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Neuromuscular Disorders : NMD|April 4, 2022
Identification of a novel mutation and genotype-phenotype relationship in MEGF10 myopathyKanako Fujii, Makito Hirano, Atsushi Terayama, et al.Neuromuscular Disorders : NMD|April 1, 2022
Clinical and neuroradiological correlates of sleep in myotonic dystrophy type 1Mark J Hamilton, Antonio Atalaia, John McLean, et al.Neuromuscular Disorders : NMD|September 18, 2018
National registry of patients with Fukuyama congenital muscular dystrophy in JapanKeiko Ishigaki, Chikoto Ihara, Harumasa Nakamura, et al.Neuromuscular Disorders : NMD|September 30, 2018
Clinical variability of early-onset congenital myasthenic syndrome due to biallelic RAPSN mutations in BrazilEduardo de Paula Estephan, Antonio Alberto Zambon, Paulo Eurípedes Marchiori, et al.Neuromuscular Disorders : NMD|March 4, 1999
Exclusion of muscle specific actinin-associated LIM protein (ALP) gene from 4q35 facioscapulohumeral muscular dystrophy (FSHD) candidate genesS Bouju, G Piétu, M Le Cunff, et al.Neuromuscular Disorders : NMD|January 5, 2000
Homozygosity for a nonsense mutation in the alpha-tropomyosin slow gene TPM3 in a patient with severe infantile nemaline myopathyP Tan, J Briner, E Boltshauser, et al.Neuromuscular Disorders : NMD|March 11, 2000
Different effects of mexiletine on two mutant sodium channels causing paramyotonia congenita and hyperkalemic periodic paralysisK Weckbecker, A Würz, B Mohammadi, et al.Neuromuscular Disorders : NMD|March 11, 2000
Effects of aerobic training on lactate and catecholaminergic exercise responses in mitochondrial myopathiesG Siciliano, M L Manca, M Renna, et al.Neuromuscular Disorders : NMD|March 11, 2000
Dermatomyositis and Whipple's diseaseT R Helliwell, R E Appleton, N C Mapstone, et al.Neuromuscular Disorders : NMD|March 11, 2000
An Italian family with Ala-47 transthyretin mutation associated with cardiomyopathy and polyneuropathyC Solaro, A Schenone, A Di Sapio, et al.Pageof 340