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Bailliere'S Clinical Haematology|October 1, 1989
Molecular cloning, expression and assembly of multimeric von Willebrand factorH Pannekoek, J VoorbergSeminars in Thrombosis and Hemostasis|August 5, 2000
Phage display technology: a tool to explore the diversity of inhibitors to blood coagulation factor VIIIJ Voorberg, E N van den BrinkEuropean Journal of Biochemistry|February 17, 1986
Characterization of three different flavodoxins from Azotobacter vinelandiiJ Klugkist, J Voorberg, H Haaker, et al.Journal of Thrombosis and Haemostasis : JTH|November 13, 2012
Dangerous liaisons: how the immune system deals with factor VIIIA Wroblewska, B M Reipert, K P Pratt, et al.The EMBO Journal|March 1, 1990
Domains involved in multimer assembly of von willebrand factor (vWF): multimerization is independent of dimerizationJ Voorberg, R Fontijn, J A van Mourik, et al.Hamostaseologie|February 28, 2013
Acquired thrombotic thrombocytopenic purpura. Development of an autoimmune responseM Schaller, J-D Studt, J Voorberg, et al.The Journal of Biological Chemistry|November 15, 1992
Characterization of recombinant von Willebrand factor corresponding to mutations in type IIA and type IIB von Willebrand diseaseA S Ribba, J Voorberg, D Meyer, et al.Journal of Thrombosis and Haemostasis : JTH|October 26, 2007
Requirements for cellular co-trafficking of factor VIII and von Willebrand factor to Weibel-Palade bodiesM van den Biggelaar, R Bierings, G Storm, et al.Journal of Thrombosis and Haemostasis : JTH|July 15, 2006
Proteolytic cleavage of factor VIII heavy chain is required to expose the binding-site for low-density lipoprotein receptor-related protein within the A2 domainN Bovenschen, G van Stempvoort, J Voorberg, et al.Journal of Thrombosis and Haemostasis : JTH|May 4, 2011
Humoral immune response to ADAMTS13 in acquired thrombotic thrombocytopenic purpuraW Pos, B M Luken, N Sorvillo, et al.Pageof 6