the first time in a 42-year-old patient. Homozygote G-6-PD deficiency in a woman]
[Systematic detection at birth of drug-induced hemolytic anemia caused by a toxic mechanism linked to an erythrocyte deficiency of glucose-6-phosphate dehydrogenase]
[The glucose-6-phosphate dehydrogenase/6-phosphogluconate dehydrogenase ratio in the identification of glucose-6-phosphate dehydrogenase heterozygosity]
[Tonsillectomy in a 6-year-old child with hemolytic anemia caused by erythrocytic glucose-6-phosphate dehydrogenase deficiency]
Anemia, Hemolytic, Autoimmune
Aortic valve replacement for a patient with glucose-6-phosphate dehydrogenase deficiency and autoimmune hemolytic anemia.
Autoimmune hemolytic anemia in a patient with a deficiency of red cell glucose-6-phosphate dehydrogenase activity.
Etiology of hemolysis in two patients with hepatitis A infection: glucose-6-phosphate dehydrogenase deficiency or autoimmune hemolytic anemia.
Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.
Mean reticulocyte volume: a specific parameter to screen for hereditary spherocytosis.
Next-generation sequencing unravels homozygous mutation in glucose-6-phosphate isomerase, GPIc.1040G>A (p.Arg347His) causing hemolysis in an Indian infant.
[Considerations on a case of autoimmune hemolytic anemia in the course of malignant granuloma with complete defect of erythrocyte glucose-6-phosphate dehydrogenase]
[Density-specific distribution of erythrocytes in different types of anemia]
Anemia, Hemolytic, Congenital
A new glucose-6-phosphate dehydrogenase variant (G6PD Nagano) associated with congenital hemolytic anemia.
A new glucose-6-phosphate dehydrogenase variant (G6PD Tsukui) associated with congenital hemolytic anemia.
A new variant of glucose-6-phosphate dehydrogenase deficiency hereditary hemolytic anemia, G6PD Cornell: erythrocyte, leukocyte, and platelet studies.
Congenital erythrocyte enzyme deficiencies.
G6PD Sendagi: a new glucose-6-phosphate dehydrogenase variant associated with congenital hemolytic anemia.
GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND NONSPHEROCYTIC CONGENITAL HEMOLYTIC ANEMIA.
Hereditary hemolytic anemia associated with glucose-6-phosphate dehydrogenase deficiency (Mediterranean type).
HEREDITARY HEMOLYTIC ANEMIA DUE TO GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY; IMPROVEMENT FOLLOWING SPLENECTOMY AND FOLIC ACID THERAPY.
Hereditary hemolytic anemia due to glucose-6-phosphate dehydrogenase Torrance: a new variant.
Intestinal iron absorption under the influence of available storage iron and erythroblastic hyperplasia. Comparative studies in children with hereditary spherocytosis, nonspherocytic enzymopenic hemolytic anemia, acquired hemolytic anemia, vitamin B12 deficiency induced megaloblastic anemia, erythroblastic hypoplasia and aplastic anemia.
Intra-erythrocytary enzymes before and after splenectomy.
Molecular aspects of erythroenzymopathies associated with hereditary hemolytic anemia.
Nonspherocytic congenital hemolytic anemia due to a new G-6-pd variant: g-6-pd alhambra.
[CONGENITAL HEMOLYTIC ANEMIA CAUSED BY GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.]
[Congenital hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency]
[Congenital hemolytic anemias with glutatione metabolism disorders (excluding glucose-6-phosphate dehydrogenase deficiency)]
[Electrophoretic and kinetic properties of the erythrocyte glucose-6-phosphate dehydrogenase of patients with hemolytic anemia related to a deficit in the activity of that enzyme]
[Glucose-6-phosphate dehydrogenase deficiency and hereditary hemolytic anemia]
[Glucose-6-phosphate dehydrogenase deficiency hereditary hemolytic anemia (author's transl)]
[Glucose-6-phosphate dehydrogenase deficiency in Japan].
[Hereditary hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency discovered in a 6-year-old child]
[Importance of the determination of glucose-6-phosphate dehydrogenase in the diagnosis of congenital hemolytic anemias]
[Non-spherocytic congenital hemolytic anemias due to G6PD deficiency. Clinical and hematologic aspects and mechanism of hyperhemolysis]
[Pathophysiology and laboratory tests of hemolytic anemia: with special reference to erythroenzymopathies]
Anemia, Hemolytic, Congenital Nonspherocytic
'Gd(-) Hôtel Dieu': a new G-6PD variant with chronic hemolysis in a Negro patient from Senegal.
A new glucose-6-phosphate dehydrogenase variant with congenital nonspherocytic hemolytic anemia (G6PD Genova). Biochemical characterization and mosaicism expression in the heterozygote.
Congenital nonspherocytic hemolytic anemia associated with erythrocyte glucose-6-phosphate dehydrogenase deficiency in a Negro family.
Congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency in a Japanese child. Clinical and metabolic studies.
Congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase East Harlem: a new deficient variant.
Disorders in the metabolism of erythrocytes in a case of congenital nonspherocytic hemolytic anemia with glucose-6-phosphate dehydrogenase deficiency.
Four new electrophoretically slow-moving glucose 6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: Gd(-) Kurume, Gd(-) Fukushima, Gd(-) Yamaguchi and Gd(-) Wakayama.
G6Pd Kanazawa: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
G6PD San Francisco: a new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
G6PD Varadero. A new variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
G6PD-Puerto Limón: a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia.
Gd(-) Rennes, a new deficient variant of glucose-6-phosphate dehydrogenase associated with congenital nonspherocytic hemolytic anemia found in France.
Severe-glucose-6-phosphate dehydrogenase (G6PD) deficiency associated with chronic hemolytic anemia, granulocyte dysfunction, and increased susceptibility to infections: description of a new molecular variant (G6PD Barcelona).
Three new electrophoretically normal glucose-6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: G6PD Ogikubo, Yokohama, and Akita.
Two new glucose 6-phosphate dehydrogenase variants associated with congenital nonspherocytic hemolytic anemia found in Japan: GD(-) Tokushima and GD(-) Tokyo.
[Congenital nonspherocytic hemolytic anemia resulting from G-6-PD inactivity]
[Congenital nonspherocytic hemolytic anemia with deficiency of glucose-6-phosphate dehydrogenase]
[Congenital nonspherocytic hemolytic anemia, cataract and glucose-6-phosphate dehydrogenase deficiency]
[Familial study in a case of congenital nonspherocytic hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency]
[On a rare form of glucose-6-phosphate dehydrogenase deficiency with congenital nonspherocytic hemolytic anemia]
Anemia, Hypochromic
Activity of glucose-6-phosphate dehydrogenase among Indians living in a malarial region of Mato Grosso and its implication to the Indian-mixed populations in Brazil.
Anemia, Iron-Deficiency
A hematological survey of preschool children of the United Arab Emirates.
Glucose 6-phosphate dehydrogenase, hexokinase activities and ATP levels as a function of cell density in thalassemia and iron deficiency anemia.
Growth-and Documentation-Deficits: Where To Start in Helping Families.
Plan and process for hematology laboratory standard in Thailand.
Prevalence of thalassaemia, iron-deficiency anaemia and glucose-6-phosphate dehydrogenase deficiency among Arab migrating nomad children, southern Islamic Republic of Iran.
Reticulocyte analysis in iron deficiency anemia and hemolytic anemia.
SPECIFIC INHIBITION OF HEPATIC GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN IRON DEFICIENCY ANEMIA IN ALBINO RATS.
The distribution of the parasitic fauna dictates the distribution of the haemochromatosis genes.
The investigation of plasma glucose-6-phosphate dehydrogenase, 6-phoshogluconate dehydrogenase, glutathione reductase in premenauposal patients with iron deficiency anemia.
[Density-specific distribution of erythrocytes in different types of anemia]
Anemia, Megaloblastic
Death from drug-induced hemolytic anemia.
Anemia, Pernicious
[Glucose-6-phosphate dehydrogenase activity of erythrocytes in pernicious anemia.]
[The importance of determination of ferritin levels in erythrocytes]
Anemia, Refractory
[Glucose-6-phosphate dehydrogenase activity in hemolytic and refractory anemias]
Anemia, Sickle Cell
A clinician's view of the mass screening of the newborn for inherited diseases: current practice and future considerations.
Acquired hemoglobin variants and exposure to glucose-6-phosphate dehydrogenase deficient red blood cell units during exchange transfusion for sickle cell disease in a patient requiring antigen-matched blood.
Adenosine monophosphate deaminase 3 activation shortens erythrocyte half-life and provides malaria resistance in mice.
Anemia and the liver. Hepatobiliary manifestations of anemia.
Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia.
Association of homozygous sickle cell anemia and glucose-6-phosphate dehydrogenase deficiency.
Birth control necessary to limit family size in tribal couples with aberrant heterosis of G-6-PD deficiency and sickle cell disorders in India: an urgency of creating awareness and imparting genetic counseling.
Burden of Hemoglobinopathies (Thalassemia, Sickle Cell Disorders and G6PD Deficiency) in Iran, 1990-2010: findings from the Global Burden of Disease Study 2010.
Campaign to control genetic blood diseases in Bahrain.
Changing trends in malaria--a decade's experience at a referral hospital.
Clinical disorders of the red cell membrane skeleton.
Clinical significance of glucose-6-phosphate dehydrogenase deficiency in Nigerian patients with sickle cell disease.
Community Expansion and Gene Geography of Sickle Cell Trait and G6PD Deficiency, and Natural Selection against Malaria: Experience from Tribal Land of India.
Complete repair of tetralogy associated with sickle cell anemia and G-6-PD deficiency.
Component therapy.
Consanguinity and major genetic disorders in Saudi children: a community-based cross-sectional study.
Do tribal communities show an inverse relationship between sickle cell disorders and glucose-6-phosphate dehydrogenase deficiency in malaria endemic areas of Central-Eastern India?
Does G gamma/A gamma ratio and Hb F level influence the severity of sickle cell anaemia.
Effect of alpha thalassaemia, G-6-PD deficiency and Hb F on the nature of sickle cell anaemia in south-western Saudi Arabia.
Effect of G-6 PD deficiency on sickle cell disease in Saudi Arabia.
Effects of glucose-6-phosphate dehydrogenase deficiency upon sickle cell anaemia.
Effects of glucose-6-phosphate dehydrogenase deficiency upon sickle cell anemia.
Enhanced erythrocyte apoptosis in sickle cell anemia, thalassemia and glucose-6-phosphate dehydrogenase deficiency.
Erythrocyte ion channels in regulation of apoptosis.
Erythrocyte oxidative stress markers in children with sickle cell disease.
Erythrocyte reduced glutathione level in sickle cell anaemia and glucose-6-phosphate dehydrogenase deficient Saudi subjects.
Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.
First report of co-morbidity of pantothenate kinase-associated neurodegeneration and three types of chronic hemolytic anemias.
Fructosamine in HbS and G6PD-deficient Saudi Arabs in the Eastern Province of Saudi Arabia.
G6PD deficiency and absence of ?-thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia.
G6PD deficiency, absence of alpha-thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia.
Genetic Blood Disorders Survey in the Sultanate of Oman.
Genetic compounds--Hb S, thalassaemias and enzymopathies: spectrum of interactions.
Genetic diversity of hemoglobinopathies, G6PD deficiency, and ABO and Rhesus blood groups in two isolates of a primitive Kharia Tribe in Sundargarh District of Northwestern Orissa, India.
Glucose 6-phosphate dehydrogenase deficiency and sickle cell anemia: frequency and features of the association in an African community.
Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Congo.
Glucose-6-phosphate dehydrogenase deficiency and homozygous sickle cell disease in Jamaica.
Glucose-6-phosphate dehydrogenase deficiency and sickle cell disease in Brazil.
Glucose-6-phosphate dehydrogenase deficiency and sickle cell disease in Burkina Faso.
Glucose-6-Phosphate Dehydrogenase Deficiency in Brazilian Children With Sickle Cell Anemia is not Associated With Clinical Ischemic Stroke or High-Risk Transcranial Doppler.
Glucose-6-phosphate dehydrogenase deficiency in Nigerian children.
Glucose-6-phosphate dehydrogenase deficiency in sickle cell disease by DNA analysis.
Glycosylated hemoglobin in Saudi sickle cell patients with glucose-6-phosphate dehydrogenase deficiency.
Haptoglobin, alpha-thalassaemia and glucose-6-phosphate dehydrogenase polymorphisms and risk of abnormal transcranial Doppler among patients with sickle cell anaemia in Tanzania.
Hematological profile of twenty-nine tribal compound cases of hemoglobinopathies and G-6-PD deficiency in rural Orissa.
Hemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in hospital births in Bahrain.
Hereditary red blood cell disorders in middle eastern patients.
High prevalence of anaemia among African migrants in Germany persists after exclusion of iron deficiency and erythrocyte polymorphisms.
Impact of glucose-6-phosphate dehydrogenase deficiency on sickle cell anaemia expression in infancy and early childhood: a prospective study.
Impaired pentose phosphate shunt function in sickle cell disease: a potential mechanism for increased Heinz body formation and membrane lipid peroxidation.
Interaction between glucose-6-phosphate dehydrogenase deficiency and sickle cell gene in Saudi Arabia.
Jordan: communities and community genetics.
Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia.
Mandibular nerve neuropathy in sickle cell disease. Local factors.
Mechanisms and pathophysiological significance of eryptosis, the suicidal erythrocyte death.
Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian population.
Mutations of a country: a mutation review of single gene disorders in the United Arab Emirates (UAE).
Neonatal screening for sickle cell disease, glucose-6-phosphate dehydrogenase deficiency and a-thalassemia in Qatif and Al Hasa.
Oxidative Stress and Suicidal Erythrocyte Death.
Pharmacoanthropology: outline, problems, and the nature of case histories.
Priapism in hematological and coagulative disorders: an update.
Pyruvate kinase deficiency in mice protects against malaria.
Rapid screening for glucose-6-phosphate dehydrogenase deficiency and haemoglobin polymorphisms in Africa by a simple high-throughput SSOP-ELISA method.
Red blood cell disorders in Rwandese neonates: screening for sickle cell disease and glucose-6-phosphate dehydrogenase deficiency.
Red blood cell indices and prevalence of hemoglobinopathies and glucose 6 phosphate dehydrogenase deficiencies in male Tanzanian residents of Dar es Salaam.
Red blood cell-derived microparticles: An overview.
Red cell genetic disorders and plasma lipids.
Regional experience with newborn screening for sickle cell disease, other hemoglobinopathies and G6PD deficiency.
Regulation of membrane-cytoskeletal interactions by tyrosine phosphorylation of erythrocyte band 3.
Role of epistatic (modifier) genes in the modulation of the phenotypic diversity of sickle cell anemia.
Sickle cell disease and glucose-6-phosphate dehydrogenase.
Sickle cell disease in Bahrain: coexistence and interaction with glucose-6-phosphate dehydrogenase (G6PD) deficiency.
Sickle cell disease, G-6-PD deficiency, and jaundice.
Some roles of free radicals in malaria.
Thalassaemia is a tropical disease.
The burden of genetic disorders in India and a framework for community control.
The effects of glucose-6-phosphate dehydrogenase deficiency on the haematological parameters and clinical manifestations in patients with sickle cell anaemia.
The hemolytic crisis of sickle cell disease: the role of glucose-6-phosphate dehydrogenase deficiency.
Therapeutic potential of manipulating suicidal erythrocyte death.
Triggers, inhibitors, mechanisms, and significance of eryptosis: the suicidal erythrocyte death.
[Association of a triple genetic erythrocyte defect: thalassemia, sickle cell disease and glucose-6-phosphate dehydrogenase deficiency in a child of Calabro-Sardinian origin]
[Erythrocyte defects and parasitemia density in patients with Plasmodium falciparum malaria in Buenaventura, Colombia]
[Etiology of hemolytic anemia]
[Evaluation of the incidence of glucose-6-phosphate dehydrogenase deficiency in children with sickle cell anemia in Brazzaville (Congo)]
[Hemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in the sub-Saharan immigrant population of the Center and South Maresme region, Catalonia, Spain]
[Neonatal screening of hemoglobinopathies and G6PD deficiency in Catalonia (Spain). Molecular study of sickle cell disease associated with alpha thalassemia and G6PD deficiency]
[Neonatal screening of hemoglobinopathies and glucose-6-phosphate dehydrogenase in Catalonia. Pilot study in anonymous not related population.]
