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Volumn , Issue , 2013, Pages 1077-1096

Thrombotic thrombocytopenic purpura, hemolytic-uremic syndrome, and related disorders

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EID: 84976534952     PISSN: None     EISSN: None     Source Type: Book    
DOI: None     Document Type: Chapter
Times cited : (6)

References (207)
  • 1
    • 0034927733 scopus 로고    scopus 로고
    • Inhibitors of von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura
    • Tsai HM, Li A, Rock G. Inhibitors of von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura. Clin Lab 2001;47:387-392.
    • (2001) Clin Lab , vol.47 , pp. 387-392
    • Tsai, H.M.1    Li, A.2    Rock, G.3
  • 2
    • 0026048114 scopus 로고
    • Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura. Canadian Apheresis Study Group
    • Rock GA, Shumak KH, Buskard NA, et al. Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura. Canadian Apheresis Study Group. N Engl J Med 1991;325:393-397.
    • (1991) N Engl J Med , vol.325 , pp. 393-397
    • Rock, G.A.1    Shumak, K.H.2    Buskard, N.A.3
  • 3
    • 25144446865 scopus 로고    scopus 로고
    • The incidence of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: All patients, idiopathic patients, and patients with severe ADAMTS-13 deficiency
    • Terrell DR, Williams LA, Vesely SK, et al. The incidence of thrombotic thrombocytopenic purpura-hemolytic uremic syndrome: all patients, idiopathic patients, and patients with severe ADAMTS-13 deficiency. J Thromb Haemost 2005;3:1432-1436.
    • (2005) J Thromb Haemost , vol.3 , pp. 1432-1436
    • Terrell, D.R.1    Williams, L.A.2    Vesely, S.K.3
  • 4
    • 0002978048 scopus 로고
    • An acute febrile pleiochromic anemia with hyaline thrombosis of the terminal arterioles and capillaries: An undescribed disease
    • Moschcowitz, E. An acute febrile pleiochromic anemia with hyaline thrombosis of the terminal arterioles and capillaries: an undescribed disease. Proc N Y Pathol Soc 1924;24: 21-24.
    • (1924) Proc N Y Pathol Soc , vol.24 , pp. 21-24
    • Moschcowitz, E.1
  • 5
    • 0021858462 scopus 로고
    • Immunohistochemistry of vascular lesions in thrombotic thrombocytopenic purpura, with special reference to factor VIII related antigen
    • Asada Y, Sumiyoshi A, Hayashi T, Suzumiya J, Kaketani K. Immunohistochemistry of vascular lesions in thrombotic thrombocytopenic purpura, with special reference to factor VIII related antigen. Thromb Res 1985;38:469-479.
    • (1985) Thromb Res , vol.38 , pp. 469-479
    • Asada, Y.1    Sumiyoshi, A.2    Hayashi, T.3    Suzumiya, J.4    Kaketani, K.5
  • 6
    • 0038354777 scopus 로고    scopus 로고
    • Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome are distinct pathologic entities. A review of 56 autopsy cases
    • Hosler GA, Cusumano AM, Hutchins GM. Thrombotic thrombocytopenic purpura and hemolytic uremic syndrome are distinct pathologic entities. A review of 56 autopsy cases. Arch Pathol Lab Med 2003;127:834-839.
    • (2003) Arch Pathol Lab Med , vol.127 , pp. 834-839
    • Hosler, G.A.1    Cusumano, A.M.2    Hutchins, G.M.3
  • 7
    • 0035035397 scopus 로고    scopus 로고
    • Von Willebrand factor and von Willebrand factor-cleaving metalloprotease activity in Escherichia coli O157:H7-associated hemolytic uremic syndrome
    • Tsai HM, Chandler WL, Sarode R, et al. von Willebrand factor and von Willebrand factor-cleaving metalloprotease activity in Escherichia coli O157:H7-associated hemolytic uremic syndrome. Pediatr Res 2001;49:653-659.
    • (2001) Pediatr Res , vol.49 , pp. 653-659
    • Tsai, H.M.1    Chandler, W.L.2    Sarode, R.3
  • 8
    • 31544475409 scopus 로고    scopus 로고
    • Thrombospondin-1 controls vascular platelet recruitment and thrombus adherence in mice by protecting (sub) endothelial VWF from cleavage by ADAMTS13
    • Bonnefoy A, Daenens K, Feys HB, et al. Thrombospondin-1 controls vascular platelet recruitment and thrombus adherence in mice by protecting (sub) endothelial VWF from cleavage by ADAMTS13. Blood 2006;107:955-964.
    • (2006) Blood , vol.107 , pp. 955-964
    • Bonnefoy, A.1    Daenens, K.2    Feys, H.B.3
  • 9
    • 33645728657 scopus 로고    scopus 로고
    • Complete deficiency in ADAMTS13 is prothrombotic, but it alone is not sufficient to cause thrombotic thrombocytopenic purpura
    • Banno F, Kokame K, Okuda T, et al. Complete deficiency in ADAMTS13 is prothrombotic, but it alone is not sufficient to cause thrombotic thrombocytopenic purpura. Blood 2006;107:3161-3166.
    • (2006) Blood , vol.107 , pp. 3161-3166
    • Banno, F.1    Kokame, K.2    Okuda, T.3
  • 10
    • 77957195023 scopus 로고    scopus 로고
    • Thrombotic thrombocytopenic purpura directly linked with ADAMTS13 inhibition in the baboon (Papio ursinus)
    • Feys HB, Roodt J, Vandeputte N, et al. Thrombotic thrombocytopenic purpura directly linked with ADAMTS13 inhibition in the baboon (Papio ursinus). Blood 2010;116:2005-2010.
    • (2010) Blood , vol.116 , pp. 2005-2010
    • Feys, H.B.1    Roodt, J.2    Vandeputte, N.3
  • 11
    • 26444551183 scopus 로고    scopus 로고
    • Shigatoxin triggers thrombotic thrombocytopenic purpura in genetically susceptible ADAMTS13-deficient mice
    • Motto DG, Chauhan AK, Zhu G, et al. Shigatoxin triggers thrombotic thrombocytopenic purpura in genetically susceptible ADAMTS13-deficient mice. J Clin Invest 2005;115:2752-2761.
    • (2005) J Clin Invest , vol.115 , pp. 2752-2761
    • Motto, D.G.1    Chauhan, A.K.2    Zhu, G.3
  • 12
    • 34249952122 scopus 로고    scopus 로고
    • Shear-induced unfolding triggers adhesion of von Willebrand factor fibers
    • Schneider SW, Nuschele S, Wixforth A, et al. Shear-induced unfolding triggers adhesion of von Willebrand factor fibers. Proc Natl Acad Sci U S A 2007;104:7899-7903.
    • (2007) Proc Natl Acad Sci U S A , vol.104 , pp. 7899-7903
    • Schneider, S.W.1    Nuschele, S.2    Wixforth, A.3
  • 13
    • 0029858896 scopus 로고    scopus 로고
    • Shear-dependent changes in the three-dimensional structure of human von Willebrand factor
    • Siedlecki CA, Lestini BJ, Kottke-Marchant KK, et al. Shear-dependent changes in the three-dimensional structure of human von Willebrand factor. Blood 1996;88:2939-2950.
    • (1996) Blood , vol.88 , pp. 2939-2950
    • Siedlecki, C.A.1    Lestini, B.J.2    Kottke-Marchant, K.K.3
  • 14
    • 0030980679 scopus 로고    scopus 로고
    • Proteolytic cleavage of recombinant type 2A von Willebrand factor mutants R834W and R834Q: Inhibition by doxycycline and by monoclonal antibody VP-1
    • Tsai HM, Sussman II, Ginsburg D, et al. Proteolytic cleavage of recombinant type 2A von Willebrand factor mutants R834W and R834Q: inhibition by doxycycline and by monoclonal antibody VP-1. Blood 1997;89:1954-1962.
    • (1997) Blood , vol.89 , pp. 1954-1962
    • Tsai, H.M.1    Sussman, I.I.2    Ginsburg, D.3
  • 15
    • 33846027518 scopus 로고    scopus 로고
    • Solution structure of human von Willebrand factor studied using small angle neutron scattering
    • Singh I, Shankaran H, Beauharnois ME, et al. Solution structure of human von Willebrand factor studied using small angle neutron scattering. J Biol Chem 2006;281:38266-38275.
    • (2006) J Biol Chem , vol.281 , pp. 38266-38275
    • Singh, I.1    Shankaran, H.2    Beauharnois, M.E.3
  • 16
    • 66149107458 scopus 로고    scopus 로고
    • Fluid shear induces conformation change in human blood protein von Willebrand factor in solution
    • Singh I, Themistou E, Porcar L, Neelamegham S. Fluid shear induces conformation change in human blood protein von Willebrand factor in solution. Biophys J 2009;96:2313-2320.
    • (2009) Biophys J , vol.96 , pp. 2313-2320
    • Singh, I.1    Themistou, E.2    Porcar, L.3    Neelamegham, S.4
  • 17
    • 23044504378 scopus 로고    scopus 로고
    • Localization of ADAMTS13 to the stellate cells of human liver
    • Uemura M, Tatsumi K, Matsumoto M, et al. Localization of ADAMTS13 to the stellate cells of human liver. Blood 2005;106:922-924.
    • (2005) Blood , vol.106 , pp. 922-924
    • Uemura, M.1    Tatsumi, K.2    Matsumoto, M.3
  • 18
    • 20444404669 scopus 로고    scopus 로고
    • ADAMTS13 is expressed in hepatic stellate cells
    • Zhou W, Inada M, Lee TP, et al. ADAMTS13 is expressed in hepatic stellate cells. Lab Invest 2005;85:780-788.
    • (2005) Lab Invest , vol.85 , pp. 780-788
    • Zhou, W.1    Inada, M.2    Lee, T.P.3
  • 19
    • 45549101029 scopus 로고    scopus 로고
    • Inflammatory cytokines inhibit ADAMTS13 synthesis in hepatic stellate cells and endothelial cells
    • Cao WJ, Niiya M, Zheng XW, Shang DZ, Zheng XL. Inflammatory cytokines inhibit ADAMTS13 synthesis in hepatic stellate cells and endothelial cells. J Thromb Haemost 2008;6:1233-1235.
    • (2008) J Thromb Haemost , vol.6 , pp. 1233-1235
    • Cao, W.J.1    Niiya, M.2    Zheng, X.W.3    Shang, D.Z.4    Zheng, X.L.5
  • 20
    • 34547636148 scopus 로고    scopus 로고
    • Podocytes express ADAMTS13 in normal renal cortex and in patients with thrombotic thrombocytopenic purpura
    • Manea M, Kristoffersson A, Schneppenheim R, et al. Podocytes express ADAMTS13 in normal renal cortex and in patients with thrombotic thrombocytopenic purpura. Br J Haematol 2007;138:651-662.
    • (2007) Br J Haematol , vol.138 , pp. 651-662
    • Manea, M.1    Kristoffersson, A.2    Schneppenheim, R.3
  • 22
    • 72949104661 scopus 로고    scopus 로고
    • Crystal structures of the noncatalytic domains of ADAMTS13 reveal multiple discontinuous exosites for von Willebrand factor
    • Akiyama M, Takeda S, Kokame K, Takagi J, Miyata T. Crystal structures of the noncatalytic domains of ADAMTS13 reveal multiple discontinuous exosites for von Willebrand factor. Proc Natl Acad Sci U S A 2009;106:19274-19279.
    • (2009) Proc Natl Acad Sci U S A , vol.106 , pp. 19274-19279
    • Akiyama, M.1    Takeda, S.2    Kokame, K.3    Takagi, J.4    Miyata, T.5
  • 23
    • 80053146780 scopus 로고    scopus 로고
    • Unraveling the scissile bond: How ADAMTS13 recognizes and cleaves von Willebrand factor
    • Crawley JT, de GR, Xiang Y, Luken BM, Lane DA. Unraveling the scissile bond: how ADAMTS13 recognizes and cleaves von Willebrand factor. Blood 2011;118:3212-3221.
    • (2011) Blood , vol.118 , pp. 3212-3221
    • Crawley, J.T.1    de, G.R.2    Xiang, Y.3    Luken, B.M.4    Lane, D.A.5
  • 24
    • 0020428664 scopus 로고
    • Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura
    • Moake JL, Rudy CK, Troll JH, et al. Unusually large plasma factor VIII:von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura. N Engl J Med 1982;307:1432-1435.
    • (1982) N Engl J Med , vol.307 , pp. 1432-1435
    • Moake, J.L.1    Rudy, C.K.2    Troll, J.H.3
  • 25
    • 0021193806 scopus 로고
    • The role of fibrinolysis in disease processes
    • Kwaan HC. The role of fibrinolysis in disease processes. Semin Thromb Hemost 1984;10:71-79.
