The present condition of and clinical guidance for autoimmune coagulation factor deficiencies in Japan
Author:
Publisher
Japanese Society on Thrombosis and Hemostasis
Subject
General Medicine
Link
https://www.jstage.jst.go.jp/article/jjsth/29/3/29_2018_JJTH_29_3_251-261/_pdf
Reference6 articles.
1. 1) Pavlova A, Delev D, Lacroix-Desmazes S, Schwaab R, Mende M, Fimmers R, Astermark J, Oldenburg J: Impact of polymorphisms of the major histocompatibility complex class II, interleukin-10, tumor necrosis factor-alpha and cytotoxic T-lymphocyte antigen-4 genes on inhibitor development in severe hemophilia A. J Thromb Haemost 7: 2006–2015, 2009.
2. 4) Lawrie AS, Green L, Mackie IJ, Liesner R, Machin SJ, Peyvandi F: Factor XIII—an under diagnosed deficiency—are we using the right assays? J Thromb Haemost 8: 2478–2482, 2010.
3. 5) Ichinose A, Kohler HP, Philippou H; Factor XIII and Fibrinogen SSC Subcommittee of the ISTH: Recommendation for ISTH/SSC Criterion 2015 for autoimmune acquired factor XIII/13 deficiency. Thromb Haemost 116: 772–774, 2016.
4. 8) Souri M, Osaki T, Ichinose A: Anti-factor XIII A subunit (FXIII-A) autoantibodies block FXIII-A2 B2 assembly and steal FXIII-A from native FXIII-A2 B2. J Thromb Haemost 13: 802–814, 2015.
5. 9) Ichinose A; Japanese Collaborative Research Group on AH13: Autoimmune acquired factor XIII deficiency due to anti-factor XIII/13 antibodies: A summary of 93 patients. Blood Rev 31: 37–45, 2017.
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