메뉴 건너뛰기




Volumn , Issue , 2008, Pages 294-312

Thrombotic Microangiopathies

Author keywords

[No Author keywords available]

Indexed keywords


EID: 70350209572     PISSN: None     EISSN: None     Source Type: Book    
DOI: 10.1016/B978-141605484-9.50028-9     Document Type: Chapter
Times cited : (4)

References (94)
  • 1
    • 0035722282 scopus 로고    scopus 로고
    • Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura
    • Ruggenenti P, Noris M, Remuzzi G Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura. Kidney Int 2001, 60:831-846.
    • (2001) Kidney Int , vol.60 , pp. 831-846
    • Ruggenenti, P.1    Noris, M.2    Remuzzi, G.3
  • 2
    • 0041411081 scopus 로고    scopus 로고
    • Long-term renal prognosis of diarrhea-associated hemolytic uremic syndrome: A systematic review, meta-analysis, and meta-regression
    • Garg AX, Suri RS, Barrowman N, et al. Long-term renal prognosis of diarrhea-associated hemolytic uremic syndrome: A systematic review, meta-analysis, 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
  • 3
    • 27744564894 scopus 로고    scopus 로고
    • Relative nephroprotection during Escherichia coli O157:H7 infections: Association with intravenous volume expansion
    • Ake JA, Jelacic S, Ciol MA, et al. Relative nephroprotection during Escherichia coli O157:H7 infections: Association with intravenous volume expansion. Pediatrics 2005, 115:e673-e680.
    • (2005) Pediatrics , vol.115
    • Ake, J.A.1    Jelacic, S.2    Ciol, M.A.3
  • 4
    • 0037208703 scopus 로고    scopus 로고
    • Adult nondiarrhea hemolytic uremic syndrome associated with Shiga toxin Escherichia coli O157:H7 bacteremia and urinary tract infection
    • Chiurchiu C, Firrincieli A, Santostefano M, et al. Adult nondiarrhea hemolytic uremic syndrome associated with Shiga toxin Escherichia coli O157:H7 bacteremia and urinary tract infection. Am J Kidney Dis 2003, 41:E4.
    • (2003) Am J Kidney Dis , vol.41
    • Chiurchiu, C.1    Firrincieli, A.2    Santostefano, M.3
  • 5
    • 0034729744 scopus 로고    scopus 로고
    • The risk of the hemolyticuremic syndrome after antibiotic treatment of Escherichia coli O157:H7 infections
    • Wong CS, Jelacic S, Habeeb RL, et al. The risk of the hemolyticuremic 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
  • 6
    • 0037190096 scopus 로고    scopus 로고
    • Risk of hemolytic uremic syndrome after antibiotic treatment of Escherichia coli O157:H7 enteritis: A meta-analysis
    • Safdar N, Said A, Gangnon RE, Maki DG Risk of hemolytic uremic syndrome after antibiotic treatment of Escherichia coli O157:H7 enteritis: A meta-analysis. JAMA 2002, 288:996-1001.
    • (2002) JAMA , vol.288 , pp. 996-1001
    • Safdar, N.1    Said, A.2    Gangnon, R.E.3    Maki, D.G.4
  • 7
    • 4844228028 scopus 로고    scopus 로고
    • Two different therapeutic regimes in patients with sequelae of hemolyticuremic syndrome
    • Caletti MG, Lejarraga H, Kelmansky D, Missoni M Two different therapeutic regimes in patients with sequelae of hemolyticuremic syndrome. Pediatr Nephrol 2004, 19:1148-1152.
    • (2004) Pediatr Nephrol , vol.19 , pp. 1148-1152
    • Caletti, M.G.1    Lejarraga, H.2    Kelmansky, D.3    Missoni, M.4
  • 8
    • 2942657338 scopus 로고    scopus 로고
    • Renoprotection by ACE inhibitors after severe hemolytic uremic syndrome
    • Van Dyck M, Proesmans W Renoprotection by ACE inhibitors after severe hemolytic uremic syndrome. Pediatr Nephrol 2004, 19:688-690.
