ammonium hydroxide has been researched along with Mucopolysaccharidoses in 3 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Mucopolysaccharidoses: Group of lysosomal storage diseases each caused by an inherited deficiency of an enzyme involved in the degradation of glycosaminoglycans (mucopolysaccharides). The diseases are progressive and often display a wide spectrum of clinical severity within one enzyme deficiency.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 3 (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 |
| O'Reilly, S | 1 |
| D'iachkova, AIa | 1 |
| Lebedev, BV | 1 |
2 reviews available for ammonium hydroxide and Mucopolysaccharidoses
| Article | Year |
|---|---|
Genetically expressed abnormalities in the fetus.
Topics: Adrenal Insufficiency; Amino Acid Metabolism, Inborn Errors; Amino Acids, Sulfur; Ammonia; Anemia, S | 1974 |
[Mental retardation and hereditary enzymopathy (review)].
Topics: Ammonia; Carboxy-Lyases; Child; Child, Preschool; Eye Diseases; Galactosemias; Growth Disorders; Har | 1971 |
1 other study available for ammonium hydroxide and Mucopolysaccharidoses
| Article | Year |
|---|---|
Neurologic disorders and liver disease.
Topics: Adipose Tissue; Ammonia; Brain Diseases; Citrulline; Fatty Liver; Galactosemias; Hepatic Encephalopa | 1971 |