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Drug Discovery Today, ISSN 1359-6446, 07/2014, Volume 19, Issue 7, pp. 985 - 989
Huntington's disease is the most frequent form of the hereditary choreas and has a multifaceted phenotype including cognitive and psychiatric impairment. The... 
Animals | Dyskinesias - diagnosis | Humans | Huntington Disease - genetics | Huntington Disease - diagnosis | Chorea - diagnosis | Genetic Testing - trends | Chorea - genetics | Mutation - genetics | Genetic Testing - methods | Dyskinesias - genetics
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 09/2018, Volume 89, Issue Suppl 1, p. A48
Background Understanding and measuring the impact of Huntington’s on people’s lives is important to patients, families and care providers. However,... 
Questionnaires | Patients | Quality of life
Journal Article
Translational Neurodegeneration, ISSN 2047-9158, 12/2013, Volume 2, Issue 1
Journal Article
Value in Health : The Journal of the International Society for Pharmacoeconomics and Outcomes Research, ISSN 1098-3015, 06/2019, Volume 22, Issue 6, p. 712
Background Although health-related quality of life is key for patients with long-term neurodegenerative conditions, measuring this is less straightforward and... 
Huntingtons disease | Validation | Discriminant analysis | Behavioural aspects | Factor analysis | Discriminant validity | Complications | Cognitive ability | Severity | Rasch model | Huntington's disease | Quality of life | Clinical assessment | Health status | Mood | Huntington's chorea | Neurodegeneration | Cognitive-Behavioural factors | Questionnaires | Psychometric properties
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 09/2018, Volume 89, Issue Suppl 1, p. A44
Background Huntington’s disease can present at almost any age but traditionally, those with an onset ≤20 years are described as having juvenile onset... 
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 09/2016, Volume 87, Issue Suppl 1, pp. A37 - A38
BackgroundDiffusion tensor imaging (DTI) could detect abnormal brain microstructural alterations. DTI studies of Huntington’s disease (HD) have yielded... 
Journal Article
European Journal of Medical Genetics, ISSN 1769-7212, 2014, Volume 57, Issue 2, pp. 103 - 112
Journal Article
Movement Disorders, ISSN 0885-3185, 07/2015, Volume 30, Issue 8, pp. 1125 - 1130
Journal Article
Frontiers in Neurology, ISSN 1664-2295, 09/2017, Volume 8
Background and purposeHuntington’s disease (HD) is a chronic progressive neurodegenerative disorder with a long presymptomatic period that opens a window for... 
caudate nucleus | Huntington’s disease | classification | pre-Huntington’s disease gene carriers | magnetization transfer imaging
Journal Article
Journal of Neurology, Neurosurgery and Psychiatry, ISSN 0022-3050, 09/2018, Volume 89, Issue Suppl 1, p. A68
Background More than a century after the first description of Huntington’s disease (HD), there is still no curative treatment of the disease; however,... 
Journal Article
Journal of Neurology, Neurosurgery & Psychiatry, ISSN 0022-3050, 09/2016, Volume 87, Issue Suppl 1, pp. A45 - A45
BackgroundThe motor signs in Huntington’s disease (HD) can be divided into predominantly choreatic and hypokinetic-rigid subtypes. It has been reported in... 
Journal Article
European journal of neurology, ISSN 1351-5101, 08/2019
Huntington's disease (HD) is a dominantly inherited neurodegenerative disorder with varied prevalence in different populations, which may be associated with... 
Journal Article
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