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Neuromuscular Disorders : NMD|November 10, 2012
Test-retest reliability and developmental evolution of the 6-min walk test in Caucasian boys aged 5-12 yearsNathalie Goemans, Katrijn Klingels, Marleen van den Hauwe, et al.
Human Genetics|August 4, 2004
Genomic rearrangements at the IGHMBP2 gene locus in two patients with SMARD1Ulf P Guenther, Markus Schuelke, Enrico Bertini, et al.
Human Molecular Genetics|November 26, 2004
Dominant collagen VI mutations are a common cause of Ullrich congenital muscular dystrophyNaomi L Baker, Matthias Mörgelin, Rachel Peat, et al.
Pediatric Diabetes|June 6, 2009
Metformin therapy to reduce weight gain and visceral adiposity in children and adolescents with neurogenic or myogenic motor deficitKristina Casteels, Steffen Fieuws, Maria van Helvoirt, et al.
Orphanet Journal of Rare Diseases|July 3, 2025
Development of the accredited duchenne centers program, a global program to achieve uniform and up-to-date care for all people living with duchenne muscular dystrophyImelda J M de Groot, Karolina Podolská, Nathalie Goemans, et al.
Plos One|January 7, 2014
Six-minute walk test: reference values and prediction equation in healthy boys aged 5 to 12 yearsNathalie Goemans, Katrijn Klingels, Marleen van den Hauwe, et al.
Frontiers in Human Neuroscience|February 16, 2018
Non-neural Muscle Weakness Has Limited Influence on Complexity of Motor Control during GaitMarije Goudriaan, Benjamin R Shuman, Katherine M Steele, et al.
Neuromuscular Disorders : NMD|February 17, 2015
Renal function in children and adolescents with Duchenne muscular dystrophyElke Braat, Liesbeth Hoste, Liesbeth De Waele, et al.
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