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Neuromuscular Disorders : NMD|July 29, 2014
Two patients with co-morbid myasthenia gravis in a Brazilian cohort of inflammatory bowel diseaseFrancisco de A A Gondim, Gisele R de Oliveira, Davi F Araújo, et al.
Neuromuscular Disorders : NMD|November 2, 2013
Statin myotoxicity: a review of genetic susceptibility factorsM Needham, F L Mastaglia
Neuromuscular Disorders : NMD|April 25, 2016
Identification of an intragenic deletion in the SGCB gene through a re-evaluation of negative next generation sequencing resultsTeresa Giugliano, Marina Fanin, Marco Savarese, et al.
Neuromuscular Disorders : NMD|August 19, 2017
Common and variable clinical, histological, and imaging findings of recessive RYR1-related centronuclear myopathy patientsOsorio Abath Neto, Cristiane de Araújo Martins Moreno, Edoardo Malfatti, et al.
Neuromuscular Disorders : NMD|August 15, 2017
A homozygous DPM3 mutation in a patient with alpha-dystroglycan-related limb girdle muscular dystrophyP Y K Van den Bergh, Y Sznajer, V Van Parys, et al.
Neuromuscular Disorders : NMD|August 1, 2017
Spinal muscular atrophy: A changing phenotype beyond the clinical trialsEduardo F Tizzano, Richard S Finkel
Neuromuscular Disorders : NMD|July 19, 2017
A 'second truncation' in TTN causes early onset recessive muscular dystrophyElizabeth Harris, Ana Töpf, Anna Vihola, et al.
Neuromuscular Disorders : NMD|November 6, 2017
Involvement of pelvic girdle and proximal leg muscles in early oculopharyngeal muscular dystrophyB M van der Sluijs, S Lassche, G J Knuiman, et al.
Neuromuscular Disorders : NMD|November 13, 2017
MEGF10 related myopathies: A new case with adult onset disease with prominent respiratory failure and review of reported phenotypesElizabeth Harris, Chiara Marini-Bettolo, Ana Töpf, et al.
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