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Neurology
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Muscle disease

Citations 131-140 of 283 total displayed.

Past content (since Jan 2001):

ARTICLES
A new dominant distal myopathy affecting posterior leg and anterior upper limb muscles
D. R. Williams, K. Reardon, L. Roberts, X. Dennet, R. Duff, N. G. Laing, and E. Byrne
Neurology 2005; 64: 1245-1254. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Aerobic training improves exercise performance in facioscapulohumeral muscular dystrophy
David B. Olsen, Mette Cathrine Ørngreen, and John Vissing
Neurology 2005; 64: 1064-1066. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
In situ identification of hepatitis C virus RNA in muscle
H. Ito, H. Ito, M. Nagano, S. Nakano, Y. Shigeyoshi, and H. Kusaka
Neurology 2005; 64: 1073-1075. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Nonsense mutations in mitochondrial DNA associated with myalgia and exercise intolerance
T. Pulkes, D. Liolitsa, A. J. Wills, I. Hargreaves, S. Heales, and M. G. Hanna
Neurology 2005; 64: 1091-1092. [Full text] [PDF]  

EDITORIALS
Titinopathies: What happens when a big gene mutates in a big family?
Duygu Selcen and Kate Bushby
Neurology 2005; 64: 596-597. [Full text] [PDF]  

ARTICLES
Titinopathies and extension of the M-line mutation phenotype beyond distal myopathy and LGMD2J
B. Udd, A. Vihola, J. Sarparanta, I. Richard, and P. Hackman
Neurology 2005; 64: 636-642. [Abstract] [Full text] [PDF]  

NEUROIMAGES
MRI in biopsy-negative dermatomyositis
E. H. Wong, A. C.F. Hui, J. F. Griffith, S. M. Wong, and C. C. Szeto
Neurology 2005; 64: 750. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Brachial plexopathy following thoracoscapular fusion in facioscapulohumeral muscular dystrophy
G. I. Wolfe, P. K. Young, S. P. Nations, W. Z. Burkhead, A. L. McVey, and R. J. Barohn
Neurology 2005; 64: 572-573. [Full text] [PDF]  

BRIEF COMMUNICATIONS
Immune-mediated rippling muscle disease
W. J. Schulte-Mattler, R. A. Kley, E. Rothenfußer-Korber, S. Böhm, T. Brüning, J. Hackemann, A. Steinbrecher, M. v. Düring, B. Voss, and M. Vorgerd
Neurology 2005; 64: 364-367. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
The lethal phenotype of a homozygous nonsense mutation in the lamin A/C gene
B. G.M. van Engelen, A. Muchir, C. J. Hutchison, A. J. van der Kooi, G. Bonne, and M. Lammens
Neurology 2005; 64: 374-376. [Abstract] [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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