ERN GUARD-Heart https://validator.w3.org/feed/docs/rss2.html Functional data improve variant classification and penetrance stratification for Brugada Syndrome  Home Left Ventricular Late Gadolinium Enhancement for Arrhythmic Risk Prediction in ARVC ARVC Previous Events Natural History of Patients With Histologically Proven Acute Eosinophilic Myocarditis Other rare cardiac diseases Catecholaminergic polymorphic ventricular tachycardia mediated by ryanodine receptor 2: a validated risk stratification CPVT Brugada HCM SS (SE) AICARM (IT) Tools SZÍVSN (HU) FAST (BG) Sudden Cardiac Death Letter for the Family Future Events Webinar series Original work Risk of myocarditis and pericarditis after the COVID-19 mRNA vaccination in the USA: a cohort study in claims databases. The Role of Molecular Autopsy in Concealed Cardiomyopathies Cocaine-Induced Sudden Cardiac Death Unravelling a SCN5A-Related Disease ERDERA 2026 Joint Transnational Call – Now Open ERN GUARD-Heart Publications Project Management Office Irish Inherited Cardiac Conditions Network Long QT Syndrome (LQTS) Experts Links Forms Generated Documents for Registries What is the risk of dangerous arrhythmias in SCN5A loss-of-function mutation carriers? Genetic analysis identifies the SLC4A3 anion exchanger as a major gene for short QT syndrome. Addressing unmet needs in pregnancy and family planning of people living with rare and low-prevalence diseases: resultsof the “ERN transversal working group on pregnancy and family planning” survey High societal costs and reduced health-related quality of life Non-amyloid specific treatment for transthyretin cardiac amyloidosis: a clinical consensus statement of the ESC Heart Failure Association Predictive value of ambulatory ECG monitoring for malignant arrhythmic events in genetic dilated cardiomyopathy ERN transversal working group on pregnancy and family planning DCM Who are our ePAG’s?Céline’s Journey: Perseverance, Resilience, and Hope SQTS Congenital heart diseases The diagnostic role of pharmacological provocation testing in cardiac electrophysiology Comparing manual versus automatic measurements of the QT-interval and QTc Sex Differences in Prognosis of Patients With Genetic Dilated Cardiomyopathy Condition-Specific Registries Impact of genotype-phenotype associations on prognosis in dilated cardiomyopathy Default Form Newsletters