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Muscle disease
Citations 221-230 of 281 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
Cerebellar ataxia and coenzyme Q10 deficiency
- C. Lamperti, A. Naini, M. Hirano, D.C. De Vivo, E. Bertini, S. Servidei, M. Valeriani, D. Lynch, B. Banwell, M. Berg, T. Dubrovsky, C. Chiriboga, C. Angelini, E. Pegoraro, and S. DiMauro
Neurology 2003; 60: 1206-1208.
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- ARTICLES
FKRP gene mutations cause congenital muscular dystrophy, mental retardation, and cerebellar cysts
- H. Topaloglu, M. Brockington, Y. Yuva, B. Talim, G. Haliloglu, D. Blake, S. Torelli, S.C. Brown, and F. Muntoni
Neurology 2003; 60: 988-992.
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- ARTICLES
Activation of nuclear factor- B in inflammatory myopathies and Duchenne muscular dystrophy
- M.C. Monici, M. Aguennouz, A. Mazzeo, C. Messina, and G. Vita
Neurology 2003; 60: 993-997.
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- NEUROIMAGES
MRI in diabetic muscle infarction
- Jill W. Miller, James Fleckenstein, Hiroyuki Nodera, and David N. Herrmann
Neurology 2003; 60: 1019.
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- CLINICAL/SCIENTIFIC NOTES
Neuroleptic malignant-like syndrome due to donepezil and maprotiline
- Norio Ohkoshi, Daisuke Satoh, Masaaki Nishi, and Shin’ichi Shoji
Neurology 2003; 60: 1050-1051.
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- ARTICLES
Myotonic dystrophy type 2: Molecular, diagnostic and clinical spectrum
- J. W. Day, K. Ricker, J. F. Jacobsen, L. J. Rasmussen, K. A. Dick, W. Kress, C. Schneider, M. C. Koch, G. J. Beilman, A. R. Harrison, J. C. Dalton, and L. P.W. Ranum
Neurology 2003; 60: 657-664.
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- ARTICLES
Clinical course correlates poorly with muscle pathology in nemaline myopathy
- M. M. Ryan, B. Ilkovski, C. D. Strickland, C. Schnell, D. Sanoudou, C. Midgett, R. Houston, D. Muirhead, X. Dennett, L. K. Shield, U. De Girolami, S. T. Iannaccone, N. G. Laing, K. N. North, and A. H. Beggs
Neurology 2003; 60: 665-673.
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- BRIEF COMMUNICATIONS
Creatine monohydrate in DM2/PROMM: A double-blind placebo-controlled clinical study
- C. Schneider–Gold, M. Beck, C. Wessig, A. George, H. Kele, K. Reiners, and K. V. Toyka
Neurology 2003; 60: 500-502.
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- BRIEF COMMUNICATIONS
Paramyotonia congenita with an SCN4A mutation affecting cardiac repolarization
- Y. Péréon, G. Lande, S. Demolombe, S. Nguyen The Tich, D. Sternberg, H. Le Marec, and A. David
Neurology 2003; 60: 340-342.
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- BRIEF COMMUNICATIONS
Myoglobinuria and COX deficiency in a patient taking cerivastatin and gemfibrozil
- J. Arenas, M.A. Fernández-Moreno, J.A. Molina, V. Fernández, P. del Hoyo, Y. Campos, P. Calvo, M.A. Martín, A. García, T. Moreno, A. Martínez-Salio, B. Börnstein, F. Bermejo, A. Cabello, and R. Garesse
Neurology 2003; 60: 124-126.
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