    • (2004) Pediatr Nephrol , vol.19 , pp. 688-690
    • Van Dyck, M.1    Proesmans, W.2
  • 9
    • 0041411080 scopus 로고    scopus 로고
    • Effect of an oral Shiga toxin-binding agent on diarrhea-associated hemolytic uremic syndrome in children: A randomized controlled trial
    • Trachtman H, Cnaan A, Christen E, et al. Effect of an oral Shiga toxin-binding agent on diarrhea-associated hemolytic uremic syndrome in children: A randomized controlled trial. JAMA 2003, 290:1337-1344.
    • (2003) JAMA , vol.290 , pp. 1337-1344
    • Trachtman, H.1    Cnaan, A.2    Christen, E.3
  • 10
    • 0023929294 scopus 로고
    • Plasma infusion for hemolyticuremic syndrome in children: Results of a multicenter controlled trial
    • Rizzoni G, Claris-Appiani A, Edefonti A, et al. Plasma infusion for hemolyticuremic syndrome in children: Results of a multicenter controlled trial. J Pediatr 1988, 112:284-290.
    • (1988) J Pediatr , vol.112 , pp. 284-290
    • Rizzoni, G.1    Claris-Appiani, A.2    Edefonti, A.3
  • 11
    • 84875791920 scopus 로고    scopus 로고
    • Von Willebrand factor (vWF)-cleaving protease activity in pediatric hemolytic uremic syndrome (HUS) [abstract]
    • Loirat C, Veyradier A, Foulard M, et al. von Willebrand factor (vWF)-cleaving protease activity in pediatric hemolytic uremic syndrome (HUS) [abstract]. Pediatr Nephrol 2001, 16:617A.
    • (2001) Pediatr Nephrol , vol.16
    • Loirat, C.1    Veyradier, A.2    Foulard, M.3
  • 12
    • 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
  • 13
    • 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
  • 14
    • 0030049869 scopus 로고    scopus 로고
    • Bilateral nephrectomy stopped disease progression in plasma-resistant hemolytic uremic syndrome with neurological signs and coma
    • Remuzzi G, Galbusera M, Salvadori M, et al. Bilateral nephrectomy stopped disease progression in plasma-resistant hemolytic uremic syndrome with neurological signs and coma. Kidney Int 1996, 49:282-286.
    • (1996) Kidney Int , vol.49 , pp. 282-286
    • Remuzzi, G.1    Galbusera, M.2    Salvadori, M.3
  • 15
    • 0141590417 scopus 로고    scopus 로고
    • Renal transplantation in patients with hemolytic uremic syndrome: High rate of recurrence and increased incidence of acute rejections
    • Artz MA, Steenbergen EJ, Hoitsma AJ, et al. Renal transplantation in patients with hemolytic uremic syndrome: High rate of recurrence and increased incidence of acute rejections. Transplantation 2003, 76:821-826.
    • (2003) Transplantation , vol.76 , pp. 821-826
    • Artz, M.A.1    Steenbergen, E.J.2    Hoitsma, A.J.3
  • 16
    • 0242694369 scopus 로고    scopus 로고
    • The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children
    • Loirat C, Niaudet P The risk of recurrence of hemolytic uremic syndrome after renal transplantation in children. Pediatr Nephrol 2003, 18:1095-1101.
    • (2003) Pediatr Nephrol , vol.18 , pp. 1095-1101
    • Loirat, C.1    Niaudet, P.2
  • 17
    • 0036952936 scopus 로고    scopus 로고
    • Shiga toxin-associated hemolytic uremic syndrome: Absence of recurrence after renal transplantation
    • Ferraris JR, Ramirez JA, Ruiz S, et al. Shiga toxin-associated hemolytic uremic syndrome: Absence of recurrence after renal transplantation. Pediatr Nephrol 2002, 17:809-814.
    • (2002) Pediatr Nephrol , vol.17 , pp. 809-814
    • Ferraris, J.R.1    Ramirez, J.A.2    Ruiz, S.3
  • 18
    • 0024601315 scopus 로고
    • Haemolytic uraemic syndrome and the Thomsen Friedenreich antigen
    • McGraw ME, Lendon M, Stevens RF, et al. Haemolytic uraemic syndrome and the Thomsen Friedenreich antigen. Pediatr Nephrol 1989, 3:135-139.
    • (1989) Pediatr Nephrol , vol.3 , pp. 135-139
    • McGraw, M.E.1    Lendon, M.2    Stevens, R.F.3
  • 19
    • 20544437666 scopus 로고    scopus 로고
    • Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome
    • Dragon-Durey MA, Loirat C, Cloarec S, et al. Anti-factor H autoantibodies associated with atypical hemolytic uremic syndrome. J Am Soc Nephrol 2005, 16:555-563.
