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Neurology
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Muscle disease

Citations 141-150 of 283 total displayed.

Past content (since Jan 2001):

CLINICAL/SCIENTIFIC NOTES
Rigid spine muscular dystrophy due to SEPN1 mutation presenting as cor pulmonale
S. L. Venance, W. J. Koopman, B. A. Miskie, R. A. Hegele, and A. F. Hahn
Neurology 2005; 64: 395-396. [Full text] [PDF]  

SPECIAL ARTICLES
Practice Parameter: Corticosteroid treatment of Duchenne dystrophy: Report of the Quality Standards Subcommittee of the American Academy of Neurology and the Practice Committee of the Child Neurology Society
R. T. Moxley, III, S. Ashwal, S. Pandya, A. Connolly, J. Florence, K. Mathews, L. Baumbach, C. McDonald, M. Sussman, and C. Wade
Neurology 2005; 64: 13-20. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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. [Full text] [PDF]  

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* Collected Resources Home

* Related collections:
 Neuromuscular disease
 All Neuromuscular Disease
 Anterior nerve cell disease
 Amyotrophic lateral sclerosis
 Myasthenia
 Lambert-Eaton syndrome
 Peripheral neuropathy
 Carpal tunnel syndrome
 Cranial neuropathy
 Guillain-Barre syndrome
 Chronic inflammatory demyelinating polyneuropathy
 Transverse myelitis
 Muscle disease


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