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Machado-Joseph disease in Brazil: from the first descriptions to the emergence as the most common spinocerebellar ataxia
(Academia Brasileira de Neurologia - ABNEURO, 2012-08-01)
Machado-Joseph disease is an autosomal dominant inherited disorder of Azorean ancestry firstly described in 1972. Since then, several Brazilian researchers have studied clinical and genetic issues related to the disease. ...
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)
Clinical evaluation of oropharyngeal dysphagia in Machado-Joseph disease
(Instituto Brasileiro de Estudos e Pesquisas de Gastroenterologia - IBEPEGE Colégio Brasileiro de Cirurgia Digestiva - CBCD Sociedade Brasileira de Motilidade Digestiva - SBMD Federação Brasileira de Gastroenterologia - FBGSociedade Brasileira de Hepatologia - SBHSociedade Brasileira de Endoscopia Digestiva - SOBED, 2010)
CONTEXT: In Machado-Joseph disease, poor posture, dystonia and peripheral neuropathy are extremely predisposing to oropharyngeal dysphagia, which is more commonly associated with muscular dystrophy. OBJECTIVE: To evaluate ...
Spinocerebellar ataxia types 2 and 3 segregating simultaneously in a single family
(Wiley-lissHobokenEUA, 2006)
Nonmotor and extracerebellar features in Machado-Joseph disease: A review
(Wiley-Blackwell, 2013-08-01)
Spinocerebellar ataxia type 3 or Machado-Joseph disease is the most common spinocerebellar ataxia worldwide, and the high frequency of nonmotor manifestations in Machado-Joseph disease demonstrates how variable is the ...
Thalamic Volume and Dystonia in Machado-Joseph Disease
(Wiley-blackwellMaldenEUA, 2011)
Anterior horn degeneration in Machado-Joseph disease
(Elsevier Science Bv, 2016)
Machado-Joseph disease versus hereditary spastic paraplegia - Case report
(Assoc Arquivos De Neuro- PsiquiatriaSao Paulo SpBrasil, 2001)