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All Genetics
Citations 431-440 of 679 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Adult-onset leukoencephalopathy with vanishing white matter with a missense mutation in EIF2B5
- H. Ohtake, T. Shimohata, K. Terajima, T. Kimura, R. Jo, R. Kaseda, O. Iizuka, M. Takano, Y. Akaiwa, H. Goto, H. Kobayashi, T. Sugai, T. Muratake, T. Hosoki, T. Shioiri, K. Okamoto, O. Onodera, K. Tanaka, T. Someya, T. Nakada, and S. Tsuji
Neurology 2004; 62: 1601-1603.
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- BRIEF COMMUNICATIONS
Distal myopathy with rimmed vacuoles (DMRV): New GNE mutations and splice variant
- H. Tomimitsu, J. Shimizu, K. Ishikawa, N. Ohkoshi, I. Kanazawa, and H. Mizusawa
Neurology 2004; 62: 1607-1610.
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- BRIEF COMMUNICATIONS
HFE mutations are not strongly associated with sporadic ALS
- A. A. Yen, E. P. Simpson, J. S. Henkel, D. R. Beers, and S. H. Appel
Neurology 2004; 62: 1611-1612.
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- BRIEF COMMUNICATIONS
Suggestive evidence for linkage to chromosome 13qter for autosomal dominant type 1 porencephaly
- U. Aguglia, A. Gambardella, G. J. Breedveld, R. L. Oliveri, E. Le Piane, D. Messina, A. Quattrone, and P. Heutink
Neurology 2004; 62: 1613-1615.
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- BRIEF COMMUNICATIONS
Genes influencing Parkinson disease onset: Replication of PARK3 and identification of novel loci
- N. Pankratz, S. K. Uniacke, C. A. Halter, A. Rudolph, C. W. Shults, P. M. Conneally, T. Foroud, W. C. Nichols, and the Parkinson Study Group
Neurology 2004; 62: 1616-1618.
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- BRIEF COMMUNICATIONS
Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
- Z. K. Wszolek, R. F. Pfeiffer, Y. Tsuboi, R. J. Uitti, R. D. McComb, A. J. Stoessl, A. J. Strongosky, A. Zimprich, B. Müller-Myhsok, M. J. Farrer, T. Gasser, D. B. Calne, and D. W. Dickson
Neurology 2004; 62: 1619-1622.
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- BRIEF COMMUNICATIONS
Alzheimer disease risk associated with APOE4 is modified by STH gene polymorphism
- D. Seripa, M. G. Matera, R. P. D’Andrea, C. Gravina, C. Masullo, A. Daniele, A. Bizzarro, M. Rinaldi, P. Antuono, D. R. Wekstein, G. Dal Forno, and V. M. Fazio
Neurology 2004; 62: 1631-1633.
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- EDITORIALS
A clever road from myopathology to genes: The myotilin story
- George Karpati and Michael Sinnreich
Neurology 2004; 62: 1248-1249.
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- VIEWS & REVIEWS
Gene therapy of the brain: The trans-vascular approach
- Felix Schlachetzki, Yun Zhang, Ruben J. Boado, and William M. Pardridge
Neurology 2004; 62: 1275-1281.
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- ARTICLES
Mutations in myotilin cause myofibrillar myopathy
- Duygu Selcen and Andrew G. Engel
Neurology 2004; 62: 1363-1371.
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