[Prevalence and morbidity of G6PD deficiency in sickle cell disease in the homozygote]
Anemia, Sideroblastic
Hereditary sideroblastic anemia and glucose-6-phosphate dehydrogenase deficiency in a Negro family.
Sideroblastic anemia segregating with glucose-6-phosphate dehydrogenase deficiency.
Aneurysm
Management of coronary artery aneurysms using abciximab in children with Kawasaki disease.
[Enzyme activity in post-infarct aneurysm and in the myocardial zone outside the infarct in experimental infarct in rats]
Antiphospholipid Syndrome
The epidemiology of recurrent pregnancy loss.
Aortic Coarctation
Influence of aortic coarctation on myocardial glucose-6-phosphate dehydrogenase.
Apnea
[Could the understanding of racial differences prevent idiosyncratic anesthetic reactions?]
Arrhythmias, Cardiac
[Biochemical markers of strophanthin arrhythmia]
[Could the understanding of racial differences prevent idiosyncratic anesthetic reactions?]
Arsenic Poisoning
[Glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activity in arsenic poisoning and in hypoxemia caused by sodium nitrite.]
Arteriosclerosis
Spectrum of genetic disorders and the impact on health care delivery: an introduction.
Arthritis
Aspirin-induced acute haemolytic anaemia in glucose-6-phosphate dehydrogenase-deficient children with systemic arthritis.
Enzyme histochemical reactions in unfixed and undecalcified cryostat sections of mouse knee joints with special reference to arthritic lesions.
Green tea extract improves the oxidative state of the liver and brain in rats with adjuvant-induced arthritis.
Arthritis, Rheumatoid
Metabolic alterations in human synovial lining cells in pigmented villonodular synovitis.
Subclinical reduced G6PD activity in rheumatoid arthritis and Sjgren's Syndrome patients: relation to clinical characteristics, disease activity and metabolic syndrome.
Ascorbic Acid Deficiency
Phagocytosis and leukocyte enzymes in ascorbic acid deficient guinea pigs.
Asthma
Asthma and oxidant stress: nutritional, environmental, and genetic risk factors.
Protein-protein interaction network analysis and identifying regulation microRNAs in asthmatic children.
The effect of dapsone in steroid-dependent asthma.
[Activity of glucose-6-phosphate dehydrogenase in erythrocytes in patients with atopic asthma and allergic rhinitis]
Astrocytoma
Oral atovaquone for the treatment of severe Pneumocystis jirovecii pneumonia in a patient with glucose-6-phosphate dehydrogenase deficiency.
Ataxia Telangiectasia
A case of ataxia telangiectasia with unbalanced glucose 6-phosphate dehydrogenase mosaicism in the granulocytic/monocytic lineages.
Combined metabolic and transcriptional profiling identifies pentose phosphate pathway activation by HSP27 phosphorylation during cerebral ischemia.
Does Ataxia Telangiectasia Mutated (ATM) protect testicular and germ cell DNA integrity by regulating the redox status?
Preexisting conditions in pediatric ALL patients: Spectrum, frequency and clinical impact.
Atherosclerosis
Clonal nature of atherosclerotic plaques.
Dehydroepiandrosterone, glucose-6-phosphate dehydrogenase, and longevity.
Estradiol prevents homocysteine-induced endothelial injury in male rats.
Glucose-6-phosphate dehydrogenase deficiency decreases vascular superoxide and atherosclerotic lesions in apolipoprotein E(-/-) mice.
Glucose-6-phosphate dehydrogenase: a novel therapeutic target in cardiovascular diseases.
Mosaicism in female hybrid hares heterozygous for glucose-6-phosphate dehydrogenase (G-6-PD). I. General properties of a hybrid hare model with special reference to atherogenesis.
Mosaicism in female hybrid hares heterozygous for glucose-6-phosphate dehydrogenase. IV. Aortic atherosclerosis in hybrid hares fed alternating cholesterol-supplemented and nonsupplemented diets.
Population dynamics of arterial cells during atherogenesis. X. Study of monotypism in atherosclerotic lesions of black women heterozygous for glucose-6-phosphate dehydrogenase (G-6-PD).
Production of inflammatory molecules in peripheral blood mononuclear cells from severely glucose-6-phosphate dehydrogenase-deficient subjects.
Avitaminosis
[Erythrocytic G-6-PD activity in experimental avitaminosis C]
Babesiosis
Isoenzyme patterns of glucose-6-phosphate dehydrogenase, malate dehydrogenase and lactate dehydrogenase in Babesia rodhaini and Babesia microti.
Bacteremia
Functional promoter haplotypes of interleukin-18 condition susceptibility to severe malarial anemia and childhood mortality.
Bacterial Infections
A prospective study of the role of bacterial infection and G6PD deficiency in severe neonatal jaundice in Nigeria.
Bacterial infections in children with glucose-6-phosphate dehydrogenase deficiency.
Diabetic ketoacidosis does not precipitate haemolysis in patients with the Mediterranean variant of glucose-6-phosphate dehydrogenase deficiency.
Effect of glucose-6-phosphate dehydrogenase deficiency on neutrophil function.
Glucose-6-phosphate dehydrogenase deficiency and bacterial infections in northern Sardinia.
Glucose-6-phosphate dehydrogenase deficiency and infection: a study of hospitalized patients in Iran.
Mechanisms of smooth muscle antibody production: a clinical study in children with infections, haemolytic syndromes, and idiopathic thrombocytopenic purpura.
Meldola Blue for the cytochemical demonstration of leukocyte dehydrogenases.
Multiple leukocyte abnormalities in chronic granulomatous disease: a familial study.
Screening for glucose-6-phosphate dehydrogenase deficiency can prevent severe neonatal jaundice.
Severe glucose-6-phosphate dehydrogenase deficiency leads to susceptibility to infection and absent NETosis.
Spectrum of neonatal hyperbilirubinemia: an analysis of 454 cases.
The metabolic and phagocytic activities of leukocytes from patients receiving corticosteroid and radiation therapy, and patients with bacterial infections.
Bartonella Infections
Is glucose-6-phosphate dehydrogenase deficiency more prevalent in Carrion's disease endemic areas in Latin America?
beta-Thalassemia
A hematological survey of preschool children of the United Arab Emirates.
Assessment of erythrocyte deformability with the laser-assisted optical rotational cell analyzer (LORCA).
beta-Thalassemia trait and hyperbilirubinemia in G-6-PD deficient newborn infants.
Biochemical genetics and mental retardation: a study of hemoglobins, Australia antigen and the enzymes pseudocholinesterase and glucose-6-phosphate dehydrogenase.
Ceramide in suicidal death of erythrocytes.
Coinheritance of Rotor syndrome, G-6-PD deficiency, and heterozygous beta thalassemia: a possible genetic interaction.
Distribution of beta-thalassemia trait and erythrocyte glucose-6-phosphate dehydrogenase deficiency in the Markham River Valley of New Guinea.
Do tribal communities show an inverse relationship between sickle cell disorders and glucose-6-phosphate dehydrogenase deficiency in malaria endemic areas of Central-Eastern India?
Elevated red blood cell 2,3-diphosphoglycerate levels in black blood donors.
Eryptosis: Ally or Enemy.
Erythrocyte programmed cell death.
Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.
Genetic resistance to malaria, oxidative stress and hemoglobin oxidation.
HbE-beta-thalassemia associated with G6PD deficiency.
Hematologic genetic disorders among Southeast Asian refugees.
Hematological profile of twenty-nine tribal compound cases of hemoglobinopathies and G-6-PD deficiency in rural Orissa.
Hemoglobin A2, E and F levels and the incidence of hemoglobin E, beta-thalassemia, and glucose-6-phosphate dehydrogenase deficiency in lymphoma.
Hemolysis following transfusion of erythrocytes from a donor with G6PD deficiency and beta-thalassemia minor.
Hereditary red cell disorders in Southeast Asian refugees and the effect on the prevalence of thalassemia disorders in the United States.
Inborn defects in the antioxidant systems of human red blood cells.
Influence of hemoglobin E trait on the antimalarial effect of artemisinin derivatives.
Influence of hemoglobin E trait on the severity of Falciparum malaria.
Innate resistance to malaria: the intraerythrocytic cycle.
Jordan: communities and community genetics.
Laboratory and field comparisons of adenosine influx in Plasmodium falciparum and Plasmodium vivax infected erythrocytes with genetic abnormalities from patients in Myanmar.
Molecular newborn screening of four genetic diseases in Guizhou Province of South China.
Occupational lead exposure, G-6PD deficiency and beta-thalassemia trait.
Pathogenesis of anemia in malaria: a concise review.
Prevalence of beta-thalassemia trait and glucose-6-phosphate dehydrogenase deficiency in Iranian Jews.
Progressive peroneal muscular atrophy (Charcot-Marie-Tooth disease) associated with beta-thalassemia trait and glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. A clinical and nerve biopsy case.
Pyruvate kinase deficiency in mice protects against malaria.
Red blood cell-derived microparticles: An overview.
Red cell acid phosphatase activity in carriers of beta-thalassemia trait and glucose-6-phosphate dehydrogenase deficiency.
Red cell membrane protein in thalassemia and glucose-6-phosphate dehydrogenase deficiency anemia.
Redox and energetic state of red blood cells in G6PD deficiency, heterozygous beta-thalassemia and the combination of both.
Reliable detection of beta-thalassemia and G6PD mutations by a DNA microarray.
Sickle cell hemoglobin, beta-thalassemia and G6PD deficiency in tribes of Maharashtra, India.
Suicide for survival--death of infected erythrocytes as a host mechanism to survive malaria.
The interaction between beta-thalassemia, G-6-PD deficiency, and favism.
Use and safety of elevated dosages of vitamin E in adults.
X-linked dyskeratosis congenita with pancytopenia.
[Aspects of the decrease of some enzyme activities in erythrocytes of subjects with beta-thalassemia]
[Beta-thalassemia and glucose-6-phosphate dehydrogenase deficiency]
[CONGENITAL AND RECESSIVE METHEMOGLOBINEMIA. ITS ASSOCIATION WITH GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND THALASSEMIA MINOR.]
[Detection of combined forms of hemoglobino- and enzymopathies in newborns]
[Genetico-epidemiological and molecular investigation of G-6-PD deficiency in a Brazilian community]
[Hemolytic anemia caused by association of a double anomaly: beta-thalassemia and deficiency of G6PD]
[Incidence of beta-thalassemia carriers and those deficient in erythrocyte glucose-6-phosphate dehydrogenase in the greater Buenos Aires area]
[Interrelation between beta-thalassemia and glucose-6-phosphate dehydrogenase deficiency and characteristics of the clinico-hemato-logic indices when the 2 are combined]
[Study of the enzymatic activities in the erythrocytes and platelets of subjects with Mediterranean anemia. V. Glucose-6-phosphate dehydrogenase and 6-phosphogluconate dehydrogenase activities of thalassemic platelets]
[The importance of determination of ferritin levels in erythrocytes]
Biotinidase Deficiency
Neonatal biochemical screening for disease.
bisphosphoglycerate mutase deficiency
Erythrocytosis due to bisphosphoglycerate mutase deficiency with concurrent glucose-6-phosphate dehydrogenase (G-6-PD) deficiency.
Blackwater Fever
Blackwater fever at the Kenyatta National Hospital in Kenya: a case report.
Falciparum malaria--present day problems. An experience with 425 cases.
Glucose-6-phosphate dehydrogenase (G6PD) mutations and haemoglobinuria syndrome in the Vietnamese population.
The role of glucose-6-phosphate dehydrogenase deficiency in blackwater fever.
Blast Crisis
Red cell enzymopathies in leukemias.
Blepharitis
Epidemiology and Associated Morbidity of Pterygium: A Large, Community-Based Case-Control Study.
Blindness
Close linkage of fragile X-mental retardation syndrome to haemophilia B and transmission through a normal male.
Genetic linkage between X-chromosome markers and bipolar affective illness.
Manic-depressive illness and linkage reanalysis in the Xq27-Xq28 region of chromosome X.
Minireview: Molecular genetics in affective illness.
New linkage data for the X-linked types of muscular dystrophy and G6PD variants, colour blindness, and Xg blood groups.
Xq28: epidemiology and sex-linkage between red-green colour blindness and G6PD deficiency.
[Geographic distribution maps of human genes in China]
Blood Group Incompatibility
Combination of ABO blood group incompatibility and glucose-6-phosphate dehydrogenase deficiency: effect on hemolysis and neonatal hyperbilirubinemia.
Comprehensive newborn screening program: ARAMCO experience, the national need and recommendations.
Evaluation of a new end-tidal carbon monoxide monitor from the bench to the bedside.
Genetic polymorphisms in Thai neonates with hyperbilirubinemia.
Management of late-preterm and term infants with hyperbilirubinaemia in resource-constrained settings.
Massive acute haemolysis and severe neonatal hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient preterm triplets.
Prenatal Training Improves New Mothers' Understanding of Jaundice.
Prospective Surveillance of Extreme Neonatal Hyperbilirubinemia inAustralia.
Spectrum of neonatal hyperbilirubinemia: an analysis of 454 cases.
Bone Resorption
Microcytophotometric analysis of human osteoclast metabolism: lack of activity in certain oxidative pathways indicates inability to sustain biosynthesis during resorption.
Boutonneuse Fever
Glucose-6-phosphate dehydrogenase deficiency in male patients with Mediterranean spotted fever in Sardinia.
Haemolysis with Mediterranean spotted fever and glucose-6-phosphate dehydrogenase deficiency.
[Malignant mediterranean boutonneuse fever in a patient with partial glucose-6-phosphate dehydrogenase deficiency]
Brain Diseases
Viral hepatitis with extreme hyperbilirubinemia, massive hemolysis and encephalopathy in a patient with a new G6PD variant.
Brain Ischemia
Knockdown of glucose-6-phosphate dehydrogenase (G6PD) following cerebral ischemic reperfusion: The pros and cons.
Redistribution of glucose-6-phosphate dehydrogenase in response to cerebral ischemia in rat brain.
[Glucose-6-phosphate dehydrogenase and catalase in the erythrocytes of patients with cerebral ischemia attacks]
Breast Diseases
Quantitative cytochemistry of glucose-6-phosphate dehydrogenase in benign and malignant breast tumours.
Breast Neoplasms
Aberrant expression of X-linked genes RbAp46, Rsk4, and Cldn2 in breast cancer.
Altered glycometabolism affects both clinical features and prognosis of triple-negative and neoadjuvant chemotherapy-treated breast cancer.
Characterization of epithelial cell islets in primary monolayer cultures of human breast carcinomas by the tetrazolium reaction for glucose 6-phosphate dehydrogenase.
Effect of branched-chain fatty acids on fatty acid biosynthesis of human breast cancer cells.
Effect of oxygen on the tetrazolium reaction for glucose 6-phosphate dehydrogenase in cryosections of human breast carcinoma, fibrocystic disease and normal breast tissue.
Effects of 17 beta-estradiol and R5020 on glucose-6-phosphate dehydrogenase activity in MCF-7 human breast cancer cells: a cytochemical assay.
Erythrocyte antioxidant enzyme activity in CMF treated breast cancer patients.
Estradiol promotes pentose phosphate pathway addiction and cell survival via reactivation of Akt in mTORC1 hyperactive cells.
Estradiol receptors and glucose-6-phosphate dehydrogenase activity in human breast tumors.
Estrogenic effects of phenolic compounds on glucose-6-phosphate dehydrogenase in MCF-7 cells and uterine glutathione peroxidase in rats.
G6PD deficiency and breast cancer.
Glucose-6-phosphate dehydrogenase activity and estrogen receptors in human breast cancer.
Glucose-6-phosphate dehydrogenase activity in human breast cancer. Lack of association with oestrogen receptor content.
Glycolaldehyde induces apoptosis in a human breast cancer cell line.
Glycolytic enzymes in human breast carcinoma cytosols: the influence of commonly used reference parameters.
Histochemical studies of human breast tumors: Activity of alkaline phosphatase, acid phosphatase and glucose-6-phosphate dehydrogenase.
Histone deacetylase inhibitor-induced cancer stem cells exhibit high pentose phosphate pathway metabolism.
