ammonium hydroxide has been researched along with Genetic Diseases, Inborn in 3 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Genetic Diseases, Inborn: Diseases that are caused by genetic mutations present during embryo or fetal development, although they may be observed later in life. The mutations may be inherited from a parent's genome or they may be acquired in utero.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (33.33) | 18.7374 |
| 1990's | 2 (66.67) | 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 |
|---|---|
| Nicolaides, K | 1 |
| Rodeck, CH | 1 |
| Morizono, H | 1 |
| Tuchman, M | 1 |
| Rajagopal, BS | 1 |
| McCann, MT | 1 |
| Listrom, CD | 1 |
| Yuan, X | 1 |
| Venugopal, D | 1 |
| Barany, G | 1 |
| Allewell, NM | 1 |
| Rosenberg, LE | 1 |
1 review available for ammonium hydroxide and Genetic Diseases, Inborn
| Article | Year |
|---|---|
Treating genetic diseases: lessons from three children.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Child; Genetic Diseases, Inborn; Genetic Therapy; Hum | 1990 |
2 other studies available for ammonium hydroxide and Genetic Diseases, Inborn
| Article | Year |
|---|---|
Prenatal diagnosis. Fetoscopy.
Topics: Amino Acid Metabolism, Inborn Errors; Ammonia; Female; Fetal Blood; Fetal Diseases; Fetoscopy; Genet | 1984 |
Expression, purification and kinetic characterization of wild-type human ornithine transcarbamylase and a recurrent mutant that produces 'late onset' hyperammonaemia.
Topics: Ammonia; Chromatography, Affinity; Cloning, Molecular; Enzyme Stability; Genetic Diseases, Inborn; H | 1997 |