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P Mauser

Showing results (141-150 of 166) with videos related to

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American Journal of Hematology|May 1, 2019
BMI is an important determinant of VWF and FVIII levels and bleeding phenotype in patients with von Willebrand diseaseFerdows Atiq, Karin Fijnvandraat, Karin P M van Galen, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 10, 2015
Joint surgery in von Willebrand disease: a multicentre cross-sectional studyK P M van Galen, K Meijer, H C Vogely, 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.
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|November 6, 2018
The prevalence and burden of hand and wrist bleeds in von Willebrand diseaseDésirée van Deukeren, Eveline P Mauser-Bunschoten, Roger E G Schutgens, et al.
Journal of Thrombosis and Haemostasis : JTH|March 30, 2010
Health-related quality of life among adult patients with moderate and severe von Willebrand diseaseE M de Wee, E P Mauser-Bunschoten, J G Van Der Bom, et al.
Research and Practice in Thrombosis and Haemostasis|December 14, 2020
ADAMTS-13 and bleeding phenotype in von Willebrand diseaseJohan Boender, Angelique Nederlof, Karina Meijer, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 15, 2018
Sports participation and physical activity in patients with von Willebrand diseaseFerdows Atiq, Eveline P Mauser-Bunschoten, Jeroen Eikenboom, et al.
Pageof 17

Showing results (141-150 of 166) with videos related to

Sort By:
Pageof 17
American Journal of Hematology|May 1, 2019
BMI is an important determinant of VWF and FVIII levels and bleeding phenotype in patients with von Willebrand diseaseFerdows Atiq, Karin Fijnvandraat, Karin P M van Galen, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 10, 2015
Joint surgery in von Willebrand disease: a multicentre cross-sectional studyK P M van Galen, K Meijer, H C Vogely, 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.
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|November 6, 2018
The prevalence and burden of hand and wrist bleeds in von Willebrand diseaseDésirée van Deukeren, Eveline P Mauser-Bunschoten, Roger E G Schutgens, et al.
Journal of Thrombosis and Haemostasis : JTH|March 30, 2010
Health-related quality of life among adult patients with moderate and severe von Willebrand diseaseE M de Wee, E P Mauser-Bunschoten, J G Van Der Bom, et al.
Research and Practice in Thrombosis and Haemostasis|December 14, 2020
ADAMTS-13 and bleeding phenotype in von Willebrand diseaseJohan Boender, Angelique Nederlof, Karina Meijer, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|November 15, 2018
Sports participation and physical activity in patients with von Willebrand diseaseFerdows Atiq, Eveline P Mauser-Bunschoten, Jeroen Eikenboom, et al.
Pageof 17