Identification of malignant cells in primary monolayer cultures of human breast tumors.
Overexpression of G6PD is associated with high risks of recurrent metastasis and poor progression-free survival in primary breast carcinoma.
Oxidant/antioxidant status in blood of patients with malignant breast tumour and benign breast disease.
Quantitative cytochemistry of glucose-6-phosphate dehydrogenase in benign and malignant breast tumours.
Quantitative reverse transcription-PCR assay for detection of mRNA encoding full-length human tissue kallikrein 7: prognostic relevance of KLK7 mRNA expression in breast cancer.
Relative value of oestrogen receptor assay, lactoferrin content, and glucose-6-phosphate dehydrogenase activity as prognostic indicators in primary breast cancer.
Role of glucose-6-phosphate dehydrogenase inhibition in the antiproliferative effects of dehydroepiandrosterone on human breast cancer cells.
Safe chemotherapy and hormone therapy for treating early breast cancer in a glucose 6-phosphate dehydrogenase-deficient patient: case report.
Sex steroid hormone modulation of NADPH pathways in MCF-7 cells.
Stimulatory effect of 1,25-dihydroxyvitamin D3 on the glucose-6-phosphate dehydrogenase activity in the MCF-7 human breast cancer cell line.
The correlation of cytologic degree of differentiation of infiltrative ductal breast carcinoma and cytochemical activity of glucose-6-phosphate dehydrogenase.
[A study on the relationship among estrogen receptor, progesterone receptor and glucose-6-phosphate dehydrogenase activity in primary breast cancer]
[Glutathione-dependent enzymes and glucose-6-phosphate dehydrogenase in breast tumors]
[Histo- and cytochemical enzymatic characteristics of breast cancer]
Bronchial Spasm
Rasburicase: potential role in managing tumor lysis in patients with hematological malignancies.
Bronchopneumonia
A Retrospective Analysis of 7 Human Immunodeficiency Virus-Negative Infants Infected by Penicillium marneffei.
Brucellosis
Brucellosis triggering hemolytic anemia in glucose-6-phosphate dehydrogenase deficiency.
Burkitt Lymphoma
Glucose-6-phosphate dehydrogenase (G-6-PD) markers in Burkitt lymphoma and other malignancies.
Immunoglobulin and glucose-6-phosphate dehydrogenase as markers of cellular origin in Burkitt lymphoma.
[Hematologic characteristics in Black Africa]
Candidiasis, Oral
A Retrospective Analysis of 7 Human Immunodeficiency Virus-Negative Infants Infected by Penicillium marneffei.
Carcinogenesis
A new lease of life for an old enzyme.
Adaptational changes in kinetic parameters of G6PDH but not of PGDH during contamination-induced carcinogenesis in livers of North Sea flatfish.
Arginase and glucose-6-phosphate dehydrogenase activities in spontaneous mammary carcinogenesis.
Chemopreventive effect of Ginkgo biloba extract against benzo(a)pyrene-induced forestomach carcinogenesis in mice: amelioration of doxorubicin cardiotoxicity.
Dehydroepiandrosterone, glucose-6-phosphate dehydrogenase, and longevity.
Development of oxygen insensitivity of the quantitative histochemical assay of G6PDH activity during colorectal carcinogenesis.
Early lesions during pancreatic carcinogenesis induced in Syrian hamster by DHPN or DOPN. I. Histologic, histochemical and radioautographic findings.
Human glucose-6-phosphate dehydrogenase (G6PD) gene transforms NIH 3T3 cells and induces tumors in nude mice.
Immunohistochemical demonstration of increased glucose-6-phosphate dehydrogenase in preneoplastic and neoplastic lesions induced by propylnitrosamines in F344 rats and Syrian hamsters.
Inhibition of 12-O-tetradecanoylphorbol-13-acetate-promoted skin tumor formation in mice by 16 alpha-fluoro-5-androsten-17-one and its reversal by deoxyribonucleosides.
Investigation of Pokemon-regulated proteins in hepatocellular carcinoma using mass spectrometry-based multiplex quantitative proteomics.
Long-term dehydroepiandrosterone and 16alpha-fluoro-5-androsten-17-one administration enhances DNA synthesis and induces expression of c-fos and c-Ha-ras in a selected population of preneoplastic lesions in liver of diethylnitrosamine-initiated rats.
Premorphological metabolic changes in human breast carcinogenesis.
Studies of tumor cell origins in mosaics.
Tumor M2-PK and glutaminolytic enzymes in the metabolic shift of tumor cells.
Carcinoma
5' structure and expression of human glucose-6-phosphate dehydrogenase mRNA.
A cytochemical study of the livers of rats treated with diethylnitrosamine/phenobarbital, with benzidine/phenobarbital, with phenobarbital, or with clofibrate.
Adaptational changes in kinetic parameters of G6PDH but not of PGDH during contamination-induced carcinogenesis in livers of North Sea flatfish.
Carbohydrate metabolism in human renal clear cell carcinomas.
Characterization of an established cell line from human renal carcinoma.
Characterization of epithelial cell islets in primary monolayer cultures of human breast carcinomas by the tetrazolium reaction for glucose 6-phosphate dehydrogenase.
Clinical response and tissue effects of etretinate treatment of patients with solar keratoses and basal cell carcinoma.
Clonal xenobiotic resistance during pollution-induced toxic injury and hepatocellular carcinogenesis in liver of female flounder (Platichthys flesus (L.)).
Combined efficacy of tamoxifen and coenzyme Q10 on the status of lipid peroxidation and antioxidants in DMBA induced breast cancer.
Comparison of enzyme phenotypes in human bladder tumours and experimentally induced hyperplastic and neoplastic lesions of the rat urinary bladder. A combined histochemical and immunohistochemical approach.
Comparison of hypoxic cell radiosensitizers, KIN-804, KIN-844, KIN-806 and TX-1877, on brain and liver metabolizing capacities in mice bearing Ehrlich ascites carcinoma.
Correlative histochemical studies on preneoplastic and neoplastic lesions in the kidney of rats treated with nitrosamines.
Cytochemical assay of glucose-6-phosphate dehydrogenase in koilocytes.
Effect of radiotherapy and chemoradiotherapy on circulating antioxidant system of human uterine cervical carcinoma.
Effect of Semecarpus anacardium Linn. nut milk extract on glutathione and its associated enzymes in experimentally induced mammary carcinoma.
Enzymatic characteristics of tubular adenomas and carcinomas of the large intestine.
Enzyme activities and level of SH groups in breast carcinomas.
Enzyme activities in human breast tumours.
Flow-cytometric determination of dehydrogenase activities in primary human gastrointestinal tumor cell lines.
Focal hepatic glycogenosis.
G6PD downregulation triggered growth inhibition and induced apoptosis by regulating STAT3 signaling pathway in esophageal squamous cell carcinoma.
Gene expression studies in prostate cancer tissue: which reference gene should be selected for normalization?
Genetic variants of glucose-6-phosphate dehydrogenase in the study of carcinoma of the cervix.
Glucose-6-phosphate dehydrogenase (G6PD) activity in tumoral tissues of G6PD-deficient subjects affected by larynx carcinoma.
Glucose-6-phosphate dehydrogenase (G6PD)-deficient epithelial cells are less tolerant to infection by Staphylococcus aureus.
Glucose-6-phosphate dehydrogenase and lactate dehydrogenase isoenzynes in rodent mammary carcinomas and the effect of oophorectomy.
Glucose-6-phosphate dehydrogenase expression is correlated with poor clinical prognosis in esophageal squamous cell carcinoma.
Glucose-6-phosphate dehydrogenase: a possible clinical indicator for prostatic carcinoma.
Hepatic foci of cellular and enzymatic alteration and nodules in rats treated with clofibrate or diethylnitrosamine followed by phenobarbital: their rate of onset and their reversibility.
Hepatocellular glycogenosis and related pattern of enzymatic changes during hepatocarcinogenesis.
Histochemical studies of human breast tumors: Activity of alkaline phosphatase, acid phosphatase and glucose-6-phosphate dehydrogenase.
Histochemistry and cytochemistry of glucose-6-phosphate dehydrogenase.
Histogenesis of dieldrin and DDT-induced hepatocellular carcinoma in Balb/c mice.
Inhibition of glucose-6-phosphate dehydrogenase from Ehrlich ascites carcinoma by ATP.
Loss of peroxisomes causes oxygen insensitivity of the histochemical assay of glucose-6-phosphate dehydrogenase activity to detect cancer cells.
Metabolomic profile of glycolysis and the pentose phosphate pathway identifies the central role of glucose-6-phosphate dehydrogenase in clear cell-renal cell carcinoma.
Multiple molecular forms of glucose-6-phosphate dehydrogenase in normal, preneoplastic, and neoplastic mammary tissues of mice.
Multiple molecular forms of lactate dehydrogenase and glucose 6-phosphate dehydrogenase in normal and abnormal human breast tissues.
One hundred and twenty-seven cultured human tumor cell lines producing tumors in nude mice.
Overexpression of G6PD Represents a Potential Prognostic Factor in Clear Cell Renal Cell Carcinoma.
Reactive oxygen species in cancer, too much or too little?
Redox cycling by motexafin gadolinium enhances cellular response to ionizing radiation by forming reactive oxygen species.
Renal cell carcinoma and oxidative stress: The lack of peroxisomes.
Semiquantitative cytochemical estimation of glucose-6-phosphate dehydrogenase activity in benign diseases and carcinoma of the breast.
Sequential histochemical and morphometric studies on preneoplastic and neoplastic lesions induced in rat colon by 1,2-dimethylhydrazine.
The correlation of membranous glycoprotein-gp-170, cytoplasmic glutathione and glucose-6-phosphate dehydrogenase levels with multidrug resistance in transitional cell carcinoma cell lines of the urinary tract.
The effect of low temperature on the enzyme activities and the level of SH groups in benign gastric ulcer and gastric carcinoma.
The histochemical G6PDH reaction but not the LDH reaction with neotetrazolium is suitable for the oxygen sensitivity test to detect cancer cells.
[Clinical studies on glucose-6-phosphate dehydrogenase in women with carcinoma of the cervix]
[Effects of glucose-6-phosphate dehydrogenase expression down-regulation on cell apoptosis and invasion ability in cutaneous squamous cell carcinoma A431 cells].
[Glucose-6-phosphate dehydrogenase and succinate dehydrogenase in metastatic cells of Lewis lung carcinoma]
[Histochemical and biochemical comparative study of glucose-6-phosphate dehydrogenase in cutaneous epitheliomas. Preliminary note]
[Histochemistry observation on the activity of deoxyribonucleases (DNase), glucose-6-phosphate dehydrogenase (G 6P DH) and acidic alpha-naphthol acetate esterase (ANAE) in nasopharyngeal carcinoma]
[Histocytospectrophotometric characteristics of lung cancer]
[Histoenzymatic studies of cervical carcinoma. II. Glucose-6-phosphate dehydrogenase, 6-phosphogluconate dehydrogenase, TPN diaphorase and DPN diaphorase]
Carcinoma, Basal Cell
Clinical response and tissue effects of etretinate treatment of patients with solar keratoses and basal cell carcinoma.
Carcinoma, Ductal
Semiquantitative cytochemical estimation of glucose-6-phosphate dehydrogenase activity in benign diseases and carcinoma of the breast.
Carcinoma, Ehrlich Tumor
Enzyme activities of six different dehydrogenases in Ehrlich ascites cells measured by flow cytometry.
Metabolic control analysis aimed at the ribose synthesis pathways of tumor cells: a new strategy for antitumor drug development.
Carcinoma, Hepatocellular
A case of minimal deviation hepatoma in man with elevated liver-type pyruvate kinase isozyme.
BAG3 elevation inhibits cell proliferation via direct interaction with G6PD in hepatocellular carcinomas.
Biochemistry and enzyme induction in MC-29 virus-induced transplantable avian hepatoma.
Changes in glucose-6-phosphate dehydrogenase expression results in altered behavior of HBV-associated liver cancer cells.
Cross-reacting material to monoclonal anti-G6PD in the absence of catalytic activity.
Distribution and partial purification of a liver membrane protein capable of inactivating cytosol enzymes.
Ecotoxicological evaluation of diethanolamine using a battery of microbiotests.
Elevated activity of the oxidative and non-oxidative pentose phosphate pathway in (pre)neoplastic lesions in rat liver.
Examination of HeLa cell contamination of human cell lines derived from primary hepatomas using glucose-6-phosphate dehydrogenase and lactate dehydrogenase isozymes.
Glucose-6-phosphate dehydrogenase activity in a hepatoma cell line: preliminary evidence for negative genetic control.
Glucose-6-phosphate dehydrogenase deficiency and malignant hepatoma in a Bantu population.
Hepatic foci of cellular and enzymatic alteration and nodules in rats treated with clofibrate or diethylnitrosamine followed by phenobarbital: their rate of onset and their reversibility.
Hepatic preneoplasia in hepatitis B virus transgenic mice.
Increased glucose 6-phosphate dehydrogenase concentration in hepatoma 3924A: enzymic and immunological evidence.
Metabolic adaptations in rat hepatomas. V. Reciprocal relationship between threonine dehydrase and glucose-6-phosphate dehydrogenase.
Overexpression of glucose-6-phosphate-dehydrogenase in rat hepatic preneoplasia and neoplasia.
Post-translational regulation of glucose-6-phosphate dehydrogenase activity in (pre)neoplastic lesions in rat liver.
Profiles of carbohydrate-metabolizing enzymes in human hepatocellular carcinomas and preneoplastic livers.
Reactive oxygen species in cancer, too much or too little?
Subchromosomal localization and order of GLA, PGK1, HPRT, and G6PD loci on the X chromosome of the American mink (Mustela vison).
The associated reactivation of two X-linked genes. The spontaneous and azacytidine-induced reexpression of ornithine transcarbamoylase and glucose-6-phosphate dehydrogenase in a rat hepatoma.
Uridine and cytidine nucleotide synthesis in renal hypertrophy: biochemical differences in response to the growth stimulus of diabetes and unilateral nephrectomy.
[Activities of dehydrogenases of the pentose phosphate pathway and transketolase in transplanted mouse hepatomas with different growth rates and in organs of tumor carriers]
[Carbohydrate metabolism enzymatic activity and its alteration under the influence of thyroid hormone during tumor growth]
[Glucose-6-phosphate dehydrogenase isoenzymes in the liver and hepatomas of mice]
[Properties of glucose-6-phosphate dehydrogenase of the liver tissue of intact rats and rats with Zaidel ascitic hepatoma]
Carcinoma, Lewis Lung
[Glucose-6-phosphate dehydrogenase and succinate dehydrogenase in metastatic cells of Lewis lung carcinoma]
Carcinoma, Medullary
Clonal origin of inherited medullary thyroid carcinoma and pheochromocytoma.
Carcinoma, Pancreatic Ductal
Enhanced citrate synthase activity in human pancreatic cancer.
Carcinoma, Renal Cell
Overexpression of G6PD Represents a Potential Prognostic Factor in Clear Cell Renal Cell Carcinoma.
Carcinoma, Small Cell
[Histocytospectrophotometric characteristics of lung cancer]
Carcinoma, Squamous Cell
G6PD downregulation triggered growth inhibition and induced apoptosis by regulating STAT3 signaling pathway in esophageal squamous cell carcinoma.
Glucose-6-phosphate dehydrogenase and the histogenesis of epidermoid carcinoma of the cervix.
Glucose-6-phosphate dehydrogenase expression is correlated with poor clinical prognosis in esophageal squamous cell carcinoma.
[Effects of glucose-6-phosphate dehydrogenase expression down-regulation on cell apoptosis and invasion ability in cutaneous squamous cell carcinoma A431 cells].
[Histocytospectrophotometric characteristics of lung cancer]
Carcinoma, Transitional Cell
Comparison of enzyme phenotypes in human bladder tumours and experimentally induced hyperplastic and neoplastic lesions of the rat urinary bladder. A combined histochemical and immunohistochemical approach.
The correlation of membranous glycoprotein-gp-170, cytoplasmic glutathione and glucose-6-phosphate dehydrogenase levels with multidrug resistance in transitional cell carcinoma cell lines of the urinary tract.
Cardiac Tamponade
Acute hemolytic anemia precipitated by myocardial infarction and pericardial tamponade in G6PD deficiency.
