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Trends in overweight and obesity prevalence in Dutch, Turkish, Moroccan and Surinamese South Asian children in the Netherlands

Archives of disease in childhood, 2009-10, Vol.94 (10), p.795-800

2009

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Declining and stabilising trends in prevalence of overweight and obesity in Dutch, Turkish, Moroccan and South Asian children 3–16 years of age between 1999 and 2011 in the Netherlands

Archives of disease in childhood, 2014-01, Vol.99 (1), p.46-51

2014

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Safety and effects of two red blood cell transfusion strategies in pediatric cardiac surgery patients: a randomized controlled trial

Intensive care medicine, 2013-11, Vol.39 (11), p.2011-2019

2013

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Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

Nature medicine, 2009-04, Vol.15 (4), p.380-383

2009

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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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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 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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Inequalities in children's mental health care: analysis of routinely collected data on prescribing and referrals to secondary care

BMC psychiatry, 2023-01, Vol.23 (1), p.22-22, Article 22

2023

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Differences in Measured and Self-Reported Height and Weight in Dutch Adolescents

Annals of nutrition and metabolism, 2006-01, Vol.50 (4), p.339-346

2006

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Household Food Security Is Inversely Associated with Undernutrition among Adolescents from Kilosa, Tanzania

The Journal of nutrition, 2012-09, Vol.142 (9), p.1741-1747

2012

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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.134-147

2024

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An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia

Circulation (New York, N.Y.), 2022-02, Vol.145 (5), p.333-344

2022

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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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Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

Human molecular genetics, 2014-06, Vol.23 (11), p.2888-2900

2014

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Predicting neurocognitive function in pediatric brain tumor early survivorship: The neurological predictor scale and the incremental validity of tumor size

Pediatric blood & cancer, 2022-09, Vol.69 (9), p.e29803-n/a

2022

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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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Trends in overweight and obesity prevalence in Dutch, Turkish, Moroccan and Surinamese South Asian children in the Netherlands

Declining and stabilising trends in prevalence of overweight and obesity in Dutch, Turkish, Moroccan and South Asian children 3–16 years of age between 1999 and 2011 in the Netherlands

Safety and effects of two red blood cell transfusion strategies in pediatric cardiac surgery patients: a randomized controlled trial

Flecainide prevents catecholaminergic polymorphic ventricular tachycardia in mice and humans

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

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

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

Inequalities in children's mental health care: analysis of routinely collected data on prescribing and referrals to secondary care

Differences in Measured and Self-Reported Height and Weight in Dutch Adolescents

Household Food Security Is Inversely Associated with Undernutrition among Adolescents from Kilosa, Tanzania

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

An International Multicenter Cohort Study on β-Blockers for the Treatment of Symptomatic Children With Catecholaminergic Polymorphic Ventricular Tachycardia

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

Loss-of-function HDAC8 mutations cause a phenotypic spectrum of Cornelia de Lange syndrome-like features, ocular hypertelorism, large fontanelle and X-linked inheritance

Predicting neurocognitive function in pediatric brain tumor early survivorship: The neurological predictor scale and the incremental validity of tumor size

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

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