Spinocerebellar ataxia type 3 in Israel: phenotype and genotype of a Jew Yemenite subpopulation

Modulation of the age at onset in spinocerebellar ataxia by CAG tracts in various genes

(2014) Sophie Tezenas du Montcel et al.   BRAIN

Mutational Origin of Machado-Joseph Disease in the Australian Aboriginal Communities of Groote Eylandt and Yirrkala

(2012) Sandra Martins et al.   ARCHIVES OF NEUROLOGY

The APOE ε2 Allele Increases the Risk of Earlier Age at Onset in Machado-Joseph Disease

(2011) Conceição Bettencourt   ARCHIVES OF NEUROLOGY

Electronystagmography findings in spinocerebellar ataxia type 3 (SCA3) and type 2 (SCA2)

(2011) Bianca Simone Zeigelboim et al.   ARQUIVOS DE NEURO-PSIQUIATRIA

Machado-Joseph Disease: from first descriptions to new perspectives

(2011) Conceição Bettencourt et al.   Orphanet Journal of Rare Diseases

Clinical and genetic characteristics in patients with Huntington’s Disease from Argentina

(2011) Emilia Gatto et al.   PARKINSONISM & RELATED DISORDERS

Levels of DNAJB family members (HSP40) correlate with disease onset in patients with spinocerebellar ataxia type 3

(2010) M. P. Zijlstra et al.   EUROPEAN JOURNAL OF NEUROSCIENCE

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

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

Head impulse test in unilateral vestibular loss: Vestibulo-ocular reflex and catch-up saccades

(2008) K. P. Weber et al.   NEUROLOGY