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Neuromuscular Disorders : NMD|January 16, 2019
A novel MFN2 mutation causes variable clinical severity in a multi-generational CMT2 familyLois Dankwa, Jessica Richardson, William W Motley, et al.Neuromuscular Disorders : NMD|January 15, 2019
Clinical spectrum of neuromuscular complications after immune checkpoint inhibitionAraya Puwanant, Michael Isfort, David Lacomis, et al.Neuromuscular Disorders : NMD|September 25, 2020
The effects of non-invasive mechanical ventilation on cardiac autonomic dysfunction in spinal muscular atrophyGulcin Benbir Senel, N Burcu Arkali, Sema Saltik, et al.Neuromuscular Disorders : NMD|September 29, 2020
Biallelic mutations in Tenascin-X cause classical-like Ehlers-Danlos syndrome with slowly progressive muscular weaknessMarion Brisset, Corinne Metay, Robert-Yves Carlier, et al.Neuromuscular Disorders : NMD|September 15, 2020
Optimizing hand-function patient outcome measures for inclusion body myositisAva Yun Lin, Catherine Sly Siener, Anna V Faino, et al.Neuromuscular Disorders : NMD|September 23, 2020
Genotype and age at diagnosis in Thai boys with Duchenne muscular dystrophy (DMD)Pattareeya Yamputchong, Theeraphong Pho-Iam, Chanin Limwongse, et al.Neuromuscular Disorders : NMD|January 19, 2020
Cylindrical spirals in two families: Clinical and genetic investigationsSarah J Beecroft, Montse Olive, Lidia Gonzalez Quereda, et al.Neuromuscular Disorders : NMD|December 29, 2019
244th ENMC international workshop: Newborn screening in spinal muscular atrophy May 10-12, 2019, Hoofdorp, The NetherlandsTamara Dangouloff, Arthur Burghes, Eduardo F Tizzano, et al.Neuromuscular Disorders : NMD|March 15, 2020
Identification of novel SMN1 subtle mutations using an allelic-specific RT-PCRYan Xu, Bing Xiao, Yu Liu, et al.Neuromuscular Disorders : NMD|April 2, 2020
Clinical and histological features of immune-mediated necrotising myopathy: A multi-centre South Australian cohort studyJessica Day, Sophia Otto, Kathy Cash, et al.Pageof 341