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From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2

European heart journal, 2019-06, Vol.40 (23), p.1832-1836

2019

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Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome

Circulation (New York, N.Y.), 2020-12, Vol.142 (25), p.2405-2415

2020

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Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

European heart journal, 2019-09, Vol.40 (35), p.2964-2975

2019

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The genetics underlying acquired long QT syndrome: impact for genetic screening

European heart journal, 2016-05, Vol.37 (18), p.1456-1464

2016

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Congenital long QT syndrome

Orphanet journal of rare diseases, 2008-07, Vol.3 (1), p.18-18, Article 18

2008

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Management of survivors of cardiac arrest - the importance of genetic investigation

Nature reviews cardiology, 2016-09, Vol.13 (9), p.560-566

2016

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The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?

International journal of cardiology, 2018-01, Vol.250, p.139-145

2018

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Mutation location and I Ks regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region

European heart journal, 2021-12, Vol.42 (46), p.4743-4755

2021

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FGF12 is a candidate Brugada syndrome locus

Heart rhythm, 2013-12, Vol.10 (12), p.1886-1894

2013

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A comprehensive electrocardiographic, molecular, and echocardiographic study of Brugada syndrome: Validation of the 2013 diagnostic criteria

Heart rhythm, 2014-07, Vol.11 (7), p.1176-1183

2014

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In a case of female-to-male sex reassignment, testosterone therapy switches on an underlying Brugada

International journal of arrhythmia, 2020-10, Vol.21 (1), p.1-4, Article 17

2020

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Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene

Stem cell research, 2018-05, Vol.29, p.157-161

2018

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Torsades de pointes following acute myocardial infarction: Evidence for a deadly link with a common genetic variant

Heart rhythm, 2012-07, Vol.9 (7), p.1104-1112

2012

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Spectrum and Prevalence of Mutations Involving BrS1- Through BrS12-Susceptibility Genes in a Cohort of Unrelated Patients Referred for Brugada Syndrome Genetic Testing

Journal of the American College of Cardiology, 2012-10, Vol.60 (15), p.1410-1418

2012

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A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome

Heart rhythm, 2009-02, Vol.6 (2), p.212-218

2009

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Evolution in Managing Long QT Syndrome

Journal of the American College of Cardiology, 2017-07, Vol.70 (4), p.463-465

2017

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Energy drinks and sudden death: If it swims like a duck

Heart rhythm, 2024-07, Vol.21 (7), p.1089-1090

2024

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Vagal Reflexes Following an Exercise Stress Test

Journal of the American College of Cardiology, 2012-12, Vol.60 (24), p.2515-2524

2012

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Prevalence of cardiac amyloidosis among adult patients referred to tertiary centres with an initial diagnosis of hypertrophic cardiomyopathy

International journal of cardiology, 2020-02, Vol.300, p.191-195

2020

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Mexiletine Shortens the QT Interval in Patients With Potassium Channel–Mediated Type 2 Long QT Syndrome

Circulation. Arrhythmia and electrophysiology, 2019-05, Vol.12 (5), p.e007280-e007280

2019

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A wearable remote monitoring system for the identification of subjects with a prolonged QT interval or at risk for drug-induced long QT syndrome

International journal of cardiology, 2018-09, Vol.266, p.89-94

2018

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Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation

European heart journal, 2024-08, Vol.45 (29), p.2647-2656

2024

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From patient-specific induced pluripotent stem cells to clinical translation in long QT syndrome Type 2

Exercise Training-Induced Repolarization Abnormalities Masquerading as Congenital Long QT Syndrome

Calmodulin mutations and life-threatening cardiac arrhythmias: insights from the International Calmodulinopathy Registry

The genetics underlying acquired long QT syndrome: impact for genetic screening

Congenital long QT syndrome

Role of common and rare variants in SCN10A: results from the Brugada syndrome QRS locus gene discovery collaborative study

Management of survivors of cardiac arrest - the importance of genetic investigation

Impact of clinical and genetic findings on the management of young patients with Brugada syndrome

The genetics underlying idiopathic ventricular fibrillation: A special role for catecholaminergic polymorphic ventricular tachycardia?

Mutation location and I Ks regulation in the arrhythmic risk of long QT syndrome type 1: the importance of the KCNQ1 S6 region

FGF12 is a candidate Brugada syndrome locus

A comprehensive electrocardiographic, molecular, and echocardiographic study of Brugada syndrome: Validation of the 2013 diagnostic criteria

In a case of female-to-male sex reassignment, testosterone therapy switches on an underlying Brugada

Generation of the human induced pluripotent stem cell (hiPSC) line PSMi002-A from a patient affected by the Jervell and Lange-Nielsen syndrome and carrier of two compound heterozygous mutations on the KCNQ1 gene

Torsades de pointes following acute myocardial infarction: Evidence for a deadly link with a common genetic variant

Spectrum and Prevalence of Mutations Involving BrS1- Through BrS12-Susceptibility Genes in a Cohort of Unrelated Patients Referred for Brugada Syndrome Genetic Testing

A KCNH2 branch point mutation causing aberrant splicing contributes to an explanation of genotype-negative long QT syndrome

Evolution in Managing Long QT Syndrome

Energy drinks and sudden death: If it swims like a duck

Vagal Reflexes Following an Exercise Stress Test

Top stories on congenital long QT syndrome

Prevalence of cardiac amyloidosis among adult patients referred to tertiary centres with an initial diagnosis of hypertrophic cardiomyopathy

Mexiletine Shortens the QT Interval in Patients With Potassium Channel–Mediated Type 2 Long QT Syndrome

A wearable remote monitoring system for the identification of subjects with a prolonged QT interval or at risk for drug-induced long QT syndrome

Long QT syndrome: importance of reassessing arrhythmic risk after treatment initiation

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