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Muscle disease
Citations 111-120 of 281 total displayed.
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Past content
(since Jan 2001):
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- BRIEF COMMUNICATIONS
A family with McLeod syndrome and calpainopathy with clinically overlapping diseases
- A. Starling, D. Schlesinger, F. Kok, M. Rita Passos-Bueno, M. Vainzof, and M. Zatz
Neurology 2005; 65: 1832-1833.
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- CLINICAL/SCIENTIFIC NOTES
Isolated dropped head due to adult-onset nemaline myopathy treated by posterior fusion
- B. Katirji, R. Hachwi, A. Al-Shekhlee, M. L. Cohen, and H. H. Bohlman
Neurology 2005; 65: 1504-1505.
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- VIEWS & REVIEWS
Sporadic late onset nemaline myopathy
- Nizar Chahin, Duygu Selcen, and Andrew G. Engel
Neurology 2005; 65: 1158-1164.
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- BRIEF COMMUNICATIONS
Early-onset toe walking in rippling muscle disease due to a new caveolin-3 gene mutation
- Ricardo E. Madrid, Christian Kubisch, and Arthur P. Hays
Neurology 2005; 65: 1301-1303.
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- BRIEF COMMUNICATIONS
Inclusion body myopathy and Paget disease is linked to a novel mutation in the VCP gene
- D. Haubenberger, R. E. Bittner, S. Rauch-Shorny, F. Zimprich, C. Mannhalter, L. Wagner, I. Mineva, K. Vass, E. Auff, and A. Zimprich
Neurology 2005; 65: 1304-1305.
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- BRIEF COMMUNICATIONS
Hypokalemic weakness in hyperaldosteronism: Activity-dependent conduction block
- Arun V. Krishnan, James G. Colebatch, and Matthew C. Kiernan
Neurology 2005; 65: 1309-1312.
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- CLINICAL/SCIENTIFIC NOTES
Sensory symptoms in acquired neuromyotonia
- Steven Herskovitz, Haodong Song, Dominique Cozien, and StephenN Scelsa
Neurology 2005; 65: 1330-1331.
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- NEUROIMAGES
Unilateral toe-walking secondary to intramuscular hemangioma in the gastrocnemius
- Fujio Umehara, Eiji Matsuura, Shinichi Kitajima, and Mitsuhiro Osame
Neurology 2005; 65: E15.
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- ARTICLES
Andersen–Tawil syndrome: New potassium channel mutations and possible phenotypic variation
- N. P. Davies, P. Imbrici, D. Fialho, C. Herd, L. G. Bilsland, A. Weber, R. Mueller, D. Hilton-Jones, J. Ealing, B. R. Boothman, P. Giunti, L. M. Parsons, M. Thomas, A. Y. Manzur, K. Jurkat-Rott, F. Lehmann-Horn, P. F. Chinnery, M. Rose, D. M. Kullmann, and M. G. Hanna
Neurology 2005; 65: 1083-1089.
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- BRIEF COMMUNICATIONS
A new congenital form of X-linked autophagic vacuolar myopathy
- C. Yan, M. Tanaka, K. Sugie, T. Nobutoki, M. Woo, N. Murase, Y. Higuchi, S. Noguchi, I. Nonaka, Y. K. Hayashi, and I. Nishino
Neurology 2005; 65: 1132-1134.
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