uric acid has been researched along with Amylo-1,6-Glucosidase Deficiency in 3 studies
Uric Acid: An oxidation product, via XANTHINE OXIDASE, of oxypurines such as XANTHINE and HYPOXANTHINE. It is the final oxidation product of purine catabolism in humans and primates, whereas in most other mammals URATE OXIDASE further oxidizes it to ALLANTOIN.
uric acid : An oxopurine that is the final oxidation product of purine metabolism.
6-hydroxy-1H-purine-2,8(7H,9H)-dione : A tautomer of uric acid having oxo groups at C-2 and C-8 and a hydroxy group at C-6.
7,9-dihydro-1H-purine-2,6,8(3H)-trione : An oxopurine in which the purine ring is substituted by oxo groups at positions 2, 6, and 8.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (66.67) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (33.33) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yamasaki, T | 1 |
| Mineo, I | 2 |
| Greene, HL | 1 |
| Kono, N | 1 |
| Hara, N | 1 |
| Shimizu, T | 1 |
| Yamada, Y | 1 |
| Kawachi, M | 1 |
| Kiyokawa, H | 1 |
| Wang, YL | 1 |
| Tarui, S | 1 |
2 reviews available for uric acid and Amylo-1,6-Glucosidase Deficiency
| Article | Year |
|---|---|
[Secondary hyperuricemia in glycogen storage disease types I, III, V and VII].
Topics: Glycogen Storage Disease Type I; Glycogen Storage Disease Type III; Glycogen Storage Disease Type V; | 2003 |
Glycogen storage disease.
Topics: Blood Glucose; Glucosephosphate Dehydrogenase Deficiency; Glycogen; Glycogen Storage Disease; Glycog | 1982 |
1 other study available for uric acid and Amylo-1,6-Glucosidase Deficiency
| Article | Year |
|---|---|
Myogenic hyperuricemia. A common pathophysiologic feature of glycogenosis types III, V, and VII.
Topics: Adult; Ammonia; Glycogen Storage Disease; Glycogen Storage Disease Type III; Glycogen Storage Diseas | 1987 |