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Muscle disease
Citations 191-200 of 281 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Limb-girdle muscular dystrophy in a 71-year-old woman with an R27Q mutation in the CAV3 gene
- D. Figarella–Branger, J. Pouget, R. Bernard, M. Krahn, C. Fernandez, N. Lévy, and J. F. Pellissier
Neurology 2003; 61: 562-564.
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- CLINICAL/SCIENTIFIC NOTES
Response to sumatriptan in headache of MELAS syndrome
- Takahiro Iizuka, Fumihiko Sakai, Motoi Endo, and Norihiro Suzuki
Neurology 2003; 61: 577-578.
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- EDITORIALS
Unicorns, dragons, polymyositis, and other mythological beasts
- Anthony A. Amato and Robert C. Griggs
Neurology 2003; 61: 288-289.
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- ARTICLES
Polymyositis: An overdiagnosed entity
- M. F.G. van der Meulen, I. M. Bronner, J. E. Hoogendijk, H. Burger, W. J. van Venrooij, A. E. Voskuyl, H. J. Dinant, W. H.J.P. Linssen, J. H.J. Wokke, and M. de Visser
Neurology 2003; 61: 316-321.
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- ARTICLES
MAP kinase phosphatase-1 is induced in abnormal fibers in inclusion body myositis
- S. Nakano, A. Shinde, H. Ito, H. Ito, and H. Kusaka
Neurology 2003; 61: 322-326.
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- BRIEF COMMUNICATIONS
GNE mutations causing distal myopathy with rimmed vacuoles with inflammation
- I. Yabe, T. Higashi, S. Kikuchi, H. Sasaki, T. Fukazawa, K. Yoshida, and K. Tashiro
Neurology 2003; 61: 384-386.
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- BRIEF COMMUNICATIONS
A neonatal form of glycogen storage disease type IV
- M. Nambu, K. Kawabe, T. Fukuda, T. B. Okuno, S. Ohta, I. Nonaka, H. Sugie, and I. Nishino
Neurology 2003; 61: 392-394.
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- BRIEF COMMUNICATIONS
A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2
- L. Palenzuela, A.L. Andreu, J. Gàmez, M.R. Vilà, T. Kunimatsu, A. Meseguer, C. Cervera, I. Fernandez Cadenas, P.F.M. van der Ven, T.G. Nygaard, E. Bonilla, and M. Hirano
Neurology 2003; 61: 404-406.
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- NEUROIMAGES
Eosinophilic fasciitis: MRI evaluation
- Tomihiro Imai, Masaki Saitoh, and Hiroyuki Matsumoto
Neurology 2003; 61: 416.
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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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