The mission of ERN GUARD-Heart is to facilitate access to highly specialised diagnosis and treatment of rare and complex heart diseases in both adult and paediatric patients across the European Union.
Articles
- Characterization and Management of Arrhythmic Events in Young Patients With Brugada Syndrome
- 2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary
- Yield of Clinical Screening for Hypertrophic Cardiomyopathy in Child First-Degree Relatives
- Effectiveness of the 2014 European Society of Cardiology guideline on sudden cardiac death in hypertrophic cardiomyopathy: a systematic review and meta-analysis
- Implantable cardioverter-defibrillators in previously undiagnosed patients with catecholaminergic polymorphic ventricular tachycardia resuscitated from sudden cardiac arrest
- Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry
- European recommendations integrating genetic testing into multidisciplinary management of sudden cardiac death
- The yield of postmortem genetic testing in sudden death cases with structural findings at autopsy
- Next-generation sequencing using microfluidic PCR enrichment for molecular autopsy
- Severe Cardiac Dysfunction and Death Caused by Arrhythmogenic Right Ventricular Cardiomyopathy Type 5 Are Improved by Inhibition of Glycogen Synthase Kinase-3β
- An International Multicenter Evaluation of Type 5 Long QT Syndrome
- Ethnic differences in patients with Brugada syndrome and arrhythmic events: New insights from Survey on Arrhythmic Events in Brugada Syndrome
- Time-to-first appropriate shock in patients implanted prophylactically with an implantable cardioverter-defibrillator: data from the Survey on Arrhythmic Events in BRUgada Syndrome (SABRUS)
- Continued misuse of orphan drug legislation: a life-threatening risk for mexiletine
- Prevalence and clinical significance of red flags in patients with hypertrophic cardiomyopathy
- Multimodality imaging in the diagnosis, risk stratification, and management of patients with dilated cardiomyopathies: an expert consensus document from the European Association of Cardiovascular Imaging
- Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia
- Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand
- ESC EORP Cardiomyopathy Registry: real‐life practice of genetic counselling and testing in adult cardiomyopathy patients
- Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study
- Inherited cardiac arrhythmias
- Transethnic Genome-Wide Association Study Provides Insights in the Genetic Architecture and Heritability of Long QT Syndrome
- Natural History and Risk Stratification in Andersen-Tawil Syndrome Type 1
Details
- Publication date
- 27 January 2021