ammonium hydroxide has been researched along with Glycogen Storage Disease Type VII in 5 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
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.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Patients with muscle phosphofructokinase deficiency are unable to achieve a spontaneous second wind under conditions that consistently produce one in patients with McArdle's disease." | 2.71 | No spontaneous second wind in muscle phosphofructokinase deficiency. ( Haller, RG; Vissing, J, 2004) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (60.00) | 18.7374 |
| 1990's | 1 (20.00) | 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 |
|---|---|
| Haller, RG | 1 |
| Vissing, J | 1 |
| Ono, A | 1 |
| Kuwajima, M | 1 |
| Kono, N | 4 |
| Mineo, I | 4 |
| Nakagawa, C | 1 |
| Tarui, S | 4 |
| Matsuzawa, Y | 1 |
| Shimizu, T | 3 |
| Kiyokawa, H | 2 |
| Yamada, Y | 3 |
| Hara, N | 3 |
| Kawachi, M | 2 |
| Nakajima, H | 1 |
| Wang, YL | 2 |
| Sumi, S | 1 |
| Nonaka, K | 1 |
2 trials available for ammonium hydroxide and Glycogen Storage Disease Type VII
| Article | Year |
|---|---|
No spontaneous second wind in muscle phosphofructokinase deficiency.
Topics: Adolescent; Adult; Ammonia; Child; Exercise Test; Fasting; Female; Glycogen Storage Disease Type V; | 2004 |
Glucose infusion paradoxically accelerates degradation of adenine nucleotide in working muscle of patients with glycogen storage disease type VII.
Topics: Adenine Nucleotides; Adult; Ammonia; Blood Glucose; Exercise Test; Fatty Acids, Nonesterified; Femal | 1995 |
3 other studies available for ammonium hydroxide and Glycogen Storage Disease Type VII
| Article | Year |
|---|---|
Erythrocyte glycolysis and its marked alterations by muscular exercise in type VII glycogenosis.
Topics: 2,3-Diphosphoglycerate; Adenine Nucleotides; Adenosine Monophosphate; Adenosine Triphosphate; Adoles | 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 |