Cardiomegaly
Human alpha B-crystallin mutation causes oxido-reductive stress and protein aggregation cardiomyopathy in mice.
Regulation of and intervention into the oxidative pentose phosphate pathway and adenine nucleotide metabolism in the heart.
Cardiomyopathies
Human alpha B-crystallin mutation causes oxido-reductive stress and protein aggregation cardiomyopathy in mice.
The NADPH metabolic network regulates human ?B-crystallin cardiomyopathy and reductive stress in Drosophila melanogaster.
Upregulation of glucose-6-phosphate dehydrogenase and NAD(P)H oxidase activity increases oxidative stress in failing human heart.
Cardiomyopathy, Alcoholic
Effect of chronic ethanol treatment under partial catalase inhibition on the activity of enzymes related to peroxide metabolism in rat liver and heart.
Cardiomyopathy, Dilated
Upregulation of glucose-6-phosphate dehydrogenase and NAD(P)H oxidase activity increases oxidative stress in failing human heart.
Cardiotoxicity
Protective role of DLalpha-lipoic acid against adriamycin-induced cardiac lipid peroxidation.
Severe Malaria Complicated by G6PD Deficiency in a Pediatric Tanzanian Immigrant.
Cardiovascular Diseases
Amifostine administration during radiotherapy for cancer patients with genetic, autoimmune, metabolic and other diseases.
Blood pressure and other cardiovascular disease risk factors in black adults with sickle cell trait or glucose-6-phosphate dehydrogenase deficiency.
Glucose-6-phosphate dehydrogenase: a novel therapeutic target in cardiovascular diseases.
High-dose vitamin therapy stimulates variant enzymes with decreased coenzyme binding affinity (increased K(m)): relevance to genetic disease and polymorphisms.
Impact of glucose-6-phosphate dehydrogenase deficiency on the pathophysiology of cardiovascular disease.
Mortality in a cohort of men expressing the glucose-6-phosphate dehydrogenase deficiency.
Occupational lead exposure and screening of glucose-6-phosphate dehydrogenase polymorphism: useful prevention or nonvoluntary discrimination?
Production of inflammatory molecules in peripheral blood mononuclear cells from severely glucose-6-phosphate dehydrogenase-deficient subjects.
Superoxide Production by NAD(P)H oxidase and Mitochondria is Increased in Genetically Obese and Hyperglycemic Rat Heart and Aorta Prior to Cardiac ...
Targeting the Pentose Phosphate Pathway in Syndrome X-related Cardiovascular Complications.
Cataract
Alphab-crystallin-assisted reactivation of glucose-6-phosphate dehydrogenase upon refolding.
Analysis of the genetic variants of glucose-6-phosphate dehydrogenase in inhabitants of the 4th Nile cataract region in Sudan.
Anemia, cataracts, and seizures in patient with glucose-6-phosphate dehydrogenase deficiency.
Bilateral cataracts associated with glucose-6-phosphate dehydrogenase deficiency.
Blood and lens lipid peroxidation and antioxidant status in normal individuals, senile and diabetic cataractous patients.
Cataracts in glucose-6-phosphate dehydrogenase deficiency.
Changes in erythrocyte glucose-6-phosphate dehydrogenase (G6PD) and reduced glutathione (GSH) activities in the development of senile and diabetic cataracts.
Changes in glutathione, glutathione-linked enzymes and hexose monophosphate shunt enzymes in senile cataract.
Decreased Glucose-6-PhosphateDehydrogenase (G6PD) Activity and Risk of Senile Cataract in Taiwan.
Effects of antioxidant supplementation on mRNA expression of glucose-6-phosphate dehydrogenase, ?-actin and 18S rRNA in the anterior capsule of the lens in cataract patients.
Effects of G-6-PD deficiency, experimentally induced or genetically transmitted, on the sorbitol pathway activity. In vitro and in vivo studies.
Erythrocyte glutathione concentrations in diabetics with cataracts, with and without glucose-6-phosphate dehydrogenase deficiency.
Fructose induced deactivation of glucose-6-phosphate dehydrogenase activity and its prevention by pyruvate: implications in cataract prevention.
G6PD deficiency in senile cataracts.
Genetic localization and phenotypic expression of X-linked cataract (Xcat) in Mus musculus.
Glucose 6-phosphate dehydrogenase deficiency and cataract of patients in northern Sardinia.
Glucose 6-phosphate dehydrogenase deficiency both in red blood cells and lenses of the normal and cataractous native population of Cukurova, the southern part of Turkey. Part I.
Glucose 6-phosphate dehydrogenase deficiency both in red blood cells and lenses of the normal and cataractous native population of Cukurova, the southern part of Turkey. Part II.
Glucose 6-phosphate dehydrogenase variants: Gd (+) Alexandra associated with neonatal jaundice and Gd (-) Camperdown in a young man with lamellar cataracts.
Glucose-6-phosphate dehydrogenase (G6PD) deficiency and senile cataract in a Sardinian male population, Italy.
Glucose-6-phosphate dehydrogenase deficiency and cataracts.
Glucose-6-phosphate dehydrogenase deficiency and idiopathic presenile cataract in Dalmatia, Croatia.
Glucose-6-phosphate dehydrogenase deficiency and incidence of cataract in Sicily.
Glucose-6-phosphate dehydrogenase deficiency with bilateral cataract.
Grape seed extract and Zinc containing nutritional food supplement delays onset and progression of Streptozocin-induced diabetic cataract in Wistar rats.
GSSG-reducing activity in lenses deficient in glucose-6-phosphate dehydrogenase.
Increased incidence of cataracts in male subjects deficient in glucose-6-phosphate dehydrogenase.
India-US case-control study of age-related cataracts. India-US Case-Control Study Group.
Letter: cataracts with a glucose-6-phosphate dehydrogenase variant.
Osmotic stress induced oxidative damage: possible mechanism of cataract formation in diabetes.
Quantitative cytochemistry of enzymes in the epithelium of ageing rat lenses.
Recent epidemiologic studies on nutrition and cataract in India, Italy and the United States.
Red blood cells and serum antioxidant defense systems of galactosaemic children.
Risk factors for age-related cortical, nuclear, and posterior subcapsular cataracts. The Italian-American Cataract Study Group.
Senile cataract and glucose-6-phosphate dehydrogenase deficiency in Indians.
The effect of diabetes mellitus and diabetic therapy on cataract formation.
The relationship between glucose-6-phosphate dehydrogenase deficiency and cataracts in Sardinia. An epidemiological and biochemical study.
The study of G6PD in erythrocyte and lens in senile and presenile cataract.
[Cataract and glucose-6-phosphate dehydrogenase deficiency in Sardinians]
[Congenital nonspherocytic hemolytic anemia, cataract and glucose-6-phosphate dehydrogenase deficiency]
Catatonia
Catatonia and Glucose-6-Phosphate Dehydrogenase Deficiency: A Report of Two Cases and a Review.
Cerebral Palsy
Anaesthetic management in a child with an atypical triad for reconstructive scoliosis surgery.
Glucose-6-phosphate dehydrogenase deficiency. WHO Working Group.
Cervical Intraepithelial Neoplasia
Cytochemical assay of glucose-6-phosphate dehydrogenase in koilocytes.
Increased activity of 6-phosphogluconate dehydrogenase and glucose-6-phosphate dehydrogenase in purified cell suspensions and single cells from the uterine cervix in cervical intraepithelial neoplasia.
Chagas Disease
Comparative study of enzymes in testes and ovaries from adult Dipetalogaster maximus (Uhler) and triatoma infestans (Klug) (Hemiptera: Reduviidae). correlation with fine structural organization.
Discovery of new uncompetitive inhibitors of glucose-6-phosphate dehydrogenase.
The identification by isoenzyme patterns of two distinct strain-groups of Trypanosoma cruzi, circulating independently in a rural area of Brazil.
Chalazion
Epidemiology and Associated Morbidity of Pterygium: A Large, Community-Based Case-Control Study.
Charcot-Marie-Tooth Disease
Progressive peroneal muscular atrophy (Charcot-Marie-Tooth disease) associated with beta-thalassemia trait and glucose-6-phosphate dehydrogenase (G-6-PD) deficiency. A clinical and nerve biopsy case.
Chediak-Higashi Syndrome
A new glucose-6-phosphate dehydrogenase deficient variant in a patient with Chediak-Higashi syndrome.
Congenital disorders of the function of polymorphonuclear neutrophils.
Chemical and Drug Induced Liver Injury
[Catalytic properties of 6-phosphogluconate dehydrogenase from rat liver in normal state and during toxic hepatitis]
[Regulatory properties of glucose-6-phosphate dehydrogenase from rat liver under conditions of the intensification of free-radical oxidation stimulated by toxic hepatitis]
[Thioctic acid action on glutathione-dependent antioxidant system functioning at toxic hepatitis of rats]
Chickenpox
Mechanisms of smooth muscle antibody production: a clinical study in children with infections, haemolytic syndromes, and idiopathic thrombocytopenic purpura.
Cholangiocarcinoma
Intestinal metaplasia and altered enzyme expression in propylnitrosamine-induced Syrian hamster cholangiocellular and gallbladder lesions.
Cholelithiasis
Effects of variant UDP-glucuronosyltransferase 1A1 gene, glucose-6-phosphate dehydrogenase deficiency and thalassemia on cholelithiasis.
Gilbert syndrome.
Increased prevalence of glucose-6-phosphate dehydrogenase deficiency in patients with cholelithiasis.
Cholestasis
Assessment of potential donors for living related liver transplantation.
Cooperating G6PD mutations associated with severe neonatal hyperbilirubinemia and cholestasis.
Jaundice associated with lobar pneumonia. A clinical, laboratory and histological study.
Metabolic changes in rat brain histaminergic neurons during subhepatic cholestasis.
[Activity of carbohydrate metabolism enzyme activity in normal and pathologic parodontal tissues]
Cholestasis, Extrahepatic
[Concentration of components of the adenylate system in the liver during cholestasis]
Cholestasis, Intrahepatic
Glucose-6-phosphate dehydrogenase deficiency and lobar pneumonia. Fine structure of the liver.
Cholesteatoma
A comparative study of enzyme histochemical features in the gerbilline and human cholesteatoma.
Cleidocranial Dysplasia
Genetic disorders in Southern Africa.
coagulation factor ixa deficiency
Cytological mapping of the human glucose-6-phosphate dehydrogenase gene distal to the fragile-X site suggests a high rate of meiotic recombination across this site.
Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree.
The human genes for hemophilia A and hemophilia B flank the X chromosome fragile site at Xq27.3.
Coinfection
Primaquine administration after falciparum malaria treatment in malaria hypoendemic areas with high incidence of falciparum and vivax mixed infection: pros and cons.
Colitis, Ulcerative
In vivo effects of curcumin on the paraoxonase, carbonic anhydrase, glucose-6-phosphate dehydrogenase and ?-glucosidase enzyme activities in dextran sulphate sodium-induced ulcerative colitis mice.
Ulcerative colitis and erythrocyte G6PD deficiency. Salicylazosulfapyridine-provoked hemolysis.
Colonic Neoplasms
Efficiency of diagnostic biomarkers among colonic schistosomiasis Egyptian patients.
Modulation of doxorubicin resistance by the glucose 6-phosphate dehydrogenase activity.
Modulation of pentose phosphate pathway during cell cycle progression in human colon adenocarcinoma cell line HT29.
Color Vision Defects
A case-control study of primary hepatocellular carcinoma in Taiwan.
Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus.
Evidence against close linkage of unipolar affective illness to human chromosome 11p markers HRAS1 and INS and chromosome Xq marker DXS52.
Evidence of a predisposing locus to bipolar disorder on Xq24-q27.1 in an extended Finnish pedigree.
Genetic studies of the Seneca Indians: haptoglobins, transferrins, G-6-PD deficiency, hemoglobinopathy, color blindness, morphological traits and dermatoglyphics.
Linkage analysis of bipolar illness with X-chromosome DNA markers: a susceptibility gene in Xq27-q28 cannot be excluded.
Linkage disequilibrium between glucose-6-phosphate dehydrogenase deficiency and congenital color blindness in Turkish population.
Old and new genetics help ordering loci at the telomere of the human X-chromosome long arm.
Studies on hemophilia A in Sardinia bearing on the problems of multiple allelism, carrier detection, and differential mutation rate in the two sexes.
The ocular findings in glucose-6-phosphate dehydrogenase deficiency.
Triplo-X constitution of mother explains apparent occurrence of two recombinants in sibship segregating at two closely X-linked loci (G6PD and deutan).
X-chromosome markers and manic-depressive illness. Rejection of linkage to Xq28 in nine bipolar pedigrees.
[Frequency of color blindness and glucose-6-phosphate dehydrogenase enzyme deficiency in non-industrialized populations in the state of Nuevo León, México]
Colorectal Neoplasms
Aspirin inhibits glucose?6?phosphate dehydrogenase activity in HCT 116 cells through acetylation: Identification of aspirin-acetylated sites.
Prognostic estimation of survival of colorectal cancer patients with the quantitative histochemical assay of G6PDH activity and the multiparameter classification program CLASSIF1.
Communicable Diseases
Community-acquired acute kidney injury in Asia.
Dental Considerations in Children with Glucose-6-phosphate Dehydrogenase Deficiency (Favism): A Review of the Literature and Case Report.
Glucose-6-phosphate dehydrogenase deficiency.
[Anesthesia in patients with glucose-6-phosphate dehydrogenase deficiency: case report and perioperative anesthesiologic management]
Condylomata Acuminata
Viral "tumorigenesis" in man: cell markers in condylomata acuminata.
Confusion
Medications and glucose-6-phosphate dehydrogenase deficiency: an evidence-based review.
Psychotic mania in glucose-6-phosphate-dehydrogenase-deficient subjects.
Congenital Abnormalities
Congenital defects of the central nervous system associated with hyperendemic goiter in a neolithic highland society of Netherlands New Guinea II. Glucose-6-phosphate dehydrogenase in the mulia population.
Erythrocyte glucose-6-phosphate dehydrogenase in lichen planus.
Heinz-body anemia: "bite cell" variant--a light and electron microscopic study.
[Hemoglobinopathies and glucose-6-phosphate dehydrogenase deficiency in the sub-Saharan immigrant population of the Center and South Maresme region, Catalonia, Spain]
Congenital Hypothyroidism
A neonatal screening in Lebanon: Results of five years' experience.
Adequacy and pitfalls of G6PD deficiency counseling in Hong Kong.
Alpha-1-antitrypsin deficiency in babies with prolonged jaundice.
Comprehensive newborn screening program: ARAMCO experience, the national need and recommendations.
Current and future perspective of newborn screening: an Indian scenario.
Neonatal screening and monitoring system in Taiwan.
Neonatal screening in Hong Kong and Macau.
Newborn screening in the Philippines.
Newborn screening: need of the hour in India.
Preliminary report on neonatal screening for congenital hypothyroidism, congenital adrenal hyperplasia and glucose-6-phosphate dehydrogenase deficiency: a Chandigarh experience.
Prevention of intellectual and other disabilities: the Singapore experience.
The status of neonatal screening in China, 2013.
[Congenital hypothyroidism missed on newborn screening: report of two cases]
Congenital, Hereditary, and Neonatal Diseases and Abnormalities
Congenital X-linked incomplete achromatopsia. Evidence for slow progression, carrier fundus findings, and possible genetic linkage with glucose-6-phosphate dehydrogenase locus.
Coproporphyria, Hereditary
[Hereditary coproporphyria with grand mal epilepsy, glucose-6-phosphate dehydrogenase deficiency and phenobarbital tolerance]
Coronary Disease
Glucose-6-phosphate dehydrogenase deficiency protects against coronary heart disease.
Glucose-6-phosphate dehydrogenase deficiency: disadvantages and possible benefits.
[Disorders of myocardial metabolism in sudden coronary death in the presence of coronary atherosclerosis: findings of quantitative histoenzymologic studies]
Cough
Community-acquired Acinetobacter pneumonia: a case report.
Crigler-Najjar Syndrome
Phenotype heterogeneity of hyperbilirubinemia condition: the lesson by coinheritance of glucose-6-phosphate dehydrogenase deficiency and Crigler-Najjar syndrome type II in an Italian patient.
Crohn Disease
Crohn's disease and G-6-PD deficiency.
