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High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutations

Scientific reports, 2018-08, Vol.8 (1), p.13019-8, Article 13019

2018

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Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation

Europace (London, England), 2013-12, Vol.15 (12), p.1805-1811

2013

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Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients

Journal of medical genetics, 2005-11, Vol.42 (11), p.863-870

2005

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Permanent junctional reciprocating tachycardia in children: a multicentre study on clinical profile and outcome

Heart (British Cardiac Society), 2006-01, Vol.92 (1), p.101-104

2006

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Low incidence of cardiac events with β-blocking therapy in children with long QT syndrome

European heart journal, 2004-08, Vol.25 (16), p.1405-1411

2004

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Impact of the control of symptomatic paroxysmal atrial fibrillation on health-related quality of life

Europace (London, England), 2010-05, Vol.12 (5), p.634-642

2010

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Novel Mechanism for Brugada Syndrome: Defective Surface Localization of an SCN5A Mutant(R1432G)

Circulation research, 2001-06, Vol.88 (12), p.e78-e83

2001

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Different Atrial and Ventricular Resting Membrane Potentials May Explain the Phenotypical Variability of a Truncating SCN5A Mutation

Heart rhythm, 2013-11, Vol.10 (11), p.1746-1746

2013

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Notched T waves on Holter recordings enhance detection of patients with LQT2 (HERG) mutations

Circulation (New York, N.Y.), 2001-02, Vol.103 (8), p.1095-1101

2001

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Dominant-Negative Suppression of Nav1.5 Channel by N-Terminal SCN5A Mutations in Brugada Syndrome

Heart rhythm, 2011, Vol.8 (11), p.1824-1824

2011

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Sinus rate and QRS duration on lead V1 predict major events in Brugada syndrome

Europace (London, England), 2023-05, Vol.25 (Supplement_1)

2023

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Clinical reasoning: seizures in a child with sensorineural deafness and agitation

Neurology, 2010-04, Vol.74 (15), p.e61

2010

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ECG descriptors of ventricular repolarization are associated with cardiac events in a gene-specific manner in long QT syndrome patients

Europace (London, England), 2022-05, Vol.24 (Supplement_1)

2022

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Paroxysmal vagal overactivity, apparent life-threatening event and sudden infant death

Biology of the neonate, 2000-07, Vol.78 (1), p.1-7

2000

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Extracorporeal cardiopulmonary resuscitation in out-of-hospital cardiac arrest: a registry study

European heart journal, 2020-06, Vol.41 (21), p.1961-1971

2020

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Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome

European heart journal, 1998-01, Vol.19 (1), p.158-165

1998

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An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia

Circulation (New York, N.Y.), 2022-02, Vol.145 (5), p.333-344

2022

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Arrhythmic sudden death in children

Archives of cardiovascular diseases, 2008, Vol.101 (2), p.121-125

2008

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Electrocardiographic predictors of Brugada type response during Na channel blockade challenge

Europace (London, England), 2005-09, Vol.7 (5), p.447-453

2005

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Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia

Circulation research, 2002-10, Vol.91 (8), p.e21-e26

2002

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Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

European heart journal, 2023-09, Vol.44 (35), p.3357-3370

2023

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Epinephrine versus norepinephrine in cardiac arrest patients with post-resuscitation shock

Intensive care medicine, 2022-03, Vol.48 (3), p.300-310

2022

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Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias

Circulation (New York, N.Y.), 2001-01, Vol.103 (1), p.89-95

2001

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Differential Effect of Targeted Temperature Management Between 32 °C and 36 °C Following Cardiac Arrest According to Initial Severity of Illness: Insights From Two International Data Sets

Chest, 2023-05, Vol.163 (5), p.1120-1129

2023

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Long-term follow-up of asymptomatic Brugada patients with inducible ventricular fibrillation under hydroquinidine

Europace (London, England), 2014-04, Vol.16 (4), p.572-577

2014

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High prevalence of ventricular repolarization abnormalities in people carrying TGFβR2 mutations

Cardiac characteristics and long-term outcome in Andersen-Tawil syndrome patients related to KCNJ2 mutation

Catecholaminergic polymorphic ventricular tachycardia: RYR2 mutations, bradycardia, and follow up of the patients

Permanent junctional reciprocating tachycardia in children: a multicentre study on clinical profile and outcome

Low incidence of cardiac events with β-blocking therapy in children with long QT syndrome

Impact of the control of symptomatic paroxysmal atrial fibrillation on health-related quality of life

Novel Mechanism for Brugada Syndrome: Defective Surface Localization of an SCN5A Mutant(R1432G)

Different Atrial and Ventricular Resting Membrane Potentials May Explain the Phenotypical Variability of a Truncating SCN5A Mutation

Notched T waves on Holter recordings enhance detection of patients with LQT2 (HERG) mutations

Dominant-Negative Suppression of Nav1.5 Channel by N-Terminal SCN5A Mutations in Brugada Syndrome

Sinus rate and QRS duration on lead V1 predict major events in Brugada syndrome

Clinical reasoning: seizures in a child with sensorineural deafness and agitation

ECG descriptors of ventricular repolarization are associated with cardiac events in a gene-specific manner in long QT syndrome patients

Paroxysmal vagal overactivity, apparent life-threatening event and sudden infant death

Extracorporeal cardiopulmonary resuscitation in out-of-hospital cardiac arrest: a registry study

Diagnostic performance of QT interval variables from 24-h electrocardiography in the long QT syndrome

An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia

Arrhythmic sudden death in children

Electrocardiographic predictors of Brugada type response during Na channel blockade challenge

Absence of Calsequestrin 2 Causes Severe Forms of Catecholaminergic Polymorphic Ventricular Tachycardia

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry

Epinephrine versus norepinephrine in cardiac arrest patients with post-resuscitation shock

Genotype-phenotype correlation in the long-QT syndrome: Gene-specific triggers for life-threatening arrhythmias

Differential Effect of Targeted Temperature Management Between 32 °C and 36 °C Following Cardiac Arrest According to Initial Severity of Illness: Insights From Two International Data Sets

Long-term follow-up of asymptomatic Brugada patients with inducible ventricular fibrillation under hydroquinidine

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