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von Willebrand factor propeptide: biology and clinical utility

Blood, 2015-10, Vol.126 (15), p.1753-1761

Haberichter, Sandra L.

2015

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New advances in the diagnosis of von Willebrand disease

Hematology, 2019-12, Vol.2019 (1), p.596-600

2019

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VWF propeptide in defining VWD subtypes

Blood, 2015-05, Vol.125 (19), p.2882-2883

Haberichter, Sandra L.

2015

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Allosteric activation of ADAMTS13 by von Willebrand factor

Proceedings of the National Academy of Sciences - PNAS, 2014-12, Vol.111 (52), p.18584-18589

2014

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Establishment of an International Reference Reagent for standardization of von Willebrand factor binding to recombinant glycoprotein Ib (VWF:GPIbM and VWF:GPIbR): Official Communication of the SSC

Journal of thrombosis and haemostasis, 2019-06, Vol.17 (6), p.1003-1005

2019

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The role of genetics in the pathogenesis and diagnosis of type 1 Von Willebrand disease

Current opinion in hematology, 2019-09, Vol.26 (5), p.331

2019

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The common VWF variant p.Y1584C: detailed pathogenic examination of an enigmatic sequence change

Journal of thrombosis and haemostasis, 2024-03, Vol.22 (3), p.666-675

2024

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ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease

Blood advances, 2021-01, Vol.5 (1), p.280-300

2021

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Longitudinal bleeding assessment in von Willebrand disease utilizing an interim bleeding score

Journal of thrombosis and haemostasis, 2022-10, Vol.20 (10), p.2246-2254

2022

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Establishment of an International Reference Reagent for standardization of von Willebrand factor binding to recombinant glycoprotein Ib (VWF:GPIbM and VWF:GPIbR)

Journal of thrombosis and haemostasis, 2019-06, Vol.17 (6), p.1003-1005

2019

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Corrigendum to Examining international practices in the management of pregnant women with von Willebrand disease [J Thromb Haemost. 2022 Jan;20(1):82-91]

Journal of thrombosis and haemostasis, 2023-04, Vol.21 (4), p.1068-1068

2023

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Examining international practices in the management of pregnant women with von Willebrand disease

Journal of thrombosis and haemostasis, 2022-01, Vol.20 (1), p.82-91

2022

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Subunit Flexibility of Multimeric von Willebrand Factor/Factor VIII Complexes

ACS omega, 2022-09, Vol.7 (35), p.31183-31196

2022

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Platelet-targeted gene therapy with human factor VIII establishes haemostasis in dogs with haemophilia A

Nature communications, 2013, Vol.4 (1), p.2773-2773, Article 2773

2013

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Crucial role for the VWF A1 domain in binding to type IV collagen

Blood, 2015-04, Vol.125 (14), p.2297-2304

2015

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Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival

Blood, 2006-11, Vol.108 (10), p.3344-3351

2006

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VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population

Blood, 2012-03, Vol.119 (9), p.2135-2140

2012

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Gain-of-function GPIb ELISA assay for VWF activity in the Zimmerman Program for the Molecular and Clinical Biology of VWD

Blood, 2011-02, Vol.117 (6), p.e67-e74

2011

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Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor

Blood, 2010-07, Vol.116 (2), p.280-286

2010

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Compromised shear-dependent cleavage of type 2N von Willebrand factor variants by ADAMTS13 in the presence of factor VIII

Thrombosis and haemostasis, 2013-07, Vol.110 (1), p.202

2013

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Screening for von Willebrand disease does not impact posttonsillectomy bleeding in a low‐risk population

Pediatric blood & cancer, 2021-12, Vol.68 (12), p.e29371-n/a

2021

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Collagen binding provides a sensitive screen for variant von Willebrand disease

Clinical chemistry (Baltimore, Md.), 2013-04, Vol.59 (4), p.684-691

2013

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Active tissue factor pathway inhibitor is expressed on the surface of coated platelets

Blood, 2007-03, Vol.109 (5), p.1931-1937

2007

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von Willebrand factor propeptide: biology and clinical utility

New advances in the diagnosis of von Willebrand disease

VWF propeptide in defining VWD subtypes

Allosteric activation of ADAMTS13 by von Willebrand factor

Establishment of an International Reference Reagent for standardization of von Willebrand factor binding to recombinant glycoprotein Ib (VWF:GPIbM and VWF:GPIbR): Official Communication of the SSC

The role of genetics in the pathogenesis and diagnosis of type 1 Von Willebrand disease

The common VWF variant p.Y1584C: detailed pathogenic examination of an enigmatic sequence change

ASH ISTH NHF WFH 2021 guidelines on the diagnosis of von Willebrand disease

Longitudinal bleeding assessment in von Willebrand disease utilizing an interim bleeding score

Establishment of an International Reference Reagent for standardization of von Willebrand factor binding to recombinant glycoprotein Ib (VWF:GPIbM and VWF:GPIbR)

Corrigendum to Examining international practices in the management of pregnant women with von Willebrand disease [J Thromb Haemost. 2022 Jan;20(1):82-91]

Gut microbiota regulate hepatic von Willebrand factor synthesis and arterial thrombus formation via Toll-like receptor-2

Clinical and laboratory variability in a cohort of patients diagnosed with type 1 VWD in the United States

Examining international practices in the management of pregnant women with von Willebrand disease

Subunit Flexibility of Multimeric von Willebrand Factor/Factor VIII Complexes

Platelet-targeted gene therapy with human factor VIII establishes haemostasis in dogs with haemophilia A

Crucial role for the VWF A1 domain in binding to type IV collagen

Assay of the von Willebrand factor (VWF) propeptide to identify patients with type 1 von Willebrand disease with decreased VWF survival

VWF mutations and new sequence variations identified in healthy controls are more frequent in the African-American population

Gain-of-function GPIb ELISA assay for VWF activity in the Zimmerman Program for the Molecular and Clinical Biology of VWD

Common VWF exon 28 polymorphisms in African Americans affecting the VWF activity assay by ristocetin cofactor

Compromised shear-dependent cleavage of type 2N von Willebrand factor variants by ADAMTS13 in the presence of factor VIII

Screening for von Willebrand disease does not impact posttonsillectomy bleeding in a low‐risk population

Collagen binding provides a sensitive screen for variant von Willebrand disease

Active tissue factor pathway inhibitor is expressed on the surface of coated platelets

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