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The contribution of classical risk factors to cardiovascular disease in familial hypercholesterolaemia: data in 2400 patients

Journal of internal medicine, 2004-12, Vol.256 (6), p.482-490

2004

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Glucose tolerance at age 58 and the decline of glucose tolerance in comparison with age 50 in people prenatally exposed to the Dutch famine

Diabetologia, 2006-04, Vol.49 (4), p.637-643

2006

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Changes in microbiota during experimental human Rhinovirus infection

BMC infectious diseases, 2015-08, Vol.15 (1), p.336-336, Article 336

2015

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Effect of acute hyperglycaemia and/or hyperinsulinaemia on proinflammatory gene expression, cytokine production and neutrophil function in humans

Diabetic medicine, 2008-02, Vol.25 (2), p.157-164

2008

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Efficient ways exist to obtain the optimal sample size in clinical trials in rare diseases

Journal of clinical epidemiology, 2008-04, Vol.61 (4), p.324-330

2008

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Association of polymorphisms in the beta-2 adrenergic receptor gene with fracture risk and bone mineral density

Osteoporosis international, 2015-07, Vol.26 (7), p.2019-2027

2015

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Long-term neurologic and cognitive outcome and quality of life in adults after pneumococcal meningitis

Clinical microbiology and infection, 2020-10, Vol.26 (10), p.1361-1367

2020

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Platelet and endothelial cell P‐selectin are required for host defense against Klebsiella pneumoniae‐induced pneumosepsis

Journal of thrombosis and haemostasis, 2015-06, Vol.13 (6), p.1128-1138

2015

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Impact of an evidence-based guideline on the management of community-acquired bacterial meningitis: a prospective cohort study

Clinical microbiology and infection, 2016-11, Vol.22 (11), p.928-933

2016

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The Fc gamma receptor IIa R131H polymorphism is associated with inhibitor development in severe hemophilia A

Journal of thrombosis and haemostasis, 2014-08, Vol.12 (8), p.1294-1301

2014

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The effects of beta-2 adrenergic agonist and antagonist on human bone metabolism: A randomized controlled trial

Bone (New York, N.Y.), 2015-02, Vol.71, p.196-200

2015

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Poly(trimethylene carbonate) and poly(D,L-lactic acid) modify human dendritic cell responses to staphylococci but do not affect Th1 and Th2 cell development

European Cells and Materials, 2018-02, Vol.35, p.103-116

2018

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Study on the Protective Effect of the KIR3DL1 Gene in Ankylosing Spondylitis

Arthritis & rheumatology (Hoboken, N.J.), 2015-11, Vol.67 (11), p.2957-2965

2015

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Clonidine increases bone resorption in humans

Osteoporosis international, 2016-03, Vol.27 (3), p.1063-1071

2016

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Estimation of Multilocus Haplotype Effects Using Weighted Penalised Log‐Likelihood: Analysis of Five Sequence Variations at the Cholesteryl Ester Transfer Protein Gene Locus

Annals of human genetics, 2003-03, Vol.67 (2), p.175-184

2003

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Family history and inherited thrombophilia

Journal of thrombosis and haemostasis, 2006-10, Vol.4 (10), p.2182-2187

2006

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High levels of protein C are determined by PROCR haplotype 3

Journal of thrombosis and haemostasis, 2011-05, Vol.9 (5), p.969-976

2011

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Sample size calculations: basic principles and common pitfalls

Nephrology, dialysis, transplantation, 2010-05, Vol.25 (5), p.1388-1393

2010

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Polymorphisms in the melatonin receptor 1B gene and the risk of delirium

Dementia and geriatric cognitive disorders, 2012-01, Vol.33 (5), p.306-310

2012

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No linkage for venous thrombosis at a candidate region on chromosome 18 in Dutch thrombophilic families

Journal of thrombosis and haemostasis, 2009-07, Vol.7 (7), p.1239-1240

2009

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New risk predictor of arrhythmias in patients with congenital Long-QT Syndrome

European heart journal, 2023-11, Vol.44 (Supplement_2)

2023

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Multiple Imputation of Missing Genotype Data for Unrelated Individuals

Annals of human genetics, 2006-05, Vol.70 (3), p.372-381

2006

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Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels

Clinical genetics, 2006-03, Vol.69 (3), p.263-270

2006

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Common genetic variants improve risk stratification after atrial switch operation for transposition of the great arteries

European heart journal, 2021-10, Vol.42 (Supplement_1)

2021

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Ventricular conduction is a marker for arrhythmic risk in overlap sodium channel disease

Europace (London, England), 2023-05, Vol.25 (Supplement_1)

2023

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The contribution of classical risk factors to cardiovascular disease in familial hypercholesterolaemia: data in 2400 patients

Glucose tolerance at age 58 and the decline of glucose tolerance in comparison with age 50 in people prenatally exposed to the Dutch famine

Changes in microbiota during experimental human Rhinovirus infection

Effect of acute hyperglycaemia and/or hyperinsulinaemia on proinflammatory gene expression, cytokine production and neutrophil function in humans

Efficient ways exist to obtain the optimal sample size in clinical trials in rare diseases

Association of polymorphisms in the beta-2 adrenergic receptor gene with fracture risk and bone mineral density

Long-term neurologic and cognitive outcome and quality of life in adults after pneumococcal meningitis

Platelet and endothelial cell P‐selectin are required for host defense against Klebsiella pneumoniae‐induced pneumosepsis

Impact of an evidence-based guideline on the management of community-acquired bacterial meningitis: a prospective cohort study

The Fc gamma receptor IIa R131H polymorphism is associated with inhibitor development in severe hemophilia A

The effects of beta-2 adrenergic agonist and antagonist on human bone metabolism: A randomized controlled trial

Poly(trimethylene carbonate) and poly(D,L-lactic acid) modify human dendritic cell responses to staphylococci but do not affect Th1 and Th2 cell development

Study on the Protective Effect of the KIR3DL1 Gene in Ankylosing Spondylitis

Clonidine increases bone resorption in humans

Estimation of Multilocus Haplotype Effects Using Weighted Penalised Log‐Likelihood: Analysis of Five Sequence Variations at the Cholesteryl Ester Transfer Protein Gene Locus

Family history and inherited thrombophilia

High levels of protein C are determined by PROCR haplotype 3

Sample size calculations: basic principles and common pitfalls

Polymorphisms in the melatonin receptor 1B gene and the risk of delirium

No linkage for venous thrombosis at a candidate region on chromosome 18 in Dutch thrombophilic families

New risk predictor of arrhythmias in patients with congenital Long-QT Syndrome

Multiple Imputation of Missing Genotype Data for Unrelated Individuals

Common variants of multiple genes that control reverse cholesterol transport together explain only a minor part of the variation of HDL cholesterol levels

Common genetic variants improve risk stratification after atrial switch operation for transposition of the great arteries

Ventricular conduction is a marker for arrhythmic risk in overlap sodium channel disease

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