hypoxanthine has been researched along with Amylo-1,6-Glucosidase Deficiency in 2 studies
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (50.00) | 18.7374 |
| 1990's | 1 (50.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Azumi, T; Hisatome, I; Kinugawa, T; Kitamura, H; Kotake, H; Mashiba, H; Miyakoda, H; Ohno, K; Saito, M; Takeda, A | 1 |
| Hara, N; Kawachi, M; Kiyokawa, H; Kono, N; Mineo, I; Shimizu, T; Tarui, S; Wang, YL; Yamada, Y | 1 |
2 other study(ies) available for hypoxanthine and Amylo-1,6-Glucosidase Deficiency
| Article | Year |
|---|---|
Excess release of hypoxanthine from exercising muscle in two gout patients with partial HGPRTase deficiency: lack of ammonium release.
Topics: Adult; Ammonia; Child; Exercise Test; Glycogen Storage Disease Type III; Gout; Humans; Hypoxanthine; Hypoxanthine Phosphoribosyltransferase; Hypoxanthines; Male; Muscles | 1991 |
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 Disease Type V; Glycogen Storage Disease Type VII; Humans; Hypoxanthine; Hypoxanthines; Inosine; Male; Middle Aged; Muscles; Physical Exertion; Rest; Uric Acid | 1987 |