    • (2005) J Am Soc Nephrol , vol.16 , pp. 555-563
    • Dragon-Durey, M.A.1    Loirat, C.2    Cloarec, S.3
  • 20
    • 34548853385 scopus 로고    scopus 로고
    • Anti-factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome
    • Jozsi M, Strobel S, Dahse HM, et al. Anti-factor H autoantibodies block C-terminal recognition function of factor H in hemolytic uremic syndrome. Blood 2007, 110:1516-1518.
    • (2007) Blood , vol.110 , pp. 1516-1518
    • Jozsi, M.1    Strobel, S.2    Dahse, H.M.3
  • 21
    • 0029925856 scopus 로고    scopus 로고
    • Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis
    • Furlan M, Robles R, Lamie B Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis. Blood 1996, 87:4223-4234.
    • (1996) Blood , vol.87 , pp. 4223-4234
    • Furlan, M.1    Robles, R.2    Lamie, B.3
  • 22
    • 0032569884 scopus 로고    scopus 로고
    • Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolyticuremic syndrome
    • Furlan M, Robles R, Galbusera M, et al. von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolyticuremic 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
  • 23
    • 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
  • 24
    • 0035885927 scopus 로고    scopus 로고
    • Specific von Willebrand factor-cleaving protease in thrombotic microangiopathies: A study of 111 cases
    • Veyradier A, Obert B, Houllier A, et al. Specific von Willebrand factor-cleaving protease in thrombotic microangiopathies: A study of 111 cases. Blood 2001, 98:1765-1772.
    • (2001) Blood , vol.98 , pp. 1765-1772
    • Veyradier, A.1    Obert, B.2    Houllier, A.3
  • 25
  • 26
    • 33947594746 scopus 로고    scopus 로고
    • Prognostic value of anti-ADAMTS 13 antibody features (Ig isotype, titer, and inhibitory effect) in a cohort of 35 adult French patients undergoing a first episode of thrombotic microangiopathy with undetectable ADAMTS 13 activity
    • Ferrari S, Scheiflinger F, Rieger M, et al. Prognostic value of anti-ADAMTS 13 antibody features (Ig isotype, titer, and inhibitory effect) in a cohort of 35 adult French patients undergoing a first episode of thrombotic microangiopathy with undetectable ADAMTS 13 activity. Blood 2007, 109:2815-2822.
    • (2007) Blood , vol.109 , pp. 2815-2822
    • Ferrari, S.1    Scheiflinger, F.2    Rieger, M.3
  • 27
    • 0029826567 scopus 로고    scopus 로고
    • Development of focal segmental sclerosis and hyalinosis in hemolytic uremic syndrome
    • Caletti MG, Gallo G, Gianantonio CA Development of focal segmental sclerosis and hyalinosis in hemolytic uremic syndrome. Pediatr Nephrol 1996, 10:687-692.
    • (1996) Pediatr Nephrol , vol.10 , pp. 687-692
    • Caletti, M.G.1    Gallo, G.2    Gianantonio, C.A.3
  • 28
    • 0025999820 scopus 로고
    • Improved survival in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Clinical experience in 108 patients
    • Bell WR, Braine HG, Ness PM, Kickler TS Improved survival in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Clinical experience in 108 patients. N Engl J Med 1991, 325:398-403.
    • (1991) N Engl J Med , vol.325 , pp. 398-403
    • Bell, W.R.1    Braine, H.G.2    Ness, P.M.3    Kickler, T.S.4
  • 29
    • 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
  • 30
    • 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
  • 31
    • 8944220236 scopus 로고    scopus 로고
    • Cryosupernatant as replacement fluid for plasma exchange in thrombotic thrombocytopenic purpura. Members of the Canadian Apheresis Group
    • Rock G, Shumak KH, Sutton DM, et al. Cryosupernatant as replacement fluid for plasma exchange in thrombotic thrombocytopenic purpura. Members of the Canadian Apheresis Group. Br J Haematol 1996, 94:383-386.
