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Journal of the American College of Cardiology|January 17, 2024
Anxiety and Depression in Adults With Congenital Heart DiseaseAdrienne H Kovacs, Koen Luyckx, Corina Thomet, et al.
European Journal of Cardiovascular Nursing|June 12, 2020
Sense of coherence in adults with congenital heart disease in 15 countries: Patient characteristics, cultural dimensions and quality of lifePhilip Moons, Silke Apers, Adrienne H Kovacs, et al.
BMC Health Services Research|June 5, 2020
Healthcare system inputs and patient-reported outcomes: a study in adults with congenital heart defect from 15 countriesLiesbet Van Bulck, Eva Goossens, Koen Luyckx, et al.
Heart (British Cardiac Society)|November 25, 2020
Bleeding and thrombotic risk in pregnant women with Fontan physiologyAndrea Girnius, Dominica Zentner, Anne Marie Valente, et al.
European Journal of Preventive Cardiology|July 22, 2025
Refining current risk stratification guidelines for pregnant women with Fontan circulation: lessons from PROFAT registryMagalie Ladouceur, Andrea Girnius, Dominica Zentner, et al.
Journal of the American Heart Association|April 26, 2022
Heart Failure and Patient-Reported Outcomes in Adults With Congenital Heart Disease from 15 CountriesChun-Wei Lu, Jou-Kou Wang, Hsiao-Ling Yang, et al.
Ebiomedicine|February 28, 2024
Genome-wide enhancer-associated tandem repeats are expanded in cardiomyopathyAleksandra Mitina, Mahreen Khan, Robert Lesurf, et al.
The Canadian Journal of Cardiology|April 23, 2022
Canadian Cardiovascular Society 2022 Guidelines for Cardiovascular Interventions in Adults With Congenital Heart DiseaseAriane Marelli, Luc Beauchesne, Jack Colman, et al.
NPJ Genomic Medicine|March 15, 2022
Whole genome sequencing delineates regulatory, copy number, and cryptic splice variants in early onset cardiomyopathyRobert Lesurf, Abdelrahman Said, Oyediran Akinrinade, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|February 2, 2023
Updated clinical practice recommendations for managing adults with 22q11.2 deletion syndromeErik Boot, Sólveig Óskarsdóttir, Joanne C Y Loo, et al.
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