Platelet-dependent von Willebrand factor activity. Nomenclature and methodology: communication from the SSC of the ISTH

Author:

Bodó I.1,Eikenboom J.2,Montgomery R.3,Patzke J.4,Schneppenheim R.5,Di Paola J.6,

Affiliation:

1. Department of Hematology and Stem Cell Transplantation; St László Hospital; Budapest Hungary

2. Department of Thrombosis and Hemostasis; Leiden University Medical School; Leiden the Netherlands

3. Department of Pediatrics - MFRC; Medical College of Wisconsin; Milwaukee WI USA

4. Department of Assay Development; Siemens Healthcare Diagnostic Products GmbH; Marburg Germany

5. Department of Pediatric Hematology and Oncology; University Medical Center Hamburg-Eppendorf; Hamburg Germany

6. Pediatrics/Genetics; University of Colorado Denver; Aurora CO USA

Publisher

Wiley

Subject

Hematology

Reference63 articles.

1. Epidemiological investigation of the prevalence of von Willebrand's disease;Rodeghiero;Blood,1987

2. Ristocetin-a new tool in the investigation of platelet aggregation;Howard;Thromb Diath Haemorrh,1971

3. Quantitative assay of a plasma factor deficient in von Willebrand's disease that is necessary for platelet aggregation. Relationship to factor VIII procoagulant activity and antigen content;Weiss;J Clin Invest,1973

4. Platelets fixed with paraformaldehyde: a new reagent for assay of von Willebrand factor and platelet aggregating factor;Allain;J Lab Clin Med,1975

5. von Willebrand disease (VWD): evidence-based diagnosis and management guidelines, the National Heart, Lung, and Blood Institute (NHLBI) Expert Panel report (USA);Nichols;Haemophilia,2008

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