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Journal Articles

Activated FVIII Released from FVIII/VWF Complex Facilitates Thrombus Development Under High Shear Flow Condition

Hiroaki Yaoi, MD, Yasuaki Shida, MD PhD, Takehisa Kitazawa, Kunihiro Hattori, PhD, Midori Shima, MD PhD, Keiji Nogami, MD PhD

Blood (2016) 128 (22): 83.

https://doi.org/10.1182/blood.V128.22.83.83

Published: 2016

Journal Articles

Laboratory Predictors Of Loss Of High Molecular Weight Multimers In Patients With Cardiovascular Disease-Associated Acquired Von Willebrand Syndrom

Ewa M. Wysokinska, MD, Dong Chen, M.D., Ph.D., Joseph L Blackshear, MD

Blood (2013) 122 (21): 335.

https://doi.org/10.1182/blood.V122.21.335.335

Published: 2013

Journal Articles

Intracranial Haemorrhage in Patients with An Inherited Bleeding Disorder: A Review of 10 Years Experience in a UK Haemophilia Comprehensive Centre.

Siamak Arami, Tina T. Biss, Kate Talks

Blood (2009) 114 (22): 3489.

https://doi.org/10.1182/blood.V114.22.3489.3489

Published: 2009

Journal Articles

Recombinant Protein Infusion and Hydrodynamic Plasmid Delivery Strategies Provide Distinct and Complementary Approaches to the Characterization of Variant Forms of Von Willeband Factor (VWF) in VWF Knockout Mice.

Cynthia M. Pruss, BSc, Carol A. Hegadorn, Andrea Labelle, Erin Burnett, Mia Golder, David Lillicrap, MD

Blood (2008) 112 (11): 2020.

https://doi.org/10.1182/blood.V112.11.2020.2020

Published: 2008

Journal Articles

Intersection of Mechanisms of Type 2A Von Willebrand Disease through Defects in Von Willebrand Factor Multimerization, Secretion, ADAMTS-13 Susceptibility, and Regulated Storage

Paula M. Jacobi, Joan Cox Gill, MD, Kenneth D. Friedman, MD, Robert R. Montgomery, MD, Sandra L. Haberichter, PhD

Blood (2008) 112 (11): 588.

https://doi.org/10.1182/blood.V112.11.588.588

Published: 2008

Journal Articles

Human von Willebrand Disease Mutations in Mouse von Willebrand Factor Alter Its Cleavage by ADAMTS13.

Cynthia M. Pruss, BSc, Carol A. Hegadorn, MLT, Colleen R.P. Notley, AHT, Rouzbeh Chegeni, PhD, Aly S. Dhala, BScH, David Lillicrap, MD

Blood (2007) 110 (11): 2708.

https://doi.org/10.1182/blood.V110.11.2708.2708

Published: 2007

Journal Articles

Biochemical Characterization of Recombinant Von Willebrand Factor (VWF) with a Type 2B Mutation (P1337L) Coexpressed with a Type 1 VWF Defect (C275R): A Complex Molecular Defect in a Patient Previously Diagnosed with Type 2A Von Willebrand Disease (VWD).

Luciano Baronciani, PhD, Augusto B. Federici, MD, Matteo Beretta, PhD, Giovanna Cozzi, PhD, Maria T. Canciani, PhD, Pier M. Mannucci, MD

Blood (2004) 104 (11): 1025.

https://doi.org/10.1182/blood.V104.11.1025.1025

Published: 2004

NARROW

Activated FVIII Released from FVIII/VWF Complex Facilitates Thrombus Development Under High Shear Flow Condition

Laboratory Predictors Of Loss Of High Molecular Weight Multimers In Patients With Cardiovascular Disease-Associated Acquired Von Willebrand Syndrom

Intracranial Haemorrhage in Patients with An Inherited Bleeding Disorder: A Review of 10 Years Experience in a UK Haemophilia Comprehensive Centre.

Recombinant Protein Infusion and Hydrodynamic Plasmid Delivery Strategies Provide Distinct and Complementary Approaches to the Characterization of Variant Forms of Von Willeband Factor (VWF) in VWF Knockout Mice.

Intersection of Mechanisms of Type 2A Von Willebrand Disease through Defects in Von Willebrand Factor Multimerization, Secretion, ADAMTS-13 Susceptibility, and Regulated Storage

Human von Willebrand Disease Mutations in Mouse von Willebrand Factor Alter Its Cleavage by ADAMTS13.

Biochemical Characterization of Recombinant Von Willebrand Factor (VWF) with a Type 2B Mutation (P1337L) Coexpressed with a Type 1 VWF Defect (C275R): A Complex Molecular Defect in a Patient Previously Diagnosed with Type 2A Von Willebrand Disease (VWD).

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ASH Publications

American Society of Hematology

Activated FVIII Released from FVIII/VWF Complex Facilitates Thrombus Development Under High Shear Flow Condition

Laboratory Predictors Of Loss Of High Molecular Weight Multimers In Patients With Cardiovascular Disease-Associated Acquired Von Willebrand Syndrom

Intracranial Haemorrhage in Patients with An Inherited Bleeding Disorder: A Review of 10 Years Experience in a UK Haemophilia Comprehensive Centre.

Recombinant Protein Infusion and Hydrodynamic Plasmid Delivery Strategies Provide Distinct and Complementary Approaches to the Characterization of Variant Forms of Von Willeband Factor (VWF) in VWF Knockout Mice.

Intersection of Mechanisms of Type 2A Von Willebrand Disease through Defects in Von Willebrand Factor Multimerization, Secretion, ADAMTS-13 Susceptibility, and Regulated Storage

Human von Willebrand Disease Mutations in Mouse von Willebrand Factor Alter Its Cleavage by ADAMTS13.

Biochemical Characterization of Recombinant Von Willebrand Factor (VWF) with a Type 2B Mutation (P1337L) Coexpressed with a Type 1 VWF Defect (C275R): A Complex Molecular Defect in a Patient Previously Diagnosed with Type 2A Von Willebrand Disease (VWD).

Email alerts

ASH Publications

American Society of Hematology

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