Muscle disease

Citations 81-90 of 283 total displayed.

Past content (since Jan 2001):

BRIEF COMMUNICATIONS
Allogeneic stem cell transplantation corrects biochemical derangements in MNGIE

M. Hirano, R. Martí, C. Casali, S. Tadesse, T. Uldrick, B. Fine, D. M. Escolar, M. L. Valentino, I. Nishino, C. Hesdorffer, J. Schwartz, R. G. Hawks, D. L. Martone, M. S. Cairo, S. DiMauro, M. Stanzani, J. H. Garvin, Jr, and D. G. Savage
Neurology 2006; 67: 1458-1460. [Abstract] [Full text] [PDF]  

BRIEF COMMUNICATIONS
Infusion of platelets transiently reduces nucleoside overload in MNGIE

M. C. Lara, B. Weiss, I. Illa, P. Madoz, L. Massuet, A. L. Andreu, M. L. Valentino, Y. Anikster, M. Hirano, and R. Martí
Neurology 2006; 67: 1461-1463. [Abstract] [Full text] [PDF]  

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]  

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