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Normal cortical excitability in Myoclonus-Dystonia — A TMS study

✍ Scribed by S.M.A. van der Salm; A.F. van Rootselaar; E.M.J. Foncke; J.H.T.M. Koelman; L.J. Bour; K.P. Bhatia; J.C. Rothwell; M.A.J. Tijssen

Book ID
116459438
Publisher
Elsevier Science
Year
2009
Tongue
English
Weight
377 KB
Volume
216
Category
Article
ISSN
0014-4886

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✍ Sabine Meunier; George Lourenco; Emmanuel Roze; Emmanuelle Apartis; Jean-Marc Tr 📂 Article 📅 2008 🏛 John Wiley and Sons 🌐 English ⚖ 116 KB

## Abstract Myoclonus‐dystonia (M‐D) is an autosomal dominant movement disorder caused by mutations in the ε‐sarcoglycan gene (__DYT11__). We explore pathophysiological characteristics of M‐D with the hypothesis that they may be different from those of sporadic or genetic dystonia. We compared five