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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.
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.
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