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Dystonia
Citations 81-90 of 136 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Phenotypic heterogeneity of dopa-responsive dystonia in monozygotic twins
- H. Grötzsch, H. Schnorf, M. A. Morris, I. Moix, J. Horvath, O. Prilipko, and P. R. Burkhard
Neurology 2004; 62: 637-639.
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- ARTICLES
Mutations in DYT1: Extension of the phenotypic and mutational spectrum
- K. Kabakci, K. Hedrich, J. C. Leung, M. Mitterer, P. Vieregge, R. Lencer, J. Hagenah, J. Garrels, K. Witt, F. Klostermann, M. Svetel, J. Friedman, V. Kostic, S.B. Bressman, X.O. Breakefield, L.J. Ozelius, P.P. Pramstaller, and C. Klein
Neurology 2004; 62: 395-400.
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- BRIEF COMMUNICATIONS
Autosomal recessive, DYT2-like primary torsion dystonia: A new family
- Naheed L. Khan, Nicholas W. Wood, and Kailash P. Bhatia
Neurology 2003; 61: 1801-1803.
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Effects of botulinum toxin on motor system excitability in patients with writer’s cramp
- Babak Boroojerdi, Leonardo G. Cohen, and Mark Hallett
Neurology 2003; 61: 1546-1550.
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- BRIEF COMMUNICATIONS
Compound heterozygous PANK2 mutations confirm HARP and Hallervorden-Spatz syndromes are allelic
- H. Houlden, S. Lincoln, M. Farrer, P.G. Cleland, J. Hardy, and R.W. Orrell
Neurology 2003; 61: 1423-1426.
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- ARTICLES
"Motor circuit" gray matter changes in idiopathic cervical dystonia
- B. Draganski, C. Thun-Hohenstein, U. Bogdahn, J. Winkler, and A. May
Neurology 2003; 61: 1228-1231.
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- BRIEF COMMUNICATIONS
Prevalence of primary focal and segmental dystonia in Oslo
- Khanh-Dung Le, Beate Nilsen, and Espen Dietrichs
Neurology 2003; 61: 1294-1296.
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Candidate gene studies in focal dystonia
- D. Sibbing, F. Asmus, I. R. König, S. Tezenas du Montcel, M. Vidailhet, S. Sangla, W. H. Oertel, A. Brice, A. Ziegler, T. Gasser, and O. Bandmann
Neurology 2003; 61: 1097-1101.
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- BRIEF COMMUNICATIONS
Risperidone-responsive segmental dystonia and pallidal deep brain stimulation
- J. C. Wöhrle, R. Weigel, E. Grips, C. Blahak, H. H. Capelle, and J. K. Krauss
Neurology 2003; 61: 546-548.
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- BRIEF COMMUNICATIONS
Mutations in the  -sarcoglycan gene found to be uncommon in seven myoclonus–dystonia families
- F. Han, A. E. Lang, L. Racacho, D. E. Bulman, and D. A. Grimes
Neurology 2003; 61: 244-246.
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