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Hemorrhagic disorders of fibrinolysis: a clinical review.
Saes JL, Schols SEM, van Heerde WL, Nijziel MR. Saes JL, et al. Among authors: van heerde wl. J Thromb Haemost. 2018 May 30. doi: 10.1111/jth.14160. Online ahead of print. J Thromb Haemost. 2018. PMID: 29847021 Free article. Review.
Factor VIII gene (F8) mutation and risk of inhibitor development in nonsevere hemophilia A.
Eckhardt CL, van Velzen AS, Peters M, Astermark J, Brons PP, Castaman G, Cnossen MH, Dors N, Escuriola-Ettingshausen C, Hamulyak K, Hart DP, Hay CR, Haya S, van Heerde WL, Hermans C, Holmström M, Jimenez-Yuste V, Keenan RD, Klamroth R, Laros-van Gorkom BA, Leebeek FW, Liesner R, Mäkipernaa A, Male C, Mauser-Bunschoten E, Mazzucconi MG, McRae S, Meijer K, Mitchell M, Morfini M, Nijziel M, Oldenburg J, Peerlinck K, Petrini P, Platokouki H, Reitter-Pfoertner SE, Santagostino E, Schinco P, Smiers FJ, Siegmund B, Tagliaferri A, Yee TT, Kamphuisen PW, van der Bom JG, Fijnvandraat K; INSIGHT Study Group. Eckhardt CL, et al. Among authors: van velzen as, van heerde wl, van der bom jg. Blood. 2013 Sep 12;122(11):1954-62. doi: 10.1182/blood-2013-02-483263. Epub 2013 Aug 7. Blood. 2013. PMID: 23926300 Free article.
Whole exome sequencing in the diagnostic workup of patients with a bleeding diathesis.
Saes JL, Simons A, de Munnik SA, Nijziel MR, Blijlevens NMA, Jongmans MC, van der Reijden BA, Smit Y, Brons PP, van Heerde WL, Schols SEM. Saes JL, et al. Among authors: van der reijden ba, van heerde wl. Haemophilia. 2019 Jan;25(1):127-135. doi: 10.1111/hae.13638. Epub 2018 Nov 15. Haemophilia. 2019. PMID: 30431218
Diagnostic work up of patients with increased bleeding tendency.
Zegers SAM, Smit Y, Saes JL, van Duren C, Schuijt TJ, van Heerde WL, Schols SEM. Zegers SAM, et al. Among authors: van heerde wl, van duren c. Haemophilia. 2020 Mar;26(2):269-277. doi: 10.1111/hae.13922. Epub 2019 Dec 30. Haemophilia. 2020. PMID: 31886943 Free PMC article.
108 results