G-6-pd deficiency and Crohn's disease.
Regional enteritis and glucose-6-phosphate dehydrogenase deficiency.
Regional enteritis and granulomatous colitis associated with erythrocyte glucose-6-phosphate dehydrogenase deficiency.
Cryptorchidism
Gene mapping and serendipity. The locus for torticollis, keloids, cryptorchidism and renal dysplasia (31430, Mckusick) is at Xq28, distal to the G6PD locus.
Cystic Fibrosis
A Rare Case of Short-Chain Acyl-COA Dehydrogenase Deficiency: The Apparent Rarity of the Disorder Results in Under Diagnosis.
Adaptations of Pseudomonas aeruginosa to the cystic fibrosis lung environment can include deregulation of zwf, encoding glucose-6-phosphate dehydrogenase.
Attitudes and beliefs of pediatricians and genetic counselors regarding testing and screening for CF and G6PD: implications for policy.
Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children.
Does familiarity breed acceptance? The influence of policy on physicians' attitudes toward newborn screening programs.
Evolutionary explanations in medical and health profession courses: are you answering your students' "why" questions?
Genetic screening for low-penetrance variants in protein-coding genes.
Gilbert syndrome.
Glucose 6-phosphate dehydrogenase deficiency and cystic fibrosis.
Jordan: communities and community genetics.
Neonatal biochemical screening for disease.
Preexisting conditions in pediatric ALL patients: Spectrum, frequency and clinical impact.
Understanding human disease mutations through the use of interspecific genetic variation.
Cysts
Growth performance, meat quality and activities of glycolytic enzymes in the blood and muscle tissue of calves infected with Sarcocystis cruzi.
Histoenzymological study of selected dehydrogenase enzymes in Pneumocystis carinii.
Some glucose metabolic enzymes in various fractions of sarcocysts of Sarcocystis fusiformis of buffalo (Bubalus bubalis).
The Ribavirin Pregnancy Registry: Findings after 5 years of enrollment, 2003-2009.
[Periapical odontogenic processes of inflammatory origin. Enzyme activity]
cytochrome-b5 reductase deficiency
Red cell enzymes.
Cytomegalovirus Infections
Cytomegalovirus infection and aplastic crisis in glucose-6-phosphate dehydrogenase deficiency.
Cytomegalovirus infection and hemolytic anemia due to glucose-6-phosphate dehydrogenase deficiency.
Hepatitis A and cytomegalovirus infection precipitating acute hemolysis in glucose-6-phosphate dehydrogenase deficiency.
Oral atovaquone for the treatment of severe Pneumocystis jirovecii pneumonia in a patient with glucose-6-phosphate dehydrogenase deficiency.
Deafness
Glucose 6-phosphate dehydrogenase deficiency with kernicterus: progressive late recovery from profound deafness.
Molecular newborn screening of four genetic diseases in Guizhou Province of South China.
Persistent and transient distal renal tubular acidosis with bicarbonate wasting.
[Infantile transitory distal renal tubular acidosis with bicarbonate loss]
Dehydration
Changes in globus pallidus with (pre)term kernicterus.
Mechanisms and pathophysiological significance of eryptosis, the suicidal erythrocyte death.
Neurological complications of kernicterus.
The role of glutathione in yeast dehydration tolerance.
The subfornical organ: biochemical and neuroendocrine comparisons with the hypothalamo-neurohypophysial system.
Therapeutic potential of manipulating suicidal erythrocyte death.
[Effect of dehydration on lipid metabolism]
[The hormonal status and carbohydrate-energy metabolism of rats after the long-term action of low doses of ionizing radiation and heat]
Delirium
Glucose-6-phosphate dehydrogenase deficiency with psychosis.
Dementia
Acute Hemolytic Anemia in Glucose-6-Phosphate Dehydrogenase Deficiency Complicated by Ginkgo biloba.
Glucose-6-phosphate dehydrogenase a novel hope on a blood-based diagnosis of Alzheimer's disease.
Dengue
A novel point mutation in a class IV glucose-6-phosphate dehydrogenase variant (G6PD So Paulo) and polymorphic G6PD variants in So Paulo State, Brazil.
Atypical dengue Fever in a splenectomized boy with glucose-6- phosphodehydrogenase deficiency and thalassemia intermedia.
Dengue Virus Type 2 (DENV2)-Induced Oxidative Responses in Monocytes from Glucose-6-Phosphate Dehydrogenase (G6PD)-Deficient and G6PD Normal Subjects.
Development of a Method to Control the RNA Extraction and Reverse Transcription Steps for the Detection of Dengue Virus Present in Human Blood Samples.
Effect of red blood cell glucose-6-phosphate dehydrogenase deficiency on patients with dengue hemorrhagic fever.
Higher Infection of Dengue Virus Serotype 2 in Human Monocytes of Patients with G6PD Deficiency.
Dermatitis, Allergic Contact
Diet in dermatology: revisited.
Dermatitis, Atopic
Diet in dermatology: revisited.
[Activity of pyruvate kinase and glucose-6-phosphate dehydrogenase in polymorphonuclear granulocytes of patients with atopic dermatitis in the active stage and in remission]
Dermatofibrosarcoma
[Enzyme patterns in connective tissue proliferations (author's transl)]
Diabetes Complications
Increased prevalence of proliferative retinopathy in patients with type 1 diabetes who are deficient in glucose-6-phosphate dehydrogenase.
Molecular chaperones protect against glycation-induced inactivation of glucose-6-phosphate dehydrogenase.
Diabetes Mellitus
Assessment of potential donors for living related liver transplantation.
Association of glucose-6-phosphate dehydrogenase deficiency with diabetes mellitus in ethnic groups of Singapore.
Association of glucose-6-phosphate dehydrogenase deficiency with diabetes mellitus.
Blood glucose normalization-induced haemolysis in three adolescents with type 1 diabetes mellitus at onset and unknown G-6-PD deficiency.
Decreased blood activity of glucose-6-phosphate dehydrogenase associates with increased risk for diabetes mellitus.
Diabetes mellitus and glucose-6-phosphate dehydrogenase deficiency: from one crisis to another.
Effects of G-6-PD deficiency, experimentally induced or genetically transmitted, on the sorbitol pathway activity. In vitro and in vivo studies.
Epidemiology of clinical hyperbilirubinaemia in Al Ain, United Arab Emirates.
Further studies of haemoglobin glycosylation: influence of diabetes mellitus and glucose-6-phosphate dehydrogenase deficiency in Nigerians.
G6PD deficiency and diabetes mellitus in northern Sardinian subjects.
G6PD deficiency: its role in the high prevalence of hypertension and diabetes mellitus.
Genetic disorders in Southern Africa.
Glucose-6-Phosphate Dehydrogenase Activity and Protein Oxidative Modification in Patients with Type 2 Diabetes Mellitus.
Glucose-6-phosphate dehydrogenase deficiency and diabetes mellitus with severe retinal complications in a Sardinian population, Italy.
Glucose-6-phosphate dehydrogenase deficiency and diabetes mellitus.
Glucose-6-Phosphate Dehydrogenase Deficiency Diagnosed in an Adolescent with Type 1 Diabetes Mellitus and Hemoglobin A1c Discordant with Blood Glucose Measurements.
Haemolysis during diabetic ketoacidosis treatment in two girls with incomplete glucose-6-phosphate dehydrogenase deficiency.
Hemolytic crisis in a non-ketotic and euglycemic child with glucose-6-phosphate dehydrogenase deficiency and onset of type 1 diabetes mellitus.
Infants at risk of significant hyperbilirubinemia in poorly-resourced countries: evidence from a scoping review.
Spectrum of genetic disorders and the impact on health care delivery: an introduction.
[Features of disruption of certain components of carbohydrate metabolism in a combination of pulmonary tuberculosis and diabetes mellitus in people with haptoglobin phenotypes]
[Lactate dehydrogenase and glucose-6-phosphate dehydrogenase activity in the erythrocytes in diabetes mellitus]
[On the activity of erythrocyte glucose-6-phosphate dehydrogenase in diabetes mellitus]
[The regulation of glucose-6-phosphate dehydrogenase and glycogen synthase activities by insulin superfamily peptides in myometrium of pregnant women and its impairments under different types of diabetes mellitus]
Diabetes Mellitus, Experimental
Effect of alloxan diabetes and cortisol on glucose-6-phosphate dehydrogenase and transketolase in rabbit liver mitochondria.
The effects of alloxan diabetes, insulin and epinephrine on glucose-6-phosphate dehydrogenase from rat liver and brain.
Tissue distribution of glucose-6-phosphate dehydrogenase isoenzymes and the effect of alloxan diabetes and insulin.
[Activity of hexokinase and glucose-6-phosphate dehydrogenase in hemopoietic cells of the bone marrow in normal rabbits and after hydrocortisone administration during starvation and alloxan diabetes]
[Isoenzymic composition of glucose-6-phosphate dehydrogenase of subcellular fractions of rabbit tissues under alloxan diabetes]
Diabetes Mellitus, Type 1
Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children.
Blood glucose normalization-induced haemolysis in three adolescents with type 1 diabetes mellitus at onset and unknown G-6-PD deficiency.
Does familiarity breed acceptance? The influence of policy on physicians' attitudes toward newborn screening programs.
Glucose-6-Phosphate Dehydrogenase Deficiency Diagnosed in an Adolescent with Type 1 Diabetes Mellitus and Hemoglobin A1c Discordant with Blood Glucose Measurements.
Haemolysis during diabetic ketoacidosis treatment in two girls with incomplete glucose-6-phosphate dehydrogenase deficiency.
Hemolytic crisis in a non-ketotic and euglycemic child with glucose-6-phosphate dehydrogenase deficiency and onset of type 1 diabetes mellitus.
Hypoglycemia-induced hemolysis in glucose-6-phosphate dehydrogenase deficiency.
Increased prevalence of proliferative retinopathy in patients with type 1 diabetes who are deficient in glucose-6-phosphate dehydrogenase.
[The regulation of glucose-6-phosphate dehydrogenase and glycogen synthase activities by insulin superfamily peptides in myometrium of pregnant women and its impairments under different types of diabetes mellitus]
Diabetes Mellitus, Type 2
Association of glucose-6-phosphate dehydrogenase deficiency with diabetes mellitus in ethnic groups of Singapore.
Caveolin-1 upregulation in diabetic fibroblasts and wounded tissues: implication for understanding the underlying mechanisms of non-healing diabetic ulcers.
Diet, diabetes, hypertension and blacks.
G6PD up-regulation promotes pancreatic beta-cell dysfunction.
Glucose-6-Phosphate Dehydrogenase Activity and Protein Oxidative Modification in Patients with Type 2 Diabetes Mellitus.
Glucose-6-phosphate dehydrogenase deficiency and type 2 diabetes.
Glyburide-induced acute haemolysis in a G6PD-deficient patient with NIDDM.
High prevalence of glucose-6-phosphate dehydrogenase deficiency without gene mutation suggests a novel genetic mechanism predisposing to ketosis-prone diabetes.
Hyperglycaemia per se does not affect erythrocyte glucose-6-phosphate dehydrogenase activity in ketosis-prone diabetes.
Real-time monitoring of glucose-6-phosphate dehydrogenase activity using liquid droplet arrays and its application to human plasma samples.
Superoxide Production by NAD(P)H oxidase and Mitochondria is Increased in Genetically Obese and Hyperglycemic Rat Heart and Aorta Prior to Cardiac ...
Synergistic activation of glucose-6-phosphate dehydrogenase and NAD(P)H oxidase by Src kinase elevates superoxide in type 2 diabetic, Zucker fa/fa, rat liver.
Targeting the Pentose Phosphate Pathway in Syndrome X-related Cardiovascular Complications.
[The regulation of glucose-6-phosphate dehydrogenase and glycogen synthase activities by insulin superfamily peptides in myometrium of pregnant women and its impairments under different types of diabetes mellitus]
Diabetes, Gestational
[The regulation of glucose-6-phosphate dehydrogenase and glycogen synthase activities by insulin superfamily peptides in myometrium of pregnant women and its impairments under different types of diabetes mellitus]
Diabetic Ketoacidosis
Diabetic ketoacidosis does not precipitate haemolysis in patients with the Mediterranean variant of glucose-6-phosphate dehydrogenase deficiency.
Diabetic ketoacidosis revealing glucose-6-phosphate dehydrogenase deficiency: description of an adult case.
G-6-PD hemolytic anemia complicating diabetic ketoacidosis.
G6PD deficiency-induced hemolysis in a Chinese diabetic patient: a case report with clinical and molecular analysis.
Haemolysis during diabetic ketoacidosis treatment in two girls with incomplete glucose-6-phosphate dehydrogenase deficiency.
Hypoglycemia-induced hemolysis in glucose-6-phosphate dehydrogenase deficiency.
[Erythrocytic glucose-6-phosphate dehydrogenase deficiency, hemolysis and diabetic ketoacidosis]
Diabetic Nephropathies
Glucose 6-phosphate dehydrogenase and the kidney.
Diabetic Retinopathy
Hyperlipidemia-Mediated Increased Advanced Lipoxidation End Products Formation, an Important Factor Associated with Decreased Erythrocyte Glucose-6-Phosphate Dehydrogenase Activity in Mild Nonproliferative Diabetic Retinopathy.
Increased prevalence of proliferative retinopathy in patients with type 1 diabetes who are deficient in glucose-6-phosphate dehydrogenase.
Disseminated Intravascular Coagulation
Consumption coagulopathy following haemolytic crisis in glucose-6-phosphate dehydrogenase deficient subjects.
Fatal haemolytic crisis with microvascular pulmonary obstruction mimicking a pulmonary embolism in a young African man with glucose-6-phosphate dehydrogenase deficiency.
Down Syndrome
Alpha-1-antitrypsin deficiency in babies with prolonged jaundice.
Congenital disorders of the function of polymorphonuclear neutrophils.
Glucose-6-phosphatedehydrogenase is also increased in erythrocytes from adolescents with Down syndrome.
Leucocyte alkaline phosphatase and erythrocyte glucose-6-phosphate dehydrogenase in Down's Syndrome.
Neonatal jaundice associated with erythrocyte glucose-6-phosphate dehydrogenase deficiency in a non-Mediterranean Caucasian infant with trisomic Down's Syndrome.
Synthesis and concentration of 5-phosphoribosyl-1-pyrophosphate in erythrocytes from patients with Down's syndrome.
The burden of genetic disorders in India and a framework for community control.
[A 12-week physical activity program increases glucose-6-phosphate-dehydrogenase activity in Down syndrome adolescents]
[Cellular enzymes and mongolism. Study on the glucose-6-phosphate dehydrogenase erythrocytes activity]
[Thermal sensitivity of enzymes in trisomy 21 leukocytes]
Drug Eruptions
Diet in dermatology: revisited.
Drug-Related Side Effects and Adverse Reactions
Dapsone therapy for malaria during pregnancy: maternal and fetal outcomes.
Duodenal Ulcer
Glucose-6-phosphate dehydrogenase deficiency and duodenal ulcer.
[Characteristics of the pentose phosphate pathway of carbohydrate metabolism in the gastric mucosa of persons with peptic ulcer]
Dysautonomia, Familial
[Could the understanding of racial differences prevent idiosyncratic anesthetic reactions?]
Dystonia
Anesthetic Management of a Child With Severe Dystonia and G6PD Deficiency for Deep Brain Stimulation.
Ectodermal Dysplasia
Hypohidrotic ectodermal dysplasia associated with glucose-6-phosphate dehydrogenase deficiency.
X-mapping in man: evidence against measurable linkage between anhidrotic ectodermal dysplasia and G6PD deficiency.
Ectodermal Dysplasia 1, Anhidrotic
Hypohidrotic ectodermal dysplasia associated with glucose-6-phosphate dehydrogenase deficiency.
Elliptocytosis, Hereditary
Abnormal haemoglobin, glucose-6-phosphate dehydrogenase deficiency and hereditary ovalocytosis in North Sumatra, Indonesia.
Abnormal hemoglobins, glucose-6-phosphate dehydrogenase deficiency and hereditary ovalocytosis in the Dayaks of Sarawak.
Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.
Glucose-6-phosphate dehydrogenase deficiency and hereditary ovalocytosis in the Ok Tedi impact region of Papua New Guinea.
