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All Neuromuscular Disease
Citations 81-90 of 158 total displayed.
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Past content
(since Jan 2000):
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- ARTICLES
Are amyotrophic lateral sclerosis patients cognitively normal?
- C. Lomen-Hoerth, J. Murphy, S. Langmore, J. H. Kramer, R. K. Olney, and B. Miller
Neurology 2003; 60: 1094-1097.
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- ARTICLES
Guillain-Barré syndrome: A prospective, population-based incidence and outcome survey
- A. Chiò, D. Cocito, M. Leone, M.T. Giordana, G. Mora, R. Mutani, and the Piemonte and Valle d’Aosta Register for Guillain-Barré Syndrome
Neurology 2003; 60: 1146-1150.
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- ARTICLES
The gene for HMSN2C maps to 12q23-24: A region of neuromuscular disorders
- C. J. Klein, J. M. Cunningham, E. J. Atkinson, D. J. Schaid, S. J. Hebbring, S. A. Anderson, D. M. Klein, P. J.B. Dyck, W. J. Litchy, S. N. Thibodeau, and P. J. Dyck
Neurology 2003; 60: 1151-1156.
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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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- HISTORICAL NEUROLOGY
Hereditary neuropathy with liability to pressure palsies: The first publication (1947)
- Peter J. Koehler
Neurology 2003; 60: 1211-1213.
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- ARTICLES
Classical infantile spinal muscular atrophy with SMN deficiency causes sensory neuronopathy
- S. Rudnik-Schöneborn, H.H. Goebel, W. Schlote, S. Molaian, H. Omran, U. Ketelsen, R. Korinthenberg, D. Wenzel, H. Lauffer, M. Kreiß-Nachtsheim, B. Wirth, and K. Zerres
Neurology 2003; 60: 983-987.
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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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- BRIEF COMMUNICATIONS
APOE genotype is a risk factor for neuropathy severity in diabetic patients
- R.S. Bedlack, D. Edelman, J.W. Gibbs, III, D. Kelling, W. Strittmatter, A.M. Saunders, and J. Morgenlander
Neurology 2003; 60: 1022-1024.
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- BRIEF COMMUNICATIONS
Myasthenia gravis: A higher than expected incidence in the elderly
- J. M. Aragonès, I. Bolíbar, X. Bonfill, E. Bufill, A. Mummany, F. Alonso, and I. Illa
Neurology 2003; 60: 1024-1026.
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