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All Genetics
Citations 311-320 of 676 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Lafora disease due to EPM2B mutations: A clinical and genetic study
- C. Gómez-Abad, P. Gómez-Garre, E. Gutiérrez-Delicado, S. Saygi, R. Michelucci, C. A. Tassinari, S. Rodríguez de Córdoba, and J. M. Serratosa
Neurology 2005; 64: 982-986.
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- BRIEF COMMUNICATIONS
Correlation of proband and sibling stroke latency: The SWISS Study
- J. F. Meschia, T. G. Brott, R. D. Brown, Jr, B. M. Kissela, J. A. Hardy, W. M. Brown, S. S. Rich for the Siblings With Ischemic Stroke Study Investigators
Neurology 2005; 64: 1061-1063.
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- EDITORIALS
Titinopathies: What happens when a big gene mutates in a big family?
- Duygu Selcen and Kate Bushby
Neurology 2005; 64: 596-597.
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- ARTICLES
Long-term effects of migraine on cognitive function: A population-based study of Danish twins
- D. Gaist, L. Pedersen, C. Madsen, I. Tsiropoulos, S. Bak, S. Sindrup, M. McGue, B. Krogh Rasmussen, and K. Christensen
Neurology 2005; 64: 600-607.
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- ARTICLES
Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2J
- B. Udd, A. Vihola, J. Sarparanta, I. Richard, and P. Hackman
Neurology 2005; 64: 636-642.
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- BRIEF COMMUNICATIONS
The impact of privacy protections on recruitment in a multicenter stroke genetics study
- D. T. Chen, B. B. Worrall, R. D. Brown, Jr, T. G. Brott, B. M. Kissela, T. S. Olson, S. S. Rich, J. F. Meschia for the SWISS Investigators
Neurology 2005; 64: 721-724.
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- BRIEF COMMUNICATIONS
The epsilon-sarcoglycan gene in myoclonic syndromes
- E. M. Valente, M. J. Edwards, P. Mir, A. DiGiorgio, S. Salvi, M. Davis, N. Russo, M. Bozi, H. -T. Kim, G. Pennisi, N. Quinn, B. Dallapiccola, and K. P. Bhatia
Neurology 2005; 64: 737-739.
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- BRIEF COMMUNICATIONS
Cystatin C as a risk factor for Alzheimer disease
- H. M. Cathcart, R. Huang, I. S. Lanham, E. H. Corder, and S. E. Poduslo
Neurology 2005; 64: 755-757.
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- EXPEDITED ARTICLES
A variant in the HS1-BP3 gene is associated with familial essential tremor
- J. J. Higgins, R. Q. Lombardi, J. Pucilowska, J. Jankovic, E. K. Tan, and J. P. Rooney
Neurology 2005; 64: 417-421.
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- ARTICLES
fMRI evidence of compensatory mechanisms in older adults at genetic risk for Alzheimer disease
- Mark W. Bondi, Wes S. Houston, Lisa T. Eyler, and Gregory G. Brown
Neurology 2005; 64: 501-508.
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