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Pharmaceutical company funding of cancer patient advocacy organizations in the Netherlands

Journal of cancer policy, 2024-09, Vol.41, p.100493, Article 100493

2024

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Untoward global effects of current guideline formulation of stereotactic radiotherapy for symptomatic brain metastases by international medical societies

Lancet Regional Health - Americas (Online), 2023-09, Vol.25, p.100584-100584, Article 100584

2023

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An analytical view of the BJH publication of ‘a clinician's view of voxelotor’

British journal of haematology, 2023-03, Vol.200 (6), p.e56-e57

2023

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Trastuzumab Deruxtecan in HER2-Low Breast Cancer

The New England journal of medicine, 2022-09, Vol.387 (12), p.1143-1144

2022

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Trastuzumab Deruxtecan in HER2-Low Breast Cancer

The New England journal of medicine, 2022-09, Vol.387 (12), p.1143-1146

2022

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Contemporary oncology trials, drug approvals and the physician-patient relationship

Lancet Regional Health - Americas (Online), 2022-07, Vol.11, p.100247-100247, Article 100247

2022

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An urgent call to raise the bar in oncology

British journal of cancer, 2021-11, Vol.125 (11), p.1477-1485

2021

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N‐terminal pro‐B‐type natriuretic peptide, tricuspid jet flow velocity, and death in adults with sickle cell disease

American journal of hematology, 2015-04, Vol.90 (4), p.E75-E76

2015

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An unusual craving

The Netherlands journal of medicine, 2015, Vol.73 (2), p.96-96

2015

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An unusual craving

Netherlands journal of medicine, 2015-02, Vol.73 (2), p.96

2015

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Nucleosomes and neutrophil activation in sickle cell disease painful crisis

Haematologica (Roma), 2013-11, Vol.98 (11), p.1797-1803

2013

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N-acetylcysteine reduces oxidative stress in sickle cell patients

Annals of hematology, 2012-07, Vol.91 (7), p.1097-1105

2012

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Increased efflux of oxidized glutathione (GSSG) causes glutathione depletion and potentially diminishes antioxidant defense in sickle erythrocytes

Biochimica et biophysica acta, 2011-11, Vol.1812 (11), p.1412-1417

2011

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Oxidative stress in sickle cell disease; pathophysiology and potential implications for disease management

American journal of hematology, 2011-06, Vol.86 (6), p.484-489

2011

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Plasma levels of pentraxin-3, an acute phase protein, are increased during sickle cell painful crisis

Blood cells, molecules, & diseases, 2011-03, Vol.46 (3), p.189-194

2011

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Urinary markers of bone resorption, pyridinoline and deoxypyridinoline, are increased in sickle cell patients with further increments during painful crisis

American journal of hematology, 2010-11, Vol.85 (11), p.902-904

2010

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Plasma levels of advanced glycation end products are associated with haemolysis‐related organ complications in sickle cell patients

British journal of haematology, 2010-10, Vol.151 (1), p.62-69

2010

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Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease

American journal of hematology, 2010-07, Vol.85 (7), p.532-535

2010

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Plasma asymmetric dimethylarginine concentrations in sickle cell disease are related to the hemolytic phenotype

Blood cells, molecules, & diseases, 2010-04, Vol.44 (4), p.229-232

2010

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Letter in response to: “Pulmonary thrombi are not detected by 3D magnetic resonance angiography in adults with sickle cell anemia and an elevated triscuspid regurgitant jet velocity”

American journal of hematology, 2010-03, Vol.85 (3), p.217-217

2010

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Plasma annexin A5 and microparticle phosphatidylserine levels are elevated in sickle cell disease and increase further during painful crisis

Biochemical and biophysical research communications, 2009-12, Vol.390 (1), p.161-164

2009

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Elevated endothelial progenitor cells during painful sickle cell crisis

Experimental hematology, 2009-09, Vol.37 (9), p.1054-1059

2009

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Circulating endothelial cells: A potential parameter of organ damage in sickle cell anemia?

Blood cells, molecules, & diseases, 2009-07, Vol.43 (1), p.63-67

2009

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Lung function tests in patients with sickle cell disease: A reply

American journal of hematology, 2009-05, Vol.84 (5), p.310-311

2009

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Elevated Circulating Stromal-Derived Factor-1 Levels in Sickle Cell Disease

Acta haematologica, 2009-01, Vol.122 (1), p.64-69

2009

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Pharmaceutical company funding of cancer patient advocacy organizations in the Netherlands

Untoward global effects of current guideline formulation of stereotactic radiotherapy for symptomatic brain metastases by international medical societies

An analytical view of the BJH publication of ‘a clinician's view of voxelotor’

Trastuzumab Deruxtecan in HER2-Low Breast Cancer

Trastuzumab Deruxtecan in HER2-Low Breast Cancer

Contemporary oncology trials, drug approvals and the physician-patient relationship

An urgent call to raise the bar in oncology

N‐terminal pro‐B‐type natriuretic peptide, tricuspid jet flow velocity, and death in adults with sickle cell disease

An unusual craving

An unusual craving

Nucleosomes and neutrophil activation in sickle cell disease painful crisis

N-acetylcysteine reduces oxidative stress in sickle cell patients

Increased efflux of oxidized glutathione (GSSG) causes glutathione depletion and potentially diminishes antioxidant defense in sickle erythrocytes

Oxidative stress in sickle cell disease; pathophysiology and potential implications for disease management

Plasma levels of pentraxin-3, an acute phase protein, are increased during sickle cell painful crisis

Urinary markers of bone resorption, pyridinoline and deoxypyridinoline, are increased in sickle cell patients with further increments during painful crisis

Plasma levels of advanced glycation end products are associated with haemolysis‐related organ complications in sickle cell patients

Pain rate and social circumstances rather than cumulative organ damage determine the quality of life in adults with sickle cell disease

Plasma asymmetric dimethylarginine concentrations in sickle cell disease are related to the hemolytic phenotype

Letter in response to: “Pulmonary thrombi are not detected by 3D magnetic resonance angiography in adults with sickle cell anemia and an elevated triscuspid regurgitant jet velocity”

Plasma annexin A5 and microparticle phosphatidylserine levels are elevated in sickle cell disease and increase further during painful crisis

Elevated endothelial progenitor cells during painful sickle cell crisis

Circulating endothelial cells: A potential parameter of organ damage in sickle cell anemia?

Lung function tests in patients with sickle cell disease: A reply

Elevated Circulating Stromal-Derived Factor-1 Levels in Sickle Cell Disease

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