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Fetal electrocardiography and artificial intelligence for prenatal detection of congenital heart disease

Acta obstetricia et gynecologica Scandinavica, 2023-11, Vol.102 (11), p.1511-1520

2023

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Prenatal detection of aortic coarctation in a well‐organized screening setting: Are we there yet?

Prenatal diagnosis, 2023-05, Vol.43 (5), p.620-628

2023

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Pregnancy in women with Brugada syndrome: Is there an increased arrhythmia risk? A case‐series report

Journal of cardiovascular electrophysiology, 2022-01, Vol.33 (1), p.123-127

2022

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Reduced kinase function in two ultra‐rare TNNI3K variants in families with congenital junctional ectopic tachycardia

Clinical genetics, 2024-07, Vol.106 (1), p.37-46

2024

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Early detection of fetal cardiac abnormalities: how effective is it and how should we manage these patients?

Prenatal diagnosis, 2014-12, Vol.34 (13), p.1235-1245

2014

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The electrical heart axis of the fetus between 18 and 24 weeks of gestation: A cohort study

PloS one, 2021-12, Vol.16 (12), p.e0256115-e0256115

2021

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Penetrance of Hypertrophic Cardiomyopathy in Children Who Are Mutation Positive

The Journal of pediatrics, 2017-09, Vol.188, p.91-95

2017

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Right ventricular dysfunction identified by abnormal strain values precedes evident growth restriction in small for gestational age fetuses

Prenatal diagnosis, 2020-12, Vol.40 (12), p.1525-1531

2020

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The standardized 12-lead fetal electrocardiogram of the healthy fetus in mid-pregnancy: A cross-sectional study

PloS one, 2020-04, Vol.15 (4), p.e0232606-e0232606

2020

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The effect of the introduction of the three‐vessel view on the detection rate of transposition of the great arteries and tetralogy of Fallot

Prenatal diagnosis, 2018-11, Vol.38 (12), p.951-957

2018

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Diagnostic Accuracy of the Standing Test in Adults Suspected for Congenital Long-QT Syndrome

Journal of the American Heart Association, 2023-07, Vol.12 (14), p.e026419-e026419

2023

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GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum

American journal of medical genetics. Part A, 2019-09, Vol.179 (9), p.1836-1845

2019

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Clinical aspects and prognosis of brugada syndrome in children

Circulation (New York, N.Y.), 2007-04, Vol.115 (15), p.2042-2048

2007

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Transposition of the great arteries: Fetal pulmonary valve growth and postoperative neo‐aortic root dilatation

Prenatal diagnosis, 2019-11, Vol.39 (12), p.1054-1063

2019

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Determination and Interpretation of the QT Interval: Comprehensive Analysis of a Large Cohort of Long QT Syndrome Patients and Controls

Circulation (New York, N.Y.), 2018-11, Vol.138 (21), p.2345-2358

2018

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The diagnostic and therapeutic aspects of loss-of-function cardiac sodium channelopathies in children

Heart rhythm, 2012-12, Vol.9 (12), p.1986-1992

2012

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Effect of age and gender on the QTc-interval in healthy individuals and patients with long-QT syndrome

Trends in cardiovascular medicine, 2018-01, Vol.28 (1), p.64-75

2018

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Comparison of Transplacental Treatment of Fetal Supraventricular Tachyarrhythmias With Digoxin, Flecainide, and Sotalol: Results of a Nonrandomized Multicenter Study

Circulation (New York, N.Y.), 2011-10, Vol.124 (16), p.1747-1754

2011

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Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2: Higher Recurrence of Events Under Metoprolol

Journal of the American College of Cardiology, 2012-11, Vol.60 (20), p.2092-2099

2012

Volltextzugriff (PDF)

Pediatric Pulmonary Hypertension in the Netherlands Epidemiology and Characterization During the Period 1991 to 2005

