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Placenta|June 25, 2021
Ex vivo human placental transfer study on recombinant Von Willebrand factor (rVWF)J Pastuschek, C Bär, C Göhner, et al.Journal of Thrombosis and Haemostasis : JTH|March 21, 2007
A common 253-kb deletion involving VWF and TMEM16B in German and Italian patients with severe von Willebrand disease type 3R Schneppenheim, G Castaman, A B Federici, et al.European Journal of Haematology|November 1, 1987
FcR-mediated clearance in thrombopenic and non-thrombopenic patients with hemophilia A and possible relation of thrombopenia to HIV seropositivityD Auch, U Budde, U Hammerstein, et al.American Journal of Clinical Pathology|October 17, 2001
Quantification and facilitated comparison of von Willebrand factor multimer patterns by densitometryJ D Studt, U Budde, R Schneppenheim, et al.Best Practice & Research. Clinical Haematology|November 1, 2001
Acquired von Willebrand syndromes: clinical features, aetiology, pathophysiology, classification and managementJ J Michiels, U Budde, M van der Planken, et al.Clinical Nephrology|January 11, 2008
Thrombotic microangiopathy in a 17-year-old patient: TTP, HUS or a bit of both?J Gerth, M Busch, F Oyen, et al.Journal of Thrombosis and Haemostasis : JTH|July 2, 2013
Deep intronic 'mutations' cause hemophilia A: application of next generation sequencing in patients without detectable mutation in F8 cDNAB Pezeshkpoor, N Zimmer, N Marquardt, et al.British Journal of Anaesthesia|February 1, 2011
Acquired type 2A von Willebrand syndrome caused by aortic valve disease corrects during valve surgeryC Solomon, U Budde, S Schneppenheim, et al.Journal of Thrombosis and Haemostasis : JTH|January 23, 2008
Diagnostic workup of patients with acquired von Willebrand syndrome: a retrospective single-centre cohort studyA Tiede, J Priesack, S Werwitzke, et al.Journal of Thrombosis and Haemostasis : JTH|July 1, 2010
Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotypeG Castaman, S H Giacomelli, P Jacobi, et al.Pageof 15