    • (1984) Semin Thromb Hemost , vol.10 , pp. 71-79
    • Kwaan, H.C.1
  • 26
    • 0023789919 scopus 로고
    • Quantitation of serum prostacyclin-binding in thrombotic thrombocytopenic purpura
    • Tsai AL, Manner CE, Rudersdorf T, Wu KK. Quantitation of serum prostacyclin-binding in thrombotic thrombocytopenic purpura. Thromb Res 1988;51:583-592.
    • (1988) Thromb Res , vol.51 , pp. 583-592
    • Tsai, A.L.1    Manner, C.E.2    Rudersdorf, T.3    Wu, K.K.4
  • 27
    • 0027281982 scopus 로고
    • Increased levels of vascular endothelial cell markers in thrombotic thrombocytopenic purpura
    • Wada H, Kaneko T, Ohiwa M, et al. Increased levels of vascular endothelial cell markers in thrombotic thrombocytopenic purpura. Am J Hematol 1993;44:101-105.
    • (1993) Am J Hematol , vol.44 , pp. 101-105
    • Wada, H.1    Kaneko, T.2    Ohiwa, M.3
  • 28
    • 0035144223 scopus 로고    scopus 로고
    • Anti-endothelial cell antibodies from patients with thrombotic thrombocytopenic purpura specifically activate small vessel endothelial cells
    • Praprotnik S, Blank M, Levy Y, et al. Anti-endothelial cell antibodies from patients with thrombotic thrombocytopenic purpura specifically activate small vessel endothelial cells. Int Immunol 2001;13:203-210.
    • (2001) Int Immunol , vol.13 , pp. 203-210
    • Praprotnik, S.1    Blank, M.2    Levy, Y.3
  • 29
    • 0023689408 scopus 로고
    • Lytic anti-endothelial cell antibodies in haemolytic-uraemic syndrome
    • Leung DY, Moake JL, Havens PL, Kim M, Pober JS. Lytic anti-endothelial cell antibodies in haemolytic-uraemic syndrome. Lancet 1988;2:183-186.
    • (1988) Lancet , vol.2 , pp. 183-186
    • Leung, D.Y.1    Moake, J.L.2    Havens, P.L.3    Kim, M.4    Pober, J.S.5
  • 30
    • 0020000118 scopus 로고
    • Pathologic effects of plasma from patients with thrombotic thrombocytopenic purpura on platelets and cultured vascular endothelial cells
    • Burns ER, Zucker-Franklin D. Pathologic effects of plasma from patients with thrombotic thrombocytopenic purpura on platelets and cultured vascular endothelial cells. Blood 1982;60:1030-1037.
    • (1982) Blood , vol.60 , pp. 1030-1037
    • Burns, E.R.1    Zucker-Franklin, D.2
  • 31
    • 0017950117 scopus 로고
    • Circulating immune complexes in thrombotic thrombocytopenic purpura (TTP)
    • Neame PB, Hirsh J. Circulating immune complexes in thrombotic thrombocytopenic purpura (TTP). Blood 1978;51:559-560.
    • (1978) Blood , vol.51 , pp. 559-560
    • Neame, P.B.1    Hirsh, J.2
  • 32
    • 0027284512 scopus 로고
    • Characterization of platelet agglutinating protein p37 purified from the plasma of a patient with thrombotic thrombocytopenic purpura
    • Siddiqui FA, Lian EC. Characterization of platelet agglutinating protein p37 purified from the plasma of a patient with thrombotic thrombocytopenic purpura. Biochem Mol Biol Int 1993;30:385-395.
    • (1993) Biochem Mol Biol Int , vol.30 , pp. 385-395
    • Siddiqui, F.A.1    Lian, E.C.2
  • 33
    • 0028126796 scopus 로고
    • Anti-CD36 antibodies in thrombotic thrombocytopenic purpura
    • Tandon NN, Rock G, Jamieson GA. Anti-CD36 antibodies in thrombotic thrombocytopenic purpura. Br J Haematol 1994;88:816-825.
    • (1994) Br J Haematol , vol.88 , pp. 816-825
    • Tandon, N.N.1    Rock, G.2    Jamieson, G.A.3
  • 34
    • 0025097163 scopus 로고
    • The platelet aggregating factor(s) of thrombotic thrombocytopenic purpura
    • Kelton JG, Moore JC, Murphy WG. The platelet aggregating factor(s) of thrombotic thrombocytopenic purpura. Prog Clin Biol Res 1990;337:141-149.
    • (1990) Prog Clin Biol Res , vol.337 , pp. 141-149
    • Kelton, J.G.1    Moore, J.C.2    Murphy, W.G.3
  • 35
    • 45549087679 scopus 로고    scopus 로고
    • Synergistic interactions between interferon-gamma and TRAIL modulate c-FLIP in endothelial cells, mediating their lineage-specific sensitivity to thrombotic thrombocytopenic purpura plasma-associated apoptosis
    • Stefanescu R, Bassett D, Modarresi R, et al. Synergistic interactions between interferon-gamma and TRAIL modulate c-FLIP in endothelial cells, mediating their lineage-specific sensitivity to thrombotic thrombocytopenic purpura plasma-associated apoptosis. Blood 2008;112:340-349.
    • (2008) Blood , vol.112 , pp. 340-349
    • Stefanescu, R.1    Bassett, D.2    Modarresi, R.3
  • 36
    • 84860474599 scopus 로고    scopus 로고
    • Complement activation in thrombotic thrombocytopenic purpura
    • Reti M, Farkas P, Csuka D, et al. Complement activation in thrombotic thrombocytopenic purpura. J Thromb Haemost 2012;10:791-798.
    • (2012) J Thromb Haemost , vol.10 , pp. 791-798
    • Reti, M.1    Farkas, P.2    Csuka, D.3
  • 37
    • 0032832924 scopus 로고    scopus 로고
    • Calpain activity in bone marrow transplantassociated thrombotic thrombocytopenic purpura
    • Zeigler Z, Kelton J, Moore J, et al. Calpain activity in bone marrow transplantassociated thrombotic thrombocytopenic purpura. Bone Marrow Transplant 1999;24:641-645.
    • (1999) Bone Marrow Transplant , vol.24 , pp. 641-645
    • Zeigler, Z.1    Kelton, J.2    Moore, J.3
  • 38
    • 0031787532 scopus 로고    scopus 로고
    • Anti-CD36 autoantibodies in thrombotic thrombocytopenic purpura and other thrombotic disorders: Identification of an 85 kD form of CD36 as a target antigen
    • Schultz DR, Arnold PI, Jy W, et al. Anti-CD36 autoantibodies in thrombotic thrombocytopenic purpura and other thrombotic disorders: identification of an 85 kD form of CD36 as a target antigen. Br J Haematol 1998;103:849-857.
    • (1998) Br J Haematol , vol.103 , pp. 849-857
    • Schultz, D.R.1    Arnold, P.I.2    Jy, W.3
  • 39
    • 0027944712 scopus 로고
    • Anti-CD36 antibodies in patients with lupus anticoagulant and thrombotic complications
    • Rock G, Chauhan K, Jamieson GA, Tandon NN. Anti-CD36 antibodies in patients with lupus anticoagulant and thrombotic complications. Br J Haematol 1994;88:878-880.
    • (1994) Br J Haematol , vol.88 , pp. 878-880
    • Rock, G.1    Chauhan, K.2    Jamieson, G.A.3    Tandon, N.N.4
  • 40
    • 32944462499 scopus 로고    scopus 로고
    • Haemolytic uraemic syndrome is an immune-mediated disease: Role of anti-CD36 antibodies
    • Rock G, Clark W, Sternbach M, Kolajova M, McLaine P. Haemolytic uraemic syndrome is an immune-mediated disease: role of anti-CD36 antibodies. Br J Haematol 2005;131:247-252.
    • (2005) Br J Haematol , vol.131 , pp. 247-252
    • Rock, G.1    Clark, W.2    Sternbach, M.3    Kolajova, M.4    McLaine, P.5
  • 41
    • 0032939729 scopus 로고    scopus 로고
    • Plasma sFas and sFas ligand levels in patients with thrombotic thrombocytopenic purpura and in those with disseminated intravascular coagulation
    • Hori Y, Wada H, Mori Y, et al. Plasma sFas and sFas ligand levels in patients with thrombotic thrombocytopenic purpura and in those with disseminated intravascular coagulation. Am J Hematol 1999;61:21-25.
    • (1999) Am J Hematol , vol.61 , pp. 21-25
    • Hori, Y.1    Wada, H.2    Mori, Y.3
  • 42
    • 0032569840 scopus 로고    scopus 로고
    • Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura
    • Tsai HM, Lian EC. Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med 1998;339: 1585-1594.
    • (1998) N Engl J Med , vol.339 , pp. 1585-1594
    • Tsai, H.M.1    Lian, E.C.2
  • 43
    • 84872899526 scopus 로고    scopus 로고
    • Autoimmune thrombotic microangiopathy: Advances in pathogenesis, diagnosis, and management
    • Tsai HM. Autoimmune thrombotic microangiopathy: advances in pathogenesis, diagnosis, and management. Semin Thromb Hemost 2012;38:469-482.
    • (2012) Semin Thromb Hemost , vol.38 , pp. 469-482
    • Tsai, H.M.1
  • 44
    • 30144431914 scopus 로고    scopus 로고
    • Decreased activity of plasma ADAMTS13 may contribute to the development of liver disturbance and multiorgan failure in patients with alcoholic hepatitis
    • Uemura M, Matsuyama T, Ishikawa M, et al. Decreased activity of plasma ADAMTS13 may contribute to the development of liver disturbance and multiorgan failure in patients with alcoholic hepatitis. Alcohol Clin Exp Res 2005;29:264S-271S.
    • (2005) Alcohol Clin Exp Res , vol.29 , pp. 264S-271S
    • Uemura, M.1    Matsuyama, T.2    Ishikawa, M.3
  • 45
    • 0036275582 scopus 로고    scopus 로고
    • Impaired activity of plasma von Willebrand factor-cleaving protease may predict the occurrence of hepatic veno-occlusive disease after stem cell transplantation
    • Park YD, Yoshioka A, Kawa K, et al. Impaired activity of plasma von Willebrand factor-cleaving protease may predict the occurrence of hepatic veno-occlusive disease after stem cell transplantation. Bone Marrow Transplant 2002;29:789-794.
    • (2002) Bone Marrow Transplant , vol.29 , pp. 789-794
    • Park, Y.D.1    Yoshioka, A.2    Kawa, K.3
  • 46
    • 30444461242 scopus 로고    scopus 로고
    • Severe secondary deficiency of von Willebrand factor-cleaving protease (ADAMTS13) in patients with sepsis-induced disseminated intravascular coagulation: Its correlation with development of renal failure
    • Ono T, Mimuro J, Madoiwa S, et al. Severe secondary deficiency of von Willebrand factor-cleaving protease (ADAMTS13) in patients with sepsis-induced disseminated intravascular coagulation: its correlation with development of renal failure. Blood 2006;107:528-534.
    • (2006) Blood , vol.107 , pp. 528-534
    • Ono, T.1    Mimuro, J.2    Madoiwa, S.3
  • 47
    • 33846901167 scopus 로고    scopus 로고
    • Acquired ADAMTS-13 deficiency in pediatric patients with severe sepsis
    • Nguyen TC, Liu A, Liu L, et al. Acquired ADAMTS-13 deficiency in pediatric patients with severe sepsis. Haematologica 2007;92:121-124.
    • (2007) Haematologica , vol.92 , pp. 121-124
    • Nguyen, T.C.1    Liu, A.2    Liu, L.3
  • 48
    • 0035525768 scopus 로고    scopus 로고
    • Changes in health and disease of the metalloprotease that cleaves von Willebrand factor
    • Mannucci PM, Canciani MT, Forza I, et al. Changes in health and disease of the metalloprotease that cleaves von Willebrand factor. Blood 2001;98: 2730-2735.
    • (2001) Blood , vol.98 , pp. 2730-2735
    • Mannucci, P.M.1    Canciani, M.T.2    Forza, I.3
  • 49
    • 33745875950 scopus 로고    scopus 로고
    • Elevated levels of von Willebrand Factor in cirrhosis support platelet adhesion despite reduced functional capacity
    • Lisman T, Bongers TN, Adelmeijer J, et al. Elevated levels of von Willebrand Factor in cirrhosis support platelet adhesion despite reduced functional capacity. Hepatology 2006;44:53-61.
    • (2006) Hepatology , vol.44 , pp. 53-61
    • Lisman, T.1    Bongers, T.N.2    Adelmeijer, J.3
  • 50
    • 0037100531 scopus 로고    scopus 로고
    • Von Willebrand factorcleaving protease (ADAMTS13) in thrombocytopenic disorders: A severely deficient activity is specific for thrombotic thrombocytopenic purpura
    • Bianchi V, Robles R, Alberio L, Furlan M, Lammle B. Von Willebrand factorcleaving protease (ADAMTS13) in thrombocytopenic disorders: a severely deficient activity is specific for thrombotic thrombocytopenic purpura. Blood 2002;100:710-713.
