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All Movement Disorders
Citations 91-100 of 174 total displayed.
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Past content
(since Jan 2000):
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- BRIEF COMMUNICATIONS
Hereditary myoclonus–dystonia associated with epilepsy
- E. M.J. Foncke, C. Klein, J. H.T.M. Koelman, P. L. Kramer, K. Schilling, B. Müller, J. Garrels, P. de Carvalho Aguiar, L. Liu, A. de Froe, J. D. Speelman, L. J. Ozelius, and M. A.J. Tijssen
Neurology 2003; 60: 1988-1990.
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- BRIEF COMMUNICATIONS
Modulation of the onset age in primary dystonia by APOE genotype
- S. Matsumoto, M. Nishimura, T. Sakamoto, K. Asanuma, Y. Izumi, H. Shibasaki, N. Kamatani, T. Nakamura, and R. Kaji
Neurology 2003; 60: 2003-2005.
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- EDITORIALS
Blind men and blinking elephants
- Craig Evinger and Joel S. Perlmutter
Neurology 2003; 60: 1732-1733.
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- ARTICLES
Striatal activation during blepharospasm revealed by fMRI
- Kerstin E. Schmidt, David E.J. Linden, Rainer Goebel, Friedhelm E. Zanella, H. Lanfermann, and Alina A. Zubcov
Neurology 2003; 60: 1738-1743.
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- CLINICAL/SCIENTIFIC NOTES
Cervical myelopathy secondary to violent tics of Tourette’s syndrome
- Michael Dobbs and Joseph R. Berger
Neurology 2003; 60: 1862-1866.
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- ARTICLES
Parkin-proven disease: Common founders but divergent phenotypes
- S. Lincoln, J. Wiley, T. Lynch, J. W. Langston, R. Chen, A. Lang, E. Rogaeva, D. S. Sa, R. P. Munhoz, J. Harris, K. Marder, C. Klein, G. Bisceglio, J. Hussey, A. West, M. Hulihan, J. Hardy, and M. Farrer
Neurology 2003; 60: 1605-1610.
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- ARTICLES
Evidence for more widespread cerebral pathology in early HD: An MRI-based morphometric analysis
- H. D. Rosas, W. J. Koroshetz, Y. I. Chen, C. Skeuse, M. Vangel, M. E. Cudkowicz, K. Caplan, K. Marek, L. J. Seidman, N. Makris, B. G. Jenkins, and J. M. Goldstein
Neurology 2003; 60: 1615-1620.
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- BRIEF COMMUNICATIONS
A novel mutation in the  -sarcoglycan gene causing myoclonus–dystonia syndrome
- L. E. Hjermind, L. M. Werdelin, H. Eiberg, B. Krag–Olsen, E. Dupont, and S. A. Sørensen
Neurology 2003; 60: 1536-1539.
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- CLINICAL/SCIENTIFIC NOTES
Acute necrotizing encephalopathy of childhood with radiographic progression over 10 hours
- Alexander G. Bassuk, Delilah M. Burrowes, and Wes McRae
Neurology 2003; 60: 1552-1553.
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- BRIEF COMMUNICATIONS
New parkin mutations and atypical phenotypes in families with autosomal recessive parkinsonism
- N. Rawal, M. Periquet, E. Lohmann, C.B. Lücking, H.A. Teive, G. Ambrosio, S. Raskin, S. Lincoln, N. Hattori, J. Guimaraes, M.W.I.M. Horstink, W. Dos Santos Bele, E. Brousolle, A. Destée, Y. Mizuno, M. Farrer, J.-F. Deleuze, G. De Michele, Y. Agid, A. Dürr, and A. Brice
Neurology 2003; 60: 1378-1381.
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