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Journal of Thrombosis and Haemostasis : JTH|March 20, 2013
Reduced prevalence of arterial thrombosis in von Willebrand diseaseY V Sanders, J Eikenboom, E M de Wee, et al.
Journal of Thrombosis and Haemostasis : JTH|April 3, 2015
CLEC4M and STXBP5 gene variations contribute to von Willebrand factor level variation in von Willebrand diseaseY V Sanders, J G van der Bom, A Isaacs, et al.
Journal of Thrombosis and Haemostasis : JTH|October 26, 2018
Clinically relevant differences between assays for von Willebrand factor activityJ Boender, J Eikenboom, J G van der Bom, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|April 10, 2015
Joint bleeds in von Willebrand disease patients have significant impact on quality of life and joint integrity: a cross-sectional studyK P M van Galen, Y V Sanders, U Vojinovic, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|March 25, 2018
Analysis of current perioperative management with Haemate<sup>®</sup> P/Humate P<sup>®</sup> in von Willebrand disease: Identifying the need for personalized treatmentH C A M Hazendonk, J M Heijdra, N C B de Jager, et al.
Journal of Thrombosis and Haemostasis : JTH|November 6, 2018
Population pharmacokinetics of factor IX in hemophilia B patients undergoing surgeryT Preijers, H C A M Hazendonk, R Liesner, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 1, 2018
Perioperative replacement therapy in haemophilia B: An appeal to "B" more preciseH C A M Hazendonk, T Preijers, R Liesner, et al.
Research and Practice in Thrombosis and Haemostasis|April 25, 2024
Tachyphylaxis and reproducibility of desmopressin response in perioperative persons with nonsevere hemophilia A: implications for clinical practiceL G R Romano, L M Schütte, R M van Hest, et al.
American Journal of Hematology|February 21, 2025
Pyruvate Kinase Function Correlates With Red Blood Cell Properties and Clinical Manifestations in Sickle Cell DiseaseM J M Traets, J F Bos, S van der Veen, et al.
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