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Flow cytometric mepacrine fluorescence can be used for the exclusion of platelet dense granule deficiency.
van Asten I, Blaauwgeers M, Granneman L, Heijnen HFG, Kruip MJHA, Beckers EAM, Coppens M, Eikenboom J, Tamminga RYJ, Pasterkamp G, Huisman A, van Galen KPM, Korporaal SJA, Schutgens REG, Urbanus RT. van Asten I, et al. Among authors: coppens m. J Thromb Haemost. 2020 Mar;18(3):706-713. doi: 10.1111/jth.14698. Epub 2019 Dec 27. J Thromb Haemost. 2020. PMID: 31815339 Free PMC article.
von Willebrand factor propeptide and the phenotypic classification of von Willebrand disease.
Sanders YV, Groeneveld D, Meijer K, Fijnvandraat K, Cnossen MH, van der Bom JG, Coppens M, de Meris J, Laros-van Gorkom BA, Mauser-Bunschoten EP, Leebeek FW, Eikenboom J; WiN study group. Sanders YV, et al. Among authors: coppens m. Blood. 2015 May 7;125(19):3006-13. doi: 10.1182/blood-2014-09-603241. Epub 2015 Feb 11. Blood. 2015. PMID: 25673639 Free article.
Clinical outcome of patients with a vitamin K antagonist-associated bleeding treated with prothrombin complex concentrate.
Brekelmans MPA, Abdoellakhan RA, Scheres LJJ, Biedermann JS, Hutten BA, Meijer K, Cate HT, Huisman MV, Kruip MJHA, Middeldorp S, Coppens M. Brekelmans MPA, et al. Among authors: coppens m. Res Pract Thromb Haemost. 2017 Nov 13;2(1):77-84. doi: 10.1002/rth2.12055. eCollection 2018 Jan. Res Pract Thromb Haemost. 2017. PMID: 30046709 Free PMC article.
Desmopressin treatment combined with clotting factor VIII concentrates in patients with non-severe haemophilia A: protocol for a multicentre single-armed trial, the DAVID study.
Schütte LM, Cnossen MH, van Hest RM, Driessens MHE, Fijnvandraat K, Polinder S, Beckers EAM, Coppens M, Eikenboom J, Laros-van Gorkom BAP, Meijer K, Nieuwenhuizen L, Mauser-Bunschoten EP, Leebeek FWG, Mathôt RAA, Kruip MJHA. Schütte LM, et al. Among authors: coppens m. BMJ Open. 2019 Apr 23;9(4):e022719. doi: 10.1136/bmjopen-2018-022719. BMJ Open. 2019. PMID: 31015264 Free PMC article.
BMI is an important determinant of VWF and FVIII levels and bleeding phenotype in patients with von Willebrand disease.
Atiq F, Fijnvandraat K, van Galen KPM, Laros-Van Gorkom BAP, Meijer K, de Meris J, Coppens M, Mauser-Bunschoten EP, Cnossen MH, van der Bom JG, Eikenboom J, Leebeek FWG; WiN study group. Atiq F, et al. Among authors: coppens m. Am J Hematol. 2019 Aug;94(8):E201-E205. doi: 10.1002/ajh.25499. Epub 2019 May 13. Am J Hematol. 2019. PMID: 31037771 Free PMC article. No abstract available.
One piece of the puzzle: Population pharmacokinetics of FVIII during perioperative Haemate P® /Humate P® treatment in von Willebrand disease patients.
de Jager NCB, Bukkems LH, Heijdra JM, Hazendonk CHCAM, Fijnvandraat K, Meijer K, Eikenboom J, Laros-van Gorkom BAP, Leebeek FWG, Cnossen MH, Mathôt RAA; OPTI-CLOT group. de Jager NCB, et al. J Thromb Haemost. 2020 Feb;18(2):295-305. doi: 10.1111/jth.14652. Epub 2019 Oct 21. J Thromb Haemost. 2020. PMID: 31557387 Free PMC article.
307 results