Hemoglobinopathies, G6PD deficiency, and hereditary elliptocytosis in Bahrain.
Hereditary elliptocytosis (the first report in Thailand) in association with erythrocyte glucose-6-phosphate dehydrogenase deficiency and hemoglobin E.
Red blood cell-derived microparticles: An overview.
Endocarditis
Clonal structure of Streptococcus sanguinis strains isolated from endocarditis cases and the oral cavity.
Endometrial Neoplasms
The effects of medroxyprogesterone acetate on enzyme activities in human endometrial carcinoma.
Endotoxemia
Endotoxemia down-regulates bone marrow lymphopoiesis but stimulates myelopoiesis: the effect of G6PD deficiency.
Endotoxin stimulates the expression of glucose-6-phosphate dehydrogenase in Kupffer and hepatic endothelial cells.
Enterocolitis, Necrotizing
Glucose-6-phosphate dehydrogenase deficiency: another risk factor for necrotizing enterocolitis?
Use of intravenous immunoglobulin in neonates at a tertiary academic hospital: a retrospective 11-year study.
Epilepsy
Acute rhabdomyolysis induced by tonic-clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency.
[Genetic questionnaire. Genetic counseling for a patient with the complex association of G-6-PD deficiency, Gronblad-Strandberg syndrome (pseudo-xanthoma elasticum) and epilepsy]
[Hereditary coproporphyria with grand mal epilepsy, glucose-6-phosphate dehydrogenase deficiency and phenobarbital tolerance]
Epilepsy, Tonic-Clonic
[Hereditary coproporphyria with grand mal epilepsy, glucose-6-phosphate dehydrogenase deficiency and phenobarbital tolerance]
Erythema
Epidermal changes in human skin following irradiation with either UVB or UVA.
Esophageal Neoplasms
Human glucose-6-phosphate dehydrogenase (G6PD) gene transforms NIH 3T3 cells and induces tumors in nude mice.
Fabry Disease
Fabry Disease and G6PD in Three Family Members with Priapism: Is the Nitric Oxide Pathway to Blame?
Reexpression of HPRT activity following cell fusion with polyethylene glycol.
Familial Mediterranean Fever
Jordan: communities and community genetics.
Fanconi Anemia
Superoxide dismutase and other biochemical disorders in a family with Fanconi's anemia.
Fatty Liver
Assessment of potential donors for living related liver transplantation.
Biochemical changes associated with the fatty liver syndrome in cows.
Biochemical changes in liver and blood during liver fattening in rats.
Some lipogenic enzyme activities in rat livers in which an excessive fat accumulation occurred due to feeding low-level amino acid mixture diets.
Favism
A comprehensive study on the major mutations in glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in the coastal provinces of Caspian Sea in the north of Iran.
A deficiency of glucose-6-phosphate dehydrogenase activity in erythrocytes from patients with favism.
Activity of divicine in Plasmodium vinckei-infected mice has implications for treatment of favism and epidemiology of G-6-PD deficiency.
Acute renal failure in favism revealing familial glucose-6-phosphate dehydrogenase deficiency.
Ahaptoglobinemia in Favism patients from Iran.
An unusual syncope cause in the ED: Favism.
Association between ACP(1) genetic polymorphism and favism.
At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria.
Biochemical characterization of a glucose-6-phosphate dehydrogenase variant with favism: G-6-PD Zähringen.
Common G6PD variant from Saudi population and its prevalence.
Discussion on Pharmacogenetic Interaction in G6PD Deficiency and Methods to Identify Potential Hemolytic Drugs.
Distinct phenotypic expression of two de novo missense mutations affecting the dimer interface of glucose-6-phosphate dehydrogenase.
Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anemia.
Family investigations of erythrocyte glucose-6-phosphate dehydrogenase in favism.
Favism in a female newborn infant whose mother ingested fava beans before delivery.
Favism in a Portuguese family due to a deficient glucose-phosphate dehydrogenase variant (Canton) or (cpanton-like) type.
Favism in the African type of glucose-6-phosphate dehydrogenase deficiency (A-).
Favism, the commonest form of severe hemolytic anemia in Palestinian children, varies in severity with three different variants of G6PD deficiency within the same community.
Favism: divicine hemotoxicity in the rat.
Favism: looking for an autosomal gene associated with glucose-6-phosphate dehydrogenase deficiency.
G6PD Aures: a new mutation (48 Ile-->Thr) causing mild G6PD deficiency is associated with favism.
G6PD deficiency and fava bean consumption do not produce hemolysis in Thailand.
G6PD deficiency and favism in the island of Rhodes (Greece).
Gas Chromatography/Mass Spectrometry-Based Metabolomic Profiling Reveals Alterations in Mouse Plasma and Liver in Response to Fava Beans.
Gd(-) Muret and gd(-) Colomiers, two new variants of glucose-6-phosphate dehydrogenase associated with favism.
Glucose 6-phosphate dehydrogenase deficiency enhances germ cell apoptosis and causes defective embryogenesis in Caenorhabditis elegans.
Glucose-6-phosphate dehydrogenase (G6PD) deficiency in southern Italy: a case of G6PD A(-) associated with favism.
Glucose-6-phosphate dehydrogenase activity during cytodifferentiation of the haemopoietic system. Studies on red and white cells in patients with favism.
Glucose-6-phosphate dehydrogenase deficiency in Sicily. Incidence, biochemical characteristics and clinical implications.
Glucose-6-phosphate dehydrogenase variants associated with favism in thai children.
Glucose-6-phosphate dehydrogenase--from oxidative stress to cellular functions and degenerative diseases.
Haemopexin behaviour in an acute hyperhaemolytic crisis secondary to favism (erythrocyte glucose-6-phosphate dehydrogenase deficiency).
Haptoglobin therapy for acute favism: a Japanese boy with glucose-6-phosphate dehydrogenase Guadalajara.
Hemoglobin A1 in subjects with G-6-PD deficiency during and after hemolytic crises due to favism.
Hemolytic crises of favism in Sicilian females heterozygous for G-6-PD deficiency.
Heterogeneity of "Mediterranean type" glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain and description of two new variants associated with favism.
Heterozygote detection in glucose-6-phosphate dehydrogenase deficiency: limitation of hair follicle analysis.
High incidence of glucose-6-phosphate dehydrogenase deficiency in Croatian island isolate: example from Vis island, Croatia.
High-dose vitamin therapy stimulates variant enzymes with decreased coenzyme binding affinity (increased K(m)): relevance to genetic disease and polymorphisms.
Identification of Mediterranean mutation in Egyptian favism patients.
Independent origin of single and double mutations in the human glucose 6-phosphate dehydrogenase gene.
Lactose absorption in patients with glucose 6-phosphate dehydrogenase deficiency with and without favism.
Leucocyte glucose-6-phosphate dehydrogenase (g-6-pd) activity in g-6-pd deficient subjects.
Malaria, favism and glucose-6-phosphate dehydrogenase deficiency.
Marked decline of favism after neonatal glucose-6-phosphate dehydrogenase screening and health education: the northern Sardinian experience.
Mechanism of action of divicine in a cell-free system and in glucose-6-phosphate dehydrogenase-deficient red cells.
Mechanisms of perturbation of erythrocyte calcium homeostasis in favism.
Medical expenses of patients with Favism admitted to 17th Shahrivar Hospital compared to G6PD enzyme screening cost, in north of Iran.
Molecular characterization of glucose-6-phosphate dehydrogenase deficiency in the Kurdish population of Western Iran.
Molecular genetics of glucose-6-phosphate dehydrogenase (G6PD) deficiency in Spain: identification of two new point mutations in the G6PD gene.
Molecular heterogeneity underlying the G6PD Mediterranean phenotype.
Molecular identification of mutations in G6PD gene in patients with favism in Iran.
Neonatal jaundice in Saudi newborns with G6PD Aures.
Oxidative stress and antioxidant defense in Egyptian favism patients.
Perioperative management of the glucose-6-phosphate dehydrogenase deficient patient: a review of literature.
Possible fenugreek induced haemolysis in a patient with previously unknown G6PD deficiency.
Prevalence of Erythrocyte Glucose-6-Phosphate Dehydrogenase (G6PD) Deficiency in the Population of Western Turkey.
Red cell acid phosphatase: another polymorphism correlated with Malaria?
Several mutations including two novel mutations of the glucose-6-phosphate dehydrogenase gene in Polish G6PD deficient subjects with chronic nonspherocytic hemolytic anemia, acute hemolytic anemia, and favism.
Tf, Gc and Cp phenotypes in favism and G-6-PD deficiency.
The erythroenzymopathies. With particular reference to glucose-6-phosphate dehydrogenase deficiency and favism.
The interaction between beta-thalassemia, G-6-PD deficiency, and favism.
The ocular findings in glucose-6-phosphate dehydrogenase deficiency.
The Protective Role of Anise Oil in Oxidative Stress and Genotoxicity Produced in Favism.
Three major glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in Mazandaran state of Iran.
Unsuspected glucose-6-phosphate dehydrogenase deficiency presenting as symptomatic methemoglobinemia with severe hemolysis after fava bean ingestion in a 6-year-old boy.
[A cytochemical study of the enzyme glucose-6-phosphate dehydrogenase in favism]
[A search for glucose-6-phosphate dehydrogenase deficiency, among Toros Seljouck Turks, in both normal and pathological conditions. The explanation of hemolytic anemias seen, in snake bite and poisonous insect bites cases. Three cases of favism and hemolytic syndrome]
[ACTION OF THE STROMA ON ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE IN NORMAL HUMAN SUBJECTS AND SUBJECTS WITH A HISTORY OF FAVISM.]
[Biochemical characterization of a new variant of glucose-6-phosphate dehydrogenase (G-6-PD) deficiency with favism: G-6-PD Bielefeld (author's transl)]
[Broad beans as a cause of acute hemolytic anemia]
[Deficiency of the enzyme glucose-6-phosphate dehydrogenase, favism, malario-resistance and the pathogenesis of certain types of jaundice.]
[Determination of glucose-6-phosphate dehydrogenase (G6PD) in the thrombocytes of children with ictero-hemoglobinuric favism]
[Family studies of erythrocyte glucose-6-phosphate dehydrogenase in favism]
[Favism (study of 8 families)]
[FAVISM AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY. FURTHER OBSERVATIONS IN ANOTHER SPANISH FAMILY.]
[FAVISM AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY. STUDY OF THIS ENZYMATIC DISTURBANCE IN A SPANISH FAMILY.]
[FAVISM IN GLUCOSE-6-PHOSPHATE DEHYDROGENASE INACTIVITY. REPORT ON 3 CASES OBSERVED IN GERMANY.]
[Favism, hemoglobin H, alpha-thalassemia and hemoglobinopathy in various Sardinian families. Studies on glucose-6-phosphate dehydrogenase]
[Favism, hemolytic attacks caused by drugs and grave neonatal jaundice in populations with high incidence of G-6-PD deficiency]
[Favism, hemolytic crises and severe jaundice of the newborn infant in the population with increased G-6-PD deficiency]
[Favism: hemolytic crisis due to glucose-6-phosphate dehydrogenase deficiency in erythrocytes]
[Favism]
[Glucose-6-phosphate dehydrogenase activity in the erythrocytes of children with favism, during and at various intervals after the hemolytic attack]
[Glucose-6-phosphate dehydrogenase deficiency of the Mediterranean type B minus. 1. Favism in childhood]
[GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY. APROPOS OF A CASE OF FAVISM.]
[Hemolytic anemia caused by glucose-6-phosphate dehydrogenase deficiency. Aprpos of 20 cases from 1969 to 1974]
[Hereditary transmission of glucose-6-phosphate dehydrogenase deficiency (G-6-PD) in the granulocytes and erythrocytes of 3 Sardinian families with a history of favism]
[Molecular analysis of glucose-6-dehydrogenase deficiency in Spain]
[New aspects of the biochemical alterations in the erythrocytes of patients with favism; almost complete absence of glucose-6-phosphate dehydrogenase.]
[New contributions on the subject of the bio-enzymology of ictero-hemoglobinuric favism. Note 3. Glucose-6-phosphate dehydrogenase activity of the hepatic parenchyma.]
[Scanning electron microscopic study of the morphological changes induced by acetylsalicylic acid in therapeutic doses in the red blood cells of a patient with a very severe G6PD deficiency and clinical manifestations of favism]
[Study of the relationships between hereditary transmission of the erythrocytic thrombocytic deficiency of glucose-6-phosphate dehydrogenase in Sardinian subjects with favism]
[Variations in enzymatic patterns in G6PD deficiency and favism]
Fetal Diseases
Brain glucose-6-phosphate dehydrogenase protects against endogenous oxidative DNA damage and neurodegeneration in aged mice.
Molecular and biochemical mechanisms in teratogenesis involving reactive oxygen species.
Oxidative damage in chemical teratogenesis.
Fetal Growth Retardation
Altered hepatic gene expression of enzymes involved in energy metabolism in the growth-retarded fetal rat.
Choline supplementation improves the lipid metabolism of intrauterine-growth-restricted pigs.
Intrauterine growth retardation alters mitochondrial gene expression and function in fetal and juvenile rat skeletal muscle.
Intrauterine growth retardation increases the susceptibility of pigs to high-fat diet-induced mitochondrial dysfunction in skeletal muscle.
Fetal Hypoxia
[Antioxidant enzymes activity of erythrocytes and indicators of blood hemodynamics of normal and hypoxic newborns in their first day of life]
Fetal Resorption
An embryoprotective role for glucose-6-phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis.
Fetomaternal Transfusion
Hematologic disorders and nonimmune hydrops fetalis.
Fibroadenoma
Relative value of oestrogen receptor assay, lactoferrin content, and glucose-6-phosphate dehydrogenase activity as prognostic indicators in primary breast cancer.
Semiquantitative cytochemical estimation of glucose-6-phosphate dehydrogenase activity in benign diseases and carcinoma of the breast.
Fibroma
Probable clonal origin of neurofibrosarcoma in a patient with hereditary neurofibromatosis.
[Enzyme patterns in connective tissue proliferations (author's transl)]
Filariasis
[Global health of unaccompanied refugee minors in Gironde (France) between 2011 and 2013].
Fragile X Syndrome
Evolutionary explanations in medical and health profession courses: are you answering your students' "why" questions?
Fragile X syndrome: search for phenotypic manifestations at loci for hypoxanthine phosphoribosyltransferase and glucose-6-phosphate dehydrogenase.
Mental retardation in heterozygotes for the fragile-X mutation: evidence in favor of an X inactivation-dependent effect.
Galactosemias
A Rare Case of Short-Chain Acyl-COA Dehydrogenase Deficiency: The Apparent Rarity of the Disorder Results in Under Diagnosis.
Detection of inborn errors of metabolism in 1,117 patients studied because of suspected inherited disease.
Diet in dermatology: revisited.
False-Positive Newborn Screen Using the Beutler Spot Assay for Galactosemia in Glucose-6-Phosphate Dehydrogenase Deficiency.
Neonatal biochemical screening for disease.
Neonatal screening and monitoring system in Taiwan.
Newborn screening in the Philippines.
Screening for galactosemia and glucose-6-phosphate dehydrogenase deficiency in newborn infants.
Two novel glucose-6-phosphate dehydrogenase variants found in newborn mass-screening for galactosaemia.
[Congenital hypothyroidism missed on newborn screening: report of two cases]
[Hereditary galactosemia in rats: biochemical mechanisms of the disease]
Gallstones
Gall stones, G-6PD deficiency and Wilson's disease.
Gallstones due to hereditary spherocytosis with glucose-6-phosphate dehydrogenase deficiency.
Gardner Syndrome
Multiclonal origin of polyps in Gardner syndrome.
Gastroesophageal Reflux
Is GERD a Factor in Osteonecrosis of the Jaw? Evidence of Pathology Linked to G6PD Deficiency and Sulfomucins.
Gastrointestinal Neoplasms
Antioxidant enzyme levels in cases with gastrointesinal cancer.
Gaucher Disease
Genetic screening for low-penetrance variants in protein-coding genes.
Genetic Diseases, Inborn
Abnormal haemoglobins, thalassaemia and G-6-PD enzyme deficiency in Rajasthan (western-India).
Adverse effects of herbal or dietary supplements in G6PD deficiency: A systematic review.
Amifostine administration during radiotherapy for cancer patients with genetic, autoimmune, metabolic and other diseases.
