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Genetics of Sudden Cardiac Death

Circulation research, 2015-06, Vol.116 (12), p.1919-1936

2015

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Missense Mutations in Plakophilin-2 Cause Sodium Current Deficit and Associate With a Brugada Syndrome Phenotype

Circulation (New York, N.Y.), 2014-03, Vol.129 (10), p.1092-1103

2014

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Desmoplakin Cardiomyopathy, a Fibrotic and Inflammatory Form of Cardiomyopathy Distinct From Typical Dilated or Arrhythmogenic Right Ventricular Cardiomyopathy

Circulation (New York, N.Y.), 2020-06, Vol.141 (23), p.1872-1884

2020

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Sodium channel mutations and arrhythmias

Nature reviews cardiology, 2009-05, Vol.6 (5), p.337-348

2009

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Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis

Circulation (New York, N.Y.), 2016-02, Vol.133 (7), p.622-630

2016

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Inherited Dysfunction of Sarcoplasmic Reticulum Ca2+ Handling and Arrhythmogenesis

Circulation research, 2011-04, Vol.108 (7), p.871-883

2011

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Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3

Journal of the American College of Cardiology, 2016-03, Vol.67 (9), p.1053-1058

2016

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Inherited conditions of arrhythmia: translating disease mechanisms to patient management

Cardiovascular research, 2020-07, Vol.116 (9), p.1539-1541

2020

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Sudden cardiac death in the young: Are we still missing the opportunity to prevent recurrences in the family?

Heart rhythm, 2021-10, Vol.18 (10), p.1645-1646

2021

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Inherited calcium channelopathies in the pathophysiology of arrhythmias

Nature reviews cardiology, 2012-10, Vol.9 (10), p.561

2012

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Warning: not all carriers of pathogenic mutations in desmosomal genes should follow the same medical advices

Cardiovascular research, 2020-05, Vol.116 (6), p.1085-1088

2020

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Risk stratification in Brugada syndrome: results of the PRELUDE (PRogrammed ELectrical stimUlation preDictive valuE) registry

Journal of the American College of Cardiology, 2012-01, Vol.59 (1), p.37-45

2012

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European Society of Cardiology Congress 2019 Together With the World Congress of Cardiology in Paris: The Scientific Chairs Give the Inside Track on Achieving Excellence and Engagement

Circulation, 2019-11, Vol.140 (19), p.1590-1592

2019

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What a Congress

European heart journal, 2019-11, Vol.40 (43), p.3507-3509

2019

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Sudden Cardiac Death and Genetic Ion Channelopathies: Long QT, Brugada, Short QT, Catecholaminergic Polymorphic Ventricular Tachycardia, and Idiopathic Ventricular Fibrillation

Circulation (New York, N.Y.), 2012-04, Vol.125 (16), p.2027-2034

2012

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Novel Insight Into the Natural History of Short QT Syndrome

Journal of the American College of Cardiology, 2014-04, Vol.63 (13), p.1300-1308

2014

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Gene therapy to treat cardiac arrhythmias

Nature reviews cardiology, 2015-09, Vol.12 (9), p.531

2015

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Beta Blocker Therapy for Long QT Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia: Are all beta blockers equivalent?

Heart rhythm, 2017-01, Vol.14 (1), p.e41-e44

2017

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Interplay Between Genetic Substrate, QTc Duration, and Arrhythmia Risk in Patients With Long QT Syndrome

Journal of the American College of Cardiology, 2018-04, Vol.71 (15), p.1663-1671

2018

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Drugs and Brugada syndrome patients: Review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)

Heart rhythm, 2009-09, Vol.6 (9), p.1335-1341

2009

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Precision Medicine in Catecholaminergic Polymorphic Ventricular Tachycardia: JACC Focus Seminar 5/5

Journal of the American College of Cardiology, 2021-05, Vol.77 (20), p.2592-2612

2021

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Genetics of Sudden Cardiac Death

Missense Mutations in Plakophilin-2 Cause Sodium Current Deficit and Associate With a Brugada Syndrome Phenotype

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy

Desmoplakin Cardiomyopathy, a Fibrotic and Inflammatory Form of Cardiomyopathy Distinct From Typical Dilated or Arrhythmogenic Right Ventricular Cardiomyopathy

Sodium channel mutations and arrhythmias

Programmed Ventricular Stimulation for Risk Stratification in the Brugada Syndrome: A Pooled Analysis

Inherited Dysfunction of Sarcoplasmic Reticulum Ca2+ Handling and Arrhythmogenesis

Gene-Specific Therapy With Mexiletine Reduces Arrhythmic Events in Patients With Long QT Syndrome Type 3

Inherited conditions of arrhythmia: translating disease mechanisms to patient management

Sudden cardiac death in the young: Are we still missing the opportunity to prevent recurrences in the family?

2022 ESC Guidelines for the management of patients with ventricular arrhythmias and the prevention of sudden cardiac death

Inherited calcium channelopathies in the pathophysiology of arrhythmias

2019 HRS expert consensus statement on evaluation, risk stratification, and management of arrhythmogenic cardiomyopathy: Executive summary

Warning: not all carriers of pathogenic mutations in desmosomal genes should follow the same medical advices

HRS/EHRA/APHRS expert consensus statement on the diagnosis and management of patients with inherited primary arrhythmia syndromes: document endorsed by HRS, EHRA, and APHRS in May 2013 and by ACCF, AHA, PACES, and AEPC in June 2013

Risk stratification in Brugada syndrome: results of the PRELUDE (PRogrammed ELectrical stimUlation preDictive valuE) registry

European Society of Cardiology Congress 2019 Together With the World Congress of Cardiology in Paris: The Scientific Chairs Give the Inside Track on Achieving Excellence and Engagement

What a Congress

Sudden Cardiac Death and Genetic Ion Channelopathies: Long QT, Brugada, Short QT, Catecholaminergic Polymorphic Ventricular Tachycardia, and Idiopathic Ventricular Fibrillation

Novel Insight Into the Natural History of Short QT Syndrome

Gene therapy to treat cardiac arrhythmias

Beta Blocker Therapy for Long QT Syndrome and Catecholaminergic Polymorphic Ventricular Tachycardia: Are all beta blockers equivalent?

Interplay Between Genetic Substrate, QTc Duration, and Arrhythmia Risk in Patients With Long QT Syndrome

Drugs and Brugada syndrome patients: Review of the literature, recommendations, and an up-to-date website (www.brugadadrugs.org)

Precision Medicine in Catecholaminergic Polymorphic Ventricular Tachycardia: JACC Focus Seminar 5/5

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