Modified clot waveform analysis to measure plasma coagulation potential in the presence of the anti‐factor IXa/factor X bispecific antibody emicizumab
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Tomoko Matsumoto | K. Nogami | M. Shima | T. Kitazawa | T. Soeda | T. Matsumoto | N. Arai | Y. Tabuchi | Tabuchi Yuka | Nobuo Arai
[1] F. Rosendaal,et al. Factor VIII products and inhibitor development in previously treated patients with severe or moderately severe hemophilia A: a systematic review , 2018, Journal of thrombosis and haemostasis : JTH.
[2] Y. Abe,et al. An Evaluation of Hemostatic Abnormalities in Patients With Hemophilia According to the Activated Partial Thromboplastin Time Waveform , 2018, Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis.
[3] H. Wada,et al. Emicizumab Prophylaxis in Hemophilia A with Inhibitors. , 2017, The New England journal of medicine.
[4] Tetsuji Sato,et al. Long-term safety and efficacy of emicizumab in a phase 1/2 study in patients with hemophilia A with or without inhibitors. , 2017, Blood advances.
[5] K. Nogami,et al. Clot waveform analysis using CS‐2000i™ distinguishes between very low and absent levels of factor VIII activity in patients with severe haemophilia A , 2017, Haemophilia : the official journal of the World Federation of Hemophilia.
[6] J. Oldenburg,et al. Emicizumab Prophylaxis in Hemophilia A with Inhibitors , 2017, The New England journal of medicine.
[7] K. Nogami,et al. Factor VIIIa-mimetic cofactor activity of a bispecific antibody to factors IX/IXa and X/Xa, emicizumab, depends on its ability to bridge the antigens , 2017, Thrombosis and Haemostasis.
[8] B. Ewenstein,et al. Pro‐ and anticoagulant factors facilitate thrombin generation and balance the haemostatic response to FEIBA® in prophylactic therapy , 2016, Haemophilia : the official journal of the World Federation of Hemophilia.
[9] Tetsuji Sato,et al. Factor VIII-Mimetic Function of Humanized Bispecific Antibody in Hemophilia A. , 2016, The New England journal of medicine.
[10] K. Yoneyama,et al. A first-in-human phase 1 study of ACE910, a novel factor VIII-mimetic bispecific antibody, in healthy subjects. , 2016, Blood.
[11] K. Nogami,et al. Phenotypic Heterogeneity of Hemostasis in Severe Hemophilia , 2015, Seminars in Thrombosis & Hemostasis.
[12] K. Nogami,et al. Optimal monitoring of bypass therapy in hemophilia A patients with inhibitors by the use of clot waveform analysis , 2014, Journal of thrombosis and haemostasis : JTH.
[13] M. Shima,et al. Anti‐factor IXa/X bispecific antibody (ACE910): hemostatic potency against ongoing bleeds in a hemophilia A model and the possibility of routine supplementation , 2014, Journal of thrombosis and haemostasis : JTH.
[14] J. Thachil,et al. Towards standardization of clot waveform analysis and recommendations for its clinical applications , 2013, Journal of thrombosis and haemostasis : JTH.
[15] K. Nogami,et al. The mild phenotype in severe hemophilia A with Arg1781His mutation is associated with enhanced binding affinity of factor VIII for factor X. , 2013, Thrombosis and haemostasis.
[16] T. Igawa,et al. Identification and Multidimensional Optimization of an Asymmetric Bispecific IgG Antibody Mimicking the Function of Factor VIII Cofactor Activity , 2013, PloS one.
[17] C. Witmer,et al. Factor VIII inhibitors in hemophilia A: rationale and latest evidence , 2013, Therapeutic advances in hematology.
[18] J. Mahlangu,et al. Guidelines for the management of hemophilia , 2013, Haemophilia : the official journal of the World Federation of Hemophilia.
[19] Tsukasa Suzuki,et al. A bispecific antibody to factors IXa and X restores factor VIII hemostatic activity in a hemophilia A model , 2012, Nature Medicine.
[20] M. Trossaërt,et al. Prevalence, biological phenotype and genotype in moderate/mild hemophilia A with discrepancy between one‐stage and chromogenic factor VIII activity , 2011, Journal of thrombosis and haemostasis : JTH.
[21] J. G. van der Bom,et al. The long-term course of factor VIII inhibitors in patients with congenital haemophilia A without immune tolerance induction. , 2010, Thrombosis and haemostasis.
[22] H. M. van den Berg,et al. A survey of adherence to haemophilia therapy in six European countries: results and recommendations , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[23] Tomoko Matsumoto,et al. New assays for monitoring haemophilia treatment , 2008, Haemophilia : the official journal of the World Federation of Hemophilia.
[24] D. Monroe. Further understanding of recombinant activated factor VII mode of action. , 2008, Seminars in hematology.
[25] C. Lee,et al. Parents of children with haemophilia – a transforming experience , 2007, Haemophilia : the official journal of the World Federation of Hemophilia.
[26] A. Giles,et al. The measurement of low levels of factor VIII or factor IX in hemophilia A and hemophilia B plasma by clot waveform analysis and thrombin generation assay , 2006, Journal of thrombosis and haemostasis : JTH.
[27] Maureane Hoffman,et al. Remodeling the Blood Coagulation Cascade , 2003, Journal of Thrombosis and Thrombolysis.
[28] A. Giles,et al. The Utility of activated Partial Thromboplastin Time (aPTT) Clot Waveform Analysis in the Investigation of Hemophilia A Patients with very Low Levels of Factor VIII Activity (FVIII:C) , 2002, Thrombosis and Haemostasis.
[29] A. Stead,et al. Properties of Optical Data from Activated Partial Thromboplastin Time and Prothrombin Time Assays , 1997, Thrombosis and Haemostasis.
[30] A. Satterfield,et al. TREATMENT , 1924, California and western medicine.