Muscle disease

Citations 161-170 of 281 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Progressive myopathy with circulating autoantibody against giantin in the Golgi apparatus

K. Sahashi, T. Ibi, K. Ohno, K. Sahashi, N. Nakao, and H. Kondo
Neurology 2004; 62: 1891-1893. [Abstract] [Full text] [PDF]  

VIEWS & REVIEWS
Clinical and histologic findings in autosomal centronuclear myopathy

P.-Y. Jeannet, G. Bassez, B. Eymard, P. Laforêt, J. A. Urtizberea, A. Rouche, P. Guicheney, M. Fardeau, and N. B. Romero
Neurology 2004; 62: 1484-1490. [Abstract] [Full text] [PDF]  

ARTICLES
Mutation of the slow myosin heavy chain rod domain underlies hyaline body myopathy

S. Bohlega, S. N. Abu-Amero, S. M. Wakil, P. Carroll, R. Al-Amr, B. Lach, Y. Al-Sayed, E. J. Cupler, and B. F. Meyer
Neurology 2004; 62: 1518-1521. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Distal myopathy with rimmed vacuoles (DMRV): New GNE mutations and splice variant

H. Tomimitsu, J. Shimizu, K. Ishikawa, N. Ohkoshi, I. Kanazawa, and H. Mizusawa
Neurology 2004; 62: 1607-1610. [Abstract] [Full text] [PDF]  

EDITORIALS
A clever road from myopathology to genes: The myotilin story

George Karpati and Michael Sinnreich
Neurology 2004; 62: 1248-1249. [Full text] [PDF]  

ARTICLES
Cerebral lactic acidosis correlates with neurological impairment in MELAS

P. Kaufmann, D. C. Shungu, M. C. Sano, S. Jhung, K. Engelstad, E. Mitsis, X. Mao, S. Shanske, M. Hirano, S. DiMauro, and D. C. De Vivo
Neurology 2004; 62: 1297-1302. [Abstract] [Full text] [PDF]  

ARTICLES
Mutations in myotilin cause myofibrillar myopathy

Duygu Selcen and Andrew G. Engel
Neurology 2004; 62: 1363-1371. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Catastrophic presentation of mitochondrial disease due to a mutation in the tRNA^His gene

R. W. Taylor, A. M. Schaefer, M. T. McDonnell, R. K.H. Petty, A. M. Thomas, E. L. Blakely, C. M. Hayes, R. McFarland, and D. M. Turnbull
Neurology 2004; 62: 1420-1423. [Abstract] [Full text] [PDF]  

ARTICLES
Leukocyte CTG repeat length correlates with severity of myotonia in myotonic dystrophy type 1

E. L. Logigian, R. T. Moxley, IV, C. L. Blood, C. A. Barbieri, W. B. Martens, A. W. Wiegner, C. A. Thornton, and R. T. Moxley, III
Neurology 2004; 62: 1081-1089. [Abstract] [Full text] [PDF]  

ARTICLES
Large-scale disruption of microtubule pathways in morphologically normal human spastin muscle

A. Molon, S. Di Giovanni, Y. W. Chen, P. M. Clarkson, C. Angelini, E. Pegoraro, and E. P. Hoffman
Neurology 2004; 62: 1097-1104. [Abstract] [Full text] [PDF]  

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