Scientific Articles

2022

Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias

Suppression and Replacement Gene Therapy for KCNH2-Mediated Arrhythmias

Posttraumatic stress disorder in pediatric patients with implantable cardioverter-defibrillators and their parents

International Evidence Based Reappraisal of Genes Associated with ARVC

Life-threatening cardiac arrhythmia and sudden death during electronic gaming

Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)

Does sports participation increase risk in patients with long QT syndrome? Results from a large French cohort

A prospective longitudinal study of health-related quality of life and psychological wellbeing after an implantable cardioverter-defibrillator (ICD) in patients with genetic heart diseases

Use of oral contraceptives in women with congenital long QT syndrome

EDITORIAL COMMENTARY Oral contraceptives and their effect on arrhythmogenesis in long QT syndrome: Does it matter?

Burst Exercise Testing Can Unmask Arrhythmias in Patients With Incompletely Penetrant Catecholaminergic Polymorphic Ventricular (CPVT)

Outcomes of Patients With Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT) Treated With β-Blockers

Experiences of athletes with arrhythmogenic cardiac conditions (SADS) in returning to play

Diagnosis and management of rare cardiomyopathies in adult and paediatric patients: the ACM Team

An International Multicenter Study on β-Blockers for the Treatment of Symptomatic Children with CPVT

Brugada Syndrome: State-of-the-Art Review Abstract

Heart transplantation outcomes in arrhythmogenic right ventricular cardiomyopathy: a contemporary national analysis

Genome-wide association analyses identify new Brugada syndrome risk loci and highlight a new mechanism of sodium channel regulation in disease susceptibility

Recent understanding of clinical sequencing and gene-based risk stratification in inherited primary arrhythmia syndrome

Clinical characteristics and risk stratification of desmoplakin cardiomyopathy

A prospective longitudinal study of health-related quality of life and psychological wellbeing after an implantable cardioverter-defibrillator (ICD) in patients with genetic heart diseases

Genome Sequencing in a Genetically Elusive Multi-Generational Long QT Syndrome Pedigree Identifies a Novel LQT2-Causative Deeply Intronic KCNH2 Variant

Diagnostic accuracy of the 12-lead ECG in the first 48 hours of life for newborns of a parent with congenital long QT syndrome

Psychosocial symptoms of ventricular arrhythmias: Integrating patient-reported outcomes in to clinical care

Role of CACNA1C in Brugada syndrome: Prevalence and phenotype of probands referred for genetic testing

Multimodality Imaging in Arrhythmogenic Right Ventricular Cardiomyopathy (ARVC)

2021

Re-Entry Anxiety in the Pandemic Aftermath

Importance of Dedicated Units for Management of SADS CircGen April 2021

2020 APHRS/HRS expert consensus statement on the investigation of decedents with sudden unexplained death and patients with sudden cardiac arrest, and of their families

KKCNQ1 Gene Therapy for LQT1 CIRCULATIONAHA.1-28-21

Life Saving Therapy Inhibition by Phones Containing Magnets

2020

An autoantibody identifies arrhythmogenic right ventricular cardiomyopathy and participates in its pathogenesis

An autoantibody profile detects Brugada syndrome and identifies abnormally expressedmyocardial proteins

Wash U-developed holograms help physicians during cardiac procedure

Validation and Disease Risk Assessment of Previously Reported Genome-Wide Genetic Variants Associated with Brugada Syndrome: SADS-TW BrS Registry

An International Multicenter Evaluation of Type 5 Long QT Syndrome

An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome

Circulation: Arrhythmia and Electrophysiology:Heart Rate Recovery After Exercise Is Associated With Arrhythmic Events in Patients With Catecholaminergic Polymorphic Ventricular Tachycardia

CIRCEP Heart Rate Recovery After Exercise in CPVT

Genetic Testing in Inherited Heart Diseases

Genetic Cardiovascular Conditions – It’s All About Family

Exercise and Arrhythmogenic Right Ventricular Cardiomyopathy

Brugada Syndrome: Clinical Care Amidst Pathophysiological Uncertainty

Pre-Test Probability and Genes and VUS’s in Familial LQTS

50 Years of Catecholaminergic Polymorphic Ventricular Tachycardia (CPVT)

Precision medicine opportunities for familial arrhythmias and cardiomyopathies identified when cost of genetic testing is removed as a barrier

A Novel Genotype -Phenotype Risk Prediction Model for Arrhythmic Events in Women with Long-QT Syndrome

Clinical limitations of genotyping- versus sequencing-based strategies for cardiomyopathy evaluation

Exertional syncope in with college varsity athletes

Implantable Cardioverter Defibrillator placement in a patient with potentially reversible causes of Long QT Syndrome

Left Cardiac Sympathectomy Denervation LQTS

MEXILETINE Shortens QT Interval

Outcomes of Sports Participation for Patients with Hypertrophic Cardiomyopathy and Implantable Cardioverter: Data from the ICD Sportys Regisrty

QTc in Patients with Turner Syndrome

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