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The Entirely Subcutaneous Implantable Cardioverter-Defibrillator: Initial Clinical Experience in a Large Dutch Cohort

Journal of the American College of Cardiology, 2012-11, Vol.60 (19), p.1933-1939

2012

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Who Are the Long-QT Syndrome Patients Who Receive an Implantable Cardioverter-Defibrillator and What Happens to Them?: Data From the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry

Circulation (New York, N.Y.), 2010-09, Vol.122 (13), p.1272-1282

2010

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Familial Evaluation in Catecholaminergic Polymorphic Ventricular Tachycardia: Disease Penetrance and Expression in Cardiac Ryanodine Receptor Mutation–Carrying Relatives

Circulation. Arrhythmia and electrophysiology, 2012-08, Vol.5 (4), p.748-756

2012

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A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation

Circulation research, 2008-06, Vol.102 (11), p.1433-1442

2008

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Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome

Circulation (New York, N.Y.), 2005-01, Vol.111 (3), p.257-263

2005

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Desmin mutations as a cause of right ventricular heart failure affect the intercalated disks

Heart rhythm, 2010-08, Vol.7 (8), p.1058-1064

2010

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The ICD for Primary Prevention in Patients With Inherited Cardiac Diseases: Indications, Use, and Outcome: A Comparison With Secondary Prevention

Circulation. Arrhythmia and electrophysiology, 2013-02, Vol.6 (1), p.91-100

2013

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Surveillance of hepatic late adverse effects in a large cohort of long-term survivors of childhood cancer: Prevalence and risk factors

European journal of cancer (1990), 2013-01, Vol.49 (1), p.185-193

2013

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The timing of surgery of antenatally diagnosed choledochal malformations: A descriptive analysis of a 26-year nationwide cohort

Journal of pediatric surgery, 2017-07, Vol.52 (7), p.1156-1160

2017

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The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening

European heart journal, 2010-04, Vol.31 (7), p.842-848

2010

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Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

Blood, 2012-12, Vol.120 (25), p.5041-5049

2012

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Long-Term Psychiatric Outcomes in Adults with History of Pediatric Traumatic Brain Injury

Journal of neurotrauma, 2021-06, Vol.38 (11), p.1515-1525

2021

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Developmental aspects of long QT syndrome type 3 and brugada syndrome on the basis of a single SCN5A mutation in childhood

Journal of the American College of Cardiology, 2005-07, Vol.46 (2), p.331-337

2005

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Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular Cardiomyopathy

JACC. Clinical electrophysiology, 2022-03, Vol.8 (3), p.306-318

2022

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Retinal structure and function in achromatopsia: implications for gene therapy

Ophthalmology (Rochester, Minn.), 2014-01, Vol.121 (1), p.234-245

2014

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Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study

JACC. Heart failure, 2024-01, Vol.12 (1), p.134

2024

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A Germline Mutation in BLOC1S3/ Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome (HPS8)

American journal of human genetics, 2006-01, Vol.78 (1), p.160-166

2006

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Prophylaxis in severe forms of von Willebrand's disease: results from the von Willebrand Disease Prophylaxis Network (VWD PN)

Haemophilia : the official journal of the World Federation of Hemophilia, 2013-01, Vol.19 (1), p.76-81

2013

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A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q

European journal of human genetics : EJHG, 2011-07, Vol.19 (7), p.820-826

2011

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Evidence that the prevalence of childhood overweight is plateauing: data from nine countries

International journal of pediatric obesity, 2011-10, Vol.6 (5-6), p.342-360

2011

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Posttransplantation lymphoproliferative disorder in pediatric recipients of solid organ transplants: timing and location of disease

American journal of roentgenology (1976), 2005-11, Vol.185 (5), p.1335-1341

2005

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Efficacy and safety of a new generation von Willebrand factor/factor VIII concentrate (Wilate®) in the management of perioperative haemostasis in von Willebrand disease patients undergoing surgery

Thrombosis and haemostasis, 2011-06, Vol.105 (6), p.1072-1079

2011

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Gender differences in the long QT syndrome: effects of β-adrenoceptor blockade

Cardiovascular research, 2002-02, Vol.53 (3), p.770-776

2002

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Prophylactic and therapeutic recombinant factor VIIa administration to patients with Glanzmann's thrombasthenia: results of an international survey

Journal of thrombosis and haemostasis, 2004-07, Vol.2 (7), p.1096-1103

2004

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The relationship between adolescent suicidal behavior and life events in childhood and adolescence

The American journal of psychiatry, 1992-01, Vol.149 (1), p.45-51

1992

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The Entirely Subcutaneous Implantable Cardioverter-Defibrillator: Initial Clinical Experience in a Large Dutch Cohort

Who Are the Long-QT Syndrome Patients Who Receive an Implantable Cardioverter-Defibrillator and What Happens to Them?: Data From the European Long-QT Syndrome Implantable Cardioverter-Defibrillator (LQTS ICD) Registry

Familial Evaluation in Catecholaminergic Polymorphic Ventricular Tachycardia: Disease Penetrance and Expression in Cardiac Ryanodine Receptor Mutation–Carrying Relatives

A Gain-of-Function TBX5 Mutation Is Associated With Atypical Holt–Oram Syndrome and Paroxysmal Atrial Fibrillation

Long-term prognosis of individuals with right precordial ST-segment-elevation Brugada syndrome

Desmin mutations as a cause of right ventricular heart failure affect the intercalated disks

The ICD for Primary Prevention in Patients With Inherited Cardiac Diseases: Indications, Use, and Outcome: A Comparison With Secondary Prevention

Surveillance of hepatic late adverse effects in a large cohort of long-term survivors of childhood cancer: Prevalence and risk factors

The timing of surgery of antenatally diagnosed choledochal malformations: A descriptive analysis of a 26-year nationwide cohort

The yield of risk stratification for sudden cardiac death in hypertrophic cardiomyopathy myosin-binding protein C gene mutation carriers: focus on predictive screening

Evaluation of participants with suspected heritable platelet function disorders including recommendation and validation of a streamlined agonist panel

Long-Term Psychiatric Outcomes in Adults with History of Pediatric Traumatic Brain Injury

Developmental aspects of long QT syndrome type 3 and brugada syndrome on the basis of a single SCN5A mutation in childhood

Clinical Characteristics and Follow-Up of Pediatric-Onset Arrhythmogenic Right Ventricular Cardiomyopathy

Retinal structure and function in achromatopsia: implications for gene therapy

Penetrance and Prognosis of MYH7 Variant-Associated Cardiomyopathies: Results From a Dutch Multicenter Cohort Study

A Germline Mutation in BLOC1S3/ Reduced Pigmentation Causes a Novel Variant of Hermansky-Pudlak Syndrome (HPS8)

Prophylaxis in severe forms of von Willebrand's disease: results from the von Willebrand Disease Prophylaxis Network (VWD PN)

A novel autosomal dominant condition consisting of congenital heart defects and low atrial rhythm maps to chromosome 9q

Evidence that the prevalence of childhood overweight is plateauing: data from nine countries

Posttransplantation lymphoproliferative disorder in pediatric recipients of solid organ transplants: timing and location of disease

Efficacy and safety of a new generation von Willebrand factor/factor VIII concentrate (Wilate®) in the management of perioperative haemostasis in von Willebrand disease patients undergoing surgery

Gender differences in the long QT syndrome: effects of β-adrenoceptor blockade

Prophylactic and therapeutic recombinant factor VIIa administration to patients with Glanzmann's thrombasthenia: results of an international survey

The relationship between adolescent suicidal behavior and life events in childhood and adolescence

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