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All Genetics
Citations 501-510 of 679 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
D4F104S1 deletion in facioscapulohumeral muscular dystrophy: Phenotype, size, and detection
- R. J.L.F. Lemmers, M. Osborn, T. Haaf, M. Rogers, R. R. Frants, G. W. Padberg, D. N. Cooper, S. M. van der Maarel, and M. Upadhyaya
Neurology 2003; 61: 178-183.
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- BRIEF COMMUNICATIONS
A clinical and genetic study of SPG5A linked autosomal recessive hereditary spastic paraplegia
- P.A. Wilkinson, A.H. Crosby, C. Turner, H. Patel, N.W. Wood, A.H. Schapira, and T.T. Warner
Neurology 2003; 61: 235-238.
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- BRIEF COMMUNICATIONS
Mutations in the  -sarcoglycan gene found to be uncommon in seven myoclonus–dystonia families
- F. Han, A. E. Lang, L. Racacho, D. E. Bulman, and D. A. Grimes
Neurology 2003; 61: 244-246.
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- BRIEF COMMUNICATIONS
Transthyretin Val122Ile, accumulated Aß, and inclusion-body myositis aspects in cultured muscle
- Valerie Askanas, W. King Engel, Janis McFerrin, and Gaetano Vattemi
Neurology 2003; 61: 257-260.
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- CLINICAL/SCIENTIFIC NOTES
Polyalanine expansion of ARX associated with cryptogenic West syndrome
- M. Kato, S. Das, K. Petras, Y. Sawaishi, and W.B. Dobyns
Neurology 2003; 61: 267-276.
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- CLINICAL/SCIENTIFIC NOTES
Serum prolactin in symptomatic and asymptomatic dopa-responsive dystonia due to a GCH1 mutation
- Y. Furukawa, M. Guttman, H. Wong, S.A. Farrell, S. Furtado, and S.J. Kish
Neurology 2003; 61: 269-270.
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- EDITORIALS
PD or not PD?: That is the question
- Caroline M. Tanner
Neurology 2003; 61: 5-6.
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- ARTICLES
Validity of family history data on PD: Evidence for a family information bias
- A. Elbaz, S.K. McDonnell, D.M. Maraganore, K.J. Strain, D.J. Schaid, J.H. Bower, J.E. Ahlskog, and W.A. Rocca
Neurology 2003; 61: 11-17.
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- ARTICLES
Accuracy of family history data on Parkinson’s disease
- K. Marder, G. Levy, E. D. Louis, H. Mejia–Santana, L. Cote, H. Andrews, J. Harris, C. Waters, B. Ford, S. Frucht, S. Fahn, and R. Ottman
Neurology 2003; 61: 18-23.
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- ARTICLES
A distinct phenotype of distal myopathy in a large Finnish family
- I. Mahjneh, H. Haravuori, A. Paetau, L.V.B. Anderson, A. Saarinen, B. Udd, and H. Somer
Neurology 2003; 61: 87-92.
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