Zobrazeno 1 - 10
of 33
pro vyhledávání: '"Brit B. Sørensen"'
Autor:
Jens Buchardt, Heidi L. Holmberg, Johan Karlsson, Mads Kjelgaard-Hansen, Kasper Lamberth, Anders B. Sorensen, Wolfram Ruf, Prafull S. Gandhi, Carsten Dan Ley, Brit B. Sørensen, Anders Lærke Nielsen, Henrik Østergaard, Ole Hvilsted Olsen
Publikováno v:
Proceedings of the National Academy of Sciences. 114:12454-12459
Recombinant factor VIIa (FVIIa) variants with increased activity offer the promise to improve the treatment of bleeding episodes in patients with inhibitor-complicated hemophilia. Here, an approach was adopted to enhance the activity of FVIIa by sele
Publikováno v:
Haemophilia. 23:769-776
Aims Concizumab, a humanized monoclonal antibody against tissue factor pathway inhibitor (TFPI), is being developed as a subcutaneously (s.c.) administered treatment for haemophilia. It demonstrated a concentration-dependent procoagulant effect in fu
Publikováno v:
Journal of Thrombosis and Haemostasis. 13:2041-2052
SummaryBackground Conventional coagulation factor assays are associated with certain limitations, as they do not always reflect the clinical heterogeneity of bleeding in hemophilic patients or correctly reflect the individual patient response to trea
Autor:
B. Hua, L. Wang, Tina Manon-Jensen, Brit B. Sørensen, Eva H. N. Olsen, Kirstine Roepstorff, Yupei Zhao, Morten A. Karsdal, S. Sun, Mads Kjelgaard-Hansen, B. Vandahl, C. N. Gudme
Publikováno v:
Haemophilia : the official journal of the World Federation of Hemophilia. 23(4)
Introduction Progressive arthropathy caused by recurrent joint bleeds is a severe complication in haemophilia. Aim We investigated whether biomarkers of cartilage and bone degradation, and inflammation were altered in haemophilia patients and whether
Autor:
Berit Olsen Krogh, Brit B. Sørensen, L. Anders Svensson, Mirella Ezban, Kristoffer W. Balling, Jens Breinholt, Helle Heibroch Petersen, Jes Thorn Clausen, Lene Hansen, Christina Jespersgaard, Birgitte Friederichsen, Albrecht Gruhler, Andrew Neil Bowler, Brian Lauritzen, Lars Christian Petersen, Søren E. Bjørn, Thomas Egebjerg, Mette B. Hermit, Ida Hilden
Publikováno v:
Blood. 119:5871-5878
Hemophilia is treated by IV replacement therapy with Factor VIII (FVIII) or Factor IX (FIX), either on demand to resolve bleeding, or as prophylaxis. Improved treatment may be provided by drugs designed for subcutaneous and less frequent administrati
Autor:
Mirella Ezban, S. Segel, Thomas Dock Steenstrup, A. Bagger-Sørensen, Egon Persson, Stefan Lethagen, Niels Kristian Klausen, Ida Hilden, M. L. S. Christiansen, Dorthe Viuff, Brit B. Sørensen, Kristoffer W. Balling, Marianne Kjalke
Publikováno v:
Haemophilia. 16:878-887
The aim of this study was to evaluate the in vitro function of the new recombinant factor VIII (FVIII) compound, N8. The specific activity of N8 as measured in a FVIII:C one-stage clot assay was 9300±400 IU mg(-1) based on the analysis of seven indi
Autor:
Mette B. Hermit, Henrik Agersø, Mikael Tranholm, Inger Thorup, Brit B. Sørensen, Mirella Ezban, Henning R. Stennicke, Peter B. Johansen, Søren E. Bjørn
Publikováno v:
Thrombosis and Haemostasis. 104:157-164
SummaryThe pharmacokinetics and pharmacodynamics of 40k-PEG-rFVIIa, a GlycoPEGylated derivative of recombinant wild-type FVIIa, were compared with rFVIIa in rabbits. The procoagulant effect was determined as the weight of the clot formed in a defined
Autor:
Mirella Ezban, Ditte M. Karpf, Brit B. Sørensen, Torben Elm, Anne Steinø, Eva H. N. Olsen, Lars Christian Petersen, Thomas N. Krogh
Publikováno v:
Thrombosis and Haemostasis. 101:818-826
SummaryThe mechanism for the elimination of factor VII (FVII) from the circulation is unknown, just as it is unclear how activation of FVII to FVIIa and subsequent complex formation with antithrombin III (AT) or α2-macroglobulin (α2M) affects clear
Autor:
Brit B. Sørensen, Robert Bayer, David Zopf, Kyle Kinealy, Matt S. Kalo, Søren E. Bjørn, Henrik Østergaard, Pernille Holm, Henning R. Stennicke
Publikováno v:
Thrombosis and Haemostasis. 100:920-928
SummaryProphylaxis with 2–4 times weekly dosing of factor (F)VIII or FIX is established as an efficacious and safe treatment in haemophilia. Although prophylaxis is not readily available for the inhibitor patient,recent studies have demonstrated a
Publikováno v:
Journal of Thrombosis and Haemostasis. 5:P-T