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Muscle disease
Citations 141-150 of 281 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Truncated ClC-1 mRNA in myotonic dystrophy exerts a dominant-negative effect on the Cl current
- Jim Berg, Hong Jiang, Charles A. Thornton, and Stephen C. Cannon
Neurology 2004; 63: 2371-2375.
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- BRIEF COMMUNICATIONS
Associations with autoimmune disorders and HLA class I and II antigens in inclusion body myositis
- U. A. Badrising, G. M.Th. Schreuder, M. J. Giphart, K. Geleijns, J. J.G.M. Verschuuren, A. R. Wintzen, and the Dutch IBM Study Group
Neurology 2004; 63: 2396-2398.
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- BRIEF COMMUNICATIONS
Sudden cardiac death in myotonic dystrophy type 2
- B. G.H. Schoser, K. Ricker, C. Schneider-Gold, C. Hengstenberg, J. Dürre, B. Bültmann, W. Kress, J. W. Day, and L. P.W. Ranum
Neurology 2004; 63: 2402-2404.
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- ARTICLES
New mutations of SCN4A cause a potassium-sensitive normokalemic periodic paralysis
- S. Vicart, D. Sternberg, E. Fournier, F. Ochsner, P. Laforet, T. Kuntzer, B. Eymard, B. Hainque, and B. Fontaine
Neurology 2004; 63: 2120-2127.
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- CLINICAL/SCIENTIFIC NOTES
SCN4A-associated hypokalemic periodic paralysis merits a trial of acetazolamide
- S. L. Venance, K. Jurkat-Rott, F. Lehmann-Horn, and R. Tawil
Neurology 2004; 63: 1977.
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- ARTICLES
Correlating phenotype and genotype in the periodic paralyses
- T. M. Miller, M. R. Dias da Silva, H. A. Miller, H. Kwiecinski, J. R. Mendell, R. Tawil, P. McManis, R. C. Griggs, C. Angelini, S. Servidei, J. Petajan, M. C. Dalakas, L. P.W. Ranum, Y. H. Fu, and L. J. Ptácek
Neurology 2004; 63: 1647-1655.
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- ARTICLES
Late-onset Pompe disease primarily affects quality of life in physical health domains
- M. L.C. Hagemans, A. C.J.W. Janssens, L. P.F. Winkel, K. A. Sieradzan, A. J.J. Reuser, P. A. Van Doorn, and A. T. Van der Ploeg
Neurology 2004; 63: 1688-1692.
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- CLINICAL/SCIENTIFIC NOTES
Charcot–Marie–Tooth features and maculopathy in a patient with Danon disease
- P. Laforêt, P. Charron, T. Maisonobe, N. B. Romero, E. Villard, P. Sebillon, V. Drouin-Garraud, O. Dubourg, M. Fardeau, M. Komajda, and B. Eymard
Neurology 2004; 63: 1535.
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- ARTICLES
Clinical and genetic heterogeneity of branching enzyme deficiency (glycogenosis type IV)
- C. Bruno, O. P. van Diggelen, D. Cassandrini, M. Gimpelev, B. Giuffrè, M. A. Donati, P. Introvini, A. Alegria, S. Assereto, L. Morandi, M. Mora, E. Tonoli, S. Mascelli, M. Traverso, E. Pasquini, M. Bado, L. Vilarinho, G. van Noort, F. Mosca, S. DiMauro, F. Zara, and C. Minetti
Neurology 2004; 63: 1053-1058.
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- BRIEF COMMUNICATIONS
Familial myopathy with tubular aggregates associated with abnormal pupils
- Nortina Shahrizaila, James Lowe, and Adrian Wills
Neurology 2004; 63: 1111-1113.
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