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Active Cascade Screening in Primary Inherited Arrhythmia Syndromes

Journal of the American College of Cardiology, 2010-06, Vol.55 (23), p.2570-2576

2010

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Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: The experience of a tertiary referral center in The Netherlands

Heart rhythm, 2010-10, Vol.7 (10), p.1383-1389

2010

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Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene

Circulation (New York, N.Y.), 2007-05, Vol.115 (19), p.2481-2489

2007

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Genotype-Phenotype Aspects of Type 2 Long QT Syndrome

Journal of the American College of Cardiology, 2009-11, Vol.54 (22), p.2052-2062

2009

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Low rate of cardiac events in first-degree relatives of diagnosis-negative young sudden unexplained death syndrome victims during follow-up

Heart rhythm, 2014-10, Vol.11 (10), p.1728-1732

2014

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Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation

International journal of cardiology, 2017-06, Vol.236, p.187-193

2017

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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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Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction

European journal of human genetics : EJHG, 2016-08, Vol.24 (8), p.1160-1166

2016

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Determination and Interpretation of the QT Interval

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

2018

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Diagnostic Value of Flecainide Testing in Unmasking SCN5A-Related Brugada Syndrome

Journal of cardiovascular electrophysiology, 2006-08, Vol.17 (8), p.857-864

2006

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Contribution of inherited heart disease to sudden cardiac death in childhood

Pediatrics (Evanston), 2007-10, Vol.120 (4), p.e967-e973

2007

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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

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Role of Genetic Testing in Patients with Ventricular Arrhythmias in Apparently Normal Hearts

Cardiac electrophysiology clinics, 2016-09, Vol.8 (3), p.515-523

2016

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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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Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study

Circulation (New York, N.Y.), 2016-09, Vol.134 (12), p.872-882

2016

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The Role of the Epinephrine Test in the Diagnosis and Management of Children Suspected of Having Congenital Long QT Syndrome

Pediatric cardiology, 2010-05, Vol.31 (4), p.462-468

2010

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The RYR2- Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome

Journal of the American College of Cardiology, 2009-11, Vol.54 (22), p.2065-2074

2009

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Abstract 11823: Are Disease-Specific Patient-Reported Outcomes Measures (PROMs) Used in Cardio Genetics? A Review

Circulation (New York, N.Y.), 2022-11, Vol.146 (Suppl_1)

2022

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Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey

Europace (London, England), 2022-02, Vol.24 (2), p.331-339

2022

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The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis

Journal of the American College of Cardiology, 2009-11, Vol.54 (22), p.2065-2074

2009

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Are disease-specific patient-reported outcomes measures (PROMs) used in cardiogenetics? A systematic review

European journal of human genetics : EJHG, 2024-06, Vol.32 (6), p.607-618

2024

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Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life-Threatening Events: Implications for Mutation-Specific Response to β-Blocker Therapy in Type 1 Long-QT Syndrome

Circulation (New York, N.Y.), 2012-04, Vol.125 (16), p.1988-1996

2012

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Yield of Molecular and Clinical Testing for Arrhythmia Syndromes: Report of 15 Years’ Experience

Circulation (New York, N.Y.), 2013-10, Vol.128 (14), p.1513-1521

2013

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Sudden unexplained death : Heritability and diagnostic yield of cardiological and genetic examination in surviving relatives

Circulation (New York, N.Y.), 2005-07, Vol.112 (2), p.207-213

2005

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Active Cascade Screening in Primary Inherited Arrhythmia Syndromes: Does It Lead to Prophylactic Treatment?

Journal of the American College of Cardiology, 2010-06, Vol.55 (23), p.2570-2576

2010

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Active Cascade Screening in Primary Inherited Arrhythmia Syndromes

Diagnostic yield in sudden unexplained death and aborted cardiac arrest in the young: The experience of a tertiary referral center in The Netherlands

Clinical aspects of type-1 long-QT syndrome by location, coding type, and biophysical function of mutations involving the KCNQ1 gene

Genotype-Phenotype Aspects of Type 2 Long QT Syndrome

Low rate of cardiac events in first-degree relatives of diagnosis-negative young sudden unexplained death syndrome victims during follow-up

Gain-of-function mutation in SCN5A causes ventricular arrhythmias and early onset atrial fibrillation

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

Asymmetry of parental origin in long QT syndrome: preferential maternal transmission of KCNQ1 variants linked to channel dysfunction

Determination and Interpretation of the QT Interval

Diagnostic Value of Flecainide Testing in Unmasking SCN5A-Related Brugada Syndrome

Contribution of inherited heart disease to sudden cardiac death in childhood

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

Role of Genetic Testing in Patients with Ventricular Arrhythmias in Apparently Normal Hearts

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

Clinical Aspects of Type 3 Long-QT Syndrome: An International Multicenter Study

The Role of the Epinephrine Test in the Diagnosis and Management of Children Suspected of Having Congenital Long QT Syndrome

The RYR2- Encoded Ryanodine Receptor/Calcium Release Channel in Patients Diagnosed Previously With Either Catecholaminergic Polymorphic Ventricular Tachycardia or Genotype Negative, Exercise-Induced Long QT Syndrome

Abstract 11823: Are Disease-Specific Patient-Reported Outcomes Measures (PROMs) Used in Cardio Genetics? A Review

Investigation on Sudden Unexpected Death in the Young (SUDY) in Europe: results of the European Heart Rhythm Association Survey

The RYR2-encoded ryanodine receptor/calcium release channel in patients diagnosed previously with either catecholaminergic polymorphic ventricular tachycardia or genotype negative, exercise-induced long QT syndrome: a comprehensive open reading frame mutational analysis

Are disease-specific patient-reported outcomes measures (PROMs) used in cardiogenetics? A systematic review

Mutations in Cytoplasmic Loops of the KCNQ1 Channel and the Risk of Life-Threatening Events: Implications for Mutation-Specific Response to β-Blocker Therapy in Type 1 Long-QT Syndrome

Yield of Molecular and Clinical Testing for Arrhythmia Syndromes: Report of 15 Years’ Experience

Sudden unexplained death : Heritability and diagnostic yield of cardiological and genetic examination in surviving relatives

Active Cascade Screening in Primary Inherited Arrhythmia Syndromes: Does It Lead to Prophylactic Treatment?

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