Anders K. Broendberg
Palle Juul Jensens Boulevard 82
Aarhus N, 8200, Denmark
Aarhus N, 8200, Denmark
Last Updated: 09/26/2026
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Found 10 publications
Outcome after out-of-hospital cardiac arrest in patients with ischaemic and non-ischaemic heart disease: A Danish tertiary-center cohort study.
Journal: International journal of cardiology. Heart & vasculature
Published: April 01, 2022
The G213D variant in Nav1.5 alters sodium current and causes an arrhythmogenic phenotype resulting in a multifocal ectopic Purkinje-related premature contraction phenotype in human-induced pluripotent stem cell-derived cardiomyocytes.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: December 01, 2021
Cardiac ryanodine receptor calcium release deficiency syndrome.
Journal: Science translational medicine
Published: December 30, 2019
Implantable cardioverter-defibrillator therapy and device-related complications in young patients with inherited cardiomyopathies or channelopathies: a 17-year cohort study.
Journal: Europace : European pacing, arrhythmias, and cardiac electrophysiology : journal of the working groups on cardiac pacing, arrhythmias, and cardiac cellular electrophysiology of the European Society of Cardiology
Published: January 09, 2018
Outcome of clinical management in relatives of sudden cardiac death victims.
Journal: International journal of cardiology
Published: December 03, 2017
Multifocal atrial and ventricular premature contractions with an increased risk of dilated cardiomyopathy caused by a Nav1.5 gain-of-function mutation (G213D).
Journal: International journal of cardiology
Published: September 24, 2017
Nationwide experience of catecholaminergic polymorphic ventricular tachycardia caused by RyR2 mutations.
Journal: Heart (British Cardiac Society)
Published: August 24, 2016
Cardiovascular risk factor control is insufficient in young patients with coronary artery disease.
Journal: Vascular health and risk management
Published: June 17, 2016
Repeated molecular genetic analysis in Brugada syndrome revealed a novel disease-associated large deletion in the SCN5A gene.
Journal: HeartRhythm case reports
Published: March 09, 2016
Molecular genetic diagnostics of the cause of ventricular arrhythmias in children
Journal: Ugeskrift for laeger
Published: September 17, 2015
Showing 1-10 of 10
Last Updated: 09/26/2026