ammonium hydroxide has been researched along with Abnormalities, Sex Chromosome in 5 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
| Excerpt | Relevance | Reference |
|---|---|---|
| "Ornithine transcarbamylase deficiency is an X-linked recessive disorder of urea biosynthesis characterized by recurrent, often fatal, hyperammonemic encephalopathy in affected males; carrier females are usually asymptomatic." | 1.29 | Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy. ( Blaser, S; Clarke, JT; Pridmore, CL, 1995) |
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 4 (80.00) | 18.7374 |
| 1990's | 1 (20.00) | 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 |
|---|---|
| Pridmore, CL | 1 |
| Clarke, JT | 1 |
| Blaser, S | 1 |
| LaBrecque, DR | 1 |
| Latham, PS | 1 |
| Riely, CA | 1 |
| Hsia, YE | 1 |
| Klatskin, G | 1 |
| Zoghbi, HY | 1 |
| Milstien, S | 1 |
| Butler, IJ | 1 |
| Smith, EO | 1 |
| Kaufman, S | 1 |
| Glaze, DG | 1 |
| Percy, AK | 1 |
| Zoghbi, H | 1 |
| Hayasaka, K | 1 |
| Metoki, K | 1 |
| Ishiguro, S | 1 |
| Kato, S | 1 |
| Chiba, T | 1 |
| Hirooka, M | 1 |
| Kikuchi, M | 1 |
| Kurobane, I | 1 |
| Narisawa, K | 1 |
| Tada, K | 1 |
1 review available for ammonium hydroxide and Abnormalities, Sex Chromosome
| Article | Year |
|---|---|
Genetic aspects of Rett syndrome.
Topics: Ammonia; Autistic Disorder; Child; Diseases in Twins; Female; Genetic Linkage; Humans; Neurocognitiv | 1988 |
4 other studies available for ammonium hydroxide and Abnormalities, Sex Chromosome
| Article | Year |
|---|---|
Ornithine transcarbamylase deficiency in females: an often overlooked cause of treatable encephalopathy.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Brain; Brain Damage, Chronic; Brain Disea | 1995 |
Heritable urea cycle enzyme deficiency-liver disease in 16 patients.
Topics: Adolescent; Adult; Ammonia; Biopsy, Needle; Carbamoyl-Phosphate Synthase (Ammonia); Child; Child, Pr | 1979 |
Cerebrospinal fluid biogenic amines and biopterin in Rett syndrome.
Topics: Adolescent; Ammonia; Biogenic Amines; Biopterins; Brain Chemistry; Child; Child, Preschool; Dihydrop | 1989 |
Partial ornithine transcarbamylase deficiency in females: diagnosis by an immunohistochemical method.
Topics: Adolescent; Amino Acid Metabolism, Inborn Errors; Ammonia; Carbamoyl-Phosphate Synthase (Ammonia); C | 1987 |