Review article on huntington's disease

This article has been cited by other articles in PMC. Go to: Abstract. Huntington disease (HD) is a rare neurodegenerative disorder of the central. Huntington.s disease is a progressive, fatal, neurodegenerative disorder caused by an expanded CAG repeat in the huntingtin gene, which Historical Article. Research Support, N.I.H. Extramural. Research Support, Non-U.S. Gov.t. Review. Huntington disease (HD) is a progressive disorder of motor, cognitive, and psychiatric disturbances. The mean age of onset is 35 to 44 years.

Full Site. Previous Article middot. Next Article middot. Volume 10, No. 1, p8398, January 2011 Review. Switch to Standard ViewSwitch to Enhanced View. Huntington.s disease: from molecular pathogenesis to clinical treatment. Dr Christopher A Ross. BMJ, , VoluMe 341. CliniCal Review. For the full versions of these articles see bmj.com. Huntington.s disease. Marianne J U Novak,1 2 Sarah J.

Huntington.s disease: underlying molecular mechanisms and Article Info Huntington.s disease (HD) is a progressive neurodegenerative. Article middot. Figures Data middot. Info middot. PDF. Loading. Abstract. Huntington.s disease (HD) is a neurodegenerative disorder caused by a We also review the different mechanisms by which the mutation in huntingtin causes toxicity.

Huntington;s disease: a clinical review

Huntington.s disease: a clinical review View Article. Abstract. Huntington Huntington.s disease (HD), which is caused by a triplet-repeat expansion in the IT15 In this article, we review the most important HD phenocopy disorders.

Clinical Review: Huntington;s disease, GPonline

Volume 2011 (2011), Article ID 563784, 7 pages Review Article Huntington.s disease (HD) is a progressive neurodegenerative disorder. Huntington disease (HD) is a dominantly inherited neurodegenerative disorder that usually presents in In this review, we seek to provide an overview of the clinical and genetic features of HD together with a Articles citing this article. Review Article. Hippocampal Neurogenesis, Cognitive Deficits and Affective. Disorder in Huntington.s Disease. Mark I. Ransome,1 Thibault Renoir,1 and.

Review ARTICLE. Front. Neurosci. 04 July Dopamine imbalance in Huntington.s disease: a mechanism for the lack of behavioral flexibility. Jane Y. Chen. Huntington.s disease is an inherited neurodegenerative disorder. disease at a clinical meeting in your practice, using this article as a guide.

Juvenile Huntington.s disease (JHD) is usually defined as. Articles not written in English were excluded, the one exception being the German.

Hippocampal Neurogenesis, Cognitive Deficits and

Huntington.s disease (HD) is an autosomal dominant neurodegenerative. Only peer-reviewed published articles were accepted for inclusion in the review. Read Article, Listen to Podcast Review We evaluated progression in Huntington.s disease using a novel longitudinal magnetic resonance imaging analysis. Genetic testing has been available for Huntington.s disease for longer than any other adult This review article provides an overview of the literature and draws.