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1989, Johns Hopkins series in contemporary medicine and public health., ISBN 0801838606, x, 251
Book
2002, 3rd ed., Oxford monographs on medical genetics, ISBN 0198510608, Volume 45, xvi, 558
Book
1993, ISBN 0521459834, Volume 23., 46
This report presents the findings of a study of people affected by Huntington's chorea and their unaffected relatives, and in particular, of the incidence of... 
Book
1981, ISBN 0387105883, xvii, 192
Book
Brain Research Bulletin, ISSN 0361-9230, 2006, Volume 72, Issue 2, pp. 165 - 171
Journal Article
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics, ISSN 1552-4841, 01/2017, Volume 174, Issue 1, pp. 75 - 92
Journal Article
Parkinsonism and Related Disorders, ISSN 1353-8020, 04/2019, Volume 61, pp. 101 - 105
The frequency of late-onset Huntington's disease (>59 years) is assumed to be low and the clinical course milder. However, previous literature on late-onset... 
Age of onset | Huntington's disease | Late-onset Huntington's disease | CLINICAL NEUROLOGY | AGE | FEATURES | Genetic research | Medical genetics
Journal Article
Journal of the Neurological Sciences, ISSN 0022-510X, 2015, Volume 363, pp. 114 - 115
Highlights • Huntington's disease (HD) is associated with the expansion of (CAG) trinucleotide (> 36) at the coding region of the IT 15 gene. • Individuals... 
Neurology | Huntington's disease | Late onset | intermediated alleles | NEUROSCIENCES | CLINICAL NEUROLOGY | Huntington Disease - diagnostic imaging | Age Factors | Humans | Aged, 80 and over | Huntington Disease - genetics | Trinucleotide Repeat Expansion - genetics | Male
Journal Article
Parkinsonism & Related Disorders, ISSN 1873-5126, 2018
BACKGROUND: The frequency of late-onset Huntington's disease (>59 years) is assumed to be low and the clinical course milder. However, previous literature... 
Neurology | Neurologi | Medical and Health Sciences | Age of onset | Medicin och hälsovetenskap | Huntington's disease | Late-onset Huntington's disease
Journal Article
Current Opinion in Neurology, ISSN 1350-7540, 2014, Volume 27, Issue 4, pp. 477 - 483
Purpose of review This review highlights the recent advances in Huntington's disease, with a particular focus on development of disease biomarkers for use in... 
neurodegeneration | premanifest Huntington's disease | prodromal Huntington's disease | biomarker | Huntington's disease | TRACK-HD | MUTANT HUNTINGTIN | PREMANIFEST | NEUROSCIENCES | CLINICAL NEUROLOGY | OBSERVATIONAL DATA | MOUSE MODEL | MOTOR | LATE-ONSET | MICE | DYSFUNCTION | Huntington Disease - therapy | Huntington Disease - genetics | Humans | Huntington Disease - physiopathology
Journal Article