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International Journal of Cardiology|December 1, 2005
Primary impairment of left ventricular function in Marfan syndromeJulie F De Backer, Daniel Devos, Patrick Segers, et al.Orphanet Journal of Rare Diseases|February 28, 2013
Twenty patients including 7 probands with autosomal dominant cutis laxa confirm clinical and molecular homogeneitySmail Hadj-Rabia, Bert L Callewaert, Emmanuelle Bourrat, et al.Journal of Medical Genetics|July 2, 2010
The revised Ghent nosology for the Marfan syndromeBart L Loeys, Harry C Dietz, Alan C Braverman, et al.European Journal of Human Genetics : EJHG|April 15, 2010
Altered TGFbeta signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiencyMarjolijn Renard, Tammy Holm, Regan Veith, et al.Orphanet Journal of Rare Diseases|December 31, 2011
Osteogenesis Imperfecta: the audiological phenotype lacks correlation with the genotypeFreya K R Swinnen, Paul J Coucke, Anne M De Paepe, et al.Human Mutation|November 14, 2008
Comprehensive clinical and molecular assessment of 32 probands with congenital contractural arachnodactyly: report of 14 novel mutations and review of the literatureBert L Callewaert, Bart L Loeys, Anna Ficcadenti, et al.The New England Journal of Medicine|August 25, 2006
Aneurysm syndromes caused by mutations in the TGF-beta receptorBart L Loeys, Ulrike Schwarze, Tammy Holm, et al.Nature Genetics|February 26, 2005
A syndrome of altered cardiovascular, craniofacial, neurocognitive and skeletal development caused by mutations in TGFBR1 or TGFBR2Bart L Loeys, Junji Chen, Enid R Neptune, et al.American Heart Journal|May 13, 2015
Design and rationale of a prospective, collaborative meta-analysis of all randomized controlled trials of angiotensin receptor antagonists in Marfan syndrome, based on individual patient data: A report from the Marfan Treatment Trialists' CollaborationAlex Pitcher, Jonathan Emberson, Ronald V Lacro, et al.Pageof 1