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Page 1
Inhibitors in nonsevere haemophilia A: outcome and eradication strategies.
van Velzen AS, Eckhardt CL, Hart DP, Peters M, Rangarajan S, Mancuso ME, Smiers FJ, Khair K, Petrini P, Jiménez-Yuste V, Hay CR, van der Bom JG, Yee TT, Fijnvandraat K; INSIGHT study group. van Velzen AS, et al. Among authors: smiers fj. Thromb Haemost. 2015 Jul;114(1):46-55. doi: 10.1160/TH14-11-0940. Epub 2015 Apr 16. Thromb Haemost. 2015. PMID: 25879247
Impact of von Willebrand disease on health-related quality of life in a pediatric population.
de Wee EM, Fijnvandraat K, de Goede-Bolder A, Mauser-Bunschoten EP, Eikenboom JC, Brons PP, Smiers FJ, Tamminga R, Oostenbrink R, Raat H, van der Bom JG, Leebeek FW; WiN Study Group. de Wee EM, et al. Among authors: smiers fj. J Thromb Haemost. 2011 Mar;9(3):502-9. doi: 10.1111/j.1538-7836.2010.04175.x. J Thromb Haemost. 2011. PMID: 21166992 Free article.
Diagnosis and management of thalassaemia.
Peters M, Heijboer H, Smiers F, Giordano PC. Peters M, et al. BMJ. 2012 Jan 25;344:e228. doi: 10.1136/bmj.e228. BMJ. 2012. PMID: 22277544 Review. No abstract available.
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: smiers fj. 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.
Bleeding spectrum in children with moderate or severe von Willebrand disease: Relevance of pediatric-specific bleeding.
Sanders YV, Fijnvandraat K, Boender J, Mauser-Bunschoten EP, van der Bom JG, de Meris J, Smiers FJ, Granzen B, Brons P, Tamminga RY, Cnossen MH, Leebeek FW; WiN Study Group. Sanders YV, et al. Among authors: smiers fj. Am J Hematol. 2015 Dec;90(12):1142-8. doi: 10.1002/ajh.24195. Epub 2015 Nov 17. Am J Hematol. 2015. PMID: 26375306 Free article.
ADAMTS-13 and bleeding phenotype in von Willebrand disease.
Boender J, Nederlof A, Meijer K, Mauser-Bunschoten EP, Cnossen MH, Fijnvandraat K, van der Bom JG, de Meris J, Laros-van Gorkom BAP, van Galen KPM, Eikenboom J, de Maat MPM, Leebeek FWG; WiN Study Group. Boender J, et al. Res Pract Thromb Haemost. 2020 Oct 31;4(8):1331-1339. doi: 10.1002/rth2.12442. eCollection 2020 Nov. Res Pract Thromb Haemost. 2020. PMID: 33313472 Free PMC article.
Platelet degranulation and bleeding phenotype in a large cohort of Von Willebrand disease patients.
Swinkels M, Atiq F, Bürgisser PE, van Moort I, Meijer K, Eikenboom J, Fijnvandraat K, van Galen KPM, de Meris J, Schols SEM, van der Bom JG, Cnossen MH, Voorberg J, Leebeek FWG, Bierings R, Jansen AJG; WiN study group. Swinkels M, et al. Br J Haematol. 2022 May;197(4):497-501. doi: 10.1111/bjh.18145. Epub 2022 Mar 22. Br J Haematol. 2022. PMID: 36165954 Free PMC article.
75 results