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Prior medication adherence of participants and non participants of a randomized controlled trial to improve patient adherence in cardiovascular risk management

BMC medical research methodology, 2019-05, Vol.19 (1), p.95-9, Article 95

2019

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Can continuous remote vital sign monitoring reduce the number of room visits to patients suspected of COVID-19: A quasi-experimental study

International journal of nursing studies, 2021-03, Vol.115, p.103868-103868, Article 103868

2021

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Indications of combined vitamin K antagonists and aspirin therapy

Journal of thrombosis and thrombolysis, 2009-05, Vol.27 (4), p.421-429

2009

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Critical aneurysmal dilatation of the thoracic aorta in young adolescents with variant hyperimmunoglobulin E syndrome

Journal of internal medicine, 2006-06, Vol.259 (6), p.615-618

2006

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A Nurse-Led Multidisciplinary Intervention to Improve Cardiovascular Disease Profile of Patients

Western journal of nursing research, 2015-06, Vol.37 (6), p.705-723

2015

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Enhanced interleukin-10 production by dendritic cells upon stimulation with Toll-like receptor 4 agonists in systemic sclerosis that is possibly implicated in CCL18 secretion

Scandinavian journal of rheumatology, 2009, Vol.38 (4), p.282-290

2009

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F-18-fluorodeoxyglucose positron emission tomography in diagnosis and follow-up of patients with different types of vasculitis

Netherlands journal of medicine, 2003-10, Vol.61 (10), p.323-329

2003

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A patient with sudden pain in the upper abdomen accompanied by vomiting

Netherlands journal of medicine, 2006-07, Vol.64 (7), p.258, 260-260

2006

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Vascular graft infection in aortoiliac and aortofemoral bypass surgery: clinical presentation, diagnostic strategies and results of surgical treatment

Netherlands journal of medicine, 2004-12, Vol.62 (11), p.446-452

2004

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Segregation analysis of plasma apolipoprotein B levels in familial combined hyperlipidemia

Arteriosclerosis, thrombosis, and vascular biology, 1997-05, Vol.17 (5), p.834

1997

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Pulmonary hypertension : its diagnosis and management, a multidisciplinary approach

Netherlands journal of medicine, 2005-06, Vol.63 (6), p.193-198

2005

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An unusual cause of a cerebral tumour in a young patient

Netherlands journal of medicine, 2006-05, Vol.64 (5)

2006

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Metabolic and genetic aspects of familial combined hyperlipidaemia with emphasis on low-density lipoprotein heterogeneity

European journal of clinical investigation, 1997-10, Vol.27 (10), p.802-811

1997

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The StethoDop: a Doppler stethoscope attachment for investigation of arterial and venous insufficiency of the lower extremities

Netherlands journal of medicine, 2004-02, Vol.62 (2), p.53-57

2004

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High D‐dimer levels increase the likelihood of pulmonary embolism

Journal of internal medicine, 2008-08, Vol.264 (2), p.195-200

2008

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Early Warning Scores at the nursing ward: what do you really want to know?

Nederlands tijdschrift voor geneeskunde, 2020-11, Vol.164

2020

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Nonobese patients with familial combined hyperlipidemia are insulin resistant compared with their nonaffected relatives

Arteriosclerosis, thrombosis, and vascular biology, 1997-07, Vol.17 (7), p.1465

1997

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An automated computerized method using Finapres for measuring cardiovascular reflexes

Clinical science (1979), 1992-08, Vol.83 (2), p.157

1992

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Comparison of gemfibrozil versus simvastatin in familial combined hyperlipidemia and effects on apolipoprotein-B-containing lipoproteins, low-density lipoprotein subfraction profile, and low-density lipoprotein oxidizability

The American journal of cardiology, 1995-02, Vol.75 (5), p.348-353

1995

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Inherited susceptibility determines the distribution of dense low-density lipoprotein subfraction profiles in familial combined hyperlipidemia

American journal of human genetics, 1996-04, Vol.58 (4), p.812-822

1996

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The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemia

Atherosclerosis, 2000-08, Vol.151 (2), p.443-450

2000

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A Common Genetic Mechanism Determines Plasma Apolipoprotein B Levels and Dense LDL Subfraction Distribution in Familial Combined Hyperlipidemia

American journal of human genetics, 1998-08, Vol.63 (2), p.586-594

1998

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The redox status of coenzyme Q10 in total LDL as an indicator of in vivo oxidative modification. Studies on subjects with familial combined hyperlipidemia

Arteriosclerosis, thrombosis, and vascular biology, 1997-01, Vol.17 (1), p.127

1997

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The lipoprotein lipase (Asn291 → Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia

Atherosclerosis, 1996-01, Vol.119 (2), p.159-167

1996

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Gender-related association between the −93T→G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia

Atherosclerosis, 1998-05, Vol.138 (1), p.91-99

1998

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Prior medication adherence of participants and non participants of a randomized controlled trial to improve patient adherence in cardiovascular risk management

Can continuous remote vital sign monitoring reduce the number of room visits to patients suspected of COVID-19: A quasi-experimental study

Indications of combined vitamin K antagonists and aspirin therapy

Critical aneurysmal dilatation of the thoracic aorta in young adolescents with variant hyperimmunoglobulin E syndrome

A Nurse-Led Multidisciplinary Intervention to Improve Cardiovascular Disease Profile of Patients

Enhanced interleukin-10 production by dendritic cells upon stimulation with Toll-like receptor 4 agonists in systemic sclerosis that is possibly implicated in CCL18 secretion

F-18-fluorodeoxyglucose positron emission tomography in diagnosis and follow-up of patients with different types of vasculitis

A patient with sudden pain in the upper abdomen accompanied by vomiting

Vascular graft infection in aortoiliac and aortofemoral bypass surgery: clinical presentation, diagnostic strategies and results of surgical treatment

Segregation analysis of plasma apolipoprotein B levels in familial combined hyperlipidemia

Pulmonary hypertension : its diagnosis and management, a multidisciplinary approach

An unusual cause of a cerebral tumour in a young patient

Metabolic and genetic aspects of familial combined hyperlipidaemia with emphasis on low-density lipoprotein heterogeneity

The StethoDop: a Doppler stethoscope attachment for investigation of arterial and venous insufficiency of the lower extremities

High D‐dimer levels increase the likelihood of pulmonary embolism

Early Warning Scores at the nursing ward: what do you really want to know?

Nonobese patients with familial combined hyperlipidemia are insulin resistant compared with their nonaffected relatives

An automated computerized method using Finapres for measuring cardiovascular reflexes

Comparison of gemfibrozil versus simvastatin in familial combined hyperlipidemia and effects on apolipoprotein-B-containing lipoproteins, low-density lipoprotein subfraction profile, and low-density lipoprotein oxidizability

Inherited susceptibility determines the distribution of dense low-density lipoprotein subfraction profiles in familial combined hyperlipidemia

The V73M mutation in the hepatic lipase gene is associated with elevated cholesterol levels in four Dutch pedigrees with familial combined hyperlipidemia

A Common Genetic Mechanism Determines Plasma Apolipoprotein B Levels and Dense LDL Subfraction Distribution in Familial Combined Hyperlipidemia

The redox status of coenzyme Q10 in total LDL as an indicator of in vivo oxidative modification. Studies on subjects with familial combined hyperlipidemia

The lipoprotein lipase (Asn291 → Ser) mutation is associated with elevated lipid levels in families with familial combined hyperlipidaemia

Gender-related association between the −93T→G/D9N haplotype of the lipoprotein lipase gene and elevated lipid levels in familial combined hyperlipidemia

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