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All Neuromuscular Disease
Citations 31-40 of 158 total displayed.
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Past content
(since Jan 2000):
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- EDITORIALS
A "nema" of hope in the treatment of late-onset nemaline myopathy
- Marinos C. Dalakas and Stephen A. Smith
Neurology 2008; 71: 472-473.
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- ARTICLES
Dehydroepiandrosterone for myotonic dystrophy type 1
- I. Pénisson-Besnier, M. Devillers, R. Porcher, D. Orlikowski, V. Doppler, C. Desnuelle, X. Ferrer, M. -C.A. Bes, F. Bouhour, C. Tranchant, E. Lagrange, A. Vershueren, D. Uzenot, P. Cintas, G. Solé, J. -Y. Hogrel, P. Laforêt, C. Vial, A. L. Vila, S. Sacconi, J. Pouget, B. Eymard, S. Chevret, and D. Annane
Neurology 2008; 71: 407-412.
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- PATIENT PAGES
Gene therapy and muscular dystrophies
- Steven Karceski
Neurology 2008; 71: e6-8e.
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- ARTICLES
Lack of toxicity of alpha-sarcoglycan overexpression supports clinical gene transfer trial in LGMD2D
- L. R. Rodino-Klapac, J-S Lee, R. C. Mulligan, K. R. Clark, and J. R. Mendell
Neurology 2008; 71: 240-247.
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- RESIDENT AND FELLOW SECTION
Video NeuroImage: Generalized tetanus in a 70-year-old woman
- G. M. De Marchis
Neurology 2008; 70: e70.
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- ARTICLES
Paraoxonase 1 (PON1) organophosphate hydrolysis is not reduced in ALS
- A. -M. Wills, J. E. Landers, H. Zhang, R. J. Richter, A. J. Caraganis, M. E. Cudkowicz, C. E. Furlong, and R. H. Brown, Jr
Neurology 2008; 70: 929-934.
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- NEUROIMAGES
Suprascapular nerve entrapment by a spinoglenoid cyst
- Alexander Semmler, Marcus von Falkenhausen, and Rolf Schröder
Neurology 2008; 70: 890.
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- ARTICLES
Motoneuron-specific NR3B gene: No association with ALS and evidence for a common null allele
- S. Niemann, J. E. Landers, M. J. Churchill, B. Hosler, P. Sapp, W. C. Speed, B. T. Lahn, K. K. Kidd, R. H. Brown, Jr, and Y. Hayashi
Neurology 2008; 70: 666-676.
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- SPECIAL ARTICLE
Practice Parameter: Assessing patients in a neurology practice for risk of falls (an evidence-based review): Report of the Quality Standards Subcommittee of the American Academy of Neurology
- David J. Thurman, Judy A. Stevens, and Jaya K. Rao
Neurology 2008; 70: 473-479.
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- ARTICLES
The hypocretin neurotransmission system in myotonic dystrophy type 1
- E. Ciafaloni, E. Mignot, V. Sansone, J. E. Hilbert, L. Lin, X. Lin, L. C. Liu, W. R. Pigeon, M. L. Perlis, and C. A. Thornton
Neurology 2008; 70: 226-230.
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