    • (2002) Blood , vol.100 , pp. 710-713
    • Bianchi, V.1    Robles, R.2    Alberio, L.3    Furlan, M.4    Lammle, B.5
  • 51
    • 62949125310 scopus 로고    scopus 로고
    • ADAMTS13 deficiency with elevated levels of ultra-large and active von Willebrand factor in P. falciparum and P. vivax malaria
    • de MQ, Groot E, Asih PB, et al. ADAMTS13 deficiency with elevated levels of ultra-large and active von Willebrand factor in P. falciparum and P. vivax malaria. Am J Trop Med Hyg 2009;80:492-498.
    • (2009) Am J Trop Med Hyg , vol.80 , pp. 492-498
    • de, M.Q.1    Groot, E.2    Asih, P.B.3
  • 52
    • 73349123465 scopus 로고    scopus 로고
    • Pathophysiology of thrombotic thrombocytopenic purpura
    • Tsai HM. Pathophysiology of thrombotic thrombocytopenic purpura. Int J Hematol 2010;91:1-19.
    • (2010) Int J Hematol , vol.91 , pp. 1-19
    • Tsai, H.M.1
  • 53
    • 77952689917 scopus 로고    scopus 로고
    • HLA-DRB1*11: A strong risk factor for acquired severe ADAMTS13 deficiency-related idiopathic thrombotic thrombocytopenic purpura in Caucasians
    • Coppo P, Busson M, Veyradier A, et al. HLA-DRB1*11: a strong risk factor for acquired severe ADAMTS13 deficiency-related idiopathic thrombotic thrombocytopenic purpura in Caucasians. J Thromb Haemost 2010;8:856-859.
    • (2010) J Thromb Haemost , vol.8 , pp. 856-859
    • Coppo, P.1    Busson, M.2    Veyradier, A.3
  • 54
    • 0032055447 scopus 로고    scopus 로고
    • Thrombotic thrombocytopenic purpura associated with ticlopidine. A review of 60 cases
    • Bennett CL, Weinberg PD, Rozenberg-Ben-Dror K, et al. Thrombotic thrombocytopenic purpura associated with ticlopidine. A review of 60 cases. Ann Intern Med 1998;128:541-544.
    • (1998) Ann Intern Med , vol.128 , pp. 541-544
    • Bennett, C.L.1    Weinberg, P.D.2    Rozenberg-Ben-Dror, K.3
  • 55
    • 0034674030 scopus 로고    scopus 로고
    • Antibody inhibitors to von Willebrand factor metalloproteinase and increased binding of von Willebrand factor to platelets in ticlopidine-associated thrombotic thrombocytopenic purpura
    • Tsai HM, Rice L, Sarode R, Chow TW, Moake JL. Antibody inhibitors to von Willebrand factor metalloproteinase and increased binding of von Willebrand factor to platelets in ticlopidine-associated thrombotic thrombocytopenic purpura. Ann Intern Med 2000;132:794-799.
    • (2000) Ann Intern Med , vol.132 , pp. 794-799
    • Tsai, H.M.1    Rice, L.2    Sarode, R.3    Chow, T.W.4    Moake, J.L.5
  • 56
    • 0034660472 scopus 로고    scopus 로고
    • Thrombotic thrombocytopenic purpura associated with clopidogrel
    • Bennett CL, Connors JM, Carwile JM, et al. Thrombotic thrombocytopenic purpura associated with clopidogrel. N Engl J Med 2000;342:1773-1777.
    • (2000) N Engl J Med , vol.342 , pp. 1773-1777
    • Bennett, C.L.1    Connors, J.M.2    Carwile, J.M.3
  • 57
    • 0030957526 scopus 로고    scopus 로고
    • Human immunodeficiency virus infection and thrombotic microangiopathy
    • Hymes KB, Karpatkin S. Human immunodeficiency virus infection and thrombotic microangiopathy. Semin Hematol 1997;34:117-125.
    • (1997) Semin Hematol , vol.34 , pp. 117-125
    • Hymes, K.B.1    Karpatkin, S.2
  • 58
    • 38349100169 scopus 로고    scopus 로고
    • Prevalence of the ADAMTS-13 missense mutation R1060W in late onset adult thrombotic thrombocytopenic purpura
    • Camilleri RS, Cohen H, MacKie IJ, et al. Prevalence of the ADAMTS-13 missense mutation R1060W in late onset adult thrombotic thrombocytopenic purpura. J Thromb Haemost 2008;6:331-338.
    • (2008) J Thromb Haemost , vol.6 , pp. 331-338
    • Camilleri, R.S.1    Cohen, H.2    MacKie, I.J.3
  • 59
    • 0035807348 scopus 로고    scopus 로고
    • Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura
    • Levy GG, Nichols WC, Lian EC, et al. Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature 2001;413:488-494.
    • (2001) Nature , vol.413 , pp. 488-494
    • Levy, G.G.1    Nichols, W.C.2    Lian, E.C.3
  • 61
    • 52449083418 scopus 로고    scopus 로고
    • ADAMTS13 P475S polymorphism causes a lowered enzymatic activity and urea lability in vitro
    • Akiyama M, Kokame K, Miyata T. ADAMTS13 P475S polymorphism causes a lowered enzymatic activity and urea lability in vitro. J Thromb Haemost 2008;6:1830-1832.
    • (2008) J Thromb Haemost , vol.6 , pp. 1830-1832
    • Akiyama, M.1    Kokame, K.2    Miyata, T.3
  • 62
    • 48649085559 scopus 로고    scopus 로고
    • Frequency of Pro475Ser polymorphism of ADAMTS13 gene and its association with ADAMTS-13 activity in the Korean population
    • Jang MJ, Kim NK, Chong SY, et al. Frequency of Pro475Ser polymorphism of ADAMTS13 gene and its association with ADAMTS-13 activity in the Korean population. Yonsei Med J 2008;49:405-408.
    • (2008) Yonsei Med J , vol.49 , pp. 405-408
    • Jang, M.J.1    Kim, N.K.2    Chong, S.Y.3
  • 63
    • 3042538950 scopus 로고    scopus 로고
    • The frequency of P475S polymorphism in von Willebrand factor-cleaving protease in the Chinese population and its relevance to arterial thrombotic disorders
    • Ruan C, Dai L, Su J, Wang Z, Ruan C. The frequency of P475S polymorphism in von Willebrand factor-cleaving protease in the Chinese population and its relevance to arterial thrombotic disorders. Thromb Haemost 2004;91: 1257-1258.
    • (2004) Thromb Haemost , vol.91 , pp. 1257-1258
    • Ruan, C.1    Dai, L.2    Su, J.3    Wang, Z.4    Ruan, C.5
  • 64
    • 0032569884 scopus 로고    scopus 로고
    • Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome
    • Furlan M, Robles R, Galbusera M, et al. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. N Engl J Med 1998;339:1578-1584.
    • (1998) N Engl J Med , vol.339 , pp. 1578-1584
    • Furlan, M.1    Robles, R.2    Galbusera, M.3
  • 65
    • 0037015057 scopus 로고    scopus 로고
    • Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity
    • Kokame K, Matsumoto M, Soejima K, et al. Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity. Proc Natl Acad Sci U S A 2002;99:11902-11907.
    • (2002) Proc Natl Acad Sci U S A , vol.99 , pp. 11902-11907
    • Kokame, K.1    Matsumoto, M.2    Soejima, K.3
  • 66
    • 30144440926 scopus 로고    scopus 로고
    • Modulation of ADAMTS13 secretion and specific activity by a combination of common amino acid polymorphisms and a missense mutation
    • Plaimauer B, Fuhrmann J, Mohr G, et al. Modulation of ADAMTS13 secretion and specific activity by a combination of common amino acid polymorphisms and a missense mutation. Blood 2006;107:118-125.
    • (2006) Blood , vol.107 , pp. 118-125
    • Plaimauer, B.1    Fuhrmann, J.2    Mohr, G.3
  • 67
    • 70350006842 scopus 로고    scopus 로고
    • IgG subclass distribution of anti-ADAMTS13 antibodies in patients with acquired thrombotic thrombocytopenic purpura
    • Ferrari S, Mudde GC, Rieger M, et al. IgG subclass distribution of anti-ADAMTS13 antibodies in patients with acquired thrombotic thrombocytopenic purpura. J Thromb Haemost 2009;7:1703-1710.
    • (2009) J Thromb Haemost , vol.7 , pp. 1703-1710
    • Ferrari, S.1    Mudde, G.C.2    Rieger, M.3
  • 68
    • 59849089873 scopus 로고    scopus 로고
    • VH1-69 germline encoded antibodies directed towards ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura
    • Pos W, Luken BM, Hovinga JA, et al. VH1-69 germline encoded antibodies directed towards ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura. J Thromb Haemost 2009;7:421-428.
    • (2009) J Thromb Haemost , vol.7 , pp. 421-428
    • Pos, W.1    Luken, B.M.2    Hovinga, J.A.3
  • 69
    • 28844502248 scopus 로고    scopus 로고
    • Enzymatically active ADAMTS13 variants are not inhibited by anti-ADAMTS13 autoantibodies: A novel therapeutic strategy?
    • Zhou W, Dong L, Ginsburg D, Bouhassira EE, Tsai HM. Enzymatically active ADAMTS13 variants are not inhibited by anti-ADAMTS13 autoantibodies: a novel therapeutic strategy? J Biol Chem 2005;280:39934-39941.
    • (2005) J Biol Chem , vol.280 , pp. 39934-39941
    • Zhou, W.1    Dong, L.2    Ginsburg, D.3    Bouhassira, E.E.4    Tsai, H.M.5
  • 70
    • 77949882442 scopus 로고    scopus 로고
    • An autoantibody epitope comprising residues R660, Y661, and Y665 in the ADAMTS13 spacer domain identifies a binding site for the A2 domain of VWF
    • Pos W, Crawley JT, Fijnheer R, et al. An autoantibody epitope comprising residues R660, Y661, and Y665 in the ADAMTS13 spacer domain identifies a binding site for the A2 domain of VWF. Blood 2010;115:1640-1649.
    • (2010) Blood , vol.115 , pp. 1640-1649
    • Pos, W.1    Crawley, J.T.2    Fijnheer, R.3
  • 71
    • 84860316787 scopus 로고    scopus 로고
    • Gain-of-function ADAMTS13 variants that are resistant to autoantibodies against ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura
    • Jian C, Xiao J, Gong L, et al. Gain-of-function ADAMTS13 variants that are resistant to autoantibodies against ADAMTS13 in patients with acquired thrombotic thrombocytopenic purpura. Blood 2012;119:3836-3843.
    • (2012) Blood , vol.119 , pp. 3836-3843
    • Jian, C.1    Xiao, J.2    Gong, L.3
  • 72
    • 77956824177 scopus 로고    scopus 로고
    • Multiple domains of ADAMTS13 are targeted by autoantibodies against ADAMTS13 in patients with acquired idiopathic thrombotic thrombocytopenic purpura
    • Zheng XL, Wu HM, Shang D, et al. Multiple domains of ADAMTS13 are targeted by autoantibodies against ADAMTS13 in patients with acquired idiopathic thrombotic thrombocytopenic purpura. Haematologica 2010;95:1555-1562.
    • (2010) Haematologica , vol.95 , pp. 1555-1562
    • Zheng, X.L.1    Wu, H.M.2    Shang, D.3
  • 73
    • 72849154313 scopus 로고
    • Studies on thrombopoiesis. I. A factor in normal human plasma required for platelet production; Chronic thrombocytopenia due to its deficiency
    • Schulman I, Pierce M, Lukens A, Currimbhoy Z. Studies on thrombopoiesis. I. A factor in normal human plasma required for platelet production; Chronic thrombocytopenia due to its deficiency. Blood 1960;16:943-957.
    • (1960) Blood , vol.16 , pp. 943-957
    • Schulman, I.1    Pierce, M.2    Lukens, A.3    Currimbhoy, Z.4
  • 74
    • 0018098453 scopus 로고
    • Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia
    • Upshaw JD Jr. Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia. N Engl J Med 1978;298:1350-1352.
    • (1978) N Engl J Med , vol.298 , pp. 1350-1352
    • Upshaw, J.D.1
  • 75
    • 80051590576 scopus 로고    scopus 로고
    • Polymorphisms and mutations of ADAMTS13 in the Japanese population and estimation of the number of patients with Upshaw-Schulman syndrome
    • Kokame K, Kokubo Y, Miyata T. Polymorphisms and mutations of ADAMTS13 in the Japanese population and estimation of the number of patients with Upshaw-Schulman syndrome. J Thromb Haemost 2011;9:1654-1656.
    • (2011) J Thromb Haemost , vol.9 , pp. 1654-1656
    • Kokame, K.1    Kokubo, Y.2    Miyata, T.3
  • 76
    • 0037226460 scopus 로고    scopus 로고
    • Thrombotic thrombocytopenic purpura in a newborn
    • Jubinsky PT, Moraille R, Tsai HM. Thrombotic thrombocytopenic purpura in a newborn. J Perinatol 2003;23:85-87.
