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Muscle disease
Citations 261-270 of 281 total displayed.
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Past content
(since Jan 2001):
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- CLINICAL/SCIENTIFIC NOTES
Intravenous immunoglobulin for dysphagia of inclusion body myositis
- P. Cherin, S. Pelletier, A. Teixeira, P. Laforet, A. Simon, S. Herson, and B. Eymard
Neurology 2002; 58: 326.
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- ARTICLES
A sporadic case of rippling muscle disease caused by a de novo caveolin-3 mutation
- M. Vorgerd, K. Ricker, F. Ziemssen, W. Kress, H. H. Goebel, W. A. Nix, C. Kubisch, B. G.H. Schoser, and W. Mortier
Neurology 2001; 57: 2273-2277.
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- BRIEF COMMUNICATIONS
Inflammation in dysferlin myopathy: Immunohistochemical characterization of 13 patients
- E. Gallardo, R. Rojas–García, N. de Luna, A. Pou, R.H. Brown, Jr., and I. Illa
Neurology 2001; 57: 2136-2138.
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- ARTICLES
Gating of myotonic Na channel mutants defines the response to mexiletine and a potent derivative
- J.-F. Desaphy, A. De Luca, P. Tortorella, D. De Vito, A. L. George, Jr., and D. Conte Camerino
Neurology 2001; 57: 1849-1857.
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- BRIEF COMMUNICATIONS
Episodes of generalized weakness in two sibs with the C164T mutation of the connexin 32 gene
- Marios Panas, Nikolaos Kalfakis, Charalampos Karadimas, and Demetris Vassilopoulos
Neurology 2001; 57: 1906-1908.
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- ARTICLES
Production of IL-6 by human myoblasts stimulated with Aß: Relevance in the pathogenesis of IBM
- P. Baron, D. Galimberti, L. Meda, E. Scarpini, G. Conti, F. Cogiamanian, and G. Scarlato
Neurology 2001; 57: 1561-1565.
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- ARTICLES
Randomized pilot trial of ßINF1a (Avonex) in patients with inclusion body myositis
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Neurology 2001; 57: 1566-1570.
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- ARTICLES
Randomized, double-blind, placebo-controlled trial of albuterol in facioscapulohumeral dystrophy
- J. T. Kissel, M. P. McDermott, J. R. Mendell, W. M. King, S. Pandya, R. C. Griggs, and R. Tawil
Neurology 2001; 57: 1434-1440.
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- ARTICLES
Sleep-disordered breathing and respiratory failure in acid maltase deficiency
- U. Mellies, R. Ragette, C. Schwake, M. Baethmann, T. Voit, and H. Teschler
Neurology 2001; 57: 1290-1295.
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- BRIEF COMMUNICATIONS
Congenital muscular dystrophy with primary partial laminin  2 chain deficiency: Molecular study
- Y. He, K. J. Jones, N. Vignier, G. Morgan, M. Chevallay, A. Barois, B. Estournet–Mathiaud, H. Hori, T. Mizuta, F. M.S. Tomé, K. N. North, and P. Guicheney
Neurology 2001; 57: 1319-1322.
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