ammonium hydroxide has been researched along with Orphan Diseases in 2 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Orphan Diseases: Rare diseases that have not been well studied.
| Excerpt | Relevance | Reference |
|---|---|---|
| "3-methylglutaconic aciduria includes a heterogeneous group of inborn errors of metabolism." | 5.05 | Coincidence of 3-methylglutaconic aciduria and duplication 5q - a case report and literature review. ( Pyrkosz, A; Sykut-Cegielska, J; Zapolnik, P, 2020) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 0 (0.00) | 18.7374 |
| 1990's | 0 (0.00) | 18.2507 |
| 2000's | 0 (0.00) | 29.6817 |
| 2010's | 1 (50.00) | 24.3611 |
| 2020's | 1 (50.00) | 2.80 |
| Authors | Studies |
|---|---|
| Zapolnik, P | 1 |
| Sykut-Cegielska, J | 1 |
| Pyrkosz, A | 1 |
| Dumont, R | 1 |
| Loly, JP | 1 |
| Delwaide, J | 1 |
| Louis, E | 1 |
1 review available for ammonium hydroxide and Orphan Diseases
| Article | Year |
|---|---|
Coincidence of 3-methylglutaconic aciduria and duplication 5q - a case report and literature review.
Topics: Abnormalities, Multiple; Adolescent; Ammonia; Chromosomes, Human, Pair 5; Comparative Genomic Hybrid | 2020 |
1 other study available for ammonium hydroxide and Orphan Diseases
| Article | Year |
|---|---|
[RENDU-OSLER DISEASE: A RARE CAUSE OF AMMONIA ENCEPHALOPATHY].
Topics: Ammonia; Hepatic Encephalopathy; Humans; Male; Middle Aged; Rare Diseases; Telangiectasia, Hereditar | 2016 |