ammonium hydroxide has been researched along with Glycogen Storage Disease Type I in 2 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Glycogen Storage Disease Type I: An autosomal recessive disease in which gene expression of glucose-6-phosphatase is absent, resulting in hypoglycemia due to lack of glucose production. Accumulation of glycogen in liver and kidney leads to organomegaly, particularly massive hepatomegaly. Increased concentrations of lactic acid and hyperlipidemia appear in the plasma. Clinical gout often appears in early childhood.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Eleven patients had Reye's syndrome, three had acute "toxic" encephalopathy (without fatty liver), two had glycogen storage disease type 1, and one had congenital hyperammonemia type 2." | 1.26 | Tissue lipids in hyperammonemic encephalopathies of childhood. ( Chaves-Carballo, E; Ellefson, RD, 1980) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (100.00) | 18.7374 |
| 1990's | 0 (0.00) | 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 |
|---|---|
| Chaves-Carballo, E | 1 |
| Ellefson, RD | 1 |
| Esato, K | 1 |
| Yasutake, S | 1 |
| Kaku, R | 1 |
| Yamaki, R | 1 |
2 other studies available for ammonium hydroxide and Glycogen Storage Disease Type I
| Article | Year |
|---|---|
Tissue lipids in hyperammonemic encephalopathies of childhood.
Topics: Adipose Tissue; Adolescent; Ammonia; Brain; Brain Diseases, Metabolic; Child; Child, Preschool; Chol | 1980 |
End-to-side anastomosis of the mesenteric vein to the inferior vena cava in the treatment of glycogen storage disease: case report.
Topics: Ammonia; Blood Glucose; Child, Preschool; Cholesterol; Glucose-6-Phosphatase; Glycogen Storage Disea | 1977 |