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Muscle disease
Citations 171-180 of 283 total displayed.
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Past content
(since Jan 2001):
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- 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.
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- 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.
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- BRIEF COMMUNICATIONS
Pilot trial of albuterol in Duchenne and Becker muscular dystrophy
- E. G. Fowler, M. C. Graves, G. T. Wetzel, and M. J. Spencer
Neurology 2004; 62: 1006-1008.
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- BRIEF COMMUNICATIONS
POMT1 mutation results in defective glycosylation and loss of laminin-binding activity in  -DG
- D. -S. Kim, Y. K. Hayashi, H. Matsumoto, M. Ogawa, S. Noguchi, N. Murakami, R. Sakuta, M. Mochizuki, D. E. Michele, K. P. Campbell, I. Nonaka, and I. Nishino
Neurology 2004; 62: 1009-1011.
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- BRIEF COMMUNICATIONS
Periodic paralysis mutation MiRP2-R83H in controls: Interpretations and general recommendation
- Karin Jurkat-Rott and Frank Lehmann-Horn
Neurology 2004; 62: 1012-1015.
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- BRIEF COMMUNICATIONS
Late-onset cerebellar ataxia with hypogonadism and muscle coenzyme Q10 deficiency
- M. Gironi, C. Lamperti, R. Nemni, M. Moggio, G. Comi, F. R. Guerini, P. Ferrante, N. Canal, A. Naini, N. Bresolin, and S. DiMauro
Neurology 2004; 62: 818-820.
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- VIEWS & REVIEWS
Caveolinopathies: Mutations in caveolin-3 cause four distinct autosomal dominant muscle diseases
- S. E. Woodman, F. Sotgia, F. Galbiati, C. Minetti, and M. P. Lisanti
Neurology 2004; 62: 538-543.
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- BRIEF COMMUNICATIONS
Ullrich disease due to deficiency of collagen VI in the sarcolemma
- H. Ishikawa, K. Sugie, K. Murayama, A. Awaya, Y. Suzuki, S. Noguchi, Y. K. Hayashi, I. Nonaka, and I. Nishino
Neurology 2004; 62: 620-623.
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- CLINICAL/SCIENTIFIC NOTES
Statin-associated rhabdomyolysis triggered by grapefruit consumption
- Jens P. Dreier and Matthias Endres
Neurology 2004; 62: 670.
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- CLINICAL/SCIENTIFIC NOTES
Respiratory function in congenital muscular dystrophy and limb girdle muscular dystrophy 2I
- C. Dohna-Schwake, R. Ragette, U. Mellies, V. Straub, H. Teschler, and T. Voit
Neurology 2004; 62: 513-514.
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