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Nederlands Tijdschrift Voor Geneeskunde|September 19, 2007
[The silent yet successful revolution of mechanical ventilation in patients with neuromuscular disorders, in particular Duchenne muscular dystrophy]B G M van EngelenClinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology|November 28, 2007
Clinical neurophysiology of fatigueM J Zwarts, G Bleijenberg, B G M van EngelenJournal of Neuromuscular Diseases|March 6, 2023
Facioscapulohumeral Disease as a myodevelopmental disease: Applying Ockham's razor to its various featuresG W Padberg, B G M van Engelen, N C VoermansNederlands Tijdschrift Voor Geneeskunde|November 18, 2008
[Mitochondrial diseases; thinking beyond organ specialism necessary]B W Smits, J A M Smeitink, B G M van EngelenThe Cochrane Database of Systematic Reviews|January 27, 2006
Drug treatment for myotoniaJ Trip, G Drost, B G M van Engelen, et al.Journal of Communication Disorders|July 18, 2006
Warming up improves speech production in patients with adult onset myotonic dystrophyB J M de Swart, B G M van Engelen, B A M MaassenNederlands Tijdschrift Voor Geneeskunde|October 6, 2005
[The spectrum of hereditary skeletal-muscle channelopathies]J Trip, G Drost, H B Ginjaar, et al.Gait & Posture|July 2, 2015
Dynamic stability during level walking and obstacle crossing in persons with facioscapulohumeral muscular dystrophyN H M Rijken, B G M van Engelen, A C H Geurts, et al.The Netherlands Journal of Medicine|December 12, 2012
MIDD or MELAS : that's not the question MIDD evolving into MELAS : a severe phenotype of the m.3243A>G mutation due to paternal co-inheritance of type 2 diabetes and a high heteroplasmy levelH M de Wit, H J Westeneng, B G M van Engelen, et al.Neuromuscular Disorders : NMD|October 11, 2025
Marion or the metamorphosis: a journey of self-reconstruction and hope in the face of FSHDM Sellenet, A Belayew, R de Haas, et al.Pageof 9