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U Budde

Showing results (101-110 of 126) with videos related to

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Human Genetics|December 1, 1994
Genetic heterogeneity of severe von Willebrand disease type III in the German populationR Schneppenheim, S Krey, F Bergmann, et al.
Thrombosis and Haemostasis|December 22, 2009
Loss of high-molecular-weight von Willebrand factor multimers mainly affects platelet aggregation in patients with aortic stenosisS Panzer, R Badr Eslam, A Schneller, et al.
Journal of Thrombosis and Haemostasis : JTH|October 16, 2010
Laboratory diagnosis of von Willebrand disease: results from a prospective and blind study in 32 laboratories worldwide using lyophilized plasmasC A Lee, A Hubbard, C A Sabin, et al.
Journal of Thrombosis and Haemostasis : JTH|January 22, 2010
Accelerated clearance alone explains ultra-large multimers in von Willebrand disease VicenzaA Gézsi, U Budde, I Deák, et al.
Thrombosis and Haemostasis|May 11, 1999
First workshop for detection of heparin-induced antibodies: validation of the heparin-induced platelet-activation test (HIPA) in comparison with a PF4/heparin ELISAP Eichler, U Budde, S Haas, et al.
Thrombosis and Haemostasis|August 26, 2000
Acquired von Willebrand syndrome: data from an international registryA B Federici, J H Rand, P Bucciarelli, et al.
Thrombosis and Haemostasis|February 11, 2000
Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 familiesR Schneppenheim, A B Federici, U Budde, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 29, 2009
Novel findings in two patients with late-diagnosed afibrinogenaemia: intraosseous haemorrhage and fingertip necrosisM Erlacher, J Heiss, I Hainmann, et al.
Journal of Thrombosis and Haemostasis : JTH|June 14, 2018
An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS-VWF studyA Szederjesi, L Baronciani, U Budde, et al.
Annals of Hematology|January 20, 1998
Excessive prolongation of the bleeding time by aspirin in essential thrombocythemia is related to a decrease of large von Willebrand factor multimers in plasmaP J van Genderen, H H van Vliet, F J Prins, et al.
Pageof 13

Showing results (101-110 of 126) with videos related to

Sort By:
Pageof 13
Human Genetics|December 1, 1994
Genetic heterogeneity of severe von Willebrand disease type III in the German populationR Schneppenheim, S Krey, F Bergmann, et al.
Thrombosis and Haemostasis|December 22, 2009
Loss of high-molecular-weight von Willebrand factor multimers mainly affects platelet aggregation in patients with aortic stenosisS Panzer, R Badr Eslam, A Schneller, et al.
Journal of Thrombosis and Haemostasis : JTH|October 16, 2010
Laboratory diagnosis of von Willebrand disease: results from a prospective and blind study in 32 laboratories worldwide using lyophilized plasmasC A Lee, A Hubbard, C A Sabin, et al.
Journal of Thrombosis and Haemostasis : JTH|January 22, 2010
Accelerated clearance alone explains ultra-large multimers in von Willebrand disease VicenzaA Gézsi, U Budde, I Deák, et al.
Thrombosis and Haemostasis|May 11, 1999
First workshop for detection of heparin-induced antibodies: validation of the heparin-induced platelet-activation test (HIPA) in comparison with a PF4/heparin ELISAP Eichler, U Budde, S Haas, et al.
Thrombosis and Haemostasis|August 26, 2000
Acquired von Willebrand syndrome: data from an international registryA B Federici, J H Rand, P Bucciarelli, et al.
Thrombosis and Haemostasis|February 11, 2000
Von Willebrand Disease type 2M "Vicenza" in Italian and German patients: identification of the first candidate mutation (G3864A; R1205H) in 8 familiesR Schneppenheim, A B Federici, U Budde, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 29, 2009
Novel findings in two patients with late-diagnosed afibrinogenaemia: intraosseous haemorrhage and fingertip necrosisM Erlacher, J Heiss, I Hainmann, et al.
Journal of Thrombosis and Haemostasis : JTH|June 14, 2018
An international collaborative study to compare different von Willebrand factor glycoprotein Ib binding activity assays: the COMPASS-VWF studyA Szederjesi, L Baronciani, U Budde, et al.
Annals of Hematology|January 20, 1998
Excessive prolongation of the bleeding time by aspirin in essential thrombocythemia is related to a decrease of large von Willebrand factor multimers in plasmaP J van Genderen, H H van Vliet, F J Prins, et al.
Pageof 13