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Page 1
Polymorphic variation within the VWF gene contributes to the failure to detect mutations in patients historically diagnosed with type 1 von Willebrand disease from the MCMDM-1VWD cohort.
Hampshire DJ, Burghel GJ, Goudemand J, Bouvet LC, Eikenboom JC, Schneppenheim R, Budde U, Peake IR, Goodeve AC; EU-VWD and ZPMCB-VWD study groups. Hampshire DJ, et al. Haematologica. 2010 Dec;95(12):2163-5. doi: 10.3324/haematol.2010.027177. Epub 2010 Sep 17. Haematologica. 2010. PMID: 20851871 Free PMC article. No abstract available.
Haemophilia A and von Willebrand's disease.
Goodeve AC, Rosén S, Verbruggen B. Goodeve AC, et al. Haemophilia. 2010 Jul;16 Suppl 5:79-84. doi: 10.1111/j.1365-2516.2010.02303.x. Haemophilia. 2010. PMID: 20590861 Review.
von Willebrand factor variant p.Arg924Gln marks an allele associated with reduced von Willebrand factor and factor VIII levels.
Hickson N, Hampshire D, Winship P, Goudemand J, Schneppenheim R, Budde U, Castaman G, Rodeghiero F, Federici AB, James P, Peake I, Eikenboom J, Goodeve A; MCMDM-1VWD and ZPMCB-VWD study groups. Hickson N, et al. J Thromb Haemost. 2010 Sep;8(9):1986-93. doi: 10.1111/j.1538-7836.2010.03927.x. J Thromb Haemost. 2010. PMID: 20492463 Free PMC article.
The genetic basis of von Willebrand disease.
Goodeve AC. Goodeve AC. Blood Rev. 2010 May;24(3):123-34. doi: 10.1016/j.blre.2010.03.003. Epub 2010 Apr 20. Blood Rev. 2010. PMID: 20409624 Review.
14 results