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Muscle disease
Citations 11-20 of 281 total displayed.
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Past content
(since Jan 2001):
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- NEUROIMAGES
Scotosensitive myoclonic seizures in MERRF
- Mohamad Z. Koubeissi, Chaiyos Khongkhatithum, Annette I. Janus, and Hans Lüders
Neurology 2009; 72: 858.
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- ARTICLES
Fat metabolism during exercise in patients with McArdle disease
- M. C. Ørngreen, T. D. Jeppesen, S. Tvede Andersen, T. Taivassalo, S. Hauerslev, N. Preisler, R. G. Haller, G. van Hall, and J. Vissing
Neurology 2009; 72: 718-724.
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- CLINICAL/SCIENTIFIC NOTES
SUPERFICIAL SIDEROSIS: SEALING THE DEFECT
- Neeraj Kumar, John I. Lane, and David G. Piepgras
Neurology 2009; 72: 671-673.
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- EDITORIALS
How much expansion to be diseased?: Toward repeat size and myotonic dystrophy type 2
- Benedikt Schoser and Tetsuo Ashizawa
Neurology 2009; 72: 484-485.
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- ARTICLES
Premutation allele pool in myotonic dystrophy type 2
- L. L. Bachinski, T. Czernuszewicz, L. S. Ramagli, T. Suominen, M. D. Shriver, B. Udd, M. J. Siciliano, and R. Krahe
Neurology 2009; 72: 490-497.
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- ARTICLES
Effect of aerobic training in patients with spinal and bulbar muscular atrophy (Kennedy disease)
- N. Preisler, G. Andersen, F. Thøgersen, C. Crone, T. D. Jeppesen, F. Wibrand, and J. Vissing
Neurology 2009; 72: 317-323.
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- CLINICAL/SCIENTIFIC NOTES
LINEZOLID INDUCING COMPLEX PARTIAL STATUS EPILEPTICUS IN A PATIENT WITH EPILEPSY
- Bassel F. Shneker, Peggy D. Baylin, and Michael E. Nakhla
Neurology 2009; 72: 378-379.
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- ARTICLES
New morphologic and genetic findings in cap disease associated with β-tropomyosin (TPM2) mutations
- M. Ohlsson, S. Quijano-Roy, N. Darin, G. Brochier, E. Lacène, D. Avila-Smirnow, M. Fardeau, A. Oldfors, and H. Tajsharghi
Neurology 2008; 71: 1896-1901.
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- ARTICLES
Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1
- D. S. Stamm, C. M. Powell, J. M. Stajich, V. L. Zismann, D. A. Stephan, B. Chesnut, A. S. Aylsworth, S. G. Kahler, K. L. Deak, J. R. Gilbert, and M. C. Speer
Neurology 2008; 71: 1764-1769.
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- ARTICLES
Autosomal recessive myosclerosis myopathy is a collagen VI disorder
- L. Merlini, E. Martoni, P. Grumati, P. Sabatelli, S. Squarzoni, A. Urciuolo, A. Ferlini, F. Gualandi, and P. Bonaldo
Neurology 2008; 71: 1245-1253.
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