Anemia in Patients with Coinherited Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency.
Antioxidant vitamins and glucose-6-phosphate dehydrogenase deficiency in full-term neonates.
Cation channels, cell volume and the death of an erythrocyte.
Chemical toxicity of red cells.
Cost-benefit analysis of G6PD screening in Lebanese newborn males.
Different effects of 26-week dietary intake of rapeseed oil and soybean oil on plasma lipid levels, glucose-6-phosphate dehydrogenase activity and cyclooxygenase-2 expression in spontaneously hypertensive rats.
Differentiation of hair growth cycle from scalp hair roots for the diagnosis of glucose-6-phosphate dehydrogenase deficiency in neonates.
Do tribal communities show an inverse relationship between sickle cell disorders and glucose-6-phosphate dehydrogenase deficiency in malaria endemic areas of Central-Eastern India?
Enhanced phagocytosis of ring-parasitized mutant erythrocytes: a common mechanism that may explain protection against falciparum malaria in sickle trait and beta-thalassemia trait.
Epigenetic therapy reprograms hereditary disease.
Evolutionary explanations in medical and health profession courses: are you answering your students' "why" questions?
G6PD deficiency: the genotype-phenotype association.
Genetic diversity of hemoglobinopathies, G6PD deficiency, and ABO and Rhesus blood groups in two isolates of a primitive Kharia Tribe in Sundargarh District of Northwestern Orissa, India.
Glucose-6-phosphate dehydrogenase deficiency--a genetic disorder of red cell metabolism.
Glucose-6-phosphate dehydrogenase deficiency: not exclusively in males.
Hereditary disorders in the Eastern Mediterranean Region.
High prevalence of glucose-6-phosphate dehydrogenase deficiency without gene mutation suggests a novel genetic mechanism predisposing to ketosis-prone diabetes.
Hypohidrotic ectodermal dysplasia associated with glucose-6-phosphate dehydrogenase deficiency.
Insertion/Deletion polymorphisms do play any role in G6PD deficiency individuals in the Kingdom of the Saudi Arabia.
Medications and glucose-6-phosphate dehydrogenase deficiency: an evidence-based review.
Methemoglobinemia in an elderly patient with glucose-6-phosphate dehydrogenase deficiency: a case report.
Molecular basis of haemoglobinopathies and G6PD deficiency in the Comorian population.
Molecular newborn screening of four genetic diseases in Guizhou Province of South China.
Multiplex primer extension reaction screening and oxidative challenge of glucose-6-phosphate dehydrogenase mutants in hemizygous and heterozygous subjects.
Neonatal screening program for G6PD deficiency in India: need and feasibility.
Oxidative stress as a potential causal factor for autoimmune hemolytic anemia and systemic lupus erythematosus.
Oxidative stress, inflammation and carcinogenesis are controlled through the pentose phosphate pathway by transaldolase.
Present status of understanding on the G6PD deficiency and natural selection.
Prevalence and Molecular Characterization of Glucose-6-Phosphate Dehydrogenase Deficiency at the China-Myanmar Border.
Prevalence of G6PD deficiency and Plasmodium falciparum parasites in asymptomatic school children living in southern Ghana.
Prevalence of glucose-6-phosphate dehydrogenase (G6PD) deficiency in southeast Iran: implications for malaria elimination.
Prevalence of glucose-6-phosphate dehydrogenase deficiency and haemoglobin S in high and moderate malaria transmission areas of Muheza, north-eastern Tanzania.
Prevalence of glucose-6-phosphate dehydrogenase deficiency and its association with Plasmodium falciparum infection among children in Iganga distric in Uganda.
Rapid screening for glucose-6-phosphate dehydrogenase deficiency and haemoglobin polymorphisms in Africa by a simple high-throughput SSOP-ELISA method.
Reappraisal of known malaria resistance loci in a large multicenter study.
Red cell genetic disorders and plasma lipids.
Sickle cell haemoglobin, thalassaemia and G-6-PD enzyme deficiency genes in Garasiya tribe inhabited malaria endemic areas of Sirohi District, Rajasthan (India).
Spatial distribution of G6PD deficiency variants across malaria-endemic regions.
Tolerability of tiaprofenic acid in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency.
Two novel glucose 6-phosphate dehydrogenase deficiency mutations and association of such mutations with F8C/G6PD haplotype in Chinese.
Why does the Iranian national program of screening newborns for G6PD enzyme deficiency miss a large number of affected infants?
[PCR-single-strand conformation (SSCP), DNA direct sequencing analysis in detecting mutation in exon 2 of g6pd gene]
[The client's viewpoint on genetic counseling. Acceptability of the service in an Oristanese community (Cabras)]
Gilbert Disease
Bilirubin conjugation, reflected by conjugated bilirubin fractions, in glucose-6-phosphate dehydrogenase-deficient neonates: a determining factor in the pathogenesis of hyperbilirubinemia.
Bilirubin levels in the acute hemolytic crisis of G6PD deficiency are related to Gilbert's syndrome.
Chronic hemolytic anemia associated with glucose 6-phosphate dehydrogenase (Guadalajara)1 159 C --> T (387 Arg --> Cys) deficiency associated with Gilbert syndrome in a Turkish patient.
Differing pathogenesis of perinatal bilirubinemia in glucose-6-phosphate dehydrogenase-deficient versus-normal neonates.
Disease-modifying influences of coexistent G6PD-deficiency, Gilbert syndrome and deletional alpha thalassemia in hereditary spherocytosis: A report of three cases.
Genetic interactions in the pathogenesis of neonatal hyperbilirubinemia: Gilbert's Syndrome and glucose-6-phosphate dehydrogenase deficiency.
Gilbert syndrome and glucose-6-phosphate dehydrogenase deficiency: a dose-dependent genetic interaction crucial to neonatal hyperbilirubinemia.
Gilbert syndrome.
Gilbert's syndrome and jaundice in glucose-6-phosphate dehydrogenase deficient neonates.
Gilbert's syndrome associated with glucose-6-phosphate dehydrogenase deficiency.
Glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome: a gene interaction underlies severe jaundice without severe hemolysis.
Glucose-6-phosphate dehydrogenase deficiency: a hidden risk for kernicterus.
Glucose-6-phosphate dehydrogenase deficiency: a potential source of severe neonatal hyperbilirubinaemia and kernicterus.
Hemolysis and hyperbilirubinemia in an African American neonate heterozygous for glucose-6-phosphate dehydrogenase deficiency.
Hyperbilirubinaemia, glucose-6-phosphate dehydrogenase deficiency and Gilbert syndrome.
Hyperbilirubinemia, glucose-6-phosphate-dehydrogenase deficiency and Gilbert's syndrome.
Preexisting conditions in pediatric ALL patients: Spectrum, frequency and clinical impact.
Severe jaundice in a patient with a previously undescribed glucose-6-phosphate dehydrogenase (G6PD) mutation and Gilbert syndrome.
Study of a family in the province of Matera presenting with glucose-6-phosphate dehydrogenase deficiency and Gilbert's syndrome.
The expression of uridine diphosphate glucuronosyltransferase gene is a major determinant of bilirubin level in heterozygous beta-thalassaemia and in glucose-6-phosphate dehydrogenase deficiency.
The interaction between Gilbert's syndrome and G6PD deficiency influences bilirubin levels.
[Glucose-6-phosphate dehydrogenase deficiency, neonatal hyperbilirubinemia and Gilbert syndrome]
Glioblastoma
Glycolysis and the pentose phosphate pathway are differentially associated with the dichotomous regulation of glioblastoma cell migration versus proliferation.
Glioma
Effect of Naringenin on metabolic markers, lipid profile and expression of GFAP in C6 glioma cells implanted rat's brain.
Enzymes of glucose metabolism in cultured human gliomas: neoplasia is accompanied by altered hexokinase, phosphofructokinase, and glucose-6-phosphate dehydrogenase levels.
Enzymes related to energy metabolism in human gliomas.
Hirsutinolide Series Inhibit Stat3 Activity, Alter GCN1, MAP1B, Hsp105, G6PD, Vimentin, TrxR1, and Importin ?-2 Expression, and Induce Antitumor Effects against Human Glioma.
Histochemical evaluation of energy metabolism in rat glioma.
Protective role of glucose-6-phosphate dehydrogenase activity in the metabolic response of C6 rat glioma cells to polyunsaturated fatty acid exposure.
Regulation of the pentose phosphate pathway in human astrocytes and gliomas.
Glomerulonephritis
Dapsone induced hemolysis in a patient with ANCA associated glomerulonephritis and normal G6PD level and implications for clinical practice: case report and review of the literature.
Dialytic support in acute renal failure.
Haemodialysis for paediatric acute kidney injury in a low resource setting: experience from a tertiary hospital in South West Nigeria.
[Arterial hypertension in glomerulonephritis]
Glucose Intolerance
Glucose-6-phosphate dehydrogenase contributes to the regulation of glucose uptake in skeletal muscle.
High glucose inhibits glucose-6-phosphate dehydrogenase, leading to increased oxidative stress and beta-cell apoptosis.
Inhibition of the oxidative and nonoxidative pentose phosphate pathways by somatostatin: a possible mechanism of antitumor action.
Intracellular metabolism in biopsies from the aorta in patients undergoing coronary bypass surgery.
Pioglitazone versus metformin in two rat models of glucose intolerance and diabetes.
glucose-6-phosphate dehydrogenase (nadp+) deficiency
"COMPLETE" ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.
'Gd(-) Hôtel Dieu': a new G-6PD variant with chronic hemolysis in a Negro patient from Senegal.
(TA)n UDP-glucuronosyltransferase 1A1 promoter polymorphism in Nigerian neonates.
(TA)n UGT 1A1 promoter polymorphism: a crucial factor in the pathophysiology of jaundice in G-6-PD deficient neonates.
1376G-->T mutation of G6PD gene in Han and Li nationalities in Hainan, China.
16alpha-bromoepiandrosterone, an antimalarial analogue of the hormone dehydroepiandrosterone, enhances phagocytosis of ring stage parasitized erythrocytes: a novel mechanism for antimalarial activity.
3'-UTR variations and G6PD deficiency.
59Fe study of red blood cells life span in glucose-6-phosphate dehydrogenase deficiency heterozygote.
6-Phosphogluconate dehydrogenase deficiency in an Italian family.
6-Phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency: possible interaction with glucose-6-phosphate dehydrogenase deficiency.
?-Lipoic acid supplementation up-regulates antioxidant capacity in adults with G6PD deficiency.
A benign sickle-cell disease in a Saudi subject with beta zero-thalassemia and glucose-6-phosphate dehydrogenase deficiency.
A case of black water fever treated with peritoneal dialysis and artemether (quinghaosu derivative).
A case of concomitant autosomal recessive osteopetrosis and G6PD deficiency.
A case of congenital dyserythropoietic anemia in a male Chinese.
A case of immune complex hemolytic anemia, thrombocytopenia, and acute renal failure associated with doxepin use.
A case of kernicterus in New Zealand: a predictable tragedy?
A Case of Mania in a Patient with Systemic Lupus Erythematosus: Can Its Inflammatory Pathogenesis be Applied to Primary Mood Disorders?
A case-control study of primary hepatocellular carcinoma in Taiwan.
A challenge to the concept of selection by malaria in glucose-6-phosphate dehydrogenase deficiency.
A child with xeroderma pigmentosum and G6PD deficiency.
A clinician's view of the mass screening of the newborn for inherited diseases: current practice and future considerations.
A combined system for the study of glutathione metabolism in erythrocytes.
A community-based study of common hereditary blood disorders in Oman.
A comparative study of acute haemolytic anaemia in patients of viral hepatitis in relation to erythrocyte glucose 6-phosphate dehydrogenase deficiency.
A comparative study of standard ERCP catheter and hydrophilic guide wire in the selective cannulation of the common bile duct.
A comparison among quantitative, dye reduction and fluorescent spot tests for G-6-PD deficiency.
A comparison of the two-generation and three-generation methods of estimating linkage values on the X chromosome in man with special reference to the loci determining the Xg blood group and glucose-6-phosphate dehydrogenase deficiency.
A comprehensive analysis of membrane and morphology of erythrocytes from patients with glucose-6-phosphate dehydrogenase deficiency.
A comprehensive study on the major mutations in glucose-6-phosphate dehydrogenase-deficient polymorphic variants identified in the coastal provinces of Caspian Sea in the north of Iran.
A controlled study of polymorphisms in serum globulin and glucose-6-phosphate dehydrogenase deficiency in leprosy.
A correlative study of A B O blood groups, sickle cell haemoglobin and glucose-6-phosphate dehydrogenase deficiency as genetic marker in Mahar community of rural population of Wardha District in Maharashtra.
A difficult diagnosis of lysinuric protein intolerance: association with glucose-6-phosphate dehydrogenase deficiency.
A DUAL HEREDITARY RED BLOOD CELL DEFECT IN ONE FAMILY: HYPOCATALASEMIA AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.
A genetic profile of the South African Ashkenazi Jewish population.
A genetic study among the Lepchas of the Darjeeling area of eastern India.
A glucose 6-phosphate dehydrogenase Gd (-) Castilla variant characterized by mild deficiency associated with drug-induced hemolytic anemia.
A glucose-6-phosphate dehydrogenase (G6PD) splice site consensus sequence mutation associated with G6PD enzyme deficiency.
A glucose-6-phosphate dehydrogenase stain for frozen human skeletal muscle biopsy specimens. A sensitive indicator of fiber degeneration.
A hematological survey of preschool children of the United Arab Emirates.
A hemolysis trigger in glucose-6-phosphate dehydrogenase enzyme deficiency. Vicia sativa (Vetch).
A Japanese neonatal case of glucose-6-phosphate dehydrogenase deficiency presenting as severe jaundice and hemolytic anemia without apparent trigger.
A large, systematic molecular-genetic study of G6PD in Indian populations identifies a new non-synonymous variant and supports recent positive selection.
A model of glucose-6-phosphate dehydrogenase deficiency in the zebrafish.
A new glucose-6-phosphate dehydrogenase deficiency variant, G6PD Mizushima, showing increases in serum ferritin and cytosol leucine aminopeptidase levels.
A new glucose-6-phosphate dehydrogenase variant (G6PD Nagano) associated with congenital hemolytic anemia.
A new glucose-6-phosphate dehydrogenase variant, G6PD Orissa (44 Ala-->Gly), is the major polymorphic variant in tribal populations in India.
A new lease of life for an old enzyme.
A new mutation responsible for severe G6PD deficiency in two ethnic Chinese with different clinical presentations: determination by a direct PCR sequencing technique.
A new simple screening method for glucose 6-phosphate dehydrogenase deficiency.
A new variant of glucose-6-phosphate dehydrogenase deficiency hereditary hemolytic anemia, G6PD Cornell: erythrocyte, leukocyte, and platelet studies.
A note on oseltamivir treatment in a boy with G6PD deficiency.
A Novel A1088T Mutation in the Glucose-6-Phosphate Dehydrogenase Gene Detected by RT-PCR Combined with DNA Sequencing.
A novel C to T substitution at nucleotide 1360 of cDNA which abolishes a natural Hha I site accounts for a new G6PD deficiency gene in Chinese.
A novel cytofluorometric assay for the detection and quantification of glucose-6-phosphate dehydrogenase deficiency.
A Novel de novo Mutation in the G6PD Gene in a Korean Boy with Glucose-6-phosphate Dehydrogenase Deficiency: Case Report.
A novel G473A mutation in the glucose-6-phosphate dehydrogenase gene.
A novel G6PD mutation leading to chronic hemolytic anemia.
A novel GLA mutation in a Fabry family with glucose-6-phosphate dehydrogenase deficiency.
A novel link between G6PD deficiency and hemolysis in patients with continuous-flow left ventricular assist devices.
A novel R198H mutation in the glucose-6-phosphate dehydrogenase gene in the tribal groups of the Nilgiris in Southern India.
A Pale Baby With Blue Blood.
A pediatrician's practical guide to diagnosing and treating hereditary spherocytosis in neonates.
A population survey of the glucose-6-phosphate dehydrogenase (G6PD) 563C>T (Mediterranean) mutation in Afghanistan.
A preliminary survey for glucose-6-phosphate dehydrogenase deficiency and haemoglobin S in Ethiopia.
