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Neuromuscular Disorders : NMD|November 11, 2019
Clinical features of Pompe disease with motor neuronopathyLi-Kai Tsai, Wuh-Liang Hwu, Ni-Chung Lee, et al.Neuromuscular Disorders : NMD|November 12, 2019
Psychiatric and neurodevelopmental aspects of Becker muscular dystrophyMadoka Mori-Yoshimura, Yukio Mizuno, Sumiko Yoshida, et al.Neuromuscular Disorders : NMD|December 17, 2019
Characteristics of respiratory muscle involvement in myotonic dystrophy type 1Carolin Henke, Jens Spiesshoefer, Hans-Joachim Kabitz, et al.Neuromuscular Disorders : NMD|March 14, 2020
Phenotypic convergence in Charcot-Marie-Tooth 2Y with novel VCP mutationJasmine Gite, Emily Milko, Lauren Brady, et al.Neuromuscular Disorders : NMD|January 9, 2020
Discontinuation of enzyme replacement therapy in adults with Pompe disease: Evaluating the European POmpe Consortium stop criteriaH A van Kooten, L Harlaar, N A M E van der Beek, et al.Neuromuscular Disorders : NMD|January 14, 2020
Megaconial congenital muscular dystrophy: Same novel homozygous mutation in CHKB gene in two unrelated Chinese patientsSophelia Hs Chan, Ronnie Sl Ho, P L Khong, et al.Neuromuscular Disorders : NMD|February 2, 2020
A novel de novo ACTA1 variant in a patient with nemaline myopathy and mitochondrial Complex I deficiencyShpresa Pula, Kathryn Urankar, Andrew Norman, et al.Neuromuscular Disorders : NMD|January 15, 2019
The clinical management of neuromuscular disorders in intensive careMaxwell S Damian, Eelco F M WijdicksNeuromuscular Disorders : NMD|January 20, 2019
Targeted gene approach with biochemical assay confirms ABCD1 mutation of X-linked adrenoleukodystrophy in a 62-year-old man with gait imbalanceMichelle L Mauermann, Zhiyv Niu, Deborah L Renaud, et al.Neuromuscular Disorders : NMD|January 2, 2019
Spinal muscular atrophy with respiratory distress type 1: A multicenter retrospective studyAgnès Viguier, Valérie Lauwers-Cances, Pascal Cintas, et al.Pageof 340