Copyright ©2013 Baishideng Publishing Group Co.
World J Hematol. Nov 6, 2013; 2(4): 99-108
Published online Nov 6, 2013. doi: 10.5315/wjh.v2.i4.99
Figure 3
Figure 3 State of the Art characterization of a family with autosomal recessive von Willebrand disease type 1 by Casonato and co-workers using a complete set of laboratory assays related to von Willebrand disease diagnosis, von Willebrand factor multimeric analysis in plasma and platelets and the response of FVIII, VWF: Ag and VWF: RCo to desmopressin acetate before and at several time points after desmopressin acetate according to standardized recommendations anno 2006. RIPA: Ristocetin induced platelet aggregation; VWF: von Willebrand factor; VWD: von Willebrand disease; DDAVP: Desmopressin acetate.