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Muscle disease
Citations 71-80 of 281 total displayed.
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Past content
(since Jan 2001):
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- ARTICLES
Broad spectrum of Pompe disease in patients with the same c.-32-13T G haplotype
- M. A. Kroos, R. J. Pomponio, M. L. Hagemans, J.L.M. Keulemans, M. Phipps, M. DeRiso, R. E. Palmer, M. G.E.M. Ausems, N. A.M.E. Van der Beek, O. P. Van Diggelen, D. J.J. Halley, A. T. Van der Ploeg, and A. J.J. Reuser
Neurology 2007; 68: 110-115.
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- ARTICLES
Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys
- Rita Horvath, Rudolf Andre Kley, Hanns Lochmüller, and Matthias Vorgerd
Neurology 2007; 68: 56-58.
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- ARTICLES
Endurance training: An effective and safe treatment for patients with LGMD2I
- M. -L. Sveen, T. D. Jeppesen, S. Hauerslev, T. O. Krag, and J. Vissing
Neurology 2007; 68: 59-61.
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- ARTICLES
Muscle imaging in dominant core myopathies linked or unlinked to the ryanodine receptor 1 gene
- D. Fischer, M. Herasse, A. Ferreiro, H. M. Barragán-Campos, J. Chiras, L. Viollet, S. Maugenre, J. -P. Leroy, N. Monnier, J. Lunardi, P. Guicheney, M. Fardeau, and N. B. Romero
Neurology 2006; 67: 2217-2220.
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- CLINICAL/SCIENTIFIC NOTES
Ptosis as a feature of late-onset glycogenosis type II
- W. B. Groen, W. G. Leen, A.M.C. Vos, J. R.M. Cruysberg, P. A. van Doorn, and B. G.M. van Engelen
Neurology 2006; 67: 2261-2262.
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- ARTICLES
Mitochondrial disease criteria: Diagnostic applications in children
- E. Morava, L. van den Heuvel, F. Hol, M. C. de Vries, M. Hogeveen, R. J. Rodenburg, and J.A.M. Smeitink
Neurology 2006; 67: 1823-1826.
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- BRIEF COMMUNICATIONS
Pregnancy and birth outcomes in women with facioscapulohumeral muscular dystrophy
- E. Ciafaloni, E. K. Pressman, A. M. Loi, A. M. Smirnow, D. J. Guntrum, N. Dilek, and R. Tawil
Neurology 2006; 67: 1887-1889.
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- ARTICLES
Early development of critical illness myopathy and neuropathy in patients with severe sepsis
- Jaffar Khan, Taylor B. Harrison, Mark M. Rich, and Marc Moss
Neurology 2006; 67: 1421-1425.
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- 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.
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- 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.
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