Muscle disease

Citations 81-90 of 281 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Diagnostic challenges in facioscapulohumeral muscular dystrophy

S. Sacconi, L. Salviati, I. Bourget, D. Figarella, Y. Péréon, R. Lemmers, S. van der Maarel, and C. Desnuelle
Neurology 2006; 67: 1464-1466. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
The association of chronic hepatitis B and myopathy

M. Capasso, A. Di Muzio, M. Comar, I. Robuffo, A. Gambi, S. Crovella, E. Pizzigallo, C. Campello, and A. Uncini
Neurology 2006; 67: 1467-1469. [Abstract] [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Lipids detected by brain MRS during coma caused by carnitine palmitoyltransferase 1 deficiency

E. Roomets, N. Lundbom, H. Pihko, S. Heikkinen, and T. Tyni
Neurology 2006; 67: 1516-1517. [Full text] [PDF]  

CLINICAL/SCIENTIFIC NOTES
Late-onset multiple acyl-CoA dehydrogenase deficiency: A frequently missed diagnosis?

S. Köppel, J. Gottschalk, G. F. Hoffmann, H. R. Waterham, H. Blobel, and S. Kölker
Neurology 2006; 67: 1519. [Full text] [PDF]  

ARTICLES
Muscle Na⁺ channelopathies: MRI detects intracellular ²³Na accumulation during episodic weakness

M. -A. Weber, S. Nielles-Vallespin, M. Essig, K. Jurkat-Rott, H. -U. Kauczor, and F. Lehmann-Horn
Neurology 2006; 67: 1151-1158. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Hypokalemic paralysis due to Gitelman syndrome: A family study

H. -Y. Ng, S. -H. Lin, C. -Y. Hsu, Y. -Z. Tsai, H. -C. Chen, and C. -T. Lee
Neurology 2006; 67: 1080-1082. [Abstract] [Full text] [PDF]  

EDITORIALS
Frontotemporal dementia: The post-tau era

Bernardino Ghetti and Hans H. Goebel
Neurology 2006; 67: 560-561. [Full text] [PDF]  

ARTICLES
A mutation in the fast skeletal muscle troponin I gene causes myopathy and distal arthrogryposis

E. Kimber, H. Tajsharghi, A. -K. Kroksmark, A. Oldfors, and M. Tulinius
Neurology 2006; 67: 597-601. [Abstract] [Full text] [PDF]  

ARTICLES
Valosin-containing protein gene mutations: Clinical and neuropathologic features

L. Guyant-Maréchal, A. Laquerrière, C. Duyckaerts, C. Dumanchin, J. Bou, F. Dugny, I. Le Ber, T. Frébourg, D. Hannequin, and D. Campion
Neurology 2006; 67: 644-651. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Do carriers of PYGM mutations have symptoms of McArdle disease?

Susanne Tvede Andersen, Morten Dunø, Marianne Schwartz, and John Vissing
Neurology 2006; 67: 716-718. [Abstract] [Full text] [PDF]  

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