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Thromb Haemost 2008; 100(06): 1213-1214
DOI: 10.1160/TH08-09-0618
DOI: 10.1160/TH08-09-0618
Letters to the Editor
On the significance of marginally low von Willebrand factor
Authors
Financial support: The study authors were supported by grants from the Icelandic Center for Research, the Landspitali Science Fund, Aventis ZLB Inc, Dade-Behring Inc., Baxter Biomedical Inc., and Grant # HL 074051 from the National Heart Lung and Blood Institute, NIH, Bethesda, MD, USA.
Weitere Informationen
Publikationsverlauf
Received:
24. September 2008
Accepted:
27. Oktober 2008
Publikationsdatum:
23. November 2017 (online)
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References
- 1 Sadler JE. Von Willebrand disease type 1: a diagnosis in search of a disease. Blood 2003; 101: 2089-2093.
- 2 Eikenboom J, Van Marion V, Putter H. et al. Linkage analysis in families diagnosed with type 1 von Willebrand disease in the European study, molecular and clinical markers for the diagnosis and management of type 1 VWD. J Thromb Haemost 2006; |p24: 774-782.
- 3 Tosetto A, Rodeghiero F, Castaman G. et al. A quantitative analysis of bleeding symptoms in type 1 von Willebrand disease: results from a multicenter European study (MCMDM-1 VWD). J Thromb Haemost 2006; 04: 766-773.
- 4 Lethagen S, Hillarp A, Ekholm C. et al. Distribution of von Willebrand factor levels in young women with and without bleeding symptoms: influence of ABO blood group and promoter haplotypes. Thromb Haemost 2008; 99: 1013-1018.
- 5 Gudmundsdottir BR, Marder VJ, Onundarson PT. Risk of excessive bleeding associated with marginally low von Willebrand factor and mild platelet dysfunction. J Thromb Haemost 2007; 05: 274-281.
- 6 Onundarson PT, Gudmundsdottir BR, Arnfinnsdottir AV. et al. Von Willebrand factor does not vary during normal menstrual cycle. Thromb Haemost 2001; 85: 183-184.