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U Budde

Showing results (91-100 of 126) with videos related to

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Journal of Thrombosis and Haemostasis : JTH|July 1, 2010
Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotypeG Castaman, S H Giacomelli, P Jacobi, et al.
Hamostaseologie|May 30, 2013
Pregnancy in Upshaw-Schulman syndromeK Kentouche, A Voigt, E Schleussner, et al.
Journal of Thrombosis and Haemostasis : JTH|October 13, 2009
Shear-induced unfolding activates von Willebrand factor A2 domain for proteolysisC Baldauf, R Schneppenheim, W Stacklies, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 16, 1996
Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand diseaseR Schneppenheim, J Brassard, S Krey, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 8, 2013
Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patientM S Enayat, S Ravanbod, M Rassoulzadegan, et al.
The Journal of Clinical Investigation|August 1, 1987
Type IIB von Willebrand factor with normal sialic acid content induces platelet aggregation in the absence of ristocetin. Role of platelet activation, fibrinogen, and two distinct membrane receptorsL De Marco, M Mazzuccato, M Grazia Del Ben, et al.
Journal of Thrombosis and Haemostasis : JTH|June 17, 2018
Acquired von Willebrand syndrome in congenital heart disease surgery: results from an observational case-seriesV Icheva, M Nowak-Machen, U Budde, et al.
Journal of Thrombosis and Haemostasis : JTH|March 21, 2012
Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formationG Castaman, S H Giacomelli, P M Jacobi, et al.
Blood|March 27, 2001
Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand diseaseR Schneppenheim, U Budde, T Obser, et al.
Hamostaseologie|May 1, 2009
Response to DDAVP in children with von Willebrand disease type 2Reinhard Schneppenheim, U Budde, Karin Beutel, et al.
Pageof 13

Showing results (91-100 of 126) with videos related to

Sort By:
Pageof 13
Journal of Thrombosis and Haemostasis : JTH|July 1, 2010
Homozygous type 2N R854W von Willebrand factor is poorly secreted and causes a severe von Willebrand disease phenotypeG Castaman, S H Giacomelli, P Jacobi, et al.
Hamostaseologie|May 30, 2013
Pregnancy in Upshaw-Schulman syndromeK Kentouche, A Voigt, E Schleussner, et al.
Journal of Thrombosis and Haemostasis : JTH|October 13, 2009
Shear-induced unfolding activates von Willebrand factor A2 domain for proteolysisC Baldauf, R Schneppenheim, W Stacklies, et al.
Proceedings of the National Academy of Sciences of the United States of America|April 16, 1996
Defective dimerization of von Willebrand factor subunits due to a Cys-> Arg mutation in type IID von Willebrand diseaseR Schneppenheim, J Brassard, S Krey, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 8, 2013
Identification of a homozygous Cys410Ser mutation in the von Willebrand factor D2 domain causing type 2A(IIC) von Willebrand disease phenotype in an Iranian patientM S Enayat, S Ravanbod, M Rassoulzadegan, et al.
The Journal of Clinical Investigation|August 1, 1987
Type IIB von Willebrand factor with normal sialic acid content induces platelet aggregation in the absence of ristocetin. Role of platelet activation, fibrinogen, and two distinct membrane receptorsL De Marco, M Mazzuccato, M Grazia Del Ben, et al.
Journal of Thrombosis and Haemostasis : JTH|June 17, 2018
Acquired von Willebrand syndrome in congenital heart disease surgery: results from an observational case-seriesV Icheva, M Nowak-Machen, U Budde, et al.
Journal of Thrombosis and Haemostasis : JTH|March 21, 2012
Reduced von Willebrand factor secretion is associated with loss of Weibel-Palade body formationG Castaman, S H Giacomelli, P M Jacobi, et al.
Blood|March 27, 2001
Expression and characterization of von Willebrand factor dimerization defects in different types of von Willebrand diseaseR Schneppenheim, U Budde, T Obser, et al.
Hamostaseologie|May 1, 2009
Response to DDAVP in children with von Willebrand disease type 2Reinhard Schneppenheim, U Budde, Karin Beutel, et al.
Pageof 13