purine has been researched along with Glycogen Storage Disease in 2 studies
1H-purine : The 1H-tautomer of purine.
3H-purine : The 3H-tautomer of purine.
9H-purine : The 9H-tautomer of purine.
7H-purine : The 7H-tautomer of purine.
Glycogen Storage Disease: A group of inherited metabolic disorders involving the enzymes responsible for the synthesis and degradation of glycogen. In some patients, prominent liver involvement is presented. In others, more generalized storage of glycogen occurs, sometimes with prominent cardiac involvement.
| 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 |
|---|---|
| HOWELL, RR | 1 |
| ASHTON, DM | 1 |
| WYNGAARDEN, JB | 1 |
| Yamasaki, T | 1 |
| Hamaguchi, T | 1 |
| Nakajima, H | 1 |
| Matsuzawa, Y | 1 |
1 review available for purine and Glycogen Storage Disease
| Article | Year |
|---|---|
[Myogenic hyperuricemia].
Topics: Adenosine Monophosphate; Adenosine Triphosphate; Energy Metabolism; Glycogen Storage Disease; Humans | 1996 |
1 other study available for purine and Glycogen Storage Disease
| Article | Year |
|---|---|
Glucose-6-phosphatase deficiency glycogen storage disease. Studies on the interrelationships of carbohydrate, lipid, and purine abnormalities.
Topics: Carbohydrates; Child; Glycogen Storage Disease; Glycogen Storage Disease Type I; Humans; Infant; Lip | 1962 |