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All Movement Disorders
Citations 121-130 of 174 total displayed.
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Past content
(since Jan 2000):
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- ARTICLES
Brain parenchyma sonography discriminates Parkinson’s disease and atypical parkinsonian syndromes
- U. Walter, L. Niehaus, T. Probst, R. Benecke, B. U. Meyer, and D. Dressler
Neurology 2003; 60: 74-77.
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- BRIEF COMMUNICATIONS
Preservation of branchimotor neurons of the nucleus ambiguus in multiple system atrophy
- Eduardo E. Benarroch, Ann M. Schmeichel, and Joseph E. Parisi
Neurology 2003; 60: 115-117.
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- BRIEF COMMUNICATIONS
Diagnostic criteria for dystonia in DYT1 families
- S. B. Bressman, D. Raymond, K. Wendt, R. Saunders–Pullman, D. de Leon, S. Fahn, L. Ozelius, and N. Risch
Neurology 2002; 59: 1780-1782.
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- BRIEF COMMUNICATIONS
Exon deletions in the GCHI gene in two of four Turkish families with dopa-responsive dystonia
- C. Klein, K. Hedrich, K. Kabakçi, K. Mohrmann, K. Wiegers, O. Landt, J. Hagenah, E. Schwinger, P. P. Pramstaller, L. J. Ozelius, K. Gucuyener, S. Aysun, and E. Demir
Neurology 2002; 59: 1783-1786.
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- VIEWS & REVIEWS
Do published criteria improve clinical diagnostic accuracy in multiple system atrophy?
- Y. Osaki, Y. Ben-Shlomo, G.K. Wenning, S.E. Daniel, A. Hughes, A.J. Lees, C.J. Mathias, and N. Quinn
Neurology 2002; 59: 1486-1491.
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- BRIEF COMMUNICATIONS
Relationship between CAG repeat length and late-stage outcomes in Huntington’s disease
- K. Marder, S. Sandler, A. Lechich, J. Klager, and S.M. Albert
Neurology 2002; 59: 1622-1624.
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- BRIEF COMMUNICATIONS
SCA-2 presenting as parkinsonism in an Alberta family: Clinical, genetic, and PET findings
- S. Furtado, M. Farrer, Y. Tsuboi, M. L. Klimek, R. de la Fuente-Fernández, J. Hussey, P. Lockhart, D. B. Calne, O. Suchowersky, A. J. Stoessl, and Z. K. Wszolek
Neurology 2002; 59: 1625-1627.
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- EDITORIALS
Penfield revisited?: Understanding and modifying behavior by deep brain stimulation for PD
- Helen S. Mayberg and Andres M. Lozano
Neurology 2002; 59: 1298-1299.
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- ARTICLES
Weight loss in early stage of Huntington’s disease
- L. Djoussé, B. Knowlton, L. A. Cupples, K. Marder, I. Shoulson, and R. H. Myers
Neurology 2002; 59: 1325-1330.
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- ARTICLES
Presymptomatic testing in Huntington’s disease and autosomal dominant cerebellar ataxias
- C. Goizet, G. Lesca, and A. Dürr
Neurology 2002; 59: 1330-1336.
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