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P08.12: Fetal and neonatal clinical evolution of isolated congenital heart disease and associated with major extracardiac malformations or genetic syndromes

Ultrasound in obstetrics & gynecology, 2010-10, Vol.36 (S1), p.198-198

2010

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DIAGNOSIS AND FOLLOW-UP OF FETAL CARDIAC TUMORS

Echocardiography (Mount Kisco, N.Y.), 2004-02, Vol.21 (2), p.212-212

2004

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An international compendium of mutations in the SCN5A -encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Heart rhythm, 2010-01, Vol.7 (1), p.33-46

2010

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Platelet reactivity and clinical outcomes after coronary artery implantation of drug-eluting stents (ADAPT-DES): a prospective multicentre registry study

The Lancet (British edition), 2013-08, Vol.382 (9892), p.614-623

2013

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Sudden death associated with short-QT syndrome linked to mutations in HERG

Circulation (New York, N.Y.), 2004-01, Vol.109 (1), p.30-35

2004

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European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases

Europace (London, England), 2022-09, Vol.24 (8), p.1307-1367

2022

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European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases

Heart rhythm, 2022-07, Vol.19 (7), p.e1-e60

2022

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Impact of Delay to Reperfusion on Reperfusion Success, Infarct Size, and Clinical Outcomes in Patients With ST-Segment Elevation Myocardial Infarction

JACC. Cardiovascular interventions, 2014-07, Vol.7 (7), p.733-740

2014

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Gain of function in I Ks secondary to a mutation in KCNE5 associated with atrial fibrillation

Heart rhythm, 2008-03, Vol.5 (3), p.427-435

2008

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Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

Heart rhythm, 2008-03, Vol.5 (3), p.427-435

2008

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Complementary prognostic utility of myocardial blush grade and ST-segment resolution after primary percutaneous coronary intervention: Analysis from the HORIZONS-AMI trial

The American heart journal, 2013-10, Vol.166 (4), p.676-683

2013

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Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome

Circulation. Arrhythmia and electrophysiology, 2008-08, Vol.1 (3), p.209-218

2008

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A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype

Circulation. Cardiovascular genetics, 2009-06, Vol.2 (3), p.270

2009

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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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Impact of Pre-Procedural Cardiopulmonary Instability in Patients With Acute Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention (from the Harmonizing Outcomes With Revascularization and Stents in Acute Myocardial Infarction Trial)

The American journal of cardiology, 2014-10, Vol.114 (7), p.962-967

2014

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Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction

Heart rhythm, 2007-08, Vol.4 (8), p.1072-1080

2007

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Cryptic 5′ splice site activation in SCN5A associated with Brugada syndrome

Journal of molecular and cellular cardiology, 2005-04, Vol.38 (4), p.555-560

2005

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Dual Variation in SCN5A and CACNB2b Underlies the Development of Cardiac Conduction Disease without Brugada Syndrome

Pacing and clinical electrophysiology, 2010-03, Vol.33 (3), p.274-285

2010

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Genetic predisposition and cellular basis for ischemia-induced ST-segment changes and arrhythmias

Journal of electrocardiology, 2007-11, Vol.40 (6), p.S26-S29

2007

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A Novel Mutation in KCNQ1 Associated with a Potent Dominant Negative Effect as the Basis for the LQT1 Form of the Long QT Syndrome

Journal of cardiovascular electrophysiology, 2007-09, Vol.18 (9), p.972-977

2007

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342: The Epidemiology of Bleeding and Clotting in Pulsatile and Continuous Flow LVAD Patients

The Journal of heart and lung transplantation, 2008, Vol.27 (2), p.S184-S184

2008

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A Mutation in the {beta}3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype

Genetics (Austin), 2009-06, Vol.2 (3), p.270

2009

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P08.12: Fetal and neonatal clinical evolution of isolated congenital heart disease and associated with major extracardiac malformations or genetic syndromes

DIAGNOSIS AND FOLLOW-UP OF FETAL CARDIAC TUMORS

An international compendium of mutations in the SCN5A -encoded cardiac sodium channel in patients referred for Brugada syndrome genetic testing

Platelet reactivity and clinical outcomes after coronary artery implantation of drug-eluting stents (ADAPT-DES): a prospective multicentre registry study

Mutations in the cardiac L-type calcium channel associated with inherited J-wave syndromes and sudden cardiac death

Sudden death associated with short-QT syndrome linked to mutations in HERG

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the state of genetic testing for cardiac diseases

European Heart Rhythm Association (EHRA)/Heart Rhythm Society (HRS)/Asia Pacific Heart Rhythm Society (APHRS)/Latin American Heart Rhythm Society (LAHRS) Expert Consensus Statement on the State of Genetic Testing for Cardiac Diseases

Impact of Delay to Reperfusion on Reperfusion Success, Infarct Size, and Clinical Outcomes in Patients With ST-Segment Elevation Myocardial Infarction

Gain of function in I Ks secondary to a mutation in KCNE5 associated with atrial fibrillation

Loss-of-function mutations in the cardiac calcium channel underlie a new clinical entity characterized by ST-segment elevation, short QT intervals, and sudden cardiac death

Gain of function in IKs secondary to a mutation in KCNE5 associated with atrial fibrillation

Complementary prognostic utility of myocardial blush grade and ST-segment resolution after primary percutaneous coronary intervention: Analysis from the HORIZONS-AMI trial

Functional Effects of KCNE3 Mutation and Its Role in the Development of Brugada Syndrome

A mutation in the beta 3 subunit of the cardiac sodium channel associated with Brugada ECG phenotype

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

Impact of Pre-Procedural Cardiopulmonary Instability in Patients With Acute Myocardial Infarction Undergoing Primary Percutaneous Coronary Intervention (from the Harmonizing Outcomes With Revascularization and Stents in Acute Myocardial Infarction Trial)

Novel mutation in the SCN5A gene associated with arrhythmic storm development during acute myocardial infarction

The Homeodomain Transcription Factor Irx5 Establishes the Mouse Cardiac Ventricular Repolarization Gradient

Cryptic 5′ splice site activation in SCN5A associated with Brugada syndrome

Dual Variation in SCN5A and CACNB2b Underlies the Development of Cardiac Conduction Disease without Brugada Syndrome

Genetic predisposition and cellular basis for ischemia-induced ST-segment changes and arrhythmias

A Novel Mutation in KCNQ1 Associated with a Potent Dominant Negative Effect as the Basis for the LQT1 Form of the Long QT Syndrome

342: The Epidemiology of Bleeding and Clotting in Pulsatile and Continuous Flow LVAD Patients

A Mutation in the {beta}3 Subunit of the Cardiac Sodium Channel Associated With Brugada ECG Phenotype

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