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Neuromuscular Disorders : NMD|November 5, 2023
The impact of clinical trial participation on quality of life and psychosocial well-being in children with Duchenne muscular dystrophy and their parentsSam Geuens, Joanna Willen, Corine Antonis, et al.Human Molecular Genetics|November 6, 2007
Increased Gs signalling in platelets and impaired collagen activation, due to a defect in the dystrophin gene, result in increased blood loss during spinal surgeryVeerle Labarque, Kathleen Freson, Chantal Thys, et al.Clinical Child Psychology and Psychiatry|September 16, 2022
Illness Perceptions and Illness Identity in Adolescents and Emerging Adults With Neuromuscular DisordersSam Geuens, Kathelijne Leyen, Koen Raymaekers, et al.Human Gene Therapy|September 4, 2014
Translational and regulatory challenges for exon skipping therapiesAnnemieke Aartsma-Rus, Alessandra Ferlini, Nathalie Goemans, et al.Advances in Experimental Medicine and Biology|January 20, 2016
Differences in Contraction-Induced Hemodynamics and Surface EMG in Duchenne Muscular DystrophyEva Van Ginderdeuren, Alexander Caicedo, Joachim Taelmans, et al.Annals of Neurology|November 18, 2015
Longitudinal effect of eteplirsen versus historical control on ambulation in Duchenne muscular dystrophyJerry R Mendell, Nathalie Goemans, Linda P Lowes, et al.Journal of Neuroengineering and Rehabilitation|October 2, 2025
Longitudinal interaction between muscle impairments and gait pathology in growing children with Duchenne muscular dystrophyInes Vandekerckhove, Geert Molenberghs, Marleen Van den Hauwe, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 6, 2019
Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers-Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrixSarah Delbaere, Tibbe Dhooge, Delfien Syx, et al.Journal of Neuromuscular Diseases|February 1, 2021
Comparison of Long-term Ambulatory Function in Patients with Duchenne Muscular Dystrophy Treated with Eteplirsen and Matched Natural History ControlsJerry R Mendell, Navid Khan, Nanshi Sha, et al.American Journal of Medical Genetics. Part A|August 2, 2005
A mitochondrial tRNA aspartate mutation causing isolated mitochondrial myopathySara Seneca, Nathalie Goemans, Rudy Van Coster, et al.Pageof 11