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A novel type 2A von Willebrand factor mutation (V1499E) associated with variable clinical expression.
van den Heuvel E, de Laat B, Eckmann CM, Michiels JJ, Schneppenheim R, Budde U, van Mourik JA, Versteegh FG. van den Heuvel E, et al. J Pediatr Hematol Oncol. 2009 Apr;31(4):277-80. doi: 10.1097/MPH.0b013e31819d9119. J Pediatr Hematol Oncol. 2009. PMID: 19346881
A comparative analysis of different automated von Willebrand factor glycoprotein Ib-binding activity assays in well typed von Willebrand disease patients.
Vangenechten I, Mayger K, Smejkal P, Zapletal O, Michiels JJ, Moore GW, Gadisseur A. Vangenechten I, et al. Among authors: michiels jj. J Thromb Haemost. 2018 Jul;16(7):1268-1277. doi: 10.1111/jth.14145. Epub 2018 Jun 6. J Thromb Haemost. 2018. PMID: 29742318 Free article. Clinical Trial.
Acquired von Willebrand disease as a cause of recurrent mucocutaneous bleeding in primary thrombocythemia: relationship with platelet count.
van Genderen PJ, Michiels JJ, van der Poel-van de Luytgaarde SC, van Vliet HH. van Genderen PJ, et al. Ann Hematol. 1994 Aug;69(2):81-4. doi: 10.1007/BF01698487. Ann Hematol. 1994. PMID: 8080884
High-dose intravenous gammaglobulin therapy for acquired von Willebrand disease.
Van Genderen PJ, Papatsonis DN, Michiels JJ, Wielenga JJ, Stibbe J, Huikeshoven FJ. Van Genderen PJ, et al. Postgrad Med J. 1994 Dec;70(830):916-20. doi: 10.1136/pgmj.70.830.916. Postgrad Med J. 1994. PMID: 7532860 Free PMC article. Review.
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