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

द्वारा 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
प्रकाशित 2013

Osteogenesis imperfecta: the audiological phenotype lacks correlation with the genotype

द्वारा 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
प्रकाशित 2011

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

द्वारा 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
प्रकाशित 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...

द्वारा 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
में प्रकाशित Am Heart J (2015)