Hereditary disease; develops in adulthood and ends in dementia.
1We conclude that quantitative assessment of chorea is feasible in Huntington's disease.
2Chorea is commonly assessed by subitems of the Unified- Huntington's Disease Rating Scale.
3She is currently involved in two areas of research; Huntington's disease and concussion.
4We compared the extent of editing in controls and cases with Huntington's disease.
5Furthermore, gut dysbiosis was recently reported in Huntington's disease transgenic mice.
6Background: Postural deficits in Huntington's disease are linked to functional impairment.
7No other drug tested in Huntington's disease has shown this effect.
8Read more about the impact of Huntington's disease on The Wireless
9A preponderance of maternal transmission was noted in late-onset Huntington's disease.
10Proteins with expanded polyglutamine domains cause eight inherited neurodegenerative diseases including Huntington's disease.
11Eighty-two percent were in favour of the principle of predictive testing for Huntington's disease.
12Overall, our findings suggest an altered gut microbiome in Huntington's disease gene expansion carriers.
13In Huntington's disease, involuntary choreatic movements are one of the hallmarks of motor dysfunction.
14The clinical features resembled those of mid-life onset Huntington's disease but progressed more slowly.
15There were no group differences on the Unified Huntington's Disease Rating total motor score.
16Approximately 25% of persons affected by Huntington's disease exhibit late onset.
Translations for huntington's disease