Page last updated: 2024-10-18

hydroxylamine and Huntington Disease

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)

Research

Studies (2)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's1 (50.00)24.3611
2020's1 (50.00)2.80

Authors

AuthorsStudies
Downs, E1
Bottrell, AD1
Naylor, K1
Sandhir, R1
Mahajan, N1
Mehrotra, A1
Aggarwal, A1
Sunkaria, A1

Other Studies

2 other studies available for hydroxylamine and Huntington Disease

ArticleYear
Identifying the Effects of Reactive Oxygen Species on Mitochondrial Dynamics and Cytoskeleton Stability in
    Cells, 2021, 08-20, Volume: 10, Issue:8

    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.
    Synapse (New York, N.Y.), 2015, Volume: 69, Issue:3

    Topics: Animals; Catalase; Cognition; Cyclic N-Oxides; Female; Free Radical Scavengers; Huntington Disease;

2015