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Muscle & Nerve|May 21, 2019
Investigation of the psychometric properties of the inclusion body myositis functional rating scale with rasch analysisGita Ramdharry, Jasper Morrow, Stacie Hudgens, et al.
Journal of Immunology (Baltimore, Md. : 1950)|January 15, 2017
Dysregulation of B Cell Repertoire Formation in Myasthenia Gravis Patients Revealed through Deep SequencingJason A Vander Heiden, Panos Stathopoulos, Julian Q Zhou, et al.
Muscle & Nerve|December 30, 2019
Magnetic resonance imaging correlates with electrical impedance myography in facioscapulohumeral muscular dystrophyJohanna Hamel, Phil Lee, Melanie D Glenn, et al.
Brain : a Journal of Neurology|June 18, 2013
Non-dystrophic myotonia: prospective study of objective and patient reported outcomesJaya R Trivedi, Brian Bundy, Jeffrey Statland, et al.
JAMA|October 4, 2012
Mexiletine for symptoms and signs of myotonia in nondystrophic myotonia: a randomized controlled trialJeffrey M Statland, Brian N Bundy, Yunxia Wang, et al.
Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration|May 18, 2013
Peer recommendations on how to improve clinical research, and Conference wrap-upDavid A Chad, Lewis P Rowland, Carmel Armon, et al.
Muscle & Nerve|April 10, 2020
Guidelines on clinical presentation and management of nondystrophic myotoniasBas C Stunnenberg, Samantha LoRusso, W David Arnold, et al.
American Journal of Human Genetics|January 9, 2008
X-linked dominant scapuloperoneal myopathy is due to a mutation in the gene encoding four-and-a-half-LIM protein 1Catarina M Quinzii, Tuan H Vu, K Christopher Min, et al.
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