ammonium hydroxide has been researched along with Autosomal Chromosome Disorders in 4 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 2 (50.00) | 18.7374 |
| 1990's | 1 (25.00) | 18.2507 |
| 2000's | 1 (25.00) | 29.6817 |
| 2010's | 0 (0.00) | 24.3611 |
| 2020's | 0 (0.00) | 2.80 |
| Authors | Studies |
|---|---|
| Qureshi, IA | 1 |
| Rao, KV | 1 |
| Sabina, RL | 1 |
| Matsuda, I | 1 |
| Sugai, M | 1 |
| Kajii, T | 1 |
| Györy, AZ | 1 |
| Edwards, KD | 1 |
2 reviews available for ammonium hydroxide and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Sparse-fur (spf) mouse as a model of hyperammonemia: alterations in the neurotransmitter systems.
Topics: Ammonia; Animals; Chromosome Aberrations; Chromosome Disorders; Disease Models, Animal; Gene Express | 1997 |
Myoadenylate deaminase deficiency. A common inherited defect with heterogeneous clinical presentation.
Topics: Alleles; Ammonia; AMP Deaminase; Chromosome Aberrations; Chromosome Disorders; Exercise Test; Genes, | 2000 |
2 other studies available for ammonium hydroxide and Autosomal Chromosome Disorders
| Article | Year |
|---|---|
Ornithine loading test in Lowe's syndrome.
Topics: Abnormalities, Multiple; Amino Acids; Ammonia; Chromosome Aberrations; Chromosome Disorders; Eye Dis | 1970 |
Renal tubular acidosis. A family with an autosomal dominant genetic defect in renal hydrogen ion transport, with proximal tubular and collecting duct dysfunction and increased metabolism of citrate and ammonia.
Topics: Acidosis, Renal Tubular; Adult; Aged; Ammonia; Chromosome Aberrations; Chromosome Disorders; Citrate | 1968 |