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Publications by Paulo C. Trevisol-Bittencourt
Frequency of the Different Mutations Causing Spinocerebellar Ataxia (SCA1, SCA2, MJD/SCA3 and DRPLA) in a Large Group of Brazilian Patients
Arquivos de Neuro-Psiquiatria
Biological Psychiatry
Neurology
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264. Translating RNAi Therapy for Spinocerebellar Ataxia 1 (SCA1) to the Clinic
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A Common Disease Haplotype Segregating in Spinocerebellar Ataxia 2 (SCA2) Pedigrees of Diverse Ethnic Origin
European Journal of Human Genetics
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Mutations inKCND3cause Spinocerebellar Ataxia Type 22
Annals of Neurology
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Brain MRI, Lumbar CSF Monoamine Concentrations, and Clinical Descriptors of Patients With Spinocerebellar Ataxia Mutations.
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Brain Derived Neurotrophic Factor (BDNF) Delays Onset of Pathogenesis in Transgenic Mouse Model of Spinocerebellar Ataxia Type 1 (SCA1)
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Frequency of KCNC3 DNA Variants as Causes of Spinocerebellar Ataxia 13 (SCA13)
PLoS ONE
Multidisciplinary
Spinocerebellar Ataxia Type 13
Spinocerebellar Ataxia Type 3
Spinocerebellar Ataxia Type 8