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Heart Rhythm|July 24, 2014
From beat rate variability in induced pluripotent stem cell-derived pacemaker cells to heart rate variability in human subjectsMeital Ben-Ari, Revital Schick, Lili Barad, et al.
Genes|August 26, 2023
Danon Disease: Entire <i>LAMP2</i> Gene Deletion with Unusual Clinical Presentation-Case Report and Review of the LiteratureAdel Shalata, Marina Bar-Shai, Yarin Hadid, et al.
Clinical Research in Cardiology : Official Journal of the German Cardiac Society|October 31, 2020
Long-term outcome of perimembranous VSD closure using the Nit-Occlud® Lê VSD coil systemRainer Kozlik-Feldmann, Avraham Lorber, Horst Sievert, et al.
International Journal of Cardiology|September 19, 2018
Depression and anxiety are associated with high health care utilization and mortality among adults with congenital heart diseaseMichal Benderly, Ofra Kalter-Leibovici, Dahlia Weitzman, et al.
European Journal of Heart Failure|October 28, 2020
A current and future outlook on upcoming technologies in remote monitoring of patients with heart failureTarek Bekfani, Marat Fudim, John G F Cleland, et al.
Journal of the American Heart Association|January 12, 2021
Health Service Utilization Patterns Among Adults With Congenital Heart Disease: A Population-Based StudyMichal Benderly, Jonathan Buber, Ofra Kalter-Leibovici, et al.
Heart Failure Reviews|February 14, 2012
From discrete dilated cardiomyopathy to successful cardiac transplantation in congenital disorders of glycosylation due to dolichol kinase deficiency (DK1-CDG)Livia Kapusta, Nili Zucker, George Frenckel, et al.
Journal of Cellular and Molecular Medicine|December 2, 2017
Investigating the cardiac pathology of SCO2-mediated hypertrophic cardiomyopathy using patients induced pluripotent stem cell-derived cardiomyocytesTova Hallas, Binyamin Eisen, Yuval Shemer, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions|April 1, 2016
Closure of Secundum Atrial Septal Defects by Using the Occlutech Occluder Devices in More Than 1300 Patients: The IRFACODE Project: A Retrospective Case SeriesNikolaus A Haas, Dagmar B Soetemann, Ismail Ates, et al.
Human Genomics|February 28, 2025
Sengers syndrome caused by biallelic TIMM29 variants and RNAi silencing in Drosophila orthologue recapitulates the human phenotypeAdel Shalata, Ann Saada, Mohammed Mahroum, et al.
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