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The Canadian Journal of Cardiology|October 11, 2021
Baffle Complications in Adults After Atrial Switch for Transposition of the Great ArteriesOdilia I Woudstra, Fabienne T E Alban, Geertruida P Bijvoet, et al.
Congenital Heart Disease|August 22, 2008
Menstrual cycle and its disorders in women with congenital heart diseaseWillem Drenthen, Elke S Hoendermis, Philip Moons, et al.
Circulation|September 28, 2011
Pediatric pulmonary hypertension in the Netherlands: epidemiology and characterization during the period 1991 to 2005Rosa Laura E van Loon, Marcus T R Roofthooft, Hans L Hillege, et al.
European Journal of Human Genetics : EJHG|March 10, 2011
A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9qJudith B A van de Meerakker, Klaartje van Engelen, Inge B Mathijssen, et al.
Journal of Magnetic Resonance Imaging : JMRI|June 30, 2025
Aortic Function in a Longitudinal 4D Flow MRI Study in Marfan Syndrome Patients Receiving ResveratrolDaan Bosshardt, Mitzi M van Andel, E M Schrauben, et al.
Angiogenesis|December 11, 2008
Molecular imaging of tumor angiogenesis using alphavbeta3-integrin targeted multimodal quantum dotsWillem J M Mulder, Karolien Castermans, Judy R van Beijnum, et al.
International Journal of Cardiology|October 12, 2010
Circumstances of death in adult congenital heart diseaseA Carla Zomer, Ilonca Vaartjes, Cuno S P M Uiterwaal, et al.
The Canadian Journal of Cardiology|June 20, 2020
Myocardial Deformation in the Systemic Right Ventricle: Strain Imaging Improves Prediction of the Failing HeartOdilia I Woudstra, Alexandra C van Dissel, Teun van der Bom, et al.
The American Journal of Cardiology|May 2, 2009
Effect of bosentan on exercise capacity and quality of life in adults with pulmonary arterial hypertension associated with congenital heart disease with and without Down's syndromeMariëlle G J Duffels, Jeroen C Vis, Rosa L E van Loon, et al.
Circulation. Cardiovascular Genetics|January 24, 2015
Beneficial Outcome of Losartan Therapy Depends on Type of FBN1 Mutation in Marfan SyndromeRomy Franken, Alexander W den Hartog, Teodora Radonic, et al.
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