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S Werwitzke

Showing results (1-10 of 13) with videos related to

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Immunobiology|September 19, 2000
CMV complications in common variable immunodeficiencyT Witte, S Werwitzke, R E Schmidt
Journal of Thrombosis and Haemostasis : JTH|January 14, 2004
Immune reconstitution inflammatory syndrome (IRIS) as a cause for inhibitor development in hemophiliaS Werwitzke, A Tiede, M Stoll, et al.
Hamostaseologie|January 8, 2015
Management of acquired haemophilia AA Tiede, R E Scharf, C Dobbelstein, et al.
Immunobiology|September 19, 2000
CD8+ T cell populations in common variable immunodeficiencyS Werwitzke, B Drescher, R E Schmidt, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 1, 2008
Thrombelastographic monitoring of recombinant factor VIIa in acquired haemophiliaH Dehmel, S Werwitzke, A Trummer, et al.
Scandinavian Journal of Immunology|June 1, 2017
Anti-FcγRIIB (CD32) Antibodies Differentially Modulate Murine FVIII-Specific Recall Response in vitroN Vollack, J Friese, S Bergmann, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 12, 2012
Increased amounts of von Willebrand factor are bound to microparticles after infusion of desmopressinA Trummer, B Haarmeijer, S Werwitzke, et al.
Clinical and Experimental Immunology|August 22, 2003
CD8beta/CD28 expression defines functionally distinct populations of peripheral blood T lymphocytesS Werwitzke, A Tiede, B E Drescher, et al.
Scandinavian Journal of Immunology|April 15, 2008
CD8alpha+beta(low) effector T cells in systemic lupus erythematosusS Werwitzke, A Tiede, R Jacobs, et al.
Journal of Thrombosis and Haemostasis : JTH|January 23, 2008
Diagnostic workup of patients with acquired von Willebrand syndrome: a retrospective single-centre cohort studyA Tiede, J Priesack, S Werwitzke, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Immunobiology|September 19, 2000
CMV complications in common variable immunodeficiencyT Witte, S Werwitzke, R E Schmidt
Journal of Thrombosis and Haemostasis : JTH|January 14, 2004
Immune reconstitution inflammatory syndrome (IRIS) as a cause for inhibitor development in hemophiliaS Werwitzke, A Tiede, M Stoll, et al.
Hamostaseologie|January 8, 2015
Management of acquired haemophilia AA Tiede, R E Scharf, C Dobbelstein, et al.
Immunobiology|September 19, 2000
CD8+ T cell populations in common variable immunodeficiencyS Werwitzke, B Drescher, R E Schmidt, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|May 1, 2008
Thrombelastographic monitoring of recombinant factor VIIa in acquired haemophiliaH Dehmel, S Werwitzke, A Trummer, et al.
Scandinavian Journal of Immunology|June 1, 2017
Anti-FcγRIIB (CD32) Antibodies Differentially Modulate Murine FVIII-Specific Recall Response in vitroN Vollack, J Friese, S Bergmann, et al.
Haemophilia : the Official Journal of the World Federation of Hemophilia|October 12, 2012
Increased amounts of von Willebrand factor are bound to microparticles after infusion of desmopressinA Trummer, B Haarmeijer, S Werwitzke, et al.
Clinical and Experimental Immunology|August 22, 2003
CD8beta/CD28 expression defines functionally distinct populations of peripheral blood T lymphocytesS Werwitzke, A Tiede, B E Drescher, et al.
Scandinavian Journal of Immunology|April 15, 2008
CD8alpha+beta(low) effector T cells in systemic lupus erythematosusS Werwitzke, A Tiede, R Jacobs, et al.
Journal of Thrombosis and Haemostasis : JTH|January 23, 2008
Diagnostic workup of patients with acquired von Willebrand syndrome: a retrospective single-centre cohort studyA Tiede, J Priesack, S Werwitzke, et al.
Pageof 2