Buscar
Mostrando ítems 21-30 de 108
Progression of Ataxia in Patients with Machado-Joseph Disease
(Wiley-lissHobokenEUA, 2009)
Volumetric MRI Changes in Spinocerebellar Ataxia (SCA3 and SCA10) Patients
(Springer, 2020-05-04)
Spinocerebellar ataxias type 3 (SCA3) and type 10 (SCA10) are the most prevalent in southern Brazil. To analyze the relationships between volumetric MRI changes and clinical and genetic findings in SCA3 and SCA10 patients. ...
Clinical and molecular characteristics of a Brazilian family with spinocerebellar ataxia type 1Características clínicas e moleculares de uma família Brasileira com ataxia espinocerebelar tipo 1
(Academia Brasileira de Neurologia - ABNEURO, 1996)
Movement Disorders in Autosomal Dominant Cerebellar Ataxias: A Systematic Review
(John Wiley & Sons Inc, 2014-09)
Autosomal dominant cerebellar ataxias (ADCAs) are clinically heterogeneous disorders classified according to genetic subtype and collectively known as SCAs. In a few SCAs, movement disorders can be the most frequent ...
Brain glyceraldehyde-3-phosphate dehydrogenase activity in human trinucleotide repeat disorders
(Amer Medical AssocChicagoEUA, 1998)
Neocortical Atrophy in Machado-Joseph Disease: A Longitudinal Neuroimaging Study
(Wiley-blackwellHobokenEUA, 2012)
Apneia Do Sono Na Doença De Machado-Joseph: Avaliação Clínica E Polissonográfica
(Universidade Federal de São Paulo (UNIFESP), 2018-02-22)
Introduction: Machado-Joseph Disease (Mjd) Or Spinocerebellar Ataxia Type 3 (Sca3) Is The Most Common Type Of Autosomal Dominant Spinocerebellar Ataxia (Acs). The Onset Of Symptoms Is Around The 3rd Or 4th Decade, Leading ...
NESSCA Validation and Responsiveness of Several Rating Scales in Spinocerebellar Ataxia Type 2
(Springer Verlag (Germany), 2017)