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Neuromuscular Disorders : NMD|October 8, 2013
Combined cap disease and nemaline myopathy in the same patient caused by an autosomal dominant mutation in the TPM3 geneEdoardo Malfatti, Ursula Schaeffer, Françoise Chapon, et al.Neuromuscular Disorders : NMD|December 17, 2009
Rigid spine syndrome revealing late-onset Pompe diseasePascal Laforêt, Valérie Doppler, Catherine Caillaud, et al.Neuromuscular Disorders : NMD|March 1, 2003
Two novel mutations in the COLQ gene cause endplate acetylcholinesterase deficiencyKeiko Ishigaki, Delphine Nicolle, Eric Krejci, et al.Muscle & Nerve|December 23, 2004
Exercise tolerance and daily life in McArdle's diseaseKaren Ollivier, Jean-Yves Hogrel, Danielle Gomez-Merino, et al.Journal of Neurology, Neurosurgery, and Psychiatry|June 22, 2010
Distal muscle involvement in granulomatous myositis can mimic inclusion body myositisSandrine Larue, Thierry Maisonobe, Olivier Benveniste, et al.Muscle & Nerve|August 18, 2016
Translation, cross-cultural adaptation, and validation of the french version of the 15-item Myasthenia Gravis Quality Of life scaleSimone Birnbaum, Idir Ghout, Sophie Demeret, et al.Muscle & Nerve|November 3, 2009
Homozygosity for dominant mutations increases severity of muscle channelopathiesMarianne Arzel-Hézode, Damien Sternberg, Nacira Tabti, et al.Immunobiology|June 19, 2012
SDF-1/CXCL12 recruits B cells and antigen-presenting cells to the thymus of autoimmune myasthenia gravis patientsJulia Miriam Weiss, Perrine Cufi, Jacky Bismuth, et al.Journal of Neuroimmunology|March 13, 2009
Association of HLA-A in autoimmune myasthenia gravis with thymomaClaire Vandiedonck, Colette Raffoux, Bruno Eymard, et al.European Heart Journal. Cardiovascular Imaging|December 28, 2018
Comprehensive evaluation of structural and functional myocardial impairments in Becker muscular dystrophy using quantitative cardiac magnetic resonance imagingBenjamin Marty, Raymond Gilles, Marcel Toussaint, et al.Pageof 21