EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
1.3.5.1 | Abortion, Habitual |
26944226 |
Infertility and recurrent miscarriage with complex II deficiency-dependent mitochondrial oxidative stress in animal models. |
causal interaction ongoing research unassigned |
1 1 0 |
1.3.5.1 | Achlorhydria |
7075932 |
Gastric acid secretion, serum gastrin and parietal cell histology in hyperthyroidism. |
diagnostic usage ongoing research unassigned |
2 4 0 |
1.3.5.1 | Acidosis |
6713488 |
A morphological, enzyme-cytochemical, and physiological study of the blood-gonad barrier in the hermaphroditic snail Lymnaea stagnalis. |
ongoing research unassigned |
2 0 |
1.3.5.1 | Acidosis |
10672232 |
The use of transgenic and mutant mice to study oxygen free radical metabolism. |
causal interaction diagnostic usage unassigned |
1 3 0 |
1.3.5.1 | Acidosis, Lactic |
1892363 |
Strongly succinate dehydrogenase-reactive blood vessels in muscles from patients with mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke-like episodes. |
diagnostic usage ongoing research unassigned |
2 2 0 |
1.3.5.1 | Acidosis, Lactic |
7616539 |
Hereditary myopathy with lactic acidosis, succinate dehydrogenase and aconitase deficiency in northern Sweden: a genealogical study. |
ongoing research therapeutic application unassigned |
1 1 0 |
1.3.5.1 | Acidosis, Lactic |
9062896 |
Expression of oxidative phosphorylation genes in muscle cell cultures from patients with mitochondrial myopathies. |
diagnostic usage ongoing research unassigned |
3 3 0 |
1.3.5.1 | Acidosis, Lactic |
14707514 |
Respiratory complex II defect in siblings associated with a symptomatic secondary block in fatty acid oxidation. |
causal interaction diagnostic usage unassigned |
1 1 0 |
1.3.5.1 | Acidosis, Lactic |
16091512 |
Predominant cerebellar volume loss as a neuroradiologic feature of pediatric respiratory chain defects. |
causal interaction diagnostic usage unassigned |
4 2 0 |
1.3.5.1 | Acidosis, Lactic |
25477904 |
Cavitating leukoencephalopathy with multiple mitochondrial dysfunction syndrome and NFU1 mutations. |
causal interaction unassigned |
4 0 |