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Neuromuscular Disorders : NMD|March 14, 2020
The mysterious death of Georges Cuvier (1832): An early case of severe Guillain-Barré syndrome?Stéphane Mathis, Jean-Michel VallatNeuromuscular Disorders : NMD|February 2, 2020
Clinical and genetic characterization of limb girdle muscular dystrophy R7 telethonin-related patients from three unrelated Chinese familiesHaizhu Chen, Guorong Xu, Feng Lin, et al.Neuromuscular Disorders : NMD|February 2, 2020
Spectral domain optical coherence tomography findings in myotonic dystrophyEdoardo Abed, Guglielmo D'Amico, Salvatore Rossi, et al.Neuromuscular Disorders : NMD|March 3, 2020
A rare case of adult onset LPIN1 associated rhabdomyolysisThomas Minton, Natalie Forrester, Sami Al Baba, et al.Neuromuscular Disorders : NMD|December 4, 2019
Evaluation of gait in Duchenne Muscular Dystrophy: Relation of 3D gait analysis to clinical assessmentAlberto Romano, Martina Favetta, Tommaso Schirinzi, et al.Neuromuscular Disorders : NMD|September 26, 2020
Congenital myasthenic syndromes in the Thai population: Clinical findings and novel mutationsNalinee Pattrakornkul, Chupong Ittiwut, Ponghatai Boonsimma, et al.Neuromuscular Disorders : NMD|January 1, 2021
Novel ACTA1 mutation causes late-presenting nemaline myopathy with unusual dark coresMatteo Garibaldi, Fabiana Fattori, Elena Maria Pennisi, et al.Neuromuscular Disorders : NMD|December 14, 2020
Sporadic late-onset nemaline myopathy with monoclonal gammopathy of undetermined significance: Report of four patientsAli Asghar Okhovat, Yalda Nilipour, Reza Boostani, et al.Neuromuscular Disorders : NMD|December 14, 2020
Impaired secretion of platelet granules in patients with Duchenne muscular dystrophy - results of a prospective diagnostic studyD C Schorling, C K Müller, A Pechmann, et al.Neuromuscular Disorders : NMD|October 31, 2020
The importance of an integrated genotype-phenotype strategy to unravel the molecular bases of titinopathiesAurélien Perrin, Raul Juntas Morales, François Rivier, et al.Pageof 340