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Neurology
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Muscle disease

Citations 21-30 of 281 total displayed.

Past content (since Jan 2001):

RESIDENT AND FELLOW SECTION
Clinical Reasoning: Rhabdomyolysis after combined treatment with simvastatin and fluconazole
O. Findling, N. Meier, J. Sellner, K. Nedeltchev, and M. Arnold
Neurology 2008; 71: e34-37e. [Full text] [PDF]  

NEUROIMAGES
Levator palpebrae myositis
Mohammed A. Almekhlafi and William A. Fletcher
Neurology 2008; 71: 1202. [Full text] [PDF]  

ARTICLES
Distinct muscle imaging patterns in myofibrillar myopathies
D. Fischer, R. A. Kley, K. Strach, C. Meyer, T. Sommer, K. Eger, A. Rolfs, W. Meyer, A. Pou, J. Pradas, C. M. Heyer, A. Grossmann, A. Huebner, W. Kress, J. Reimann, R. Schröder, B. Eymard, M. Fardeau, B. Udd, L. Goldfarb, M. Vorgerd, and M. Olivé
Neurology 2008; 71: 758-765. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
KING-DENBOROUGH SYNDROME CAUSED BY A NOVEL MUTATION IN THE RYANODINE RECEPTOR GENE
C. E. D’Arcy, A. Bjorksten, E. M. Yiu, A. Bankier, R. Gillies, C. A. McLean, L. K. Shield, and M. M. Ryan
Neurology 2008; 71: 776-777. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
SPORADIC LATE-ONSET NEMALINE MYOPATHY EFFECTIVELY TREATED BY MELPHALAN AND STEM CELL TRANSPLANT
N. C. Voermans, M. Minnema, M. Lammens, H. J. Schelhaas, A.v.d. Kooi, H. M. Lokhorst, and B. G. van Engelen
Neurology 2008; 71: 532-534. [Full text] [PDF]  

EDITORIALS
Congenital muscular dystrophy in a new age
John W. Day
Neurology 2008; 71: 308-309. [Full text] [PDF]  

ARTICLES
Diagnosis and etiology of congenital muscular dystrophy
R. A. Peat, J. M. Smith, A. G. Compton, N. L. Baker, R. A. Pace, D. J. Burkin, S. J. Kaufman, S. R. Lamandé, and K. N. North
Neurology 2008; 71: 312-321. [Abstract] [Full text] [PDF]  

PATIENT PAGES
Gene therapy and muscular dystrophies
Steven Karceski
Neurology 2008; 71: e6-8e. [Full text] [PDF]  

EDITORIALS
Sarcoglycans take center stage in gene transfer therapy
Oliver J. Müller and Hanns Lochmüller
Neurology 2008; 71: 234-235. [Full text] [PDF]  

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. [Abstract] [Full text] [PDF]  

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* Collected Resources Home

* Related collections:
 Neuromuscular disease
 All Neuromuscular Disease
 Anterior nerve cell disease
 Amyotrophic lateral sclerosis
 Myasthenia
 Lambert-Eaton syndrome
 Peripheral neuropathy
 Carpal tunnel syndrome
 Cranial neuropathy
 Guillain-Barre syndrome
 Chronic inflammatory demyelinating polyneuropathy
 Transverse myelitis
 Muscle disease


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