Page last updated: 2024-10-16

carbamates and Huntington Disease

carbamates has been researched along with Huntington Disease in 3 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 Excerpts

ExcerptRelevanceReference
" In the R6/2 mouse HD model, induced DREAM haplodeficiency or blockade of DREAM activity by chronic administration of the drug repaglinide delayed onset of motor dysfunction, reduced striatal atrophy, and prolonged life span."1.43Activating transcription factor 6 derepression mediates neuroprotection in Huntington disease. ( Arrabal, MD; Casado-Vela, J; Cercós, P; De la Cruz, A; Dopazo, XM; González, P; González, T; Gutierrez-Rodriguez, M; Higueras, E; Li, JY; Mellström, B; Morón-Oset, J; Naranjo, JR; Oliveros, JC; Prieto, A; Rábano, A; Valenzuela, C; Villar, D; Zhang, H, 2016)

Research

Studies (3)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's1 (33.33)29.6817
2010's2 (66.67)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
López-Hurtado, A1
Burgos, DF1
González, P2
Dopazo, XM2
González, V1
Rábano, A2
Mellström, B2
Naranjo, JR2
Zhang, H1
Villar, D1
Morón-Oset, J1
Higueras, E1
Oliveros, JC1
Arrabal, MD1
Prieto, A1
Cercós, P1
González, T1
De la Cruz, A1
Casado-Vela, J1
Valenzuela, C1
Gutierrez-Rodriguez, M1
Li, JY1
Rot, U1
Kobal, J1
Sever, A1
Pirtosek, Z1
Mesec, A1

Other Studies

3 other studies available for carbamates and Huntington Disease

ArticleYear
Inhibition of DREAM-ATF6 interaction delays onset of cognition deficit in a mouse model of Huntington's disease.
    Molecular brain, 2018, 03-09, Volume: 11, Issue:1

    Topics: Activating Transcription Factor 6; Animals; Carbamates; Cognition Disorders; Disease Models, Animal;

2018
Activating transcription factor 6 derepression mediates neuroprotection in Huntington disease.
    The Journal of clinical investigation, 2016, Volume: 126, Issue:2

    Topics: Activating Transcription Factor 6; Animals; Carbamates; CHO Cells; Corpus Striatum; Cricetulus; Dise

2016
Rivastigmine in the treatment of Huntington's disease.
    European journal of neurology, 2002, Volume: 9, Issue:6

    Topics: Carbamates; Cholinesterase Inhibitors; Humans; Huntington Disease; Phenylcarbamates; Rivastigmine

2002