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Archives of Neurology|November 16, 2005
Treatment of myasthenia gravis exacerbation with intravenous immunoglobulin: a randomized double-blind clinical trialPhilippe Gajdos, Christine Tranchant, Bernard Clair, et al.Neuromuscular Disorders : NMD|March 17, 2004
Vocal cord and diaphragm paralysis, as clinical features of a French family with autosomal recessive Charcot-Marie-Tooth disease, associated with a new mutation in the GDAP1 geneTanya Stojkovic, Philippe Latour, Ghislaine Viet, 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.Journal of Neuromuscular Diseases|June 16, 2020
Ganglionopathies Associated with MERRF Syndrome: An Original ReportMaud Michaud, Tanya Stojkovic, Thierry Maisonobe, et al.Journal of Neuromuscular Diseases|August 29, 2022
Muscle MRI as a Diagnostic Challenge in Emery-Dreifuss Muscular DystrophyMaria João Pinto, Yves Fromes, Isabelle Ackermann-Bonan, et al.Journal of Neurology|September 26, 2022
Sjögren syndrome and RFC1-CANVAS sensory ganglionopathy: co-occurrence or misdiagnosis?Gorka Fernández-Eulate, Rabab Debs, Thierry Maisonobe, et al.Journal of the Peripheral Nervous System : JPNS|October 10, 2019
Hereditary sensory autonomic neuropathy type II: Report of two novel mutations in the FAM134B geneCatarina Falcão de Campos, Marie Vidailhet, Annick Toutain, et al.Genetic Testing and Molecular Biomarkers|July 15, 2009
Identification of different genomic deletions and one duplication in the dysferlin gene using multiplex ligation-dependent probe amplification and genomic quantitative PCRMartin Krahn, Ana Borges, Claire Navarro, et al.Neuromuscular Disorders : NMD|November 13, 2018
Isokinetic assessment of trunk muscles in facioscapulohumeral muscular dystrophy type 1 patientsJulien Esnault, Besma Missaoui, Samy Bendaya, et al.The Journal of Molecular Diagnostics : JMD|September 9, 2022
Identification of a CCG-Enriched Expanded Allele in Patients with Myotonic Dystrophy Type 1 Using Amplification-Free Long-Read SequencingYu-Chih Tsai, Laure de Pontual, Cheryl Heiner, et al.Pageof 25