    • (2003) J Perinatol , vol.23 , pp. 85-87
    • Jubinsky, P.T.1    Moraille, R.2    Tsai, H.M.3
  • 77
    • 3843152878 scopus 로고    scopus 로고
    • Thrombocytopenia and severe hyperbilirubinemia in the neonatal period secondary to congenital thrombotic thrombocytopenic purpura and ADAMTS13 deficiency
    • Schiff DE, Roberts WD, Willert J, Tsai HM. Thrombocytopenia and severe hyperbilirubinemia in the neonatal period secondary to congenital thrombotic thrombocytopenic purpura and ADAMTS13 deficiency. J Pediatr Hematol Oncol 2004;26:535-538.
    • (2004) J Pediatr Hematol Oncol , vol.26 , pp. 535-538
    • Schiff, D.E.1    Roberts, W.D.2    Willert, J.3    Tsai, H.M.4
  • 78
    • 79960635121 scopus 로고    scopus 로고
    • Natural history of UpshawSchulman syndrome based on ADAMTS13 gene analysis in Japan
    • Fujimura Y, Matsumoto M, Isonishi A, et al. Natural history of UpshawSchulman syndrome based on ADAMTS13 gene analysis in Japan. J Thromb Haemost 2011;9(Suppl 1):283-301.
    • (2011) J Thromb Haemost , vol.9 , pp. 283-301
    • Fujimura, Y.1    Matsumoto, M.2    Isonishi, A.3
  • 79
    • 0037339175 scopus 로고    scopus 로고
    • Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome
    • Veyradier A, Obert B, Haddad E, et al. Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome. J Pediatr 2003;142: 310-317.
    • (2003) J Pediatr , vol.142 , pp. 310-317
    • Veyradier, A.1    Obert, B.2    Haddad, E.3
  • 80
    • 63049087674 scopus 로고    scopus 로고
    • Mechanisms of microvascular thrombosis in thrombotic thrombocytopenic purpura
    • Tsai HM. Mechanisms of microvascular thrombosis in thrombotic thrombocytopenic purpura. Kidney Int Suppl 2009;S11-S14.
    • (2009) Kidney Int Suppl , pp. S11-S14
    • Tsai, H.M.1
  • 81
    • 23944468642 scopus 로고    scopus 로고
    • Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvement
    • Noris M, Bucchioni S, Galbusera M, et al. Complement factor H mutation in familial thrombotic thrombocytopenic purpura with ADAMTS13 deficiency and renal involvement. J Am Soc Nephrol 2005;16:1177-1183.
    • (2005) J Am Soc Nephrol , vol.16 , pp. 1177-1183
    • Noris, M.1    Bucchioni, S.2    Galbusera, M.3
  • 82
    • 0012580388 scopus 로고    scopus 로고
    • ADAMTS13 gene mutation in congenital thrombotic thrombocytopenic purpura with previously reported normal VWF cleaving protease activity
    • Savasan S, Lee SK, Ginsburg D, Tsai HM. ADAMTS13 gene mutation in congenital thrombotic thrombocytopenic purpura with previously reported normal VWF cleaving protease activity. Blood 2003;101:4449-4451.
    • (2003) Blood , vol.101 , pp. 4449-4451
    • Savasan, S.1    Lee, S.K.2    Ginsburg, D.3    Tsai, H.M.4
  • 83
    • 0034847605 scopus 로고    scopus 로고
    • Congenital microangiopathic hemolytic anemia and thrombocytopenia with unusually large von Willebrand factor multimers and von Willebrand factor-cleaving protease
    • Savasan S, Taub JW, Buck S, et al. Congenital microangiopathic hemolytic anemia and thrombocytopenia with unusually large von Willebrand factor multimers and von Willebrand factor-cleaving protease. J Pediatr Hematol Oncol 2001;23:364-367.
    • (2001) J Pediatr Hematol Oncol , vol.23 , pp. 364-367
    • Savasan, S.1    Taub, J.W.2    Buck, S.3
  • 84
    • 77949903692 scopus 로고    scopus 로고
    • Survival and relapse in patients with thrombotic thrombocytopenic purpura
    • Hovinga JA, Vesely SK, Terrell DR, Lammle B, George JN. Survival and relapse in patients with thrombotic thrombocytopenic purpura. Blood 2010;115:1500-1511.
    • (2010) Blood , vol.115 , pp. 1500-1511
    • Hovinga, J.A.1    Vesely, S.K.2    Terrell, D.R.3    Lammle, B.4    George, J.N.5
  • 85
    • 0942276833 scopus 로고    scopus 로고
    • VWF73, a region from D1596 to R1668 of von Willebrand factor, provides a minimal substrate for ADAMTS-13
    • Kokame K, Matsumoto M, Fujimura Y, Miyata T. VWF73, a region from D1596 to R1668 of von Willebrand factor, provides a minimal substrate for ADAMTS-13. Blood 2004;103:607-612.
    • (2004) Blood , vol.103 , pp. 607-612
    • Kokame, K.1    Matsumoto, M.2    Fujimura, Y.3    Miyata, T.4
  • 86
    • 1842637235 scopus 로고    scopus 로고
    • An enzyme immunoassay of ADAMTS13 distinguishes patients with thrombotic thrombocytopenic purpura from normal individuals and carriers of ADAMTS13 mutations
    • Zhou W, Tsai HM. An enzyme immunoassay of ADAMTS13 distinguishes patients with thrombotic thrombocytopenic purpura from normal individuals and carriers of ADAMTS13 mutations. Thromb Haemost 2004;91:806-811.
    • (2004) Thromb Haemost , vol.91 , pp. 806-811
    • Zhou, W.1    Tsai, H.M.2
  • 87
    • 17144408687 scopus 로고    scopus 로고
    • FRETS-VWF73, a first fluorogenic substrate for ADAMTS13 assay
    • Kokame K, Nobe Y, Kokubo Y, Okayama A, Miyata T. FRETS-VWF73, a first fluorogenic substrate for ADAMTS13 assay. Br J Haematol 2005;129:93-100.
    • (2005) Br J Haematol , vol.129 , pp. 93-100
    • Kokame, K.1    Nobe, Y.2    Kokubo, Y.3    Okayama, A.4    Miyata, T.5
  • 88
    • 33746348610 scopus 로고    scopus 로고
    • Novel monoclonal antibody-based enzyme immunoassay for determining plasma levels of ADAMTS13 activity
    • Kato S, Matsumoto M, Matsuyama T, et al. Novel monoclonal antibody-based enzyme immunoassay for determining plasma levels of ADAMTS13 activity. Transfusion 2006;46:1444-1452.
    • (2006) Transfusion , vol.46 , pp. 1444-1452
    • Kato, S.1    Matsumoto, M.2    Matsuyama, T.3
  • 89
    • 33645092626 scopus 로고    scopus 로고
    • Relation between ADAMTS13 activity and ADAMTS13 antigen levels in healthy donors and patients with thrombotic microangiopathies (TMA)
    • Rieger M, Ferrari S, Kremer Hovinga JA, et al. Relation between ADAMTS13 activity and ADAMTS13 antigen levels in healthy donors and patients with thrombotic microangiopathies (TMA). Thromb Haemost 2006;95:212-220.
    • (2006) Thromb Haemost , vol.95 , pp. 212-220
    • Rieger, M.1    Ferrari, S.2    Kremer Hovinga, J.A.3
  • 90
    • 33646459182 scopus 로고    scopus 로고
    • ADAMTS13-binding IgG are present in patients with thrombotic thrombocytopenic purpura
    • Tsai HM, Raoufi M, Zhou W, et al. ADAMTS13-binding IgG are present in patients with thrombotic thrombocytopenic purpura. Thromb Haemost 2006;95:886-892.
    • (2006) Thromb Haemost , vol.95 , pp. 886-892
    • Tsai, H.M.1    Raoufi, M.2    Zhou, W.3
  • 91
    • 23744486523 scopus 로고    scopus 로고
    • ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases
    • Rieger M, Mannucci PM, Kremer Hovinga JA, et al. ADAMTS13 autoantibodies in patients with thrombotic microangiopathies and other immunomediated diseases. Blood 2005;106:1262-1267.
    • (2005) Blood , vol.106 , pp. 1262-1267
    • Rieger, M.1    Mannucci, P.M.2    Kremer Hovinga, J.A.3
  • 92
    • 0017727056 scopus 로고
    • Plasmapheresis in the treatment of thrombotic thrombocytopenic purpura
    • Bukowski RM, King JW, Hewlett JS. Plasmapheresis in the treatment of thrombotic thrombocytopenic purpura. Blood 1977;50:413-417.
    • (1977) Blood , vol.50 , pp. 413-417
    • Bukowski, R.M.1    King, J.W.2    Hewlett, J.S.3
  • 93
    • 0017588199 scopus 로고
    • Treatment of thrombotic thrombocytopenic purpura with plasma
    • Byrnes JJ, Khurana M. Treatment of thrombotic thrombocytopenic purpura with plasma. N Engl J Med 1977;297:1386-1389.
    • (1977) N Engl J Med , vol.297 , pp. 1386-1389
    • Byrnes, J.J.1    Khurana, M.2
  • 94
    • 0025290887 scopus 로고
    • Effectiveness of the cryosupernatant fraction of plasma in the treatment of refractory thrombotic thrombocytopenic purpura
    • Byrnes JJ, Moake JL, Klug P, Periman P. Effectiveness of the cryosupernatant fraction of plasma in the treatment of refractory thrombotic thrombocytopenic purpura. Am J Hematol 1990;34:169-174.
    • (1990) Am J Hematol , vol.34 , pp. 169-174
    • Byrnes, J.J.1    Moake, J.L.2    Klug, P.3    Periman, P.4
  • 95
    • 0021959985 scopus 로고
    • Effects of fresh-frozen plasma and its cryosupernatant fraction on von Willebrand factor multimeric forms in chronic relapsing thrombotic thrombocytopenic purpura
    • Moake JL, Byrnes JJ, Troll JH, et al. Effects of fresh-frozen plasma and its cryosupernatant fraction on von Willebrand factor multimeric forms in chronic relapsing thrombotic thrombocytopenic purpura. Blood 1985;65:1232-1236.
    • (1985) Blood , vol.65 , pp. 1232-1236
    • Moake, J.L.1    Byrnes, J.J.2    Troll, J.H.3
  • 96
    • 20244390173 scopus 로고    scopus 로고
    • Does cryosupernatant plasma improve outcome in thrombotic thrombocytopenic purpura? No answer yet
    • Rock G, Anderson D, Clark W, et al. Does cryosupernatant plasma improve outcome in thrombotic thrombocytopenic purpura? No answer yet. Br J Haematol 2005;129:79-86.
    • (2005) Br J Haematol , vol.129 , pp. 79-86
    • Rock, G.1    Anderson, D.2    Clark, W.3
  • 97
    • 0035029529 scopus 로고    scopus 로고
    • Cryoprecipitate poor plasma does not improve early response in primary adult thrombotic thrombocytopenic purpura (TTP)
    • Zeigler ZR, Shadduck RK, Gryn JF, et al. Cryoprecipitate poor plasma does not improve early response in primary adult thrombotic thrombocytopenic purpura (TTP). J Clin Apher 2001;16:19-22.
    • (2001) J Clin Apher , vol.16 , pp. 19-22
    • Zeigler, Z.R.1    Shadduck, R.K.2    Gryn, J.F.3
  • 98
    • 0036786146 scopus 로고    scopus 로고
    • Successful treatment of severe thrombotic thrombocytopenic purpura with the monoclonal antibody rituximab
    • Chemnitz J, Draube A, Scheid C, et al. Successful treatment of severe thrombotic thrombocytopenic purpura with the monoclonal antibody rituximab. Am J Hematol 2002;71:105-108.
    • (2002) Am J Hematol , vol.71 , pp. 105-108
    • Chemnitz, J.1    Draube, A.2    Scheid, C.3
  • 99
    • 70349122967 scopus 로고    scopus 로고
    • Rituximab for refractory and or relapsing thrombotic thrombocytopenic purpura related to immune-mediated severe ADAMTS13-deficiency: A report of four cases and a systematic review of the literature
    • Elliott MA, Heit JA, Pruthi RK, et al. Rituximab for refractory and or relapsing thrombotic thrombocytopenic purpura related to immune-mediated severe ADAMTS13-deficiency: a report of four cases and a systematic review of the literature. Eur J Haematol 2009; 83:365-372.
    • (2009) Eur J Haematol , vol.83 , pp. 365-372
    • Elliott, M.A.1    Heit, J.A.2    Pruthi, R.K.3
  • 100
    • 0036428821 scopus 로고    scopus 로고
    • Rituximab therapy for refractory thrombotic thrombocytopenic purpura
    • Gutterman LA, Kloster B, Tsai HM. Rituximab therapy for refractory thrombotic thrombocytopenic purpura. Blood Cells Mol Dis 2002;28:385-391.
