|
Muscle disease
Citations 1-10 of 264 total displayed.
|
Most recent content
(2 Dec 2008):
|
- 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.
[Abstract]
[Full text]
[PDF]
|
Past content
(since Jan 2001):
|
- 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.
[Abstract]
[Full text]
[PDF]
- 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.
[Abstract]
[Full text]
[PDF]
- 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]
|
|
