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

بواسطة 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
منشور في 2013

Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype

بواسطة 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
منشور في 2011

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

بواسطة 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
منشور في 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...

بواسطة 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
الحاوية / القاعدة Am Heart J (2015)