Autosomal dominant cerebellar ataxias: a systematic review of clinical features

The Ever Expanding Spinocerebellar Ataxias. Editorial

(2012) Antoni Matilla-Dueñas   CEREBELLUM

Fixing the broken system of genetic locus symbols: Parkinson disease and dystonia as examples

(2012) C. Marras et al.   NEUROLOGY

Genetics of the Dominant Ataxias

(2012) Dineke Verbeek et al.   SEMINARS IN NEUROLOGY

Tutorial in biostatistics: sample sizes for parallel group clinical trials with binary data

(2012) Steven A. Julious et al.   STATISTICS IN MEDICINE

Update on degenerative ataxias

(2011) Thomas Klockgether   CURRENT OPINION IN NEUROLOGY

The natural history of spinocerebellar ataxia type 1, 2, 3, and 6: A 2-year follow-up study

(2011) H. Jacobi et al.   NEUROLOGY

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

(2010) Alexandra Durr   LANCET NEUROLOGY

Spinocerebellar ataxia type 10: Frequency of epilepsy in a large sample of Brazilian patients

(2010) Hélio A.G. Teive et al.   MOVEMENT DISORDERS

Autosomal dominant cerebellar ataxia: frequency analysis and clinical characterization of 45 families from Portugal

(2009) J. Vale et al.   EUROPEAN JOURNAL OF NEUROLOGY

Clinical and genetic characteristics of non-Asian dentatorubral-pallidoluysian atrophy: A systematic review

(2009) Mark Wardle et al.   MOVEMENT DISORDERS

Early symptoms in spinocerebellar ataxia type 1, 2, 3, and 6

(2008) Christoph Globas et al.   MOVEMENT DISORDERS