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American Journal of Medical Genetics. Part A|June 10, 2016
RIN2 syndrome: Expanding the clinical phenotypeSimonetta Rosato, Delfien Syx, Ivan Ivanovski, 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.
European Journal of Pain (London, England)|April 20, 2022
Exploring pain mechanisms in hypermobile Ehlers-Danlos syndrome: A case-control studyInge De Wandele, Marlies Colman, Linda Hermans, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|May 1, 2018
Vascular aspects of the Ehlers-Danlos SyndromesFransiska Malfait
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.
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.
The Biochemical Journal|October 29, 2010
Identification of binding partners interacting with the α1-N-propeptide of type V collagenSofie Symoens, Marjolijn Renard, Christelle Bonod-Bidaud, et al.
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