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Neuromuscular Disorders : NMD|June 25, 2014
Limb girdle muscular dystrophy due to LAMA2 mutations: diagnostic difficulties due to associated peripheral neuropathySophelia H S Chan, A Reghan Foley, Rahul Phadke, et al.Neuromuscular Disorders : NMD|December 19, 2018
Electromyography and muscle biopsy in paediatric neuromuscular disorders - Evaluation of current practice and literature reviewPatricia Hafner, Rahul Phadke, Adnan Manzur, et al.Neuromuscular Disorders : NMD|May 11, 2015
SIL1-related Marinesco-Sjoegren syndrome (MSS) with associated motor neuronopathy and bradykinetic movement disorderSusan Byrne, Nomazulu Dlamini, Daniel Lumsden, et al.Developmental Medicine and Child Neurology|October 3, 2021
Isolated bulbar palsy and dysphagia in children with respiratory symptomsStacey Zimmels, Ian M Balfour-Lynn, Loucas Christodoulou, et al.Developmental Medicine and Child Neurology|February 7, 2019
Acquired neuromyotonia in children with CASPR2 and LGI1 antibodiesSnehal Surana, Ratna Kumar, Matthew Pitt, et al.Intensive Care Medicine|April 21, 2022
The brain in pediatric critical care: unique aspects of assessment, monitoring, investigations, and follow-upKate L Brown, Shruti Agrawal, Matthew P Kirschen, et al.Pediatric Research|December 26, 2018
Recommendations for the design of therapeutic trials for neonatal seizuresJanet S Soul, Ronit Pressler, Marilee Allen, et al.Journal of Inherited Metabolic Disease|November 17, 2011
Further delineation of pontocerebellar hypoplasia type 6 due to mutations in the gene encoding mitochondrial arginyl-tRNA synthetase, RARS2Emma Glamuzina, Ruth Brown, Kieran Hogarth, et al.Muscle & Nerve|November 20, 2019
Early electrodiagnosis in the management of neonatal brachial plexus palsy: A systematic reviewRuth van der Looven, Laura Le Roy, Emma Tanghe, et al.Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|May 14, 2019
Guidelines for single fiber EMGDonald B Sanders, Kimiyoshi Arimura, LiYing Cui, et al.Pageof 8