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All Genetics
Citations 461-470 of 676 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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- BRIEF COMMUNICATIONS
Japanese SCA families with an unusual phenotype linked to a locus overlapping with SCA15 locus
- K. Hara, T. Fukushima, T. Suzuki, T. Shimohata, M. Oyake, H. Ishiguro, K. Hirota, A. Miyashita, R. Kuwano, H. Kurisaki, H. Yomono, J. Goto, I. Kanazawa, and S. Tsuji
Neurology 2004; 62: 648-651.
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- EDITORIALS
DJ-1: The second gene for early onset Parkinson disease
- Oliver Bandmann
Neurology 2004; 62: 357-358.
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- ARTICLES
DJ-1 (PARK7) mutations are less frequent than Parkin (PARK2) mutations in early-onset Parkinson disease
- K. Hedrich, A. Djarmati, N. Schäfer, R. Hering, C. Wellenbrock, P. H. Weiss, R. Hilker, P. Vieregge, L. J. Ozelius, P. Heutink, V. Bonifati, E. Schwinger, A. E. Lang, J. Noth, S. B. Bressman, P. P. Pramstaller, O. Riess, and C. Klein
Neurology 2004; 62: 389-394.
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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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- ARTICLES
Genetic influences on memory performance in familial Alzheimer disease
- J. H. Lee, A. Flaquer, Y. Stern, B. Tycko, and R. Mayeux
Neurology 2004; 62: 414-421.
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- BRIEF COMMUNICATIONS
Clinical features of Creutzfeldt-Jakob disease with V180I mutation
- K. Jin, Y. Shiga, S. Shibuya, K. Chida, Y. Sato, H. Konno, K. Doh-ura, T. Kitamoto, and Y. Itoyama
Neurology 2004; 62: 502-505.
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- ARTICLES
Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family
- B. P.C. van de Warrenburg, D. S. Verbeek, S. J. Piersma, F. A.M. Hennekam, P. L. Pearson, N. V.A.M. Knoers, H. P.H. Kremer, and R. J. Sinke
Neurology 2003; 61: 1760-1765.
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- VIEWS & REVIEWS
The CNS phenotype of X-linked Charcot-Marie-Tooth disease: More than a peripheral problem
- Robert A. Taylor, Erin M. Simon, Harold G. Marks, and Steven S. Scherer
Neurology 2003; 61: 1475-1478.
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- ARTICLES
A CAV3 microdeletion differentially affects skeletal muscle and myocardium
- R. Cagliani, N. Bresolin, A. Prelle, A. Gallanti, F. Fortunato, M. Sironi, P. Ciscato, G. Fagiolari, S. Bonato, S. Galbiati, S. Corti, C. Lamperti, M. Moggio, and G. P. Comi
Neurology 2003; 61: 1513-1519.
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