ammonium hydroxide has been researched along with Fabry Disease in 2 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Fabry Disease: An X-linked inherited metabolic disease caused by a deficiency of lysosomal ALPHA-GALACTOSIDASE A. It is characterized by intralysosomal accumulation of globotriaosylceramide and other GLYCOSPHINGOLIPIDS in blood vessels throughout the body leading to multi-system complications including renal, cardiac, cerebrovascular, and skin disorders.
| 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 |
|---|---|
| Gardner, LI | 1 |
| Menkes, JH | 1 |
1 review available for ammonium hydroxide and Fabry Disease
| Article | Year |
|---|---|
Genetically expressed abnormalities in the fetus.
Topics: Adrenal Insufficiency; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Ammonia; Anemia, S | 1974 |
1 other study available for ammonium hydroxide and Fabry Disease
| Article | Year |
|---|---|
Biochemical approaches to the nosology of nervous system defects, III.
Topics: Ammonia; Biopsy; Brain; Brain Chemistry; Brain Diseases; Cells, Cultured; Chromatography; Fabry Dise | 1971 |