    • (2002) Blood Cells Mol Dis , vol.28 , pp. 385-391
    • Gutterman, L.A.1    Kloster, B.2    Tsai, H.M.3
  • 101
    • 1642318493 scopus 로고    scopus 로고
    • Rituximab for chronic recurring thrombotic thrombocytopenic purpura: A case report and review of the literature
    • Yomtovian R, Niklinski W, Silver B, Sarode R, Tsai HM. Rituximab for chronic recurring thrombotic thrombocytopenic purpura: a case report and review of the literature. Br J Haematol 2004;124:787-795.
    • (2004) Br J Haematol , vol.124 , pp. 787-795
    • Yomtovian, R.1    Niklinski, W.2    Silver, B.3    Sarode, R.4    Tsai, H.M.5
  • 102
    • 24744472059 scopus 로고    scopus 로고
    • Efficiency of curative and prophylactic treatment with rituximab in ADAMTS13-deficient thrombotic thrombocytopenic purpura: A study of 11 cases
    • Fakhouri F, Vernant JP, Veyradier A, et al. Efficiency of curative and prophylactic treatment with rituximab in ADAMTS13-deficient thrombotic thrombocytopenic purpura: a study of 11 cases. Blood 2005;106:1932-1937.
    • (2005) Blood , vol.106 , pp. 1932-1937
    • Fakhouri, F.1    Vernant, J.P.2    Veyradier, A.3
  • 103
    • 23044433307 scopus 로고    scopus 로고
    • Rituximab prevents recurrence of thrombotic thrombocytopenic purpura: A case report
    • Galbusera M, Bresin E, Noris M, et al. Rituximab prevents recurrence of thrombotic thrombocytopenic purpura: a case report. Blood 2005;106: 925-928.
    • (2005) Blood , vol.106 , pp. 925-928
    • Galbusera, M.1    Bresin, E.2    Noris, M.3
  • 104
    • 80051866867 scopus 로고    scopus 로고
    • A phase 2 study of the safety and efficacy of rituximab with plasma exchange in acute acquired thrombotic thrombocytopenic purpura
    • Scully M, McDonald V, Cavenagh J, et al. A phase 2 study of the safety and efficacy of rituximab with plasma exchange in acute acquired thrombotic thrombocytopenic purpura. Blood 2011;118:1746-1753.
    • (2011) Blood , vol.118 , pp. 1746-1753
    • Scully, M.1    McDonald, V.2    Cavenagh, J.3
  • 105
    • 0038813798 scopus 로고    scopus 로고
    • Rituximab induces remission of cerebral ischemia caused by thrombotic thrombocytopenic purpura
    • Tsai HM, Shulman K. Rituximab induces remission of cerebral ischemia caused by thrombotic thrombocytopenic purpura. Eur J Haematol 2003;70:183-185.
    • (2003) Eur J Haematol , vol.70 , pp. 183-185
    • Tsai, H.M.1    Shulman, K.2
  • 106
    • 56749143816 scopus 로고    scopus 로고
    • Effect of prophylactic cyclosporine therapy on ADAMTS13 biomarkers in patients with idiopathic thrombotic thrombocytopenic purpura
    • Cataland SR, Jin M, Lin S, et al. Effect of prophylactic cyclosporine therapy on ADAMTS13 biomarkers in patients with idiopathic thrombotic thrombocytopenic purpura. Am J Hematol 2008;83:911-915.
    • (2008) Am J Hematol , vol.83 , pp. 911-915
    • Cataland, S.R.1    Jin, M.2    Lin, S.3
  • 107
    • 0041665105 scopus 로고    scopus 로고
    • Role of splenectomy in patients with refractory or relapsed thrombotic thrombocytopenic purpura
    • Aqui NA, Stein SH, Konkle BA, Abrams CS, Strobl FJ. Role of splenectomy in patients with refractory or relapsed thrombotic thrombocytopenic purpura. J Clin Apheresis 2003;18:51-54.
    • (2003) J Clin Apheresis , vol.18 , pp. 51-54
    • Aqui, N.A.1    Stein, S.H.2    Konkle, B.A.3    Abrams, C.S.4    Strobl, F.J.5
  • 108
    • 79551536840 scopus 로고    scopus 로고
    • N-acetylcysteine reduces the size and activity of von Willebrand factor in human plasma and mice
    • Chen J, Reheman A, Gushiken FC, et al. N-acetylcysteine reduces the size and activity of von Willebrand factor in human plasma and mice. J Clin Invest 2011;121:593-603.
    • (2011) J Clin Invest , vol.121 , pp. 593-603
    • Chen, J.1    Reheman, A.2    Gushiken, F.C.3
  • 109
    • 78649677591 scopus 로고    scopus 로고
    • Targeting von Willebrand factor and platelet glycoprotein Ib receptor
    • Firbas C, Siller-Matula JM, Jilma B. Targeting von Willebrand factor and platelet glycoprotein Ib receptor. Expert Rev Cardiovasc Ther 2010;8: 1689-1701.
    • (2010) Expert Rev Cardiovasc Ther , vol.8 , pp. 1689-1701
    • Firbas, C.1    Siller-Matula, J.M.2    Jilma, B.3
  • 110
    • 0001478161 scopus 로고
    • Hamolytisch-uramische syndrome: Bilaterale Nierenrindennekrosen bei akutenerworbenen hamolytischen anamien
    • Gasser C, Gautier E, Steck A, et al. Hamolytisch-uramische syndrome: Bilaterale Nierenrindennekrosen bei akutenerworbenen hamolytischen anamien. Schweiz Med Woch 1955;85:905-909.
    • (1955) Schweiz Med Woch , vol.85 , pp. 905-909
    • Gasser, C.1    Gautier, E.2    Steck, A.3
  • 111
    • 15244348050 scopus 로고    scopus 로고
    • Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome
    • Tarr PI, Gordon CA, Chandler WL. Shiga-toxin-producing Escherichia coli and haemolytic uraemic syndrome. Lancet 2005;365:1073-1086.
    • (2005) Lancet , vol.365 , pp. 1073-1086
    • Tarr, P.I.1    Gordon, C.A.2    Chandler, W.L.3
  • 112
    • 80052150179 scopus 로고    scopus 로고
    • Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in Germany
    • Rasko DA, Webster DR, Sahl JW, et al. Origins of the E. coli strain causing an outbreak of hemolytic-uremic syndrome in Germany. N Engl J Med 2011;365:709-717.
    • (2011) N Engl J Med , vol.365 , pp. 709-717
    • Rasko, D.A.1    Webster, D.R.2    Sahl, J.W.3
  • 113
    • 84856266240 scopus 로고    scopus 로고
    • Outbreak of haemolytic uraemic syndrome due to Shiga toxin-producing Escherichia coli O104:H4 among French tourists returning from Turkey, September 2011
    • Jourdan-da SN, Watrin M, Weill FX, et al. Outbreak of haemolytic uraemic syndrome due to Shiga toxin-producing Escherichia coli O104:H4 among French tourists returning from Turkey, September 2011. Euro Surveill 2012;17:pii=20065.
    • (2012) Euro Surveill , vol.17 , pp. 20065
    • Jourdan-da, S.N.1    Watrin, M.2    Weill, F.X.3
  • 114
    • 84861029084 scopus 로고    scopus 로고
    • Outbreak of Shiga toxin-producing Escherichia coli O104:H4 associated with organic fenugreek sprouts, France, June 2011
    • King LA, Nogareda F, Weill FX, et al. Outbreak of Shiga toxin-producing Escherichia coli O104:H4 associated with organic fenugreek sprouts, France, June 2011. Clin Infect Dis 2012;54:1588-1594.
    • (2012) Clin Infect Dis , vol.54 , pp. 1588-1594
    • King, L.A.1    Nogareda, F.2    Weill, F.X.3
  • 115
    • 80955168000 scopus 로고    scopus 로고
    • Epidemic profile of Shiga-toxinproducing Escherichia coli O104:H4 outbreak in Germany
    • Frank C, Werber D, Cramer JP, et al. Epidemic profile of Shiga-toxinproducing Escherichia coli O104:H4 outbreak in Germany. N Engl J Med 2011;365:1771-1780.
    • (2011) N Engl J Med , vol.365 , pp. 1771-1780
    • Frank, C.1    Werber, D.2    Cramer, J.P.3
  • 116
  • 117
    • 0002394738 scopus 로고
    • Pathology of the hemolytic uremic syndrome
    • Kaplan B, Trompeter R, Moake J, eds. New York: Marcel Dekker
    • Habib R. Pathology of the hemolytic uremic syndrome. In: Kaplan B, Trompeter R, Moake J, eds. Hemolytic uremic syndrome and thrombotic thrombocytopenic purpura. New York: Marcel Dekker, 1992:315-353.
    • (1992) Hemolytic uremic syndrome and thrombotic thrombocytopenic purpura , pp. 315-353
    • Habib, R.1
  • 118
    • 0030766460 scopus 로고    scopus 로고
    • Renal histopathology in fatal cases of diarrhoea-associated haemolytic uraemic syndrome. British Association for Paediatric Nephrology
    • Inward CD, Howie AJ, Fitzpatrick MM, et al. Renal histopathology in fatal cases of diarrhoea-associated haemolytic uraemic syndrome. British Association for Paediatric Nephrology. Pediatr Nephrol 1997;11:556-559.
    • (1997) Pediatr Nephrol , vol.11 , pp. 556-559
    • Inward, C.D.1    Howie, A.J.2    Fitzpatrick, M.M.3
  • 119
    • 0023801292 scopus 로고
    • Direct cytotoxic action of Shiga toxin on human vascular endothelial cells
    • Obrig TG, Del Vecchio PJ, Brown JE, et al. Direct cytotoxic action of Shiga toxin on human vascular endothelial cells. Infect Immun 1988;56: 2373-2378.
    • (1988) Infect Immun , vol.56 , pp. 2373-2378
    • Obrig, T.G.1    Del Vecchio, P.J.2    Brown, J.E.3
  • 120
    • 0027169708 scopus 로고
    • Shiga toxin-associated hemolytic uremic syndrome: Interleukin-1 beta enhancement of Shiga toxin cytotoxicity toward human vascular endothelial cells in vitro
    • Kaye SA, Louise CB, Boyd B, Lingwood CA, Obrig TG. Shiga toxin-associated hemolytic uremic syndrome: interleukin-1 beta enhancement of Shiga toxin cytotoxicity toward human vascular endothelial cells in vitro. Infect Immun 1993;61:3886-3891.
    • (1993) Infect Immun , vol.61 , pp. 3886-3891
    • Kaye, S.A.1    Louise, C.B.2    Boyd, B.3    Lingwood, C.A.4    Obrig, T.G.5
  • 121
    • 0025946126 scopus 로고
    • Shiga toxin-associated hemolytic-uremic syndrome: Combined cytotoxic effects of Shiga toxin, interleukin-1 beta, and tumor necrosis factor alpha on human vascular endothelial cells in vitro
    • Louise CB, Obrig TG. Shiga toxin-associated hemolytic-uremic syndrome: combined cytotoxic effects of Shiga toxin, interleukin-1 beta, and tumor necrosis factor alpha on human vascular endothelial cells in vitro. Infect Immun 1991;59:4173-4179.
    • (1991) Infect Immun , vol.59 , pp. 4173-4179
    • Louise, C.B.1    Obrig, T.G.2
  • 122
    • 79960435714 scopus 로고    scopus 로고
    • Alternative pathway activation of complement by Shiga toxin promotes exuberant C3a formation that triggers microvascular thrombosis
    • Morigi M, Galbusera M, Gastoldi S, et al. Alternative pathway activation of complement by Shiga toxin promotes exuberant C3a formation that triggers microvascular thrombosis. J Immunol 2011;187:172-180.
    • (2011) J Immunol , vol.187 , pp. 172-180
    • Morigi, M.1    Galbusera, M.2    Gastoldi, S.3
  • 123
    • 0035885951 scopus 로고    scopus 로고
    • Verotoxin-1-induced up-regulation of adhesive molecules renders microvascular endothelial cells thrombogenic at high shear stress
    • Morigi M, Galbusera M, Binda E, et al. Verotoxin-1-induced up-regulation of adhesive molecules renders microvascular endothelial cells thrombogenic at high shear stress. Blood 2001;98:1828-1835.
    • (2001) Blood , vol.98 , pp. 1828-1835
    • Morigi, M.1    Galbusera, M.2    Binda, E.3
  • 124
    • 77957272189 scopus 로고    scopus 로고
    • Shiga toxin-associated hemolytic uremic syndrome: Pathophysiology of endothelial dysfunction
    • Zoja C, Buelli S, Morigi M. Shiga toxin-associated hemolytic uremic syndrome: pathophysiology of endothelial dysfunction. Pediatr Nephrol 2010;25:2231-2240.
