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Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy

Neurology, 2009-01, Vol.72 (3), p.224-231

2009

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Combined leadless pacemaker and subcutaneous implantable defibrillator therapy: feasibility, safety, and performance

Europace (London, England), 2016-11, Vol.18 (11), p.1740-1747

2016

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Pharmacological treatment of short-coupled idiopathic ventricular fibrillation: A review

Indian pacing and electrophysiology journal, 2023-05, Vol.23 (3), p.77-83

2023

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Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy

Neurology, 2011-07, Vol.77 (1), p.62-66

2011

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De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome

Clinical genetics, 2014-11, Vol.86 (5), p.492-495

2014

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THE SCN5A1795INSD/+ MUTATION RESULTS IN INCREASED INTRACELLULAR CALCIUM CONCENTRATIONS IN HUMAN CARDIOMYOCYTES DERIVED FROM INDUCED PLURIPOTENT STEM CELLS

Heart rhythm, 2014-11, Vol.11 (11), p.2136-2136

2014

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An unexpected ECG finding

Netherlands heart journal, 2015-12, Vol.23 (12), p.608-608

2015

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S.P.26 Frequency, nature, severity and progression of cardiac involvement in sarcoglycanopathies

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.894-894

2012

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Prediction of Pathogenicity of Missense Variants in Arrhythmogenic Right Ventricular Cardiomyopathy

Heart rhythm, 2012-11, Vol.9 (11), p.1917-1917

2012

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Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

Circulation (New York, N.Y.), 2010-02, Vol.121 (5), p.635-643

2010

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Read-through of SCN5A Nonsense Mutations with the Chemical Compound PTC124

Heart rhythm, 2011, Vol.8 (11), p.1819-1819

2011

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Provocation testing is irreplaceable to uncover or refute Brugada syndrome – an electrocardiographic validation study during ajmaline provocation

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study

American journal of obstetrics and gynecology, 2020-03, Vol.222 (3), p.263.e1-263.e11

2020

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Long-term follow-up of paediatric patients with a subcutaneous implantable cardioverter-defibrillator

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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P5856Identification of genetic etiology of malignant arrhythmia in dilated cardiomyopathy

European heart journal, 2017-08, Vol.38 (suppl_1)

2017

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Defibrillation threshold in elective subcutaneous implantable defibrillator generator replacements: Time to reduce the size of the pulse generator?

International journal of cardiology, 2024-03, Vol.398, p.131639-131639, Article 131639

2024

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Worsening tricuspid regurgitation after ICD implantation is rather due to transvenous lead than natural progression

International journal of cardiology, 2023-04, Vol.376, p.76-80

2023

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Hinge point fibrosis is highly prevalent in male elite water polo players

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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Atenolol is not effective in reducing ventricular arrhythmia severity on exercise stress test in patients with catecholaminergic polymorphic ventricular tachycardia

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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P6380How to determine the QT interval: comprehensive analysis of a large cohort of Long QT syndrome patients and controls

European heart journal, 2017-08, Vol.38 (suppl_1)

2017

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Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene

Forensic science international, 2017-06, Vol.275, p.187-194

2017

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High Distress in Parents Whose Children Undergo Predictive Testing for Long QT Syndrome

Community genetics, 2005-01, Vol.8 (2), p.103-113

2005

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Novel KCNQ1 and HERG missense mutations in Dutch long-QT families

Human mutation, 1999, Vol.13 (4), p.301-310

1999

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Andersen-Tawil syndrome: Overlapping clinical features with Noonan syndrome?

European journal of medical genetics, 2022-01, Vol.65 (1), p.104382-104382, Article 104382

2022

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1215Neurodevelopmental disorders in patients with RYR2-associated catecholaminergic polymorphic ventricular tachycardia

European heart journal, 2017-08, Vol.38 (suppl_1)

2017

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Identification of a possible pathogenic link between congenital long QT syndrome and epilepsy

Combined leadless pacemaker and subcutaneous implantable defibrillator therapy: feasibility, safety, and performance

Pharmacological treatment of short-coupled idiopathic ventricular fibrillation: A review

Cardiac abnormalities in a follow-up study on carriers of Duchenne and Becker muscular dystrophy

De novo mutation in the KCNQ1 gene causal to Jervell and Lange-Nielsen syndrome

THE SCN5A1795INSD/+ MUTATION RESULTS IN INCREASED INTRACELLULAR CALCIUM CONCENTRATIONS IN HUMAN CARDIOMYOCYTES DERIVED FROM INDUCED PLURIPOTENT STEM CELLS

An unexpected ECG finding

S.P.26 Frequency, nature, severity and progression of cardiac involvement in sarcoglycanopathies

Prediction of Pathogenicity of Missense Variants in Arrhythmogenic Right Ventricular Cardiomyopathy

Long-Term Prognosis of Patients Diagnosed With Brugada Syndrome: Results From the FINGER Brugada Syndrome Registry

Read-through of SCN5A Nonsense Mutations with the Chemical Compound PTC124

Provocation testing is irreplaceable to uncover or refute Brugada syndrome – an electrocardiographic validation study during ajmaline provocation

Mothers with long QT syndrome are at increased risk for fetal death: findings from a multicenter international study

Long-term follow-up of paediatric patients with a subcutaneous implantable cardioverter-defibrillator

P5856Identification of genetic etiology of malignant arrhythmia in dilated cardiomyopathy

Defibrillation threshold in elective subcutaneous implantable defibrillator generator replacements: Time to reduce the size of the pulse generator?

Worsening tricuspid regurgitation after ICD implantation is rather due to transvenous lead than natural progression

Hinge point fibrosis is highly prevalent in male elite water polo players

Atenolol is not effective in reducing ventricular arrhythmia severity on exercise stress test in patients with catecholaminergic polymorphic ventricular tachycardia

P6380How to determine the QT interval: comprehensive analysis of a large cohort of Long QT syndrome patients and controls

Genotype-phenotype dilemma in a case of sudden cardiac death with the E1053K mutation and a deletion in the SCN5A gene

High Distress in Parents Whose Children Undergo Predictive Testing for Long QT Syndrome

Novel KCNQ1 and HERG missense mutations in Dutch long-QT families

Andersen-Tawil syndrome: Overlapping clinical features with Noonan syndrome?

1215Neurodevelopmental disorders in patients with RYR2-associated catecholaminergic polymorphic ventricular tachycardia

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