IPSC reprogramming of two patients with spondyloepiphyseal dysplasia congenita (SEDC)

por De Kinderen, Pauline, Rabaut, Laura, Perik, Melanie H.A.M., Peeters, Silke, Ponsaerts, Peter, Loeys, Bart, Mortier, Geert, Meester, Josephina A.N., Verstraeten, Aline
Publicado 2023

Variable clinical expression of a Belgian TGFB3 founder variant suggests the presence of a genetic modifier

por Perik, Melanie H. A. M., Govaerts, Emmanuela, Laga, Steven, Goovaerts, Inge, Saenen, Johan, Van Craenenbroeck, Emeline, Meester, Josephina A. N., Luyckx, Ilse, Rodrigus, Inez, Verstraeten, Aline, Van Laer, Lut, Loeys, Bart L.
Publicado 2023

Novel LOX Variants in Five Families with Aortic/Arterial Aneurysm and Dissection with Variable Connective Tissue Findings

por Van Gucht, Ilse, Krebsova, Alice, Diness, Birgitte Rode, Laga, Steven, Adlam, Dave, Kempers, Marlies, Samani, Nilesh J., Webb, Tom R., Baranowska, Ania A., Van Den Heuvel, Lotte, Perik, Melanie, Luyckx, Ilse, Peeters, Nils, Votypka, Pavel, Macek, Milan, Meester, Josephina, Van Laer, Lut, Verstraeten, Aline, Loeys, Bart L.
Publicado 2021