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Matrix Biology Plus|December 1, 2021
Four decades in the making: Collagen III and mechanisms of vascular Ehlers Danlos SyndromeRamla Omar, Fransiska Malfait, Tom Van Agtmael
Genetics in Medicine : Official Journal of the American College of Medical Genetics|October 6, 2017
Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome: a systematic reviewSanne D'hondt, Tim Van Damme, Fransiska Malfait
Neuromuscular Disorders : NMD|June 18, 2013
Compound heterozygous mutations of the TNXB gene cause primary myopathyIsabelle Pénisson-Besnier, Valérie Allamand, Philippe Beurrier, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2016
Expanding the clinical and mutational spectrum of the Ehlers-Danlos syndrome, dermatosparaxis typeTim Van Damme, Alain Colige, Delfien Syx, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|September 18, 2010
Clinical and genetic aspects of Ehlers-Danlos syndrome, classic typeFransiska Malfait, Richard J Wenstrup, Anne De Paepe
Annual Review of Genomics and Human Genetics|May 24, 2015
The Genetics of Soft Connective Tissue DisordersOlivier Vanakker, Bert Callewaert, Fransiska Malfait, et al.
Orphanet Journal of Rare Diseases|July 24, 2014
Recommendations for anesthesia and perioperative management in patients with Ehlers-Danlos syndrome(s)Thomas Wiesmann, Marco Castori, Fransiska Malfait, et al.
Frontiers in Molecular Neuroscience|September 4, 2023
Analysis of matrisome expression patterns in murine and human dorsal root gangliaRobin Vroman, Rahel S Hunter, Matthew J Wood, et al.
Matrix Biology : Journal of the International Society for Matrix Biology|March 20, 2018
Type III collagen affects dermal and vascular collagen fibrillogenesis and tissue integrity in a mutant Col3a1 transgenic mouse modelSanne D'hondt, Brecht Guillemyn, Delfien Syx, et al.
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