    • (2010) Pediatr Nephrol , vol.25 , pp. 2231-2240
    • Zoja, C.1    Buelli, S.2    Morigi, M.3
  • 125
    • 70350693665 scopus 로고    scopus 로고
    • Shiga toxin activates complement and binds factor H: Evidence for an active role of complement in hemolytic uremic syndrome
    • Orth D, Khan AB, Naim A, et al. Shiga toxin activates complement and binds factor H: evidence for an active role of complement in hemolytic uremic syndrome. J Immunol 2009;182:6394-6400.
    • (2009) J Immunol , vol.182 , pp. 6394-6400
    • Orth, D.1    Khan, A.B.2    Naim, A.3
  • 126
    • 77955786950 scopus 로고    scopus 로고
    • Different classes of antibiotics differentially influence shiga toxin production
    • McGannon CM, Fuller CA, Weiss AA. Different classes of antibiotics differentially influence shiga toxin production. Antimicrob Agents Chemother 2010;54:3790-3798.
    • (2010) Antimicrob Agents Chemother , vol.54 , pp. 3790-3798
    • McGannon, C.M.1    Fuller, C.A.2    Weiss, A.A.3
  • 128
    • 0028172823 scopus 로고
    • Escherichia coli O 157:H7-associated hemolytic-uremic syndrome after ingestion of contaminated hamburgers
    • Brandt JR, Fouser LS, Watkins SL, et al. Escherichia coli O 157:H7-associated hemolytic-uremic syndrome after ingestion of contaminated hamburgers. J Pediatr 1994;125:519-526.
    • (1994) J Pediatr , vol.125 , pp. 519-526
    • Brandt, J.R.1    Fouser, L.S.2    Watkins, S.L.3
  • 129
    • 0023617473 scopus 로고
    • A severe outbreak of Escherichia coli O157:H7--associated hemorrhagic colitis in a nursing home
    • Carter AO, Borczyk AA, Carlson JA, et al. A severe outbreak of Escherichia coli O157:H7--associated hemorrhagic colitis in a nursing home. N Engl J Med 1987;317:1496-1500.
    • (1987) N Engl J Med , vol.317 , pp. 1496-1500
    • Carter, A.O.1    Borczyk, A.A.2    Carlson, J.A.3
  • 130
    • 0037012136 scopus 로고    scopus 로고
    • Prothrombotic coagulation abnormalities preceding the hemolytic-uremic syndrome
    • Chandler WL, Jelacic S, Boster DR, et al. Prothrombotic coagulation abnormalities preceding the hemolytic-uremic syndrome. N Engl J Med 2002;346:23-32.
    • (2002) N Engl J Med , vol.346 , pp. 23-32
    • Chandler, W.L.1    Jelacic, S.2    Boster, D.R.3
  • 131
    • 0028889067 scopus 로고
    • Lessons learned in the management of hemolytic uremic syndrome in children
    • Tapper D, Tarr P, Avner E, Brandt J, Waldhausen J. Lessons learned in the management of hemolytic uremic syndrome in children. J Pediatr Surg 1995;30:158-163.
    • (1995) J Pediatr Surg , vol.30 , pp. 158-163
    • Tapper, D.1    Tarr, P.2    Avner, E.3    Brandt, J.4    Waldhausen, J.5
  • 132
    • 5744228953 scopus 로고    scopus 로고
    • CT and MRI in haemolytic uraemic syndrome with central nervous system involvement: Distribution of lesions and prognostic value of imaging findings
    • Steinborn M, Leiz S, Rudisser K, et al. CT and MRI in haemolytic uraemic syndrome with central nervous system involvement: distribution of lesions and prognostic value of imaging findings. Pediatr Radiol 2004;34:805-810.
    • (2004) Pediatr Radiol , vol.34 , pp. 805-810
    • Steinborn, M.1    Leiz, S.2    Rudisser, K.3
  • 133
    • 70350041489 scopus 로고    scopus 로고
    • Recommendations for diagnosis of shiga toxin--producing Escherichia coli infections by clinical laboratories
    • Gould LH, Bopp C, Strockbine N, et al. Recommendations for diagnosis of shiga toxin--producing Escherichia coli infections by clinical laboratories. MMWR Recomm Rep 2009;58:1-14.
    • (2009) MMWR Recomm Rep , vol.58 , pp. 1-14
    • Gould, L.H.1    Bopp, C.2    Strockbine, N.3
  • 134
    • 0023689035 scopus 로고
    • Treatment of the childhood haemolytic uraemic syndrome with plasma. A multicentre randomized controlled trial. The French Society of Paediatric Nephrology
    • Loirat C, Sonsino E, Hinglais N, et al. Treatment of the childhood haemolytic uraemic syndrome with plasma. A multicentre randomized controlled trial. The French Society of Paediatric Nephrology. Pediatr Nephrol 1988;2: 279-285.
    • (1988) Pediatr Nephrol , vol.2 , pp. 279-285
    • Loirat, C.1    Sonsino, E.2    Hinglais, N.3
  • 135
    • 0033576164 scopus 로고    scopus 로고
    • Effectiveness of therapeutic plasma exchange in the 1996 Lanarkshire Escherichia coli O157:H7 outbreak
    • Dundas S, Murphy J, Soutar RL, et al. Effectiveness of therapeutic plasma exchange in the 1996 Lanarkshire Escherichia coli O157:H7 outbreak. Lancet 1999;354:1327-1330.
    • (1999) Lancet , vol.354 , pp. 1327-1330
    • Dundas, S.1    Murphy, J.2    Soutar, R.L.3
  • 136
  • 137
    • 84861128113 scopus 로고    scopus 로고
    • Effects of antibiotics on Shiga toxin 2 production and bacteriophage induction by epidemic Escherichia coli O104:H4 strain
    • Bielaszewska M, Idelevich EA, Zhang W, et al. Effects of antibiotics on Shiga toxin 2 production and bacteriophage induction by epidemic Escherichia coli O104:H4 strain. Antimicrob Agents Chemother 2012;56:3277-3282.
    • (2012) Antimicrob Agents Chemother , vol.56 , pp. 3277-3282
    • Bielaszewska, M.1    Idelevich, E.A.2    Zhang, W.3
  • 138
    • 84864408776 scopus 로고    scopus 로고
    • Therapeutic concentrations of antibiotics inhibit Shiga toxin release from enterohemorrhagic E. coli O104:H4 from the 2011 German outbreak
    • Corogeanu D, Willmes R, Wolke M, et al. Therapeutic concentrations of antibiotics inhibit Shiga toxin release from enterohemorrhagic E. coli O104:H4 from the 2011 German outbreak. BMC Microbiol 2012;12:160.
    • (2012) BMC Microbiol , vol.12 , pp. 160
    • Corogeanu, D.1    Willmes, R.2    Wolke, M.3
  • 139
    • 0034729744 scopus 로고    scopus 로고
    • The risk of the hemolytic-uremic syndrome after antibiotic treatment of Escherichia coli O157:H7 infections
    • Wong CS, Jelacic S, Habeeb RL, Watkins SL, Tarr PI. The risk of the hemolytic-uremic syndrome after antibiotic treatment of Escherichia coli O157:H7 infections. N Engl J Med 2000;342:1930-1936.
    • (2000) N Engl J Med , vol.342 , pp. 1930-1936
    • Wong, C.S.1    Jelacic, S.2    Habeeb, R.L.3    Watkins, S.L.4    Tarr, P.I.5
  • 140
    • 0041411081 scopus 로고    scopus 로고
    • Long-term renal prognosis of diarrhea-associated hemolytic uremic syndrome: A systematic review, metaanalysis, and meta-regression
    • Garg AX, Suri RS, Barrowman N, et al. Long-term renal prognosis of diarrhea-associated hemolytic uremic syndrome: a systematic review, metaanalysis, and meta-regression. JAMA 2003;290:1360-1370.
    • (2003) JAMA , vol.290 , pp. 1360-1370
    • Garg, A.X.1    Suri, R.S.2    Barrowman, N.3
  • 142
    • 61949191989 scopus 로고    scopus 로고
    • Post-infectious irritable bowel syndrome following water contamination
    • Marshall JK. Post-infectious irritable bowel syndrome following water contamination. Kidney Int Suppl 2009;S42-S43.
    • (2009) Kidney Int Suppl , pp. S42-S43
    • Marshall, J.K.1
  • 143
    • 63049120489 scopus 로고    scopus 로고
    • Risk of pregnancy-related hypertension within five years of exposure to bacteria-contaminated drinking water
    • Moist LM, Sontrop JM, Garg AX, et al. Risk of pregnancy-related hypertension within five years of exposure to bacteria-contaminated drinking water. Kidney Int Suppl 2009;S47-S49.
    • (2009) Kidney Int Suppl , pp. S47-S49
    • Moist, L.M.1    Sontrop, J.M.2    Garg, A.X.3
  • 144
    • 77958587405 scopus 로고    scopus 로고
    • Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
    • Noris M, Caprioli J, Bresin E, et al. Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clin J Am Soc Nephrol 2010;5:1844-1859.
    • (2010) Clin J Am Soc Nephrol , vol.5 , pp. 1844-1859
    • Noris, M.1    Caprioli, J.2    Bresin, E.3
  • 145
    • 77952556624 scopus 로고    scopus 로고
    • Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations
    • Fakhouri F, Roumenina L, Provot F, et al. Pregnancy-associated hemolytic uremic syndrome revisited in the era of complement gene mutations. J Am Soc Nephrol 2010;21:859-867.
    • (2010) J Am Soc Nephrol , vol.21 , pp. 859-867
    • Fakhouri, F.1    Roumenina, L.2    Provot, F.3
  • 146
    • 1842738527 scopus 로고    scopus 로고
    • Clinico-pathological findings in diarrhoea-negative haemolytic uraemic syndrome
    • Taylor CM, Chua C, Howie AJ, Risdon RA. Clinico-pathological findings in diarrhoea-negative haemolytic uraemic syndrome. Pediatr Nephrol 2004;19:419-425.
    • (2004) Pediatr Nephrol , vol.19 , pp. 419-425
    • Taylor, C.M.1    Chua, C.2    Howie, A.J.3    Risdon, R.A.4
  • 147
    • 77957577058 scopus 로고    scopus 로고
    • Atypical hemolytic uremic syndrome associated with mutations in complement regulator genes
    • Le QM, Roumenina L, Noris M, Fremeaux-Bacchi V. Atypical hemolytic uremic syndrome associated with mutations in complement regulator genes. Semin Thromb Hemost 2010;36:641-652.
    • (2010) Semin Thromb Hemost , vol.36 , pp. 641-652
    • Le, Q.M.1    Roumenina, L.2    Noris, M.3    Fremeaux-Bacchi, V.4
  • 148
    • 77952682366 scopus 로고    scopus 로고
    • Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome
    • Maga TK, Nishimura CJ, Weaver AE, Frees KL, Smith RJ. Mutations in alternative pathway complement proteins in American patients with atypical hemolytic uremic syndrome. Hum Mutat 2010;31:E1445-E1460.
    • (2010) Hum Mutat , vol.31 , pp. E1445-E1460
    • Maga, T.K.1    Nishimura, C.J.2    Weaver, A.E.3    Frees, K.L.4    Smith, R.J.5
  • 149
    • 78649863686 scopus 로고    scopus 로고
    • Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome
    • Dragon-Durey MA, Sethi SK, Bagga A, et al. Clinical features of anti-factor H autoantibody-associated hemolytic uremic syndrome. J Am Soc Nephrol 2010;21:2180-2187.
    • (2010) J Am Soc Nephrol , vol.21 , pp. 2180-2187
    • Dragon-Durey, M.A.1    Sethi, S.K.2    Bagga, A.3
  • 150
    • 75649133611 scopus 로고    scopus 로고
    • Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome
    • Moore I, Strain L, Pappworth I, et al. Association of factor H autoantibodies with deletions of CFHR1, CFHR3, CFHR4, and with mutations in CFH, CFI, CD46, and C3 in patients with atypical hemolytic uremic syndrome. Blood 2010;115:379-387.
    • (2010) Blood , vol.115 , pp. 379-387
    • Moore, I.1    Strain, L.2    Pappworth, I.3
  • 151
    • 33644964155 scopus 로고    scopus 로고
    • Insights into hemolytic uremic syndrome: Segregation of three independent predisposition factors in a large, multiple affected pedigree
    • Esparza-Gordillo J, Jorge EG, Garrido CA, et al. Insights into hemolytic uremic syndrome: segregation of three independent predisposition factors in a large, multiple affected pedigree. Mol Immunol 2006;43:1769-1775.
    • (2006) Mol Immunol , vol.43 , pp. 1769-1775
    • Esparza-Gordillo, J.1    Jorge, E.G.2    Garrido, C.A.3
  • 152
    • 84655168091 scopus 로고    scopus 로고
    • Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS
    • Ermini L, Goodship TH, Strain L, et al. Common genetic variants in complement genes other than CFH, CD46 and the CFHRs are not associated with aHUS. Mol Immunol 2012;49:640-648.
