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Von Willebrand’s Disease

The New England journal of medicine, 2016-11, Vol.375 (21), p.2067-2080

2016

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Prevalence of persistent platelet reactivity despite use of aspirin: A systematic review

The American heart journal, 2007-02, Vol.153 (2), p.175-181

2007

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Clopidogrel nonresponsiveness in patients undergoing percutaneous coronary intervention with stenting: A systematic review and meta-analysis

The American heart journal, 2007-08, Vol.154 (2), p.221-231

2007

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Elevated factor VIII levels and the risk of thrombosis

Arteriosclerosis, thrombosis, and vascular biology, 2001-05, Vol.21 (5), p.731-738

2001

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Heparin-Induced Thrombocytopenia

The New England journal of medicine, 2015-11, Vol.373 (19), p.1882-1884

2015

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von Willebrand disease

Nature reviews. Disease primers, 2024-07, Vol.10 (1), p.51, Article 51

2024

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Atherothrombosis model by silencing of protein C in APOE3-Leiden.CETP transgenic mice

Journal of thrombosis and thrombolysis, 2021-10, Vol.52 (3), p.715-719

2021

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Proteomic Screen Identifies IGFBP7 as a Novel Component of Endothelial Cell-Specific Weibel-Palade Bodies

Journal of proteome research, 2012-05, Vol.11 (5), p.2925-2936

2012

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The spectrum of neutralizing and non-neutralizing anti-FVIII antibodies in a nationwide cohort of 788 persons with hemophilia A

Frontiers in immunology, 2024-02, Vol.15, p.1355813-1355813

2024

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An evidence-based approach to pre-pregnancy counselling for patients with systemic lupus erythematosus

Rheumatology (Oxford, England), 2018-10, Vol.57 (10), p.1707-1720

2018

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Lowering the increased intracellular pH of human‐induced pluripotent stem cell‐derived endothelial cells induces formation of mature Weibel‐Palade bodies

Stem cells translational medicine, 2020-07, Vol.9 (7), p.758-772

2020

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Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand Disease

PloS one, 2015-12, Vol.10 (12), p.e0143913-e0143913

2015

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ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with A and B antigens

Thrombosis and haemostasis, 2007-04, Vol.97 (4), p.534-541

2007

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Factor VIII alters tubular organization and functional properties of von Willebrand factor stored in Weibel-Palade bodies

Blood, 2011-11, Vol.118 (22), p.5947-5956

2011

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Socioeconomic participation of persons with hemophilia: Results from the sixth hemophilia in the Netherlands study

Research and practice in thrombosis and haemostasis, 2022-08, Vol.6 (6), p.e12741-n/a, Article e12741

2022

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The value of family history as a risk indicator for venous thrombosis

Archives of internal medicine (1960), 2009-03, Vol.169 (6), p.610

2009

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Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort

Haematologica (Roma), 2010-12, Vol.95 (12), p.2163-2165

2010

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Variant mapping using mass spectrometry–based proteotyping as a diagnostic tool in von Willebrand disease

Journal of thrombosis and haemostasis, 2024-07, Vol.22 (7), p.1894-1908

2024

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Variations in glycosylation of von Willebrand factor with O-linked sialylated T antigen are associated with its plasma levels

Blood, 2007-03, Vol.109 (6), p.2430-2437

2007

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Efficacy of recombinant activated Factor VII in patients with massive uncontrolled bleeding: a retrospective observational analysis

Transfusion (Philadelphia, Pa.), 2009-03, Vol.49 (3), p.570-577

2009

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Impact of allele-selective silencing of von Willebrand factor in mice based on a single nucleotide allelic difference in von Willebrand factor

Thrombosis research, 2024-04, Vol.236, p.201-208

2024

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Clinical value of early viscoelastometric point‐of‐care testing during postpartum hemorrhage for the prediction of severity of bleeding: A multicenter prospective cohort study in the Netherlands

Acta obstetricia et gynecologica Scandinavica, 2021-09, Vol.100 (9), p.1656-1664

2021

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Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease: Results from 3WINTERS‐IPS, an international and collaborative cross‐sectional study

Journal of thrombosis and haemostasis, 2020-09, Vol.18 (9), p.2145-2154

2020

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SYMPHONY consortium: Orchestrating personalized treatment for patients with bleeding disorders

Journal of thrombosis and haemostasis, 2022-09, Vol.20 (9), p.2001-2011

2022

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The association between haemorrhage and markers of endothelial insufficiency and inflammation in patients with hypoproliferative thrombocytopenia: a cohort study

British journal of haematology, 2020-04, Vol.189 (1), p.171-181

2020

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Von Willebrand’s Disease

Prevalence of persistent platelet reactivity despite use of aspirin: A systematic review

Clopidogrel nonresponsiveness in patients undergoing percutaneous coronary intervention with stenting: A systematic review and meta-analysis

Elevated factor VIII levels and the risk of thrombosis

Heparin-Induced Thrombocytopenia

von Willebrand disease

Atherothrombosis model by silencing of protein C in APOE3-Leiden.CETP transgenic mice

Proteomic Screen Identifies IGFBP7 as a Novel Component of Endothelial Cell-Specific Weibel-Palade Bodies

The spectrum of neutralizing and non-neutralizing anti-FVIII antibodies in a nationwide cohort of 788 persons with hemophilia A

An evidence-based approach to pre-pregnancy counselling for patients with systemic lupus erythematosus

Lowering the increased intracellular pH of human‐induced pluripotent stem cell‐derived endothelial cells induces formation of mature Weibel‐Palade bodies

Identification and Characterization of Novel Variations in Platelet G-Protein Coupled Receptor (GPCR) Genes in Patients Historically Diagnosed with Type 1 von Willebrand Disease

ABO blood group genotypes, plasma von Willebrand factor levels and loading of von Willebrand factor with A and B antigens

Factor VIII alters tubular organization and functional properties of von Willebrand factor stored in Weibel-Palade bodies

Socioeconomic participation of persons with hemophilia: Results from the sixth hemophilia in the Netherlands study

The value of family history as a risk indicator for venous thrombosis

Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort

Variant mapping using mass spectrometry–based proteotyping as a diagnostic tool in von Willebrand disease

Variations in glycosylation of von Willebrand factor with O-linked sialylated T antigen are associated with its plasma levels

Efficacy of recombinant activated Factor VII in patients with massive uncontrolled bleeding: a retrospective observational analysis

Impact of allele-selective silencing of von Willebrand factor in mice based on a single nucleotide allelic difference in von Willebrand factor

Clinical value of early viscoelastometric point‐of‐care testing during postpartum hemorrhage for the prediction of severity of bleeding: A multicenter prospective cohort study in the Netherlands

Bleeding symptoms in patients diagnosed as type 3 von Willebrand disease: Results from 3WINTERS‐IPS, an international and collaborative cross‐sectional study

SYMPHONY consortium: Orchestrating personalized treatment for patients with bleeding disorders

The association between haemorrhage and markers of endothelial insufficiency and inflammation in patients with hypoproliferative thrombocytopenia: a cohort study

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