    • (1996) Br J Haematol , vol.94 , pp. 383-386
    • Rock, G.1    Shumak, K.H.2    Sutton, D.M.3
  • 32
    • 84948721566 scopus 로고
    • Treatment outcomes in patients with adult thrombotic thrombocytopenic purpura-hemolytic uremic syndrome
    • Hayward CP, Sutton DM, Carter WH, et al. Treatment outcomes in patients with adult thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Arch Intern Med 1994, 154:982-987.
    • (1994) Arch Intern Med , vol.154 , pp. 982-987
    • Hayward, C.P.1    Sutton, D.M.2    Carter, W.H.3
  • 33
    • 0032522952 scopus 로고    scopus 로고
    • Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura
    • Furlan M, Robles R, Solenthaler M, Lammle B Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura. Blood 1998, 91:2839-2846.
    • (1998) Blood , vol.91 , pp. 2839-2846
    • Furlan, M.1    Robles, R.2    Solenthaler, M.3    Lammle, B.4
  • 34
    • 0023323440 scopus 로고
    • Thrombotic microangiopathy in pregnancy and the postpartum period
    • Weiner CP Thrombotic microangiopathy in pregnancy and the postpartum period. Semin Hematol 1987, 24:119-129.
    • (1987) Semin Hematol , vol.24 , pp. 119-129
    • Weiner, C.P.1
  • 35
    • 0042703238 scopus 로고    scopus 로고
    • The association of pregnancy with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome
    • George JN The association of pregnancy with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Curr Opin Hematol 2003, 10:339-344.
    • (2003) Curr Opin Hematol , vol.10 , pp. 339-344
    • George, J.N.1
  • 36
    • 0030000015 scopus 로고    scopus 로고
    • The pathophysiology and management of thrombotic thrombocytopenic purpura
    • Ruggenenti P, Remuzzi G The pathophysiology and management of thrombotic thrombocytopenic purpura. Eur J Haematol 1996, 56:191-207.
    • (1996) Eur J Haematol , vol.56 , pp. 191-207
    • Ruggenenti, P.1    Remuzzi, G.2
  • 37
    • 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, et al. 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
  • 38
    • 18544410535 scopus 로고    scopus 로고
    • Withdrawal of interferon-alpha results in prompt resolution of thrombocytopenia and hemolysis but not renal failure in hemolytic uremic syndrome caused by interferon-alpha
    • Ohashi N, Yonemura K, Sugiura T, et al. Withdrawal of interferon-alpha results in prompt resolution of thrombocytopenia and hemolysis but not renal failure in hemolytic uremic syndrome caused by interferon-alpha. Am J Kidney Dis 2003, 41:E10.
    • (2003) Am J Kidney Dis , vol.41
    • Ohashi, N.1    Yonemura, K.2    Sugiura, T.3
  • 39
    • 0035856207 scopus 로고    scopus 로고
    • Complement factor H and the haemolytic uraemic syndrome
    • Taylor CM Complement factor H and the haemolytic uraemic syndrome. Lancet 2001, 358:1200-1202.
    • (2001) Lancet , vol.358 , pp. 1200-1202
    • Taylor, C.M.1
  • 40
    • 33746534053 scopus 로고    scopus 로고
    • Hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, and antiphospholipid antibody syndromes
    • Lippincott Williams & Wilkins, Philadelphia, E.G. Neilson, W.G. Couser (Eds.)
    • Ruggenenti P, Galli M, Remuzzi G Hemolytic uremic syndrome, thrombotic thrombocytopenic purpura, and antiphospholipid antibody syndromes. Immunologic Renal Diseases 2001, 1179-1208. Lippincott Williams & Wilkins, Philadelphia. E.G. Neilson, W.G. Couser (Eds.).
    • (2001) Immunologic Renal Diseases , pp. 1179-1208
    • Ruggenenti, P.1    Galli, M.2    Remuzzi, G.3
  • 41
    • 0031970553 scopus 로고    scopus 로고
    • Genetic studies into inherited and sporadic hemolytic uremic syndrome
    • Warwicker P, Goodship TH, Donne RL, et al. Genetic studies into inherited and sporadic hemolytic uremic syndrome. Kidney Int 1998, 53:836-844.