    • (2012) Mol Immunol , vol.49 , pp. 640-648
    • Ermini, L.1    Goodship, T.H.2    Strain, L.3
  • 153
    • 79957691055 scopus 로고    scopus 로고
    • Common polymorphisms in C3, factor B, and factor H collaborate to determine systemic complement activity and disease risk
    • Heurich M, Martinez-Barricarte R, Francis NJ, et al. Common polymorphisms in C3, factor B, and factor H collaborate to determine systemic complement activity and disease risk. Proc Natl Acad Sci U S A 2011;108:8761-8766.
    • (2011) Proc Natl Acad Sci U S A , vol.108 , pp. 8761-8766
    • Heurich, M.1    Martinez-Barricarte, R.2    Francis, N.J.3
  • 154
    • 34047200899 scopus 로고    scopus 로고
    • Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome
    • Zipfel PF, Edey M, Heinen S, et al. Deletion of complement factor H-related genes CFHR1 and CFHR3 is associated with atypical hemolytic uremic syndrome. PLoS Genet 2007;3:e41.
    • (2007) PLoS Genet , vol.3 , pp. e41
    • Zipfel, P.F.1    Edey, M.2    Heinen, S.3
  • 155
    • 38949155911 scopus 로고    scopus 로고
    • Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency
    • Jozsi M, Licht C, Strobel S, et al. Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/CFHR3 deficiency. Blood 2008;111:1512-1514.
    • (2008) Blood , vol.111 , pp. 1512-1514
    • Jozsi, M.1    Licht, C.2    Strobel, S.3
  • 156
    • 67650508077 scopus 로고    scopus 로고
    • The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome
    • Dragon-Durey MA, Blanc C, Marliot F, et al. The high frequency of complement factor H related CFHR1 gene deletion is restricted to specific subgroups of patients with atypical haemolytic uraemic syndrome. J Med Genet 2009;46:447-450.
    • (2009) J Med Genet , vol.46 , pp. 447-450
    • Dragon-Durey, M.A.1    Blanc, C.2    Marliot, F.3
  • 157
    • 75749153964 scopus 로고    scopus 로고
    • Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome
    • Bienaime F, Dragon-Durey MA, Regnier CH, et al. Mutations in components of complement influence the outcome of Factor I-associated atypical hemolytic uremic syndrome. Kidney Int 2010;77:339-349.
    • (2010) Kidney Int , vol.77 , pp. 339-349
    • Bienaime, F.1    Dragon-Durey, M.A.2    Regnier, C.H.3
  • 158
    • 80052272216 scopus 로고    scopus 로고
    • Factor H-related protein 1 neutralizes anti-factor H autoantibodies in autoimmune hemolytic uremic syndrome
    • Strobel S, Abarrategui-Garrido C, Fariza-Requejo E, et al. Factor H-related protein 1 neutralizes anti-factor H autoantibodies in autoimmune hemolytic uremic syndrome. Kidney Int 2011;80:397-404.
    • (2011) Kidney Int , vol.80 , pp. 397-404
    • Strobel, S.1    Abarrategui-Garrido, C.2    Fariza-Requejo, E.3
  • 159
    • 1542318912 scopus 로고    scopus 로고
    • Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: Report and genetic analysis of 16 cases
    • Dragon-Durey MA, Fremeaux-Bacchi V, Loirat C, et al. Heterozygous and homozygous factor H deficiencies associated with hemolytic uremic syndrome or membranoproliferative glomerulonephritis: report and genetic analysis of 16 cases. J Am Soc Nephrol 2004;15:787-795.
    • (2004) J Am Soc Nephrol , vol.15 , pp. 787-795
    • Dragon-Durey, M.A.1    Fremeaux-Bacchi, V.2    Loirat, C.3
  • 160
    • 33745697887 scopus 로고    scopus 로고
    • Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II)
    • Licht C, Heinen S, Jozsi M, et al. Deletion of Lys224 in regulatory domain 4 of Factor H reveals a novel pathomechanism for dense deposit disease (MPGN II). Kidney Int 2006;70:42-50.
    • (2006) Kidney Int , vol.70 , pp. 42-50
    • Licht, C.1    Heinen, S.2    Jozsi, M.3
  • 161
    • 84863115476 scopus 로고    scopus 로고
    • Causes of alternative pathway dysregulation in dense deposit disease
    • Zhang Y, Meyer NC, Wang K, et al. Causes of alternative pathway dysregulation in dense deposit disease. Clin J Am Soc Nephrol 2012;7:265-274.
    • (2012) Clin J Am Soc Nephrol , vol.7 , pp. 265-274
    • Zhang, Y.1    Meyer, N.C.2    Wang, K.3
  • 162
    • 84857113842 scopus 로고    scopus 로고
    • Membranoproliferative glomerulonephritis and C3 glomerulopathy: Resolving the confusion
    • Sethi S, Nester CM, Smith RJ. Membranoproliferative glomerulonephritis and C3 glomerulopathy: resolving the confusion. Kidney Int 2012;81:434-441.
    • (2012) Kidney Int , vol.81 , pp. 434-441
    • Sethi, S.1    Nester, C.M.2    Smith, R.J.3
  • 164
    • 0346656641 scopus 로고    scopus 로고
    • Familial mesangiocapillary glomerulonephritis with initial presentation as haemolytic uraemic syndrome
    • Cooper M, McGraw ME, Unsworth DJ, Mathieson P. Familial mesangiocapillary glomerulonephritis with initial presentation as haemolytic uraemic syndrome. Nephrol Dial Transplant 2004;19:230-233.
    • (2004) Nephrol Dial Transplant , vol.19 , pp. 230-233
    • Cooper, M.1    McGraw, M.E.2    Unsworth, D.J.3    Mathieson, P.4
  • 165
    • 84863716162 scopus 로고    scopus 로고
    • Genetic insights into age-related macular degeneration: Controversies addressing risk, causality, and therapeutics
    • Gorin MB. Genetic insights into age-related macular degeneration: controversies addressing risk, causality, and therapeutics. Mol Aspects Med 2012;33:467-486.
    • (2012) Mol Aspects Med , vol.33 , pp. 467-486
    • Gorin, M.B.1
  • 166
    • 84863338297 scopus 로고    scopus 로고
    • Complement factor H genetic variant and age-related macular degeneration: Effect size, modifiers and relationship to disease subtype
    • Sofat R, Casas JP, Webster AR, et al. Complement factor H genetic variant and age-related macular degeneration: effect size, modifiers and relationship to disease subtype. Int J Epidemiol 2012;41:250-262.
    • (2012) Int J Epidemiol , vol.41 , pp. 250-262
    • Sofat, R.1    Casas, J.P.2    Webster, A.R.3
  • 167
    • 84857802385 scopus 로고    scopus 로고
    • Relevance of complement factor H-related 1 (CFHR1) genotypes in age-related macular degeneration
    • Martinez-Barricarte R, Recalde S, Fernandez-Robredo P, et al. Relevance of complement factor H-related 1 (CFHR1) genotypes in age-related macular degeneration. Invest Ophthalmol Vis Sci 2012;53:1087-1094.
    • (2012) Invest Ophthalmol Vis Sci , vol.53 , pp. 1087-1094
    • Martinez-Barricarte, R.1    Recalde, S.2    Fernandez-Robredo, P.3
  • 168
    • 0028214132 scopus 로고
    • Hereditary complement factor I deficiency
    • Vyse TJ, Spath PJ, Davies KA, et al. Hereditary complement factor I deficiency. QJM 1994;87:385-401.
    • (1994) QJM , vol.87 , pp. 385-401
    • Vyse, T.J.1    Spath, P.J.2    Davies, K.A.3
  • 169
    • 35748972967 scopus 로고    scopus 로고
    • Recent advances in the diagnosis, monitoring, and management of patients with paroxysmal nocturnal hemoglobinuria
    • Richards SJ, Hill A, Hillmen P. Recent advances in the diagnosis, monitoring, and management of patients with paroxysmal nocturnal hemoglobinuria. Cytometry B Clin Cytom 2007;72:291-298.
    • (2007) Cytometry B Clin Cytom , vol.72 , pp. 291-298
    • Richards, S.J.1    Hill, A.2    Hillmen, P.3
  • 170
    • 84873637642 scopus 로고    scopus 로고
    • A phase II study of eculizumab in patients with atypical hemolytic uremic syndrome receiving chronic plasma exchange/infusion
    • Loirat C, Muus P, Legendre C, et al. A phase II study of eculizumab in patients with atypical hemolytic uremic syndrome receiving chronic plasma exchange/infusion. Haematologica 2011;96:S2-S0980.
    • (2011) Haematologica , vol.96 , pp. S2-S0980
    • Loirat, C.1    Muus, P.2    Legendre, C.3
  • 171
    • 77950857026 scopus 로고    scopus 로고
    • The management of pregnancy in paroxysmal nocturnal haemoglobinuria on long term eculizumab
    • Kelly R, Arnold L, Richards S, et al. The management of pregnancy in paroxysmal nocturnal haemoglobinuria on long term eculizumab. Br J Haematol 2010;149:446-450.
    • (2010) Br J Haematol , vol.149 , pp. 446-450
    • Kelly, R.1    Arnold, L.2    Richards, S.3
  • 172
    • 77956320935 scopus 로고    scopus 로고
    • Pregnancy in PNH: Another eculizumab baby
    • Marasca R, Coluccio V, Santachiara R, et al. Pregnancy in PNH: another eculizumab baby. Br J Haematol 2010;150:707-708.
    • (2010) Br J Haematol , vol.150 , pp. 707-708
    • Marasca, R.1    Coluccio, V.2    Santachiara, R.3
  • 173
    • 80052473232 scopus 로고    scopus 로고
    • Prophylactic eculizumab prior to kidney transplantation for atypical hemolytic uremic syndrome
    • Weitz M, Amon O, Bassler D, Koenigsrainer A, Nadalin S. Prophylactic eculizumab prior to kidney transplantation for atypical hemolytic uremic syndrome. Pediatr Nephrol 2011;26:1325-1329.
    • (2011) Pediatr Nephrol , vol.26 , pp. 1325-1329
    • Weitz, M.1    Amon, O.2    Bassler, D.3    Koenigsrainer, A.4    Nadalin, S.5
  • 174
    • 79958202220 scopus 로고    scopus 로고
    • Pre-emptive eculizumab and plasmapheresis for renal transplant in atypical hemolytic uremic syndrome
    • Nester C, Stewart Z, Myers D, et al. Pre-emptive eculizumab and plasmapheresis for renal transplant in atypical hemolytic uremic syndrome. Clin J Am Soc Nephrol 2011;6:1488-1494.
    • (2011) Clin J Am Soc Nephrol , vol.6 , pp. 1488-1494
    • Nester, C.1    Stewart, Z.2    Myers, D.3
  • 175
    • 0015876763 scopus 로고
    • Intravascular haemolysis and thrombocytopenia in left ventricular outflow obstruction
    • Jacobson RJ, Rath CE, Perloff JK. Intravascular haemolysis and thrombocytopenia in left ventricular outflow obstruction. Br Heart J 1973;35: 849-854.
    • (1973) Br Heart J , vol.35 , pp. 849-854
    • Jacobson, R.J.1    Rath, C.E.2    Perloff, J.K.3
  • 176
    • 0028376072 scopus 로고
    • Renal vascular complications of systemic lupus erythematosus
    • Appel GB, Pirani CL, D'Agati V. Renal vascular complications of systemic lupus erythematosus. J Am Soc Nephrol 1994;4:1499-1515.
    • (1994) J Am Soc Nephrol , vol.4 , pp. 1499-1515
    • Appel, G.B.1    Pirani, C.L.2    D'Agati, V.3
  • 177
    • 0019314001 scopus 로고
    • Thrombocytopenia associated with SwanGanz catheterization in patients
    • Kim YL, Richman KA, Marshall BE. Thrombocytopenia associated with SwanGanz catheterization in patients. Anesthesiology 1980;53:261-262.
    • (1980) Anesthesiology , vol.53 , pp. 261-262
    • Kim, Y.L.1    Richman, K.A.2    Marshall, B.E.3
  • 178
    • 0032126712 scopus 로고    scopus 로고
    • Association of thrombocytopenia with the use of intra-aortic balloon pumps
    • Vonderheide RH, Thadhani R, Kuter DJ. Association of thrombocytopenia with the use of intra-aortic balloon pumps. Am J Med 1998;105:27-32.
    • (1998) Am J Med , vol.105 , pp. 27-32
    • Vonderheide, R.H.1    Thadhani, R.2    Kuter, D.J.3
  • 180
    • 66349088505 scopus 로고    scopus 로고
    • An assessment of cardiopulmonary bypass-induced changes in platelet function using whole blood and classical light transmission aggregometry: The results of a pilot study
    • Velik-Salchner C, Maier S, Innerhofer P, et al. An assessment of cardiopulmonary bypass-induced changes in platelet function using whole blood and classical light transmission aggregometry: the results of a pilot study. Anesth Analg 2009;108:1747-1754.
