Progression of early features of spinocerebellar ataxia type 2 in individuals at risk: a longitudinal study
- 1 May 2014
- journal article
- Published by Elsevier in The Lancet Neurology
- Vol. 13 (5) , 482-489
Abstract
No abstract availableKeywords
This publication has 25 references indexed in Scilit:
- Epidemiology and population genetics of degenerative ataxias2012
- A Comprehensive Review of Spinocerebellar Ataxia Type 2 in CubaThe Cerebellum, 2011
- Subtle rapid eye movement sleep abnormalities in presymptomatic spinocerebellar ataxia type 2 gene carriersMovement Disorders, 2010
- Motor Decline in Clinically Presymptomatic Spinocerebellar Ataxia Type 2 Gene CarriersPLOS ONE, 2009
- Molecular epidemiology of spinocerebellar ataxias in Cuba: Insights into SCA2 founder effect in HolguinNeuroscience Letters, 2009
- Saccade velocity is reduced in presymptomatic spinocerebellar ataxia type 2Clinical Neurophysiology, 2009
- Spinocerebellar ataxias caused by polyglutamine expansions: A review of therapeutic strategiesThe Cerebellum, 2008
- Electrophysiological features in patients and presymptomatic relatives with spinocerebellar ataxia type 2Journal of the Neurological Sciences, 2007
- Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesisThe Lancet Neurology, 2004
- Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2Nature Genetics, 1996