    • (1998) Kidney Int , vol.53 , pp. 836-844
    • Warwicker, P.1    Goodship, T.H.2    Donne, R.L.3
  • 42
    • 33847237272 scopus 로고    scopus 로고
    • The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: Update and integration of membrane cofactor protein and factor I mutations with structural models
    • Saunders RE, Abarrategui-Garrido C, Fremeaux-Bacchi V, et al. The interactive Factor H-atypical hemolytic uremic syndrome mutation database and website: Update and integration of membrane cofactor protein and factor I mutations with structural models. Hum Mutat 2007, 28:222-234.
    • (2007) Hum Mutat , vol.28 , pp. 222-234
    • Saunders, R.E.1    Abarrategui-Garrido, C.2    Fremeaux-Bacchi, V.3
  • 43
    • 0035121908 scopus 로고    scopus 로고
    • Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome
    • Perez-Caballero D, Gonzalez-Rubio C, et al. Clustering of missense mutations in the C-terminal region of factor H in atypical hemolytic uremic syndrome. Am J Hum Genet 2001, 68:478-484.
    • (2001) Am J Hum Genet , vol.68 , pp. 478-484
    • Perez-Caballero, D.1    Gonzalez-Rubio, C.2
  • 44
    • 0042329931 scopus 로고    scopus 로고
    • Haemolytic uraemic syndrome and mutations of the factor H gene: A registry-based study of German speaking countries
    • Neumann HP, Salzmann M, Bohnert-Iwan B, et al. Haemolytic uraemic syndrome and mutations of the factor H gene: A registry-based study of German speaking countries. J Med Genet 2003, 40:676-681.
    • (2003) J Med Genet , vol.40 , pp. 676-681
    • Neumann, H.P.1    Salzmann, M.2    Bohnert-Iwan, B.3
  • 45
    • 33747159590 scopus 로고    scopus 로고
    • Genetics of HUS: The impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome
    • Caprioli J, Noris M, Brioschi S, et al. Genetics of HUS: The impact of MCP, CFH, and IF mutations on clinical presentation, response to treatment, and outcome. Blood 2006, 108:1267-1279.
    • (2006) Blood , vol.108 , pp. 1267-1279
    • Caprioli, J.1    Noris, M.2    Brioschi, S.3
  • 46
    • 2442433542 scopus 로고    scopus 로고
    • The human complement factor H: Functional roles, genetic variations and disease associations
    • Rodriguez de Cordoba S, Esparza-Gordillo J, Goicoechea de Jorge E, et al. The human complement factor H: Functional roles, genetic variations and disease associations. Mol Immunol 2004, 41:355-367.
    • (2004) Mol Immunol , vol.41 , pp. 355-367
    • Rodriguez de Cordoba, S.1    Esparza-Gordillo, J.2    Goicoechea de Jorge, E.3
  • 47
    • 1642518600 scopus 로고    scopus 로고
    • Attachment of the soluble complement regulator factor H to cell and tissue surfaces: Relevance for pathology
    • Jozsi M, Manuelian T, Heinen S, et al. Attachment of the soluble complement regulator factor H to cell and tissue surfaces: Relevance for pathology. Histol Histopathol 2004, 19:251-258.
    • (2004) Histol Histopathol , vol.19 , pp. 251-258
    • Jozsi, M.1    Manuelian, T.2    Heinen, S.3
  • 48
    • 33750855444 scopus 로고    scopus 로고
    • Atypical haemolytic uraemic syndrome associated with a hybrid complement gene
    • Venables JP, Strain L, Routledge D, et al. Atypical haemolytic uraemic syndrome associated with a hybrid complement gene. PLoS Med 2006, 3:e431.
    • (2006) PLoS Med , vol.3
    • Venables, J.P.1    Strain, L.2    Routledge, D.3
  • 49
    • 0242570482 scopus 로고    scopus 로고
    • Familial haemolytic uraemic syndrome and an MCP mutation
    • Noris M, Brioschi S, Caprioli J, et al. Familial haemolytic uraemic syndrome and an MCP mutation. Lancet 2003, 362:1542-1547.
    • (2003) Lancet , vol.362 , pp. 1542-1547
    • Noris, M.1    Brioschi, S.2    Caprioli, J.3
  • 50
    • 0242331610 scopus 로고    scopus 로고
    • Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome
    • Richards A, Kemp EJ, Liszewski MK, et al. Mutations in human complement regulator, membrane cofactor protein (CD46), predispose to development of familial hemolytic uremic syndrome. Proc Natl Acad Sci U S A 2003, 100:12966-12971.