    • (2009) Anesth Analg , vol.108 , pp. 1747-1754
    • Velik-Salchner, C.1    Maier, S.2    Innerhofer, P.3
  • 181
    • 0022415630 scopus 로고
    • Hemostasis defects associated with cardiac surgery, prosthetic devices, and other extracorporeal circuits
    • Bick RL. Hemostasis defects associated with cardiac surgery, prosthetic devices, and other extracorporeal circuits. Semin Thromb Hemost 1985;11:249-280.
    • (1985) Semin Thromb Hemost , vol.11 , pp. 249-280
    • Bick, R.L.1
  • 182
    • 0026385873 scopus 로고
    • Modulation of platelet surface adhesion receptors during cardiopulmonary bypass
    • Rinder CS, Mathew JP, Rinder HM, et al. Modulation of platelet surface adhesion receptors during cardiopulmonary bypass. Anesthesiology 1991;75: 563-570.
    • (1991) Anesthesiology , vol.75 , pp. 563-570
    • Rinder, C.S.1    Mathew, J.P.2    Rinder, H.M.3
  • 184
    • 0032818162 scopus 로고    scopus 로고
    • Anticoagulation and anticoagulation reversal with cardiac surgery involving cardiopulmonary bypass: An update
    • Despotis GJ, Joist JH. Anticoagulation and anticoagulation reversal with cardiac surgery involving cardiopulmonary bypass: an update. J Cardiothorac Vasc Anesth 1999;13:18-29.
    • (1999) J Cardiothorac Vasc Anesth , vol.13 , pp. 18-29
    • Despotis, G.J.1    Joist, J.H.2
  • 185
    • 33750432178 scopus 로고    scopus 로고
    • Biocompatibility of heparin-coated cardiopulmonary bypass circuits in coronary patients with left ventricular dysfunction is superior to PMEA-coated circuits
    • Kutay V, Noyan T, Ozcan S, et al. Biocompatibility of heparin-coated cardiopulmonary bypass circuits in coronary patients with left ventricular dysfunction is superior to PMEA-coated circuits. J Card Surg 2006;21:572-577.
    • (2006) J Card Surg , vol.21 , pp. 572-577
    • Kutay, V.1    Noyan, T.2    Ozcan, S.3
  • 186
    • 33846346165 scopus 로고    scopus 로고
    • Minimally invasive closed circuit versus standard extracorporeal circulation for aortic valve replacement
    • Castiglioni A, Verzini A, Pappalardo F, et al. Minimally invasive closed circuit versus standard extracorporeal circulation for aortic valve replacement. Ann Thorac Surg 2007;83:586-591.
    • (2007) Ann Thorac Surg , vol.83 , pp. 586-591
    • Castiglioni, A.1    Verzini, A.2    Pappalardo, F.3
  • 187
    • 33846946851 scopus 로고    scopus 로고
    • Relatively increased von Willebrand factor activity after off-pump coronary artery bypass graft surgery
    • Lo B, Nierich AP, Kalkman CJ, Fijnheer R. Relatively increased von Willebrand factor activity after off-pump coronary artery bypass graft surgery. Thromb Haemost 2007;97:21-26.
    • (2007) Thromb Haemost , vol.97 , pp. 21-26
    • Lo, B.1    Nierich, A.P.2    Kalkman, C.J.3    Fijnheer, R.4
  • 188
    • 20444388310 scopus 로고    scopus 로고
    • Assessment of hemostatic activation during cardiopulmonary bypass for coronary artery bypass grafting with bivalirudin: Results of a pilot study
    • Koster A, Yeter R, Buz S, et al. Assessment of hemostatic activation during cardiopulmonary bypass for coronary artery bypass grafting with bivalirudin: results of a pilot study. J Thorac Cardiovasc Surg 2005;129: 1391-1394.
    • (2005) J Thorac Cardiovasc Surg , vol.129 , pp. 1391-1394
    • Koster, A.1    Yeter, R.2    Buz, S.3
  • 189
    • 0033542876 scopus 로고    scopus 로고
    • Use of point-of-care test in identification of patients who can benefit from desmopressin during cardiac surgery: A randomised controlled trial
    • Despotis GJ, Levine V, Saleem R, Spitznagel E, Joist JH. Use of point-of-care test in identification of patients who can benefit from desmopressin during cardiac surgery: a randomised controlled trial. Lancet 1999;354:106-110.
    • (1999) Lancet , vol.354 , pp. 106-110
    • Despotis, G.J.1    Levine, V.2    Saleem, R.3    Spitznagel, E.4    Joist, J.H.5
  • 190
    • 0033524140 scopus 로고    scopus 로고
    • Pharmacological strategies to decrease excessive blood loss in cardiac surgery: A meta-analysis of clinically relevant endpoints
    • Levi M, Cromheecke ME, de JE, et al. Pharmacological strategies to decrease excessive blood loss in cardiac surgery: a meta-analysis of clinically relevant endpoints. Lancet 1999;354:1940-1947.
    • (1999) Lancet , vol.354 , pp. 1940-1947
    • Levi, M.1    Cromheecke, M.E.2    de, J.E.3
  • 191
    • 0033547701 scopus 로고    scopus 로고
    • Is epsilonminocaproic acid as effective as aprotinin in reducing bleeding with cardiac surgery?: A meta-analysis
    • Munoz JJ, Birkmeyer NJ, Birkmeyer JD, O'Connor GT, Dacey LJ. Is epsilonminocaproic acid as effective as aprotinin in reducing bleeding with cardiac surgery?: a meta-analysis. Circulation 1999;99:81-89.
    • (1999) Circulation , vol.99 , pp. 81-89
    • Munoz, J.J.1    Birkmeyer, N.J.2    Birkmeyer, J.D.3    O'Connor, G.T.4    Dacey, L.J.5
  • 192
    • 0035098728 scopus 로고    scopus 로고
    • Comparison of epsilon aminocaproic acid and low-dose aprotinin in cardiopulmonary bypass: Efficiency, safety and cost
    • Ray MJ, O'Brien MF. Comparison of epsilon aminocaproic acid and low-dose aprotinin in cardiopulmonary bypass: efficiency, safety and cost. Ann Thorac Surg 2001;71:838-843.
    • (2001) Ann Thorac Surg , vol.71 , pp. 838-843
    • Ray, M.J.1    O'Brien, M.F.2
  • 193
    • 31344467254 scopus 로고    scopus 로고
    • The risk associated with aprotinin in cardiac surgery
    • Mangano DT, Tudor IC, Dietzel C. The risk associated with aprotinin in cardiac surgery. N Engl J Med 2006;354:353-365.
    • (2006) N Engl J Med , vol.354 , pp. 353-365
    • Mangano, D.T.1    Tudor, I.C.2    Dietzel, C.3
  • 194
    • 16844371506 scopus 로고    scopus 로고
    • Combined administration of nitric oxide gas and iloprost during cardiopulmonary bypass reduces platelet dysfunction: A pilot clinical study
    • Chung A, Wildhirt SM, Wang S, Koshal A, Radomski MW. Combined administration of nitric oxide gas and iloprost during cardiopulmonary bypass reduces platelet dysfunction: a pilot clinical study. J Thorac Cardiovasc Surg 2005;129:782-790.
    • (2005) J Thorac Cardiovasc Surg , vol.129 , pp. 782-790
    • Chung, A.1    Wildhirt, S.M.2    Wang, S.3    Koshal, A.4    Radomski, M.W.5
  • 195
    • 84858155345 scopus 로고    scopus 로고
    • Von Willebrand factor, shear stress, and ADAMTS13 in hemostasis and thrombosis
    • Tsai HM. von Willebrand factor, shear stress, and ADAMTS13 in hemostasis and thrombosis. ASAIO J 2012;58:163-169.
    • (2012) ASAIO J , vol.58 , pp. 163-169
    • Tsai, H.M.1
  • 196
    • 0036232272 scopus 로고    scopus 로고
    • Acquired von Willebrand syndrome: Experience from 2 years in a single laboratory compared with data from the literature and an international registry
    • Budde U, Bergmann F, Michiels JJ. Acquired von Willebrand syndrome: experience from 2 years in a single laboratory compared with data from the literature and an international registry. Semin Thromb Hemost 2002;28:227-238.
    • (2002) Semin Thromb Hemost , vol.28 , pp. 227-238
    • Budde, U.1    Bergmann, F.2    Michiels, J.J.3
  • 197
    • 77956393954 scopus 로고    scopus 로고
    • Comparative analysis of von Willebrand factor profiles in pulsatile and continuous left ventricular assist device recipients
    • Crow S, Milano C, Joyce L, et al. Comparative analysis of von Willebrand factor profiles in pulsatile and continuous left ventricular assist device recipients. ASAIO J 2010;56:441-445.
    • (2010) ASAIO J , vol.56 , pp. 441-445
    • Crow, S.1    Milano, C.2    Joyce, L.3
  • 198
    • 77957561535 scopus 로고    scopus 로고
    • Acquired von Willebrand syndrome after continuous-flow mechanical device support contributes to a high prevalence of bleeding during long-term support and at the time of transplantation
    • Uriel N, Pak SW, Jorde UP, et al. Acquired von Willebrand syndrome after continuous-flow mechanical device support contributes to a high prevalence of bleeding during long-term support and at the time of transplantation. J Am Coll Cardiol 2010;56:1207-1213.
    • (2010) J Am Coll Cardiol , vol.56 , pp. 1207-1213
    • Uriel, N.1    Pak, S.W.2    Jorde, U.P.3
  • 200
    • 58249093243 scopus 로고    scopus 로고
    • Gastrointestinal bleeding rates in recipients of nonpulsatile and pulsatile left ventricular assist devices
    • Crow S, John R, Boyle A, et al. Gastrointestinal bleeding rates in recipients of nonpulsatile and pulsatile left ventricular assist devices. J Thorac Cardiovasc Surg 2009;137:208-215.
    • (2009) J Thorac Cardiovasc Surg , vol.137 , pp. 208-215
    • Crow, S.1    John, R.2    Boyle, A.3
  • 202
    • 0027956290 scopus 로고
    • Thrombocytopenia after hepatic cryotherapy for colorectal metastases: Correlates with hepatocellular injury
    • Cozzi PJ, Stewart GJ, Morris DL. Thrombocytopenia after hepatic cryotherapy for colorectal metastases: correlates with hepatocellular injury. World J Surg 1994;18:774-776.
    • (1994) World J Surg , vol.18 , pp. 774-776
    • Cozzi, P.J.1    Stewart, G.J.2    Morris, D.L.3
  • 203
    • 79959770145 scopus 로고    scopus 로고
    • Evidence of platelet activation at medically used hypothermia and mechanistic data indicating ADP as a key mediator and therapeutic target
    • Straub A, Krajewski S, Hohmann JD, et al. Evidence of platelet activation at medically used hypothermia and mechanistic data indicating ADP as a key mediator and therapeutic target. Arterioscler Thromb Vasc Biol 2011;31:1607-1616.
    • (2011) Arterioscler Thromb Vasc Biol , vol.31 , pp. 1607-1616
    • Straub, A.1    Krajewski, S.2    Hohmann, J.D.3
  • 204
    • 68849116522 scopus 로고    scopus 로고
    • Hypothermic cardiopulmonary bypass as a determinant of late thrombocytopenia following cardiac operations in pediatric patients
    • Ranucci M, Carlucci C, Isgro G, et al. Hypothermic cardiopulmonary bypass as a determinant of late thrombocytopenia following cardiac operations in pediatric patients. Acta Anaesthesiol Scand 2009;53:1060-1067.
    • (2009) Acta Anaesthesiol Scand , vol.53 , pp. 1060-1067
    • Ranucci, M.1    Carlucci, C.2    Isgro, G.3
  • 206
    • 0018926567 scopus 로고
    • Kinetics and in vivo redistribution of (111)Indium-labelled human platelets after intravenous protamine sulphate
    • Heyns AD, Lotter MG, Badenhorst PN, et al. Kinetics and in vivo redistribution of (111)Indium-labelled human platelets after intravenous protamine sulphate. Thromb Haemost 1980;44:65-68.
    • (1980) Thromb Haemost , vol.44 , pp. 65-68
    • Heyns, A.D.1    Lotter, M.G.2    Badenhorst, P.N.3
  • 207
    • 0019517620 scopus 로고
    • Dysbaric osteonecrosis: A consequence of intravascular bubble formation, endothelial damage, and platelet thrombosis
    • Slichter SJ, Stegall P, Smith K, Huang TW, Harker LA. Dysbaric osteonecrosis: a consequence of intravascular bubble formation, endothelial damage, and platelet thrombosis. J Lab Clin Med 1981;98:568-590.
    • (1981) J Lab Clin Med , vol.98 , pp. 568-590
    • Slichter, S.J.1    Stegall, P.2    Smith, K.3    Huang, T.W.4    Harker, L.A.5


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