ammonium hydroxide has been researched along with Amylo-1,6-Glucosidase Deficiency in 3 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 2 (66.67) | 18.7374 |
1990's | 1 (33.33) | 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 |
---|---|
Gutton, P | 1 |
Hisatome, I | 1 |
Kitamura, H | 1 |
Saito, M | 1 |
Kinugawa, T | 1 |
Miyakoda, H | 1 |
Kotake, H | 1 |
Mashiba, H | 1 |
Azumi, T | 1 |
Ohno, K | 1 |
Takeda, A | 1 |
Mineo, I | 1 |
Kono, N | 1 |
Hara, N | 1 |
Shimizu, T | 1 |
Yamada, Y | 1 |
Kawachi, M | 1 |
Kiyokawa, H | 1 |
Wang, YL | 1 |
Tarui, S | 1 |
3 other studies available for ammonium hydroxide and Amylo-1,6-Glucosidase Deficiency
Article | Year |
---|---|
[Reflections apropos of observations of children with hereditary metabolic diseases].
Topics: Adolescent; Ammonia; Child; Child Development; Child, Preschool; Female; Fructose Intolerance; Glyco | 1978 |
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; | 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 Diseas | 1987 |