EC Number |
Disease |
PubMed ID |
Title of Publication |
Category |
Confidence Level |
---|
3.2.1.106 | Glycogen Storage Disease |
4245 |
Physico-chemical and immunological properties of acid alpha-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease). |
ongoing research therapeutic application unassigned |
3 1 0 |
3.2.1.106 | Glycogen Storage Disease Type II |
4245 |
Physico-chemical and immunological properties of acid alpha-glucosidase from various human tissues in relation to glycogenosis type II (Pompe's disease). |
ongoing research therapeutic application unassigned |
3 1 0 |
3.2.1.106 | Glycogen Storage Disease Type II |
34626 |
Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts. |
causal interaction diagnostic usage ongoing research therapeutic application |
3 4 4 2 |
3.2.1.106 | mannosyl-oligosaccharide glucosidase deficiency |
34626 |
Characterization of the molecular defect in infantile and adult acid alpha-glucosidase deficiency fibroblasts. |
causal interaction diagnostic usage ongoing research therapeutic application |
3 4 4 2 |
3.2.1.106 | Glycogen Storage Disease Type II |
36157 |
Use of immobilized antibodies in investigating acid alpha-glucosidase in urine in relation to Pompe's disease. |
diagnostic usage unassigned |
3 0 |
3.2.1.106 | Glycogen Storage Disease Type II |
60470 |
Acid maltase deficiency in non-identical adult twins. A morphological and biochemical study. |
ongoing research unassigned |
2 0 |
3.2.1.106 | mannosyl-oligosaccharide glucosidase deficiency |
60470 |
Acid maltase deficiency in non-identical adult twins. A morphological and biochemical study. |
ongoing research unassigned |
2 0 |
3.2.1.106 | Glycogen Storage Disease |
350041 |
Biochemical, immunological, and cell genetic studies in glycogenosis type II. |
diagnostic usage ongoing research unassigned |
1 4 0 |
3.2.1.106 | Glycogen Storage Disease Type II |
350041 |
Biochemical, immunological, and cell genetic studies in glycogenosis type II. |
diagnostic usage ongoing research unassigned |
1 4 0 |
3.2.1.106 | Glycogen Storage Disease Type II |
352582 |
Pompe's disease: diagnosis in kidney and leucocytes using 4-methylumbelliferyl-alpha-D-glucopyranoside. |
diagnostic usage unassigned |
4 0 |