Page last updated: 2024-10-20

trimethyloxamine and Huntington Disease

trimethyloxamine has been researched along with Huntington Disease in 1 studies

trimethyloxamine: used in manufacture of quaternary ammonium cpds; insect attractant; warming agent for gas; oxidant; structure
trimethylamine N-oxide : A tertiary amine oxide resulting from the oxidation of the amino group of trimethylamine.

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 (1)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (100.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Paul, S1

Reviews

1 review available for trimethyloxamine and Huntington Disease

ArticleYear
Polyglutamine-mediated neurodegeneration: use of chaperones as prevention strategy.
    Biochemistry. Biokhimiia, 2007, Volume: 72, Issue:4

    Topics: Animals; Dimethyl Sulfoxide; HSP40 Heat-Shock Proteins; HSP70 Heat-Shock Proteins; Humans; Huntingto

2007