Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneity

Por Hadj-Rabia, Smail, Callewaert, Bert L, Bourrat, Emmanuelle, Kempers, Marlies, Plomp, Astrid S, Layet, Valerie, Bartholdi, Deborah, Renard, Marjolijn, Backer, Julie De, Malfait, Fransiska, Vanakker, Olivier M, Coucke, Paul J, De Paepe, Anne M, Bodemer, Christine
Publicado em 2013

Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype

Por Swinnen, Freya KR, Coucke, Paul J, De Paepe, Anne M, Symoens, Sofie, Malfait, Fransiska, Gentile, Filomena V, Sangiorgi, Luca, D'Eufemia, Patrizia, Celli, Mauro, Garretsen, Ton JTM, Cremers, Cor WRJ, Dhooge, Ingeborg JM, De Leenheer, Els MR
Publicado em 2011

Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency

Por Renard, Marjolijn, Holm, Tammy, Veith, Regan, Callewaert, Bert L, Adès, Lesley C, Baspinar, Osman, Pickart, Angela, Dasouki, Majed, Hoyer, Juliane, Rauch, Anita, Trapane, Pamela, Earing, Michael G, Coucke, Paul J, Sakai, Lynn Y, Dietz, Harry C, De Paepe, Anne M, Loeys, Bart L
Publicado em 2010

Design and rationale of a prospective, collaborative meta-analysis of all randomized controlled trials of angiotensin receptor antagonists in Marfan syndrome, based on individual p...

Por Pitcher, Alex, Emberson, Jonathan, Lacro, Ronald V., Sleeper, Lynn A., Stylianou, Mario, Mahony, Lynn, Pearson, Gail D., Groenink, Maarten, Mulder, Barbara J., Zwinderman, Aeilko H., De Backer, Julie, De Paepe, Anne M., Arbustini, Eloisa, Erdem, Guliz, Jin, Xu Yu, Flather, Marcus D., Mullen, Michael J., Child, Anne H., Forteza, Alberto, Evangelista, Arturo, Chiu, Hsin-Hui, Wu, Mei-Hwan, Sandor, George, Bhatt, Ami B., Creager, Mark A., Devereux, Richard B., Loeys, Bart, Forfar, J. Colin, Neubauer, Stefan, Watkins, Hugh, Boileau, Catherine, Jondeau, Guillaume, Dietz, Harry C., Baigent, Colin
Publicado no Am Heart J (2015)