Page last updated: 2024-10-21

sk&f 81297 and Huntington Disease

sk&f 81297 has been researched along with Huntington Disease in 1 studies

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
Bibb, JA1
Yan, Z1
Svenningsson, P1
Snyder, GL1
Pieribone, VA1
Horiuchi, A1
Nairn, AC1
Messer, A1
Greengard, P1

Other Studies

1 other study available for sk&f 81297 and Huntington Disease

ArticleYear
Severe deficiencies in dopamine signaling in presymptomatic Huntington's disease mice.
    Proceedings of the National Academy of Sciences of the United States of America, 2000, Jun-06, Volume: 97, Issue:12

    Topics: Animals; Benzazepines; Calcium Channels; Corpus Striatum; Dopamine; Dopamine and cAMP-Regulated Phos

2000