Muscle disease

Citations 251-260 of 283 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores

H. Jungbluth, C. R. Müller, B. Halliger–Keller, M. Brockington, S. C. Brown, L. Feng, A. Chattopadhyay, E. Mercuri, A. Y. Manzur, A. Ferreiro, N. G. Laing, M. R. Davis, H. P. Roper, V. Dubowitz, G. Bydder, C. A. Sewry, and F. Muntoni
Neurology 2002; 59: 284-287. [Abstract] [Full text] [PDF]  

ARTICLES
Clinicopathological features of genetically confirmed Danon disease

K. Sugie, A. Yamamoto, K. Murayama, S. J. Oh, M. Takahashi, M. Mora, J. E. Riggs, J. Colomer, C. Iturriaga, A. Meloni, C. Lamperti, S. Saitoh, E. Byrne, S. DiMauro, I. Nonaka, M. Hirano, and I. Nishino
Neurology 2002; 58: 1773-1778. [Abstract] [Full text] [PDF]  

ARTICLES
A forearm exercise screening test for mitochondrial myopathy

Tina D. Jensen, Pedram Kazemi-Esfarjani, Elwira Skomorowska, and John Vissing
Neurology 2002; 58: 1533-1538. [Abstract] [Full text] [PDF]  

ARTICLES
Impairment of slow inactivation as a common mechanism for periodic paralysis in DIIS4-S5

S. Bendahhou, T. R. Cummins, R. W. Kula, Y.-H. Fu, and L. J. Ptácek
Neurology 2002; 58: 1266-1272. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Exercise-induced muscle "burning," fatigue, and hyper-CKemia: mtDNA T10010C mutation in tRNA^Gly

Y. Nishigaki, E. Bonilla, S. Shanske, D. A. Gaskin, S. DiMauro, and M. Hirano
Neurology 2002; 58: 1282-1285. [Abstract] [Full text] [PDF]  

ARTICLES
A pilot randomized trial of oxandrolone in inclusion body myositis

S. B. Rutkove, R. A. Parker, R. A. Nardin, C. E. Connolly, K. J. Felice, and E. M. Raynor
Neurology 2002; 58: 1081-1087. [Abstract] [Full text] [PDF]  

ARTICLES
Resting oxygen consumption and in vivo ADP are increased in myopathy due to complex I deficiency

M. J. Roef, D.-J. Reijngoud, J. A.L. Jeneson, R. Berger, and K. de Meer
Neurology 2002; 58: 1088-1093. [Abstract] [Full text] [PDF]  

ARTICLES
Myosin heavy chain IIa gene mutation E706K is pathogenic and its expression increases with age

H. Tajsharghi, L.-E. Thornell, N. Darin, T. Martinsson, M. Kyllerman, J. Wahlström, and A. Oldfors
Neurology 2002; 58: 780-786. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Effects of L-arginine on the acute phase of strokes in three patients with MELAS

Y. Koga, M. Ishibashi, I. Ueki, S. Yatsuga, R. Fukiyama, Y. Akita, and T. Matsuishi
Neurology 2002; 58: 827-828. [Full text] [PDF]  

ARTICLES
Three lipoprotein receptors and cholesterol in inclusion-body myositis muscle

M. Jaworska-Wilczynska, G. M. Wilczynski, W. K. Engel, D. K. Strickland, K. H. Weisgraber, and V. Askanas
Neurology 2002; 58: 438-445. [Abstract] [Full text] [PDF]  

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