ammonium hydroxide has been researched along with Dysautonomia, Familial in 1 studies
azane : Saturated acyclic nitrogen hydrides having the general formula NnHn+2.
Dysautonomia, Familial: An autosomal disorder of the peripheral and autonomic nervous systems limited to individuals of Ashkenazic Jewish descent. Clinical manifestations are present at birth and include diminished lacrimation, defective thermoregulation, orthostatic hypotension (HYPOTENSION, ORTHOSTATIC), fixed pupils, excessive SWEATING, loss of pain and temperature sensation, and absent reflexes. Pathologic features include reduced numbers of small diameter peripheral nerve fibers and autonomic ganglion neurons. (From Adams et al., Principles of Neurology, 6th ed, p1348; Nat Genet 1993;4(2):160-4)
| Timeframe | Studies, this research(%) | All Research% |
|---|---|---|
| pre-1990 | 1 (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 |
|---|---|
| Harris, DJ | 1 |
| Yang, BI | 1 |
| Wolf, B | 1 |
| Snodgrass, PJ | 1 |
1 other study available for ammonium hydroxide and Dysautonomia, Familial
| Article | Year |
|---|---|
Dysautonomia in an infant with secondary hyperammonemia due to propionyl coenzyme A carboxylase deficiency.
Topics: Acyl Coenzyme A; Amino Acid Metabolism, Inborn Errors; Amino Acids; Ammonia; Carbamoyl-Phosphate Syn | 1980 |