Hereditary disease; develops in adulthood and ends in dementia.
1We conclude that quantitative assessment of chorea is feasible in Huntington's disease.
2She is currently involved in two areas of research; Huntington's disease and concussion.
3We compared the extent of editing in controls and cases with Huntington's disease.
4Furthermore, gut dysbiosis was recently reported in Huntington's disease transgenic mice.
5Background: Postural deficits in Huntington's disease are linked to functional impairment.
6No other drug tested in Huntington's disease has shown this effect.
7Read more about the impact of Huntington's disease on The Wireless
8A preponderance of maternal transmission was noted in late-onset Huntington's disease.
9Proteins with expanded polyglutamine domains cause eight inherited neurodegenerative diseases including Huntington's disease.
10Eighty-two percent were in favour of the principle of predictive testing for Huntington's disease.
11Overall, our findings suggest an altered gut microbiome in Huntington's disease gene expansion carriers.
12In Huntington's disease, involuntary choreatic movements are one of the hallmarks of motor dysfunction.
13The clinical features resembled those of mid-life onset Huntington's disease but progressed more slowly.
14Approximately 25% of persons affected by Huntington's disease exhibit late onset.
15Psychotic symptoms are more common in patients with Huntington's disease than in the general population.
16Methods: Data were obtained from the European Huntington's disease network REGISTRY study for 6540 subjects.
Translations for Huntington's disease