Clinical characteristics of patients with spinocerebellar ataxias 1, 2, 3 and 6 in the US; a prospective observational study

The Rare Diseases Clinical Research Network Contact Registry update: Features and functionality

(2012) Rachel L. Richesson et al.   Contemporary Clinical Trials

Association between Proton Magnetic Resonance Spectroscopy Measurements and CAG Repeat Number in Patients with Spinocerebellar Ataxias 2, 3, or 6

(2012) Po-Shan Wang et al.   PLoS One

Milestones in ataxia

(2011) Thomas Klockgether et al.   MOVEMENT DISORDERS

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

(2011) H. Jacobi et al.   NEUROLOGY

Progression Rate of Neurological Deficits in a 10-Year Cohort of SCA3 Patients

(2010) Laura Bannach Jardim et al.   CEREBELLUM

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

(2010) Alexandra Durr   LANCET NEUROLOGY

Responsiveness of different rating instruments in spinocerebellar ataxia patients

(2010) T. Schmitz-Hubsch et al.   NEUROLOGY

The Spinocerebellar Ataxias

(2009) Henry L Paulson   JOURNAL OF NEURO-OPHTHALMOLOGY

SCA Functional Index: A useful compound performance measure for spinocerebellar ataxia

(2008) T. Schmitz-Hubsch et al.   NEUROLOGY