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All Genetics
Citations 171-180 of 679 total displayed.
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Past content
(since Jan 2001):
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- ARTICLE
CMT1X phenotypes represent loss of GJB1 gene function
- M. E. Shy, C. Siskind, E. R. Swan, K. M. Krajewski, T. Doherty, D. R. Fuerst, P. J. Ainsworth, R. A. Lewis, S. S. Scherer, and A. F. Hahn
Neurology 2007; 68: 849-855.
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- ARTICLES
DNA microarray analysis identifies candidate regions and genes in unexplained mental retardation
- H. Engels, A. Brockschmidt, A. Hoischen, C. Landwehr, K. Bosse, C. Walldorf, G. Toedt, B. Radlwimmer, P. Propping, P. Lichter, and R. G. Weber
Neurology 2007; 68: 743-750.
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- ARTICLES
Distal arthrogryposis and muscle weakness associated with a ß-tropomyosin mutation
- H. Tajsharghi, E. Kimber, D. Holmgren, M. Tulinius, and A. Oldfors
Neurology 2007; 68: 772-775.
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- CLINICAL/SCIENTIFIC NOTES
DRD3 variant and risk of essential tremor
- E. -K. Tan, K. M. Prakash, S. Fook-Chong, Y. Yih, E. Chua, S. Y. Lum, M. C. Wong, R. Pavanni, and Y. Zhao
Neurology 2007; 68: 790-791.
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- EDITORIALS
Pushing the genetic frontier with facioscapulohumeral muscular dystrophy
- Steven A. Greenberg and George W. Padberg
Neurology 2007; 68: 544-545.
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- ARTICLES
Expression profile of FSHD supports a link between retinal vasculopathy and muscular dystrophy
- R. J. Osborne, S. Welle, S. L. Venance, C. A. Thornton, and R. Tawil
Neurology 2007; 68: 569-577.
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- ARTICLES
Genotype-phenotype study in an FSHD family with a proximal deletion encompassing p13E-11 and D4Z4
- K. L. Deak, R. J.L.F Lemmers, J. M. Stajich, R. Klooster, R. Tawil, R. R. Frants, M. C. Speer, S. M. van der Maarel, and J. R. Gilbert
Neurology 2007; 68: 578-582.
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- CLINICAL/SCIENTIFIC NOTES
Impact of apolipoprotein gene on cognitive impairment and recovery after traumatic brain injury
- Jennie Ponsford, Dion Rudzki, Karen Bailey, and Kim T. Ng
Neurology 2007; 68: 619-620.
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- ARTICLES
Myoclonus-dystonia, obsessive-compulsive disorder, and alcohol dependence in SGCE mutation carriers
- C. W. Hess, D. Raymond, P. de Carvalho Aguiar, S. Frucht, J. Shriberg, G. A. Heiman, R. Kurlan, C. Klein, S. B. Bressman, L. J. Ozelius, and R. Saunders-Pullman
Neurology 2007; 68: 522-524.
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- ARTICLES
Lack of aggregation of ischemic stroke subtypes within affected sibling pairs
- P. G. Wiklund, W. M. Brown, T. G. Brott, B. Stegmayr, R. D. Brown, Jr, S. Nilsson-Ardnor, J. A. Hardy, B. M. Kissela, A. Singleton, D. Holmberg, S. S. Rich, and J. F. Meschia
Neurology 2007; 68: 427-431.
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