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Arthritis Care & Research|January 11, 2012
Muscle-tendon tissue properties in the hypermobility type of Ehlers-Danlos syndromeLies Rombaut, Fransiska Malfait, Inge De Wandele, et al.Human Mutation|June 15, 2012
Comprehensive molecular analysis demonstrates type V collagen mutations in over 90% of patients with classic EDS and allows to refine diagnostic criteriaSofie Symoens, Delfien Syx, Fransiska Malfait, et al.Journal of Cranio-Maxillo-Facial Surgery : Official Publication of the European Association for Cranio-Maxillo-Facial Surgery|May 20, 2016
Cephalometrics in Stickler syndrome: Objectification of the typical facial appearanceFrederic R Acke, Ingeborg J Dhooge, Fransiska Malfait, et al.Clinical Rheumatology|February 4, 2014
Chronic pain in patients with the hypermobility type of Ehlers-Danlos syndrome: evidence for generalized hyperalgesiaLies Rombaut, Mark Scheper, Inge De Wandele, et al.American Journal of Medical Genetics. Part A|March 22, 2019
Ptosis as a unique hallmark for autosomal recessive WNT1-associated osteogenesis imperfectaSheela Nampoothiri, Brecht Guillemyn, Nursel Elcioglu, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|February 14, 2017
Ehlers-Danlos syndrome, classical typeJessica M Bowen, Glenda J Sobey, Nigel P Burrows, et al.Seminars in Arthritis and Rheumatism|June 28, 2014
Autonomic symptom burden in the hypermobility type of Ehlers-Danlos syndrome: a comparative study with two other EDS types, fibromyalgia, and healthy controlsInge De Wandele, Patrick Calders, Wim Peersman, et al.Arthritis Care & Research|April 16, 2020
Does Muscle Strength Change Over Time in Patients With Hypermobile Ehlers-Danlos Syndrome/Hypermobility Spectrum Disorder? An Eight-Year Follow-Up StudyMarie Coussens, Patrick Calders, Bruno Lapauw, et al.American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|November 19, 2021
Pain in the Ehlers-Danlos syndromes: Mechanisms, models, and challengesFransiska Malfait, Marlies Colman, Robin Vroman, et al.Human Molecular Genetics|January 23, 2019
Bi-allelic AEBP1 mutations in two patients with Ehlers-Danlos syndromeDelfien Syx, Inge De Wandele, Sofie Symoens, et al.Pageof 15