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- W2092016575 abstract "Spinocerebellar Ataxia type 3 (SCA3) or Machado–Joseph Disease (MJD) is a clinically heterogeneous autosomal dominantly inherited progressive ataxia disorder [ [1] Schöls L. Bauer P. Schmidt T. Schulte T. Riess O. Autosomal dominant cerebellar ataxias: clinical features, genetics, and pathogenesis. Lancet Neurol. 2004; 3: 291-304 Abstract Full Text Full Text PDF PubMed Scopus (823) Google Scholar ]. The disease comprises a wide range of neurological motor and non-motor symptoms. Among the neurological signs of SCA3/MJD, extrapyramidal features have been frequently described, particularly dystonia and parkinsonism [ [2] Wang Y.G. Du J. Wang J.L. Chen J. Chen C. Luo Y.Y. Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic. J Neurol Sci. 2009; 285: 121-124 Abstract Full Text PDF PubMed Scopus (14) Google Scholar ]. Although rare, other movement disorders (MD), may also emerge during the course of the disease, such as tremor, chorea and myoclonus [ [2] Wang Y.G. Du J. Wang J.L. Chen J. Chen C. Luo Y.Y. Six cases of SCA3/MJD patients that mimic hereditary spastic paraplegia in clinic. J Neurol Sci. 2009; 285: 121-124 Abstract Full Text PDF PubMed Scopus (14) Google Scholar ]." @default.
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- W2092016575 date "2011-11-01" @default.
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- W2092016575 title "Akathisia: An unusual movement disorder in Machado–Joseph disease" @default.
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- W2092016575 doi "https://doi.org/10.1016/j.parkreldis.2011.05.011" @default.
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