Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome: a systematic review

por D'hondt, Sanne, Van Damme, Tim, Malfait, Fransiska
Publicado 2018

The Ehlers–Danlos Syndromes against the Backdrop of Inborn Errors of Metabolism

por Van Damme, Tim, Colman, Marlies, Syx, Delfien, Malfait, Fransiska
Publicado 2022

Glycosaminoglycan linkage region of urinary bikunin as a potentially useful biomarker for β3GalT6‐deficient spondylodysplastic Ehlers–Danlos syndrome

por Nikpour, Mahnaz, Noborn, Fredrik, Nilsson, Jonas, Van Damme, Tim, Kaye, Olivier, Syx, Delfien, Malfait, Fransiska, Larson, Göran
Publicado 2022

The clinical and mutational spectrum of B3GAT3 linkeropathy: two case reports and literature review

por Colman, Marlies, Van Damme, Tim, Steichen-Gersdorf, Elisabeth, Laccone, Franco, Nampoothiri, Sheela, Syx, Delfien, Guillemyn, Brecht, Symoens, Sofie, Malfait, Fransiska
Publicado 2019

Analysis of chromosomal radiosensitivity of healthy BRCA2 mutation carriers and non-carriers in BRCA families with the G2 micronucleus assay

por Baert, Annelot, Depuydt, Julie, Van Maerken, Tom, Poppe, Bruce, Malfait, Fransiska, Van Damme, Tim, De Nobele, Sylvia, Perletti, Gianpaolo, De Leeneer, Kim, Claes, Kathleen B.M., Vral, Anne
Publicado 2017

Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta

por Syx, Delfien, Ishikawa, Yoshihiro, Gebauer, Jan, Boudko, Sergei P., Guillemyn, Brecht, Van Damme, Tim, D’hondt, Sanne, Symoens, Sofie, Nampoothiri, Sheela, Gould, Douglas B., Baumann, Ulrich, Bächinger, Hans Peter, Malfait, Fransiska
Publicado 2021

Increased chromosomal radiosensitivity in asymptomatic carriers of a heterozygous BRCA1 mutation

por Baert, Annelot, Depuydt, Julie, Van Maerken, Tom, Poppe, Bruce, Malfait, Fransiska, Storm, Katrien, van den Ende, Jenneke, Van Damme, Tim, De Nobele, Sylvia, Perletti, Gianpaolo, De Leeneer, Kim, Claes, Kathleen B. M., Vral, Anne
Publicado 2016