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Dystonia
Citations 91-100 of 136 total displayed.
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Past content
(since Jan 2001):
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- CLINICAL/SCIENTIFIC NOTES
Serum prolactin in symptomatic and asymptomatic dopa-responsive dystonia due to a GCH1 mutation
- Y. Furukawa, M. Guttman, H. Wong, S.A. Farrell, S. Furtado, and S.J. Kish
Neurology 2003; 61: 269-270.
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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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- CLINICAL/SCIENTIFIC NOTES
Bilateral pallidal stimulation for blepharospasm–oromandibular dystonia (Meige syndrome)
- Hans-Holger Capelle, Ralf Weigel, and Joachim K. Krauss
Neurology 2003; 60: 2017-2018.
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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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- BRIEF COMMUNICATIONS
Palmaris brevis spasm: An occupational syndrome
- R. Liguori, V. Donadio, V. Di Stasi, C. Cianchi, and P. Montagna
Neurology 2003; 60: 1705-1707.
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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
Camptocormia, axial dystonia, and parkinsonism: Phenotypic heterogeneity of a parkin mutation
- R. Inzelberg, N. Hattori, P. Nisipeanu, S. Abo Mouch, S.C. Blumen, R.L. Carasso, and Y. Mizuno
Neurology 2003; 60: 1393-1394.
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