A prolonged neonatal jaundice associated with a rare G6PD mutation.
A prospective study of the role of bacterial infection and G6PD deficiency in severe neonatal jaundice in Nigeria.
A randomised trial of an eight-week, once weekly primaquine regimen to prevent relapse of plasmodium vivax in Northwest Frontier Province, Pakistan.
A randomized trial of a single-dose rasburicase versus five-daily doses in patients at risk for tumor lysis syndrome.
A randomized, triple-blind, placebo-controlled trial of prophylactic oral phenobarbital to reduce the need for phototherapy in G6PD-deficient neonates.
A rapid screening dye test for the detection of glucose-6-phosphate dehydrogenase deficiency in red cells.
A RE-EVALUATION OF THE RELATIONSHIP BETWEEN GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY AND THE BEHAVIORAL MANIFESTATIONS OF SCHIZOPHRENIA.
A Retrospective Analysis of 7 Human Immunodeficiency Virus-Negative Infants Infected by Penicillium marneffei.
A review of G6PD deficiency in Pakistani perspective.
A review of Orang Asli newborns admitted to a neonatal unit in a Malaysian general hospital.
A Review of Pharmacogenetics of Antimalarials and Associated Clinical Implications.
A sensitive cytochemical staining method for glucose-6-phosphate dehydrogenase activity in individual erythrocytes. II. Further improvements of the staining procedure and some observations with glucose-6-phosphate dehydrogenase deficiency.
A series of new screening procedures for pyruvate kinase deficiency, glucose-6-phosphate dehydrogenase deficiency, and glutathione reductase deficiency.
A simple and rapid dye test for glucose-6-phosphate dehydrogenase deficiency for routine use.
A simple fluorimetric assay for pyridoxamine phosphate oxidase in erythrocyte haemolysates: effects of riboflavin supplementation and of glucose 6-phosphate dehydrogenase deficiency.
A simple laboratory procedure for the recognition of A - (African type) G-6PD deficiency in acute haemolytic crisis.
A SIMPLE MICROMETHOD FOR THE DETECTION OF ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.
A simple screening procedure for adenylate kinase, hexokinase and glucose-6-phosphate dehydrogenase deficiencies.
A simple visual screening test for glucose-6-phosphate dehydrogenase deficiency employing ascorbate and cyanide.
A single dose of Sn-mesoporphyrin prevents development of severe hyperbilirubinemia in glucose-6-phosphate dehydrogenase-deficient newborns.
A single mutation is responsible for the high prevalence of G6PD deficiency in the Vataliya Prajapatis--an endogamous caste group from Western India.
A study of nine polymorphic systems in the population of the Po Delta.
A study of some genetic characteristics of the Fur and Baggara tribes of the Sudan.
A study of subjects with erythrocyte glucose-6-phosphate dehydrogenase deficiency. II. Investigation of leukocyte enzymes.
A study of subjects with erythrocyte glucose-6-phosphate dehydrogenase deficiency: investigation of platelet enzymes.
A survey for erythrocyte glucose-6-phosphate dehydrogenase deficiency in Rumania.
A survey of glucose-6-phosphate dehydrogenase deficiency & sickle-cell trait on a local population of Tirupati.
A survey of glucose-6-phosphate dehydrogenase deficiency and some of its correlates in a Maharashtra village.
A Survey of Practice and Knowledge of Refugee and Migrant Pregnant Mothers Surrounding Neonatal Jaundice on the Thailand-Myanmar Border.
A survey of the incidence of sickle cell trait and glucose-6-phosphate dehydrogenase deficiency in Zambia.
A tetrazolium-linked cytochemical method for estimation of glucose-6-phosphate dehydrogenase activity in individual erythrocytes: applications in the study of heterozygotes for glucose-6-phosphate dehydrogenase deficiency.
ABNORMAL HAEMOGLOBIN AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY IN MALAYAN ABORIGINES.
Abnormal haemoglobin, glucose-6-phosphate dehydrogenase deficiency and hereditary ovalocytosis in North Sumatra, Indonesia.
Abnormal haemoglobin, thalassaemia and G-6-PD deficiency in Libya.
Abnormal hemoglobins, glucose-6-phosphate dehydrogenase deficiency and hereditary ovalocytosis in the Dayaks of Sarawak.
Abnormal hemoglobins, thalasemia trait & G6PD deficiency in young Pakistani males.
ABNORMAL ORAL GLUCOSE TOLERANCE RESPONSE IN ERYTHROCYTE GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY.
ABO incompatibility and glucose-6-phosphate dehydrogenase deficiency presenting as Hydrops Foetalis.
Absence of parvovirus and cytomegalovirus in red-cell aplastic crises in glucose-6-phosphate dehydrogenase deficiency.
Acalypha indica induced haemolysis in G6PD deficiency.
Access to orphan drugs in the Middle East: Challenge and perspective.
Acetamonophen and G-6-PD deficiency.
Active transport of nitrofurantoin into human milk.
Activity of divicine in Plasmodium vinckei-infected mice has implications for treatment of favism and epidemiology of G-6-PD deficiency.
Activity of glucose-6-phosphate dehydrogenase among Indians living in a malarial region of Mato Grosso and its implication to the Indian-mixed populations in Brazil.
Acute episodic hemolysis in the African black rhinoceros as an analogue of human glucose-6-phosphate dehydrogenase deficiency.
Acute haemolysis induced by high dose ascorbic acid in glucose-6-phosphate dehydrogenase deficiency.
Acute haemolysis with Ambilhar treatment in glucose-6-phosphate dehydrogenase deficiency.
Acute haemolytic anaemia and myolysis due to G6PD deficiency.
Acute haemolytic crisis in a Thai patient with homozygous haemoglobin Constant Spring (Hb CS/CS): a case report.
Acute hemolysis in a patient with a newly diagnosed glioblastoma.
Acute hemolytic anemia complicating viral hepatitis in patients with glucose-6-phosphate dehydrogenase deficiency.
Acute Hemolytic Anemia in Glucose-6-Phosphate Dehydrogenase Deficiency Complicated by Ginkgo biloba.
Acute hemolytic anemia induced by a pyrazolonic drug in a child with glucose-6-phosphate dehydrogenase deficiency.
Acute hemolytic anemia precipitated by myocardial infarction and pericardial tamponade in G6PD deficiency.
Acute intravascular haemolysis in glucose-6-phosphate dehydrogenase deficiency.
Acute intravascular haemolysis in Vanuatu following a single dose of primaquine in individuals with glucose-6-phosphate dehydrogenase deficiency.
Acute massive haemolysis in children with glucose-6-phosphate dehydrogenase deficiency.
Acute renal failure following analgesic overdose in G6PD deficiency.
Acute renal failure in favism revealing familial glucose-6-phosphate dehydrogenase deficiency.
Acute renal failure in north Indian children.
Acute renal failure in tropical Africa.
Acute reversible renal failure and Stevens-Johnson syndrome in a patient having glucose-6-phosphate dehydrogenase deficiency.
Acute rhabdomyolysis induced by tonic-clonic epileptic seizures in a patient with glucose-6-phosphate dehydrogenase deficiency.
Acute viral hepatitis E presenting with haemolytic anaemia and acute renal failure in a patient with glucose-6-phosphate dehydrogenase deficiency.
Acute viral hepatitis with severe hyperbilirubinemia and massive hemolysis in glucose-6-phosphate dehydrogenase deficiency.
Acute viral hepatitis, glucose-6-phosphate dehydrogenase deficiency and prolonged acute renal failure: a case report.
Aczone, a topical gel formulation of the antibacterial, anti-inflammatory dapsone for the treatment of acne.
Addressing the burden of neonatal hyperbilirubinaemia in countries with significant glucose-6-phosphate dehydrogenase deficiency.
Adenosine monophosphate deaminase 3 activation shortens erythrocyte half-life and provides malaria resistance in mice.
Adequacy and pitfalls of G6PD deficiency counseling in Hong Kong.
Adult-onset Still's disease associated with G6PD deficiency: a case report and literature review.
Advanced glycation end products inhibit glucose-6-phosphate dehydrogenase activity and expression in human umbilical vein endothelial cells.
Adverse effects of herbal or dietary supplements in G6PD deficiency: A systematic review.
African glucose-6-phosphate dehydrogenase alleles associated with protection from severe malaria in heterozygous females in Tanzania.
Agar in control of hyperbilirubinemia of full-term newborn infants with erythrocyte G-6-PD deficiency.
Agriculture-related anaemias.
Alcoholic liver disease in black men with G6PD deficiency.
Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility.
Alpha-1-antitrypsin deficiency in babies with prolonged jaundice.
alpha-Thalassaemia and hyperbilirubinaemia in G-6-PD-deficient newborns.
Alpha-thalassemia in Papua New Guinea.
Alpha-thalassemia minor and neonatal hyperbilirubinemia.
Alternative DNA-based newborn screening for glucose-6-phosphate dehydrogenase deficiency.
Amino acid conservation and clinical severity of human glucose-6-phosphate dehydrogenase mutations.
Amoxycillin in treatment of typhoid fever in patients with haematological contraindications to chloramphenicol.
An anthropological perspective on the epidemiology of hemoglobin defects and glucose-6-phosphate dehydrogenase deficiencies in the northern half of the African continent.
An Ashkenazi Jewish woman presenting with favism.
An embryoprotective role for glucose-6-phosphate dehydrogenase in developmental oxidative stress and chemical teratogenesis.
An epidemiological study of G-6-PD deficiency, sickle cell haemoglobin, and ABO blood groups in relation to malaria incidence in Muslim and Christian communities of Kheda, Gujarat, (India).
An etiologic study of hemoglobinuria and blackwater fever in the Kivu Mountains, Zaire.
An evaluation of screening procedures for red cell glucose-6-phosphate dehydrogenase deficiency in the newborn infant.
An evaluation of the dorset sheep as a predictive animal model for the response of G-6-PD deficient human erythrocytes to a proposed systemic toxic ozone intermediate, methyl oleate hydroperoxide.
An evaluation of the dorset sheep as a predictive animal model for the response of glucose-6-phosphate dehydrogenase-deficient human erythrocytes to a proposed systemic toxic ozone intermediate, methyl oleate ozonide.
An examination of the role of vitamin E in glucose-6-phosphate dehydrogenase deficiency.
An improved, simple screening method for detection of glucose-6-phosphate dehydrogenase deficiency.
An In vivo Drug Screening Model Using Glucose-6-Phosphate Dehydrogenase Deficient Mice to Predict the Hemolytic Toxicity of 8-Aminoquinolines.
An intriguing case of Prurigo pigmentosa in a Sicilian young patient.
An investigation into the riboflavin status of young Egyptians from the oasis with glucose-6-phosphate dehydrogenase deficiency.
An optimised age-based dosing regimen for single low-dose primaquine for blocking malaria transmission in Cambodia.
An optimised system for refolding of human glucose 6-phosphate dehydrogenase.
An unusual distribution of glucose-6-phosphate dehydrogenase deficiency of south Indian newborn population.
An unusual syncope cause in the ED: Favism.
An update on the prevalence of glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice in Tehran neonates.
Anaemia, a common but often unrecognized risk in diabetic patients: A review.
Anaemic crisis in sickle cell disease.
Anaesthesia and glucose-6-phosphate dehydrogenase deficiency. A case report and review of the literature.
Anaesthetic management in a child with an atypical triad for reconstructive scoliosis surgery.
Anaesthetic management in patients with glucose-6-phosphate dehydrogenase deficiency undergoing neurosurgical procedures.
Analysis of common mutations and associated haplotypes in Chinese patients with glucose-6-phosphate dehydrogenase deficiency.
Analysis of G6PD enzyme deficiency in Saudi population.
Analysis of malaria associated genetic traits in Cabo Verde, a melting pot of European and sub Saharan settlers.
Anemia and the liver. Hepatobiliary manifestations of anemia.
Anemia during actue infections. Role of glucose-6-phosphate dehydrogenase deficiency in Negroes.
Anemia in adolescence. 2. Hemoglobinopathies and other causes.
Anemia in newborn.
Anemia in Patients with Coinherited Thalassemia and Glucose-6-Phosphate Dehydrogenase Deficiency.
Anemia in pregnancy.
Anemia, cataracts, and seizures in patient with glucose-6-phosphate dehydrogenase deficiency.
Anesthesia and glucose-6-phosphate dehydrogenase deficiency in a child with congenital heart disease.
Anesthetic Management of a Child With Severe Dystonia and G6PD Deficiency for Deep Brain Stimulation.
Angiographic preoperative bowel segment localization using methylene blue, isosulfan blue, and fluorescein.
Aniline-induced methaemoglobinaemia in a glucose-6-phosphate dehydrogenase enzyme deficient patient.
Antimalarial NADPH-Consuming Redox-Cyclers as Superior G6PD Deficiency Copycats.
Antimalarial red cells.
Antioxidant enzymatic systems and oxidative stress in erythrocytes with G6PD deficiency: effect of deferoxamine.
Antioxidant vitamins and glucose-6-phosphate dehydrogenase deficiency in full-term neonates.
Antiplatelet and invasive treatment in patients with glucose-6-phosphate dehydrogenase (G6PD) deficiency and acute coronary syndrome. The safety of aspirin.
Aortic valve replacement for a patient with glucose-6-phosphate dehydrogenase deficiency and autoimmune hemolytic anemia.
Apert syndrome with glucose-6-phosphate dehydrogenase deficiency: a case report.
Apparent hemolysis in an AIDS patient receiving trimethoprim/sulfamethoxazole: case report and literature review.
Ascorbic-acid-induced haemolysis in G-6-PD deficiency.
Aseptic meningitis, hemolytic anemia, hepatitis, and orthostatic hypotension in a patient treated with trimethoprim-sulfamethoxazole.
Aspects of sickle cell gene in Saudi Arabia--interaction with glucose-6-phosphate dehydrogenase deficiency.
ASPECTS OF THE POPULATION DYNAMICS OF THE ABNORMAL HEMOGLOBIN AND GLUCOSE-6-PHOSPHATE DEHYDROGENASE DEFICIENCY GENES.
Aspects of tropical paediatrics.
Aspirin and glucose-6-phosphate dehydrogenase deficiency.
Aspirin-induced acute haemolytic anaemia in glucose-6-phosphate dehydrogenase-deficient children with systemic arthritis.
Assessment of erythrocyte deformability with the laser-assisted optical rotational cell analyzer (LORCA).
Assessment of G6PD screening program in premature infants in a NICU.
Assessment of Point-of-Care Diagnostics for G6PD Deficiency in Malaria Endemic Rural Eastern Indonesia.
Assessment of potential donors for living related liver transplantation.
Assessment of the humoral and cell-mediated immunity against the Plasmodium falciparum vaccine candidates circumsporozoite protein and SPf66 in adults living in highly endemic malarious areas of Papua New Guinea.
Assessment of the relative success of sporozoite inoculations in individuals exposed to moderate seasonal transmission.
Association between ACP(1) genetic polymorphism and favism.
Association Between G6PD Deficiency and Hyperbilirubinemia in Neonates: A Meta-Analysis.
Association between glucose-6-phosphate dehydrogenase deficiency and neonatal jaundice: interaction with multiple risk factors.
Association of G6PD with lower haemoglobin concentration but not increased haemolysis in patients with sickle cell anaemia.
Association of glucose-6-phosphate dehydrogenase deficiency and X-linked chronic granulomatous disease in a child with anemia and recurrent infections.
Association of glucose-6-phosphate dehydrogenase deficiency with diabetes mellitus in ethnic groups of Singapore.
Association of glucose-6-phosphate dehydrogenase deficiency with diabetes mellitus.
Association of homozygous sickle cell anemia and glucose-6-phosphate dehydrogenase deficiency.
Association of naphthalene with acute hemolytic anemia.
Association of red cell glucose-6-phosphate dehydrogenase with haemoglobinopathies.
At least five polymorphic mutants account for the prevalence of glucose-6-phosphate dehydrogenase deficiency in Algeria.
Attempts to predict the hemolytic potential of drugs in glucose-6-phosphate dehydrogenase deficiency of the Mediterranean type by an in vitro test.
Attitudes and beliefs of pediatricians and genetic counselors regarding testing and screening for CF and G6PD: implications for policy.
Attitudes of genetic counselors towards expanding newborn screening and offering predictive genetic testing to children.