[1] Dorgalaleh A, Rashidpanah J.Blood coagulation factor ⅩⅢ and factor ⅩⅢ deficiency[J]. Blood Rev,2016,30(6):461-475. [2] Levy JH, Greenberg C.Biology of Factor ⅩⅢ and clinical manifestations of Factor ⅩⅢ deficiency[J]. Transfusion,2013,53(5):1120-1131. [3] Schroeder V, Kohler HP.Factor ⅩⅢ: Structure and Function[J]. Semin Thromb Hemost,2016,42(4):422-428. [4] Komáromi I, Bagoly Z, Muszbek L, et al.Factor ⅩⅢ: novel structural and functional aspects[J]. J Thromb Haemost,2011,9(1):9-20. [5] Dickneite G, Herwald H, Korte W, et al.Coagulation factor ⅩⅢ: a multifunctional transglutaminase with clinical potential in a range of conditions[J]. Thromb Haemost,2015,113(4):686-697. [6] Muszbek L, Bereczky Z, Bagoly Z, et al.Factor ⅩⅢ: a coa-gulation factor with multiple plasmatic and cellular functions[J]. Physiol Rev,2011,91(3):931-972. [7] Schroeder V, Kohler HP.New developments in the area of factor ⅩⅢ[J]. J Thromb Haemost,2013,11(2):234-244. [8] Byrnes JR, Wolberg AS.Newly-Recognized Roles of Factor ⅩⅢ in Thrombosis[J]. Semin Thromb Hemost,2016,42(4):445-454. [9] Kohler HP, Ichinose A, Seitz R, et al.Diagnosis and classification of factor ⅩⅢ deficiencies[J]. J Thromb Haemost,2011,9(7):1404-1406. [10] Ichinose A, Japanese Collaborative Research Group (JCRG) on AH13 Hemorrhagic Acquired Coagulopathies.Inhibitors of Factor ⅩⅢ/13 in older patients[J]. Semin Thromb Hemost,2014,40(6):704-711. [11] 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[J]. Blood Rev,2017,31(1):37-45. [12] Muszbek L, Pénzes K, Katona é.Auto- and alloantibodies against factor ⅩⅢ: laboratory diagnosis and clinical consequences[J]. J Thromb Haemost,2018,16(5):822-832. [13] Tone KJ, James TE, Fergusson DA, et al.Acquired Factor ⅩⅢ Inhibitor in Hospitalized and Perioperative Patients: A Systematic Review of Case Reports and Case Series[J]. Transfus Med Rev,2016,30(3):123-131. [14] Souri M, Osaki T, Ichinose A, et al.Anti-factor ⅩⅢ A subunit (F ⅩⅢ-A) autoantibodies block FⅩⅢ-A2 B2 assembly and steal F ⅩⅢ-A from native F ⅩⅢ-A2 B2[J]. J Thromb Haemost,2015,13(5):802-814. [15] Ajzner E, Schlammadinger A, Kerényi A, et al.Severe bleeding complications caused by an autoantibody against the B subunit of plasma factor ⅩⅢ: a novel form of acquired factor ⅩⅢ deficiency[J]. Blood, 2009,113(3):723-725. [16] Boehlen F, Casini A, Chizzolini C, et al.Acquired factor ⅩⅢ deficiency: a therapeutic challenge[J]. Thromb Haem-ost,2013,109(3):479-487. [17] Muszbek L, Katona é.Diagnosis and Management of Congenital and Acquired F ⅩⅢ Deficiencies[J]. Semin Thromb Hemost,2016,42(4):429-439. [18] Katona é, Pénzes K, Molnár é, et al.Measurement of factor ⅩⅢ activity in plasma[J]. Clin Chem Lab Med,2012, 50(7):1191-1202. [19] Kessel R, Hu C, Shore-Lesserson L, et al.A child with acquired factor ⅩⅢ deficiency: case report and literature review[J]. Haemophilia, 2013,19(6):814-826. [20] Osaki T, Sugiyama D, Magari Y, et al.Rapid immunochromatographic test for detection of anti-factor ⅩⅢ A subunit antibodies can diagnose 90% of cases with autoimmune haemorrhaphilia ⅩⅢ/13[J]. Thromb Haemost,2015,113(6):1347-1356. [21] Franchini M, Mannucci PM.Acquired haemophilia A: a 2013 update[J]. Thromb Haemost,2013,110(6):1114-1120. [22] Christiansen J, Kahn R, Schmidtchen A, et al.Idiopathic angioedema and urticarial vasculitis in a patient with a history of acquired haemophilia[J]. Acta Derm Venereol,2015,95(2):227-228. [23] Cohen JI.Cinical practice: Herpes zoster[J]. N Engl J Med,2013,369(3):255-263. [24] de Jager T, Pericleous L, Kokot-Kierepa M, et al. The burden and management of F ⅩⅢ deficiency[J]. Haemophilia,2014,20(6):733-740. [25] Inbal A, Oldenburg J, Carcao M, et al.Recombinant factor ⅩⅢ: a safe and novel treatment for congenital factor ⅩⅢ deficiency[J]. Blood, 2012,119(22):5111-5117. |