    • (2003) Proc Natl Acad Sci U S A , vol.100 , pp. 12966-12971
    • Richards, A.1    Kemp, E.J.2    Liszewski, M.K.3
  • 51
    • 2342650263 scopus 로고    scopus 로고
    • Mutations in CD46, a complement regulatory protein, predispose to atypical HUS
    • Goodship TH, Liszewski MK, Kemp EJ, et al. Mutations in CD46, a complement regulatory protein, predispose to atypical HUS. Trends Mol Med 2004, 10:226-231.
    • (2004) Trends Mol Med , vol.10 , pp. 226-231
    • Goodship, T.H.1    Liszewski, M.K.2    Kemp, E.J.3
  • 52
    • 19444369542 scopus 로고    scopus 로고
    • Complement factor I: A susceptibility gene for atypical haemolytic uraemic syndrome
    • Fremeaux-Bacchi V, Dragon-Durey MA, Blouin J, et al. Complement factor I: A susceptibility gene for atypical haemolytic uraemic syndrome. J Med Genet 2004, 41:e84.
    • (2004) J Med Genet , vol.41
    • Fremeaux-Bacchi, V.1    Dragon-Durey, M.A.2    Blouin, J.3
  • 53
    • 27744452766 scopus 로고    scopus 로고
    • Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome
    • Kavanagh D, Kemp EJ, Mayland E, et al. Mutations in complement factor I predispose to development of atypical hemolytic uremic syndrome. J Am Soc Nephrol 2005, 16:2150-2155.
    • (2005) J Am Soc Nephrol , vol.16 , pp. 2150-2155
    • Kavanagh, D.1    Kemp, E.J.2    Mayland, E.3
  • 54
    • 33846094404 scopus 로고    scopus 로고
    • Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome
    • Goicoechea de Jorge E, Harris CL, Esparza-Gordillo J, et al. Gain-of-function mutations in complement factor B are associated with atypical hemolytic uremic syndrome. Proc Natl Acad Sci U S A 2007, 104:240-245.
    • (2007) Proc Natl Acad Sci U S A , vol.104 , pp. 240-245
    • Goicoechea de Jorge, E.1    Harris, C.L.2    Esparza-Gordillo, J.3
  • 55
    • 0242601270 scopus 로고    scopus 로고
    • Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: The C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease
    • Caprioli J, Castelletti F, Bucchioni S, et al. Complement factor H mutations and gene polymorphisms in haemolytic uraemic syndrome: The C-257T, the A2089G and the G2881T polymorphisms are strongly associated with the disease. Hum Mol Genet 2003, 12:3385-3395.
    • (2003) Hum Mol Genet , vol.12 , pp. 3385-3395
    • Caprioli, J.1    Castelletti, F.2    Bucchioni, S.3
  • 56
    • 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
  • 57
    • 0035089983 scopus 로고    scopus 로고
    • Familial hemolytic uremic syndrome associated with complement factor H deficiency
    • Landau D, Shalev H, Levy-Finer G, et al. Familial hemolytic uremic syndrome associated with complement factor H deficiency. J Pediatr 2001, 138:412-417.
    • (2001) J Pediatr , vol.138 , pp. 412-417
    • Landau, D.1    Shalev, H.2    Levy-Finer, G.3
  • 58
    • 34247381485 scopus 로고    scopus 로고
    • Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate
    • Cho HY, Lee BS, Moon KC, et al. Complete factor H deficiency-associated atypical hemolytic uremic syndrome in a neonate. Pediatr Nephrol 2007, 22:874-880.
    • (2007) Pediatr Nephrol , vol.22 , pp. 874-880
    • Cho, H.Y.1    Lee, B.S.2    Moon, K.C.3
  • 59
    • 0036230235 scopus 로고    scopus 로고
    • Successful treatment of factor H-related haemolytic uraemic syndrome
    • Stratton JD, Warwicker P Successful treatment of factor H-related haemolytic uraemic syndrome. Nephrol Dial Transplant 2002, 17:684-685.
    • (2002) Nephrol Dial Transplant , vol.17 , pp. 684-685
    • Stratton, J.D.1    Warwicker, P.2
  • 60
    • 34548400755 scopus 로고    scopus 로고
    • Outcome of renal transplantation in patients with non-Shiga