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Pain|June 3, 2020
Pain-related behaviors and abnormal cutaneous innervation in a murine model of classical Ehlers-Danlos syndromeDelfien Syx, Rachel E Miller, Alia M Obeidat, et al.
The Journal of Pain|June 28, 2023
Sensory Profiling in Classical Ehlers-Danlos Syndrome: A Case-Control Study Revealing Pain Characteristics, Somatosensory Changes, and Impaired Pain ModulationMarlies Colman, Delfien Syx, Inge De Wandele, et al.
Medrxiv : the Preprint Server for Health Sciences|March 3, 2023
Sensory profiling in classical Ehlers-Danlos syndrome: a case-control study revealing pain characteristics, somatosensory changes, and impaired pain modulationMarlies Colman, Delfien Syx, Inge de Wandele, et al.
Orphanet Journal of Rare Diseases|May 23, 2013
Helical mutations in type I collagen that affect the processing of the amino-propeptide result in an Osteogenesis Imperfecta/Ehlers-Danlos Syndrome overlap syndromeFransiska Malfait, Sofie Symoens, Nathalie Goemans, et al.
Rheumatology (Oxford, England)|April 21, 2016
Orthostatic intolerance and fatigue in the hypermobility type of Ehlers-Danlos SyndromeInge De Wandele, Lies Rombaut, Tine De Backer, et al.
Orphanet Journal of Rare Diseases|October 2, 2013
Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humansSofie Symoens, Fransiska Malfait, Sanne D'hondt, et al.
Clinical and Experimental Rheumatology|November 17, 2023
Microvascular status and skin thickness in adults with hypermobile Ehlers-Danlos syndrome: a pilot investigationAlberto Sulli, Elvis Hysa, Andrea Cere, et al.
Molecular Genetics & Genomic Medicine|November 19, 2017
Genetic analysis of osteogenesis imperfecta in the Palestinian population: molecular screening of 49 affected familiesOsama Essawi, Sofie Symoens, Maha Fannana, et al.
Clinical Dysmorphology|March 24, 2010
Short stature, severe aortic root dilation, skin hyperextensibility, extreme joint laxity and craniofacial dysmorphic features: a probable new syndromeElke Verstraeten, Sofie Symoens, Marjolijn Renard, et al.
Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|February 7, 2015
Defective Proteolytic Processing of Fibrillar Procollagens and Prodecorin Due to Biallelic BMP1 Mutations Results in a Severe, Progressive Form of Osteogenesis ImperfectaDelfien Syx, Brecht Guillemyn, Sofie Symoens, et al.
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