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U Budde

Showing results (1-10 of 126) with videos related to

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Beitrage Zu Infusionstherapie Und Klinische Ernahrung|January 1, 1986
[Thrombopheresis with the CS-3000 cell separator. Changes in primary hemostasis in the donor and in concentrates in 8-day storage]U Budde
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 17, 2008
Diagnosis of von Willebrand disease subtypes: implications for treatmentU Budde
MMW Fortschritte Der Medizin|March 22, 2000
[Fatigue syndrome--a kind of grief?]U Budde-Bastian
Vox Sanguinis|October 26, 1999
Measuring of factor VIII inhibitors according to the Bethesda method in patients with product-related inhibitors in comparison to non-product related inhibitorsU Budde, E Drewke
Journal of Thrombosis and Haemostasis : JTH|July 26, 2011
von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional proteinR Schneppenheim, U Budde
Deutsche Zahnarztliche Zeitschrift|January 1, 1982
[Oral surgery interventions in Willebrand-Jürgens syndrome]G Wahl, U Budde
Beitrage Zur Infusionstherapie Und Transfusionsmedizin = Contributions to Infusion Therapy and Transfusion Medicine|January 1, 1994
Von Willebrand factor multimers in virus-inactivated plasmas and F VIII concentratesU Budde, E Drewke
Hamostaseologie|March 19, 2004
[Classification of von Willebrand disease]R Schneppenheim, U Budde
Hamostaseologie|July 11, 2014
Interactions of von Willebrand factor and ADAMTS13 in von Willebrand disease and thrombotic thrombocytopenic purpuraU Budde, R Schneppenheim
Hamostaseologie|July 28, 2011
[Von Willebrand factor and ADAMTS13 balancing primary haemostasis]R Schneppenheim, U Budde
Pageof 13

Showing results (1-10 of 126) with videos related to

Sort By:
Pageof 13
Beitrage Zu Infusionstherapie Und Klinische Ernahrung|January 1, 1986
[Thrombopheresis with the CS-3000 cell separator. Changes in primary hemostasis in the donor and in concentrates in 8-day storage]U Budde
Haemophilia : the Official Journal of the World Federation of Hemophilia|September 17, 2008
Diagnosis of von Willebrand disease subtypes: implications for treatmentU Budde
MMW Fortschritte Der Medizin|March 22, 2000
[Fatigue syndrome--a kind of grief?]U Budde-Bastian
Vox Sanguinis|October 26, 1999
Measuring of factor VIII inhibitors according to the Bethesda method in patients with product-related inhibitors in comparison to non-product related inhibitorsU Budde, E Drewke
Journal of Thrombosis and Haemostasis : JTH|July 26, 2011
von Willebrand factor: the complex molecular genetics of a multidomain and multifunctional proteinR Schneppenheim, U Budde
Deutsche Zahnarztliche Zeitschrift|January 1, 1982
[Oral surgery interventions in Willebrand-Jürgens syndrome]G Wahl, U Budde
Beitrage Zur Infusionstherapie Und Transfusionsmedizin = Contributions to Infusion Therapy and Transfusion Medicine|January 1, 1994
Von Willebrand factor multimers in virus-inactivated plasmas and F VIII concentratesU Budde, E Drewke
Hamostaseologie|March 19, 2004
[Classification of von Willebrand disease]R Schneppenheim, U Budde
Hamostaseologie|July 11, 2014
Interactions of von Willebrand factor and ADAMTS13 in von Willebrand disease and thrombotic thrombocytopenic purpuraU Budde, R Schneppenheim
Hamostaseologie|July 28, 2011
[Von Willebrand factor and ADAMTS13 balancing primary haemostasis]R Schneppenheim, U Budde
Pageof 13