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Congenital Heart Disease|August 14, 2012
Hypoplasia of the aorta in a patient diagnosed with LMNA gene mutationGuillaume Coutance, Fabien Labombarda, Emmanuelle Cauderlier, et al.
European Heart Journal. Cardiovascular Imaging|January 25, 2014
Major congenital coronary artery anomalies in a paediatric and adult population: a prospective echocardiographic studyFabien Labombarda, Guillaume Coutance, Arnaud Pellissier, et al.
Archives of Cardiovascular Diseases|August 11, 2020
The value of electrocardiography and echocardiography in distinguishing Fabry disease from sarcomeric hypertrophic cardiomyopathyNicolas Junqua, Damien Legallois, Sophie Segard, et al.
Frontiers in Cardiovascular Medicine|November 17, 2022
Recurrent acute myocarditis: An under-recognized clinical entity associated with the later diagnosis of a genetic arrhythmogenic cardiomyopathyPierre Ollitrault, Mayane Al Khoury, Yann Troadec, et al.
Journal of Clinical Neuromuscular Disease|May 25, 2017
Cardiac Abnormalities in Type 1 Facioscapulohumeral Muscular DystrophyFabien Labombarda, Maxime Maurice, Jean-Philippe Simon, et al.
The American Journal of Cardiology|August 22, 2009
Transradial intervention for minimizing bleeding complications in percutaneous coronary interventionMartial Hamon, Guillaume Coutance
Respiratory Medicine|December 13, 2017
Heart rate and risk of death among patients with Pulmonary Hypertension: A 12-lead ECG analysisHelene Bouchery-Bardet, Christian Creveuil, Fabrice Bauer, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|August 19, 2016
Delayed spontaneous perforation of polyvinyl alcohol membrane-Covered atrial septal defect closure devicesFabien Labombarda, Vincent Roule, Farzin Beygui
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