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All Genetics
Citations 171-180 of 676 total displayed.
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Past content
(since Jan 2001):
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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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- ARTICLES
Multiplex ligation-dependent probe amplification detects DCX gene deletions in band heterotopia
- D. Mei, E. Parrini, M. Pasqualetti, G. Tortorella, E. Franzoni, U. Giussani, C. Marini, S. Migliarini, and R. Guerrini
Neurology 2007; 68: 446-450.
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- ARTICLES
Preclinical validation of a multiplex real-time assay to quantify SMN mRNA in patients with SMA
- L. R. Simard, M-C Bélanger, S. Morissette, M. Wride, T. W. Prior, and K. J. Swoboda
Neurology 2007; 68: 451-456.
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- ARTICLES
Familial effects on the clinical course of multiple sclerosis
- A. E. Hensiek, S. R. Seaman, L. F. Barcellos, A. Oturai, M. Eraksoi, E. Cocco, L. Vecsei, G. Stewart, B. Dubois, J. Bellman-Strobl, M. Leone, O. Andersen, K. Bencsik, D. Booth, E. G. Celius, H. F. Harbo, S. L. Hauser, R. Heard, J. Hillert, K. -M. Myhr, M. G. Marrosu, J. R. Oksenberg, C. Rajda, S. J. Sawcer, P. S. Sørensen, F. Zipp, and D.A.S. Compston
Neurology 2007; 68: 376-383.
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