Circulation (New York, N.Y.), 2011-10, Vol.124 (16), p.1755-1764

2011

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Prognosis and clinical management of asymptomatic family members with RYR2 -mediated catecholaminergic polymorphic ventricular tachycardia: a review

Cardiology in the young, 2024-04, p.1-8

2024

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Repeatability of ventricular arrhythmia characteristics on the exercise-stress test in RYR2-mediated catecholaminergic polymorphic ventricular tachycardia

Europace (London, England), 2023-02, Vol.25 (2), p.619-626

2023

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Chromosomal abnormalities and copy number variations in fetal left-sided congenital heart defects

Prenatal diagnosis, 2016-02, Vol.36 (2), p.177-185

2016

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In Children and Adolescents From Brugada Syndrome–Families, Only SCN5A Mutation Carriers Develop a Type-1 ECG Pattern Induced By Fever

Circulation (New York, N.Y.), 2020-07, Vol.142 (1), p.89-91

2020

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Diagnostic accuracy of the response to the brief tachycardia provoked by standing in children suspected for long QT syndrome

Heart rhythm O2, 2021-04, Vol.2 (2), p.149-159

2021

Volltextzugriff (PDF)

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Fetal electrocardiography and artificial intelligence for prenatal detection of congenital heart disease

Prenatal detection of aortic coarctation in a well‐organized screening setting: Are we there yet?

Pregnancy in women with Brugada syndrome: Is there an increased arrhythmia risk? A case‐series report

Reduced kinase function in two ultra‐rare TNNI3K variants in families with congenital junctional ectopic tachycardia

Early detection of fetal cardiac abnormalities: how effective is it and how should we manage these patients?

The electrical heart axis of the fetus between 18 and 24 weeks of gestation: A cohort study

Penetrance of Hypertrophic Cardiomyopathy in Children Who Are Mutation Positive

Right ventricular dysfunction identified by abnormal strain values precedes evident growth restriction in small for gestational age fetuses

The standardized 12-lead fetal electrocardiogram of the healthy fetus in mid-pregnancy: A cross-sectional study

The effect of the introduction of the three‐vessel view on the detection rate of transposition of the great arteries and tetralogy of Fallot

Diagnostic Accuracy of the Standing Test in Adults Suspected for Congenital Long-QT Syndrome

GATA6 mutations: Characterization of two novel patients and a comprehensive overview of the GATA6 genotypic and phenotypic spectrum

Clinical aspects and prognosis of brugada syndrome in children

Transposition of the great arteries: Fetal pulmonary valve growth and postoperative neo‐aortic root dilatation

Determination and Interpretation of the QT Interval: Comprehensive Analysis of a Large Cohort of Long QT Syndrome Patients and Controls

The diagnostic and therapeutic aspects of loss-of-function cardiac sodium channelopathies in children

Effect of age and gender on the QTc-interval in healthy individuals and patients with long-QT syndrome

Comparison of Transplacental Treatment of Fetal Supraventricular Tachyarrhythmias With Digoxin, Flecainide, and Sotalol: Results of a Nonrandomized Multicenter Study

Not All Beta-Blockers Are Equal in the Management of Long QT Syndrome Types 1 and 2: Higher Recurrence of Events Under Metoprolol

Pediatric Pulmonary Hypertension in the Netherlands Epidemiology and Characterization During the Period 1991 to 2005

Prognosis and clinical management of asymptomatic family members with RYR2 -mediated catecholaminergic polymorphic ventricular tachycardia: a review

Repeatability of ventricular arrhythmia characteristics on the exercise-stress test in RYR2-mediated catecholaminergic polymorphic ventricular tachycardia

Chromosomal abnormalities and copy number variations in fetal left-sided congenital heart defects

In Children and Adolescents From Brugada Syndrome–Families, Only SCN5A Mutation Carriers Develop a Type-1 ECG Pattern Induced By Fever

Diagnostic accuracy of the response to the brief tachycardia provoked by standing in children suspected for long QT syndrome

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