hydroxylamine has been researched along with Huntington Disease in 2 studies
amino alcohol : An alcohol containing an amino functional group in addition to the alcohol-defining hydroxy group.
Huntington Disease: A familial disorder inherited as an autosomal dominant trait and characterized by the onset of progressive CHOREA and DEMENTIA in the fourth or fifth decade of life. Common initial manifestations include paranoia; poor impulse control; DEPRESSION; HALLUCINATIONS; and DELUSIONS. Eventually intellectual impairment; loss of fine motor control; ATHETOSIS; and diffuse chorea involving axial and limb musculature develops, leading to a vegetative state within 10-15 years of disease onset. The juvenile variant has a more fulminant course including SEIZURES; ATAXIA; dementia; and chorea. (From Adams et al., Principles of Neurology, 6th ed, pp1060-4)
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 |
---|---|
Downs, E | 1 |
Bottrell, AD | 1 |
Naylor, K | 1 |
Sandhir, R | 1 |
Mahajan, N | 1 |
Mehrotra, A | 1 |
Aggarwal, A | 1 |
Sunkaria, A | 1 |
2 other studies available for hydroxylamine and Huntington Disease
Article | Year |
---|---|
Identifying the Effects of Reactive Oxygen Species on Mitochondrial Dynamics and Cytoskeleton Stability in
Topics: Alzheimer Disease; Antimycin A; Benzene Derivatives; Charcot-Marie-Tooth Disease; Cytoskeleton; Dict | 2021 |
4-hydroxy tempo improves mitochondrial and neurobehavioral deficits in experimental model of Huntington's disease.
Topics: Animals; Catalase; Cognition; Cyclic N-Oxides; Female; Free Radical Scavengers; Huntington Disease; | 2015 |