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Wedging the door open on platelet‐type von Willebrand disease

British journal of haematology, 2023-11, Vol.203 (4), p.501-503

2023

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Low von Willebrand factor—unraveling an enigma wrapped in a conundrum

Journal of thrombosis and haemostasis, 2024-09

2024

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Calcium-activated chloride channel regulator 1 (CLCA1) forms non-covalent oligomers in colonic mucus and has mucin 2–processing properties

The Journal of biological chemistry, 2019-11, Vol.294 (45), p.17075-17089

2019

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Differential sensitivity of von Willebrand factor activity assays to reduced VWF molecular weight forms: A large international cross-laboratory study

Thrombosis research, 2018-06, Vol.166, p.96-105

2018

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von Willebrand Disease: A Concise Review and Update for the Practicing Physician

Clinical and Applied Thrombosis/Hemostasis, 2017-11, Vol.23 (8), p.900-910

2017

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Phenotypic identification of platelet-type von Willebrand disease and its discrimination from type 2B von Willebrand disease: a question of 2B or not 2B? A story of nonidentical twins? Or two sides of a multidenominational or multifaceted primary-hemostasis coin?

Seminars in thrombosis and hemostasis, 2008-02, Vol.34 (1), p.113-127

Favaloro, Emmanuel J

2008

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Clinical and Laboratory Presentation and Underlying Mechanism in Patients with Low VWF

Thrombosis and haemostasis, 2024-04, Vol.124 (4), p.340-350

2024

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β-Cyclodextrin functionalized magnetic polyamine-amine dendrimers for high enrichment and effective analysis of trace bisphenolic pollutants in beverages

Chemosphere (Oxford), 2023-07, Vol.328, p.138537-138537, Article 138537

2023

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How I manage severe von Willebrand disease

British journal of haematology, 2019-11, Vol.187 (4), p.418-430

2019

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How we diagnose 2M von Willebrand disease (VWD): Use of a strategic algorithmic approach to distinguish 2M VWD from other VWD types

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-01, Vol.27 (1), p.137-148

2021

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Type 2M and Type 2A von Willebrand Disease: Similar but Different

Seminars in thrombosis and hemostasis, 2016-07, Vol.42 (5), p.483-497

2016

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Guideline for laboratory diagnosis and monitoring of von Willebrand disease: A joint guideline from the United Kingdom Haemophilia Centre Doctors' Organisation and the British Society for Haematology

British journal of haematology, 2024-05, Vol.204 (5), p.1714-1731

2024

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R1205H (Vicenza) causes conformational changes in the von Willebrand factor D′D3 domains and enhances von Willebrand factor binding to clearance receptors LRP1 and SR-AI

Journal of thrombosis and haemostasis, 2024-10, Vol.22 (10), p.2752-2760

2024

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Medical Toxicology of Natural Substances: Foods, Fungi, Medicinal Herbs, Plants, and Venomous Animals

Barceloux, Donald G

1. Aufl., 2008

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The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge

European journal of haematology, 2018-11, Vol.101 (5), p.684-690

2018

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A Compound Heterozygosis of Two Novel Mutations in vWF Exacerbates vWD in a Chinese Pedigree

Clinical laboratory (Heidelberg), 2024-01, Vol.70 (2/2024)

2024

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Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients

Thrombosis and haemostasis, 2018-08, Vol.118 (8), p.1382-1389

2018

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2B von Willebrand disease diagnosis: Considerations reflecting on 2021 multisociety guidelines

Research and practice in thrombosis and haemostasis, 2021-12, Vol.5 (8), p.e12635-n/a, Article e12635

2021

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Laboratory tests used to help diagnose von Willebrand disease: an update

Pathology, 2016-06, Vol.48 (4), p.303-318

2016

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Application of genetic testing for the diagnosis of von Willebrand disease

Journal of thrombosis and haemostasis, 2024-08, Vol.22 (8), p.2115-2128

2024

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Evaluating errors in the laboratory identification of von Willebrand disease using contemporary von Willebrand factor assays

Pathology, 2022-04, Vol.54 (3), p.308-317

2022

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Laboratory Testing for von Willebrand Disease Using a Composite Rapid 3-Test Chemiluminescence-Based von Willebrand Factor Assay Panel

Methods in molecular biology (Clifton, N.J.), 2023, Vol.2663, p.647

2023

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Reported prevalence of von Willebrand disease worldwide in relation to income classification

Haemophilia : the official journal of the World Federation of Hemophilia, 2023-07, Vol.29 (4), p.975-986

2023

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Utility of the platelet function analyser (PFA-100/200) for exclusion or detection of von Willebrand disease: A study 22 years in the making

Thrombosis research, 2020-04, Vol.188, p.17-24

Favaloro, Emmanuel J.

2020

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Navigating the Myriad of von Willebrand Factor Assays

Hämostaseologie, 2020-11, Vol.40 (4), p.431-442

Favaloro, Emmanuel J.

2020

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Wedging the door open on platelet‐type von Willebrand disease

Low von Willebrand factor—unraveling an enigma wrapped in a conundrum

Calcium-activated chloride channel regulator 1 (CLCA1) forms non-covalent oligomers in colonic mucus and has mucin 2–processing properties

Differential sensitivity of von Willebrand factor activity assays to reduced VWF molecular weight forms: A large international cross-laboratory study

von Willebrand Disease: A Concise Review and Update for the Practicing Physician

Phenotypic identification of platelet-type von Willebrand disease and its discrimination from type 2B von Willebrand disease: a question of 2B or not 2B? A story of nonidentical twins? Or two sides of a multidenominational or multifaceted primary-hemostasis coin?

Clinical and Laboratory Presentation and Underlying Mechanism in Patients with Low VWF

β-Cyclodextrin functionalized magnetic polyamine-amine dendrimers for high enrichment and effective analysis of trace bisphenolic pollutants in beverages

How I manage severe von Willebrand disease

How we diagnose 2M von Willebrand disease (VWD): Use of a strategic algorithmic approach to distinguish 2M VWD from other VWD types

Type 2M and Type 2A von Willebrand Disease: Similar but Different

Guideline for laboratory diagnosis and monitoring of von Willebrand disease: A joint guideline from the United Kingdom Haemophilia Centre Doctors' Organisation and the British Society for Haematology

R1205H (Vicenza) causes conformational changes in the von Willebrand factor D′D3 domains and enhances von Willebrand factor binding to clearance receptors LRP1 and SR-AI

Medical Toxicology of Natural Substances: Foods, Fungi, Medicinal Herbs, Plants, and Venomous Animals

The elusive and heterogeneous pattern of type 2M von Willebrand disease: A diagnostic challenge

A Compound Heterozygosis of Two Novel Mutations in vWF Exacerbates vWD in a Chinese Pedigree

Genetic Variation in the Syntaxin-Binding Protein STXBP5 in Type 1 von Willebrand Disease Patients

2B von Willebrand disease diagnosis: Considerations reflecting on 2021 multisociety guidelines

Laboratory tests used to help diagnose von Willebrand disease: an update

Application of genetic testing for the diagnosis of von Willebrand disease

Evaluating errors in the laboratory identification of von Willebrand disease using contemporary von Willebrand factor assays

Laboratory Testing for von Willebrand Disease Using a Composite Rapid 3-Test Chemiluminescence-Based von Willebrand Factor Assay Panel

Reported prevalence of von Willebrand disease worldwide in relation to income classification

Utility of the platelet function analyser (PFA-100/200) for exclusion or detection of von Willebrand disease: A study 22 years in the making

Navigating the Myriad of von Willebrand Factor Assays

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