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Muscle disease
Citations 41-50 of 281 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
What causes paramyotonia in the United Kingdom?: Common and new SCN4A mutations revealed
- E. Matthews, S. V. Tan, D. Fialho, M. G. Sweeney, R. Sud, A. Haworth, E. Stanley, G. Cea, M. B. Davis, and M. G. Hanna
Neurology 2008; 70: 50-53.
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- EDITORIALS
Revisiting the immunopathogenesis of the inflammatory myopathies
- Reinhard Hohlfeld and Klaus Dornmair
Neurology 2007; 69: 1966-1967.
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- VIEWS & REVIEWS
Proposed immunologic models of the inflammatory myopathies and potential therapeutic implications
- Steven A. Greenberg
Neurology 2007; 69: 2008-2019.
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- ARTICLES
A novel founder SCN4A mutation causes painful cold-induced myotonia in French-Canadians
- E. Rossignol, J. Mathieu, I. Thiffault, M. Tétreault, M. -J. Dicaire, N. Chrestian, N. Dupré, J. Puymirat, and B. Brais
Neurology 2007; 69: 1937-1941.
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- ARTICLES
T cell receptor profiling in muscle and blood lymphocytes in sporadic inclusion body myositis
- M. Salajegheh, G. Rakocevic, R. Raju, A. Shatunov, L. G. Goldfarb, and M. C. Dalakas
Neurology 2007; 69: 1672-1679.
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- ARTICLES
Cognitive impairment in familial ALS
- M. W. Wheaton, A. R. Salamone, D. M. Mosnik, R. O. McDonald, S. H. Appel, H. I. Schmolck, G. M. Ringholz, and P. E. Schulz
Neurology 2007; 69: 1411-1417.
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- ARTICLES
New POMT2 mutations causing congenital muscular dystrophy: Identification of a founder mutation
- A. Yanagisawa, C. Bouchet, P.Y.K. Van den Bergh, J. -M. Cuisset, L. Viollet, F. Leturcq, N. B. Romero, S. Quijano-Roy, M. Fardeau, N. Seta, and P. Guicheney
Neurology 2007; 69: 1254-1260.
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- VIEWS AND REVIEWS
Phenotypic clustering of lamin A/C mutations in neuromuscular patients
- S. Benedetti, I. Menditto, M. Degano, C. Rodolico, L. Merlini, A. D’Amico, L. Palmucci, A. Berardinelli, E. Pegoraro, C. P. Trevisan, L. Morandi, I. Moroni, G. Galluzzi, E. Bertini, A. Toscano, M. Olivè, G. Bonne, F. Mari, R. Caldara, R. Fazio, I. Mammì, P. Carrera, D. Toniolo, G. Comi, A. Quattrini, M. Ferrari, and S. C. Previtali
Neurology 2007; 69: 1285-1292.
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- ARTICLES
Hypomethylation is restricted to the D4Z4 repeat array in phenotypic FSHD
- J. C. de Greef, M. Wohlgemuth, O. A. Chan, K. B. Hansson, D. Smeets, R. R. Frants, C. M. Weemaes, G. W. Padberg, and S. M. van der Maarel
Neurology 2007; 69: 1018-1026.
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- ARTICLES
Primary collagen VI deficiency is the second most common congenital muscular dystrophy in Japan
- M. Okada, G. Kawahara, S. Noguchi, K. Sugie, K. Murayama, I. Nonaka, Y. K. Hayashi, and I. Nishino
Neurology 2007; 69: 1035-1042.
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