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Muscle disease
Citations 231-240 of 281 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Modafinil reduces excessive somnolence and enhances mood in patients with myotonic dystrophy
- J. R. MacDonald, J. D. Hill, and M. A. Tarnopolsky
Neurology 2002; 59: 1876-1880.
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- EDITORIALS
Sweetening the pot in muscle: Genetic defects of protein glycosylation causing muscle disease
- George Karpati and Paul Holland
Neurology 2002; 59: 1674-1676.
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- ARTICLES
Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy
- I. Nishino, S. Noguchi, K. Murayama, A. Driss, K. Sugie, Y. Oya, T. Nagata, K. Chida, T. Takahashi, Y. Takusa, T. Ohi, J. Nishimiya, N. Sunohara, E. Ciafaloni, M. Kawai, M. Aoki, and I. Nonaka
Neurology 2002; 59: 1689-1693.
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- BRIEF COMMUNICATIONS
GNE mutations in an American family with quadriceps-sparing IBM and lack of mutations in s-IBM
- Olavo M. Vasconcelos, Raghavan Raju, and Marinos C. Dalakas
Neurology 2002; 59: 1776-1779.
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- ARTICLES
Mitochondrial disorders: A proposal for consensus diagnostic criteria in infants and children
- Nicole I. Wolf and Jan A.M. Smeitink
Neurology 2002; 59: 1402-1405.
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- ARTICLES
Diagnostic criteria for respiratory chain disorders in adults and children
- F.P. Bernier, A. Boneh, X. Dennett, C.W. Chow, M.A. Cleary, and D.R. Thorburn
Neurology 2002; 59: 1406-1411.
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- ARTICLES
Molecular profiles of inflammatory myopathies
- S. A. Greenberg, D. Sanoudou, J. N. Haslett, I. S. Kohane, L. M. Kunkel, A. H. Beggs, and A. A. Amato
Neurology 2002; 59: 1170-1182.
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- ARTICLES
Mitochondrial DNA depletion: Mutations in thymidine kinase gene with myopathy and SMA
- M. Mancuso, L. Salviati, S. Sacconi, D. Otaegui, P. Camaño, A. Marina, S. Bacman, C.T. Moraes, J.R. Carlo, M. Garcia, M. Garcia-Alvarez, L. Monzon, A.B. Naini, M. Hirano, E. Bonilla, A.L. Taratuto, S. DiMauro, and T.H. Vu
Neurology 2002; 59: 1197-1202.
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- ARTICLES
Exercise tolerance in carnitine palmitoyltransferase II deficiency with IV and oral glucose
- Mette C. Ørngreen, David B. Olsen, and John Vissing
Neurology 2002; 59: 1046-1051.
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- BRIEF COMMUNICATIONS
A novel murine myotonia congenita without molecular defects in the ClC-1 and the SCN4A
- T. Shirakawa, K. Sakai, Y. Kitagawa, A. Hori, and G. Hirose
Neurology 2002; 59: 1091-1094.
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