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Use of riluzole for the treatment of hereditary ataxias: a systematic review
(2022)
Ataxia is a constellation of symptoms that involves a lack of coordination, imbalance, and difficulty walking. Hereditary ataxia occurs when a person is born with defective genes, and this degenerative disorder may progress ...
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 ...
Dentatorubro-Pallidoluysian Atrophy (DRPLA) among 700 Families with Ataxia in Brazil
(Springer, 2017)
Dentatorubro-pallidoluysian atrophy (DRPLA) is a spinocerebellar ataxia (SCA) very rare in non-Asian populations. To date, DRPLA was undetected in the general Brazilian population. Adult-onset ataxic patients have been ...
Autosomal dominant cerebellar ataxias: a systematic review of clinical features
(Wiley, 2014-02)
BACKGROUND AND PURPOSE: To assess, through systematic review, distinctive or common clinical signs of autosomal dominant cerebellar ataxias (ADCAs), also referred to as spinocerebellar ataxias (SCAs) in genetic nomenclature. ...
Analysis of pre-test interviews in a cohort of Brazilian patients with movement disorders
(Springer Verlag, 2016)
Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes
(Springer Verlag (Germany), 2018)
Machado-Joseph disease versus hereditary spastic paraplegia: case reportDoença de Machado-Joseph versus paraplegia espástica hereditária: relato de caso
(Academia Brasileira de Neurologia - ABNEURO, 2001)