Walter O. Arruda

Frequency of spinocerebellar ataxia type 1, dentatorubropallidoluysian atrophy, and Machado-Joseph disease mutations in a large group of spinocerebellar ataxia patients

Isabel Silveira, Íscia Lopes‐Cendes, Stephen J. Kish et al. · Neurology · 1996 · 105 citations

Life Sciences, Genetics, Neurology +17

Clinical phenotype of Brazilian families with spinocerebellar ataxia 10

Hélio A.G. Teive, B. B. Roa, Salmo Raskin et al. · Neurology · 2004 · 98 citations

Life Sciences, Genetics, Molecular Genetics +15

Spinocerebellar ataxias – genotype-phenotype correlations in 104 Brazilian families

Hélio A.G. Teive, Renato P. Munhoz, Walter O. Arruda et al. · Clinics · 2012 · 73 citations · Full text

Life Sciences, Genetics, Molecular Genetics +15

Frequency of the different mutations causing spinocerebellar ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a large group of Brazilian patients

Íscia Lopes‐Cendes, H. Teive, María Elisa Calcagnotto et al. · Arquivos de Neuro-Psiquiatria · 1997 · 52 citations · Full text

Life Sciences, Genetics, Neurology +17

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

Hélio A.G. Teive, Renato P. Munhoz, Salmo Raskin et al. · Movement Disorders · 2010 · 46 citations · Full text

Life Sciences, Genetics, Neurology +9