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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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Elevated factor VIII levels and the risk of thrombosis

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

2001

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Gynaecological and obstetric bleeding in moderate and severe von Willebrand disease

Thrombosis and haemostasis, 2011-11, Vol.106 (5), p.885

2011

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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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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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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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Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

Journal of thrombosis and haemostasis, 2006-10, Vol.4 (10), p.2103-2114

2006

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Increased levels of factor VIII and fibrinogen in patients with venous thrombosis are not caused by acute phase reactions

Thrombosis and haemostasis, 1999-05, Vol.81 (5), p.680

1999

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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

2007

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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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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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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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The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: an international, multicenter study

Journal of thrombosis and haemostasis, 2005-12, Vol.3 (12), p.2619-2626

2005

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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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Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD

Thrombosis research, 2010-09, Vol.126 (3), p.227-231

2010

Volltextzugriff (PDF)

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

Volltextzugriff (PDF)

Coagulation parameters of thawed fresh-frozen plasma during storage at different temperatures

Transfusion medicine (Oxford, England), 2007-06, Vol.17 (3), p.182-186

2007

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Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigation

Thrombosis and haemostasis, 1999-09, Vol.82 (3), p.1065

1999

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Plasma levels of microparticle-associated tissue factor activity in patients with clinically suspected pulmonary embolism

Thrombosis research, 2010-10, Vol.126 (4), p.345-349

2010

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Heritability of elevated factor VIII antigen levels in factor V Leiden families with thrombophilia

British journal of haematology, 2000-06, Vol.109 (3), p.519-522

2000

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Factor V antigen levels and venous thrombosis: risk profile, interaction with factor V leiden, and relation with factor VIII antigen levels

Arteriosclerosis, thrombosis, and vascular biology, 2000-05, Vol.20 (5), p.1382

2000

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Familial clustering of factor VIII and von Willebrand factor levels

Thrombosis and haemostasis, 1998-02, Vol.79 (2), p.323

1998

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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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Homozygous C2362F von Willebrand factor induces intracellular retention of mutant von Willebrand factor resulting in autosomal recessive severe von Willebrand disease

British journal of haematology, 2006-05, Vol.133 (4), p.409-418

2006

Volltextzugriff (PDF)

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Von Willebrand’s Disease

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

Elevated factor VIII levels and the risk of thrombosis

Gynaecological and obstetric bleeding in moderate and severe von Willebrand disease

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

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

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

Update on the pathophysiology and classification of von Willebrand disease: a report of the Subcommittee on von Willebrand Factor

Increased levels of factor VIII and fibrinogen in patients with venous thrombosis are not caused by acute phase reactions

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

Heparin-Induced Thrombocytopenia

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

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

The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: an international, multicenter study

von Willebrand disease

Validation of a rapid test (VWF-LIA) for the quantitative determination of von Willebrand factor antigen in type 1 von Willebrand disease diagnosis within the European multicenter study MCMDM-1VWD

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

Coagulation parameters of thawed fresh-frozen plasma during storage at different temperatures

Inconsistency of association between type 1 von Willebrand disease phenotype and genotype in families identified in an epidemiological investigation

Plasma levels of microparticle-associated tissue factor activity in patients with clinically suspected pulmonary embolism

Heritability of elevated factor VIII antigen levels in factor V Leiden families with thrombophilia

Factor V antigen levels and venous thrombosis: risk profile, interaction with factor V leiden, and relation with factor VIII antigen levels

Familial clustering of factor VIII and von Willebrand factor levels

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

Homozygous C2362F von Willebrand factor induces intracellular retention of mutant von Willebrand factor resulting in autosomal recessive severe von Willebrand disease

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