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Spinocerebellar ataxias - genotype-phenotype correlations in 104 Brazilian families
(Hospital Clinicas, Univ Sao PauloSao PauloBrasil, 2012)
Spinocerebellar ataxias: genotype-phenotype correlations in 104 Brazilian families
(Faculdade de Medicina / USP, 2012)
NESSCA Validation and Responsiveness of Several Rating Scales in Spinocerebellar Ataxia Type 2
(Springer Verlag (Germany), 2017)
Características clínicas de 63 pacientes con ataxia
(2018)
Background: Ataxia can be classified as genetic, sporadic or acquired.
Aim: To report the clinical features of a group of patients with ataxia. Material
and Methods: Review of medical records of patients consulting in a ...
Características clínicas de 63 pacientes con ataxia
(2018)
Background: Ataxia can be classified as genetic, sporadic or acquired.
Aim: To report the clinical features of a group of patients with ataxia. Material and Methods: Review of medical records of patients consulting in a ...
NESSCA Validation and Responsiveness of Several Rating Scales in Spinocerebellar Ataxia Type 2
(Springer, 2017)
Spinocerebellar ataxia type 2 (SCA2), caused by a CAG expansion (CAGexp) at ATXN2, has a complex clinical picture. While validated ataxia scales are available, comprehensive instruments to measure all SCA2 neurological ...
Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil
(Wiley, 2017)
Background and purpose: Spinocerebellar ataxia type 10 is a neurodegenerative disorder that is due to an expanded ATTCT repeat tract in the ATXN10 gene. Our aim was to describe clinical characteristics and intragenic ...
Spinocerebellar ataxia type 10: common haplotype and disease progression rate in Peru and Brazil
(Wiley Online Library, 2023)