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

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

Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans

por Symoens, Sofie, Malfait, Fransiska, D’hondt, Sanne, Callewaert, Bert, Dheedene, Annelies, Steyaert, Wouter, Bächinger, Hans Peter, De Paepe, Anne, Kayserili, Hulya, Coucke, Paul J
Publicado 2013

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