Body Mass Index is Inversely Correlated with the Expanded CAG Repeat Length in SCA3/MJD Patients

Autosomal dominant cerebellar ataxias: polyglutamine expansions and beyond

(2010) Alexandra Durr   LANCET NEUROLOGY

Serum insulin-like system alterations in patients with spinocerebellar ataxia type 3

(2010) Jonas Alex Morales Saute et al.   MOVEMENT DISORDERS

Reversibility of symptoms in a conditional mouse model of spinocerebellar ataxia type 3

(2009) Jana Boy et al.   HUMAN MOLECULAR GENETICS

Dietary intake in adults at risk for Huntington disease: Analysis of PHAROS Research Participants

(2009) K. Marder et al.   NEUROLOGY

A neurological examination score for the assessment of spinocerebellar ataxia 3 (SCA3)

(2008) C. Kieling et al.   EUROPEAN JOURNAL OF NEUROLOGY

Weight loss in Huntington disease increases with higher CAG repeat number

(2008) N. A. Aziz et al.   NEUROLOGY