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Journal Abstract Search

210 related items for PubMed ID: 33219619

  • 1. Factor VIII pharmacokinetics associates with genetic modifiers of VWF and FVIII clearance in an adult hemophilia A population.
    Ogiwara K, Swystun LL, Paine AS, Kepa S, Choi SJ, Rejtö J, Hopman W, Pabinger I, Lillicrap D.
    J Thromb Haemost; 2021 Mar; 19(3):654-663. PubMed ID: 33219619
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  • 3. Heterogeneity in the half-life of factor VIII concentrate in patients with hemophilia A is due to variability in the clearance of endogenous von Willebrand factor.
    Elsheikh E, Lavin M, Heck LA, Larkin N, Mullaney B, Doherty D, Kennedy M, Keenan C, Guest T, O'Mahony B, Fazavana J, Fallon PG, Preston RJS, Gormley J, Ryan K, O'Connell NM, Singleton E, Byrne M, McGowan M, Roche S, Doyle M, Crowley MP, O'Shea SI, Reipert BM, Johnsen JM, Pipe SW, Di Paola J, Turecek PL, O'Donnell JS, iPATH study group.
    J Thromb Haemost; 2023 May; 21(5):1123-1134. PubMed ID: 36775768
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  • 4. von Willebrand Factor and Factor VIII Clearance in Perioperative Hemophilia A Patients.
    van Moort I, Bukkems LH, Heijdra JM, Schutgens REG, Laros-van Gorkom BAP, Nieuwenhuizen L, van der Meer FJM, Fijnvandraat K, Ypma P, de Maat MPM, Leebeek FWG, Meijer K, Eikenboom J, Mathôt RAA, Cnossen MH, OPTI-CLOT Study Group.
    Thromb Haemost; 2020 Jul; 120(7):1056-1065. PubMed ID: 32480417
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  • 6. Von Willebrand factor propeptide and pathophysiological mechanisms in European and Iranian patients with type 3 von Willebrand disease enrolled in the 3WINTERS-IPS study.
    Pagliari MT, Rosendaal FR, Ahmadinejad M, Badiee Z, Baghaipour MR, Baronciani L, Benítez Hidalgo O, Bodó I, Budde U, Castaman G, Eshghi P, Goudemand J, Karimi M, Keikhaei B, Lassila R, Leebeek FWG, Lopez Fernandez MF, Mannucci PM, Marino R, Oldenburg J, Peake I, Santoro C, Schneppenheim R, Tiede A, Toogeh G, Tosetto A, Trossaert M, Yadegari H, Zetterberg EMK, Peyvandi F, Federici AB, Eikenboom J.
    J Thromb Haemost; 2022 May; 20(5):1106-1114. PubMed ID: 35092343
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  • 7. The contribution of the sinusoidal endothelial cell receptors CLEC4M, stabilin-2, and SCARA5 to VWF-FVIII clearance in thrombosis and hemostasis.
    Swystun LL, Michels A, Lillicrap D.
    J Thromb Haemost; 2023 Aug; 21(8):2007-2019. PubMed ID: 37085036
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  • 17. von Willebrand factor: evidence for variable clearance in vivo according to Y/C1584 phenotype and ABO blood group.
    Davies JA, Collins PW, Hathaway LS, Bowen DJ.
    J Thromb Haemost; 2008 Jan; 6(1):97-103. PubMed ID: 17949477
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  • 20. Influence of blood group, von Willebrand factor levels, and age on factor VIII levels in non-severe haemophilia A.
    Rejtő J, Königsbrügge O, Grilz E, Hofer S, Mauracher LM, Gabler C, Schuster G, Feistritzer C, Sunder-Plaßmann R, Quehenberger P, Gebhart J, Ay C, Pabinger I.
    J Thromb Haemost; 2020 May; 18(5):1081-1086. PubMed ID: 32073230
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