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Journal of the American College of Cardiology|May 29, 2012
Aggressive cardiovascular phenotype of aneurysms-osteoarthritis syndrome caused by pathogenic SMAD3 variantsDenise van der Linde, Ingrid M B H van de Laar, Aida M Bertoli-Avella, et al.Open Heart|March 24, 2021
Patient information portal for congenital aortic and pulmonary valve disease: a stepped-wedge cluster randomised trialJonathan R G Etnel, Lidia R Bons, Frederiek De Heer, et al.International Journal of Cardiology|January 26, 2016
Non-sustained ventricular tachycardia in patients with congenital heart disease: An important sign?Christophe P Teuwen, Tanwier T T K Ramdjan, Marco Götte, et al.International Journal of Cardiology|December 27, 2025
Live(r) with a Fontan circulation: A European survey and a proposed expert consensus on liver surveillance in collaboration with the EuroFontan groupClaudia Montanaro, Pietro Paolo Tamborrino, Suman Verma, et al.JACC. Advances|June 28, 2024
Clinical Course of TGA After Arterial Switch Operation in the Current EraLeo J Engele, Roel L F van der Palen, Renée S Joosen, et al.Nature Genetics|January 11, 2011
Mutations in SMAD3 cause a syndromic form of aortic aneurysms and dissections with early-onset osteoarthritisIngrid M B H van de Laar, Rogier A Oldenburg, Gerard Pals, et al.Circulation Research|May 3, 2012
NPHP4 variants are associated with pleiotropic heart malformationsVanessa M French, Ingrid M B H van de Laar, Marja W Wessels, et al.Journal of Medical Genetics|December 15, 2011
Phenotypic spectrum of the SMAD3-related aneurysms-osteoarthritis syndromeIngrid M B H van de Laar, Denise van der Linde, Edwin H G Oei, et al.Heart (British Cardiac Society)|November 6, 2025
Cardiac resynchronisation therapy among adults with a systemic right ventricle: a multicentre experienceFlavia Fusco, Giancarlo Scognamiglio, Mikael Dellborg, et al.Journal of the American College of Cardiology|April 4, 2015
Mutations in a TGF-β ligand, TGFB3, cause syndromic aortic aneurysms and dissectionsAida M Bertoli-Avella, Elisabeth Gillis, Hiroko Morisaki, et al.Pageof 54