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Neurology
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All Genetics

Citations 311-320 of 679 total displayed.

Past content (since Jan 2001):

EDITORIALS
Spinocerebellar ataxia type 14: Opening a new door in dominant ataxia research?
Massimo Pandolfo and Bart P.C. van de Warrenburg
Neurology 2005; 64: 1113-1114. [Full text] [PDF]  

ARTICLES
Neurologic features of horizontal gaze palsy and progressive scoliosis with mutations in ROBO3
T. M. Bosley, M. A.M. Salih, J. C. Jen, D. D.M. Lin, D. Oystreck, K. K. Abu-Amero, D. B. MacDonald, Z. al Zayed, H. al Dhalaan, T. Kansu, B. Stigsby, and R. W. Baloh
Neurology 2005; 64: 1196-1203. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
The clinical and genetic spectrum of spinocerebellar ataxia 14
D. -H. Chen, P. J. Cimino, L. P.W. Ranum, H. Y. Zoghbi, I. Yabe, L. Schut, R. L. Margolis, H. P. Lipe, A. Feleke, M. Matsushita, J. Wolff, C. Morgan, D. Lau, M. Fernandez, H. Sasaki, W. H. Raskind, and T. D. Bird
Neurology 2005; 64: 1258-1260. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

EDITORIALS
Titinopathies: What happens when a big gene mutates in a big family?
Duygu Selcen and Kate Bushby
Neurology 2005; 64: 596-597. [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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* Collected Resources Home

* Related collections:
 Genetics
 All Genetics
 Neurofibromatosis
 Other neurocutaneous disorders
 Genetic linkage
 Association studies in genetics
 Gene expression studies
 Gene therapy
 Mitochondrial disorders
 Ion channel gene defects
 Spinocerebellar ataxia
 Trinucleotide repeat diseases
 Chromosomes


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