uric acid has been researched along with Glycogen Storage Disease Type VII in 5 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.
Glycogen Storage Disease Type VII: An autosomal recessive glycogen storage disease in which there is deficient expression of 6-phosphofructose 1-kinase in muscle (PHOSPHOFRUCTOKINASE-1, MUSCLE TYPE) resulting in abnormal deposition of glycogen in muscle tissue. These patients have severe congenital muscular dystrophy and are exercise intolerant.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (80.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 1 (20.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Yamasaki, T | 1 |
| Mineo, I | 5 |
| Hara, N | 3 |
| Kono, N | 4 |
| Kiyokawa, H | 2 |
| Kawachi, M | 2 |
| Yamada, Y | 3 |
| Nakajima, H | 2 |
| Shimizu, T | 3 |
| Kuwajima, M | 1 |
| Wang, YL | 2 |
| Tarui, S | 3 |
| Sumi, S | 1 |
| Nonaka, K | 1 |
1 review available for uric acid and Glycogen Storage Disease Type VII
| 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 |
4 other studies available for uric acid and Glycogen Storage Disease Type VII
| Article | Year |
|---|---|
Myogenic hyperuricemia: a comparative study between type V and type VII glycogenosis.
Topics: Adolescent; Adult; Exercise; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Glyc | 1989 |
[Glycogenosis (molecular mechanism of muscle glycogenosis)].
Topics: Adenosine Triphosphate; Amino Acid Sequence; Glycogen; Glycogen Storage Disease; Glycogen Storage Di | 1988 |
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 |
Excess purine degradation in exercising muscles of patients with glycogen storage disease types V and VII.
Topics: Adult; Ammonia; Female; Glycogen Storage Disease; Glycogen Storage Disease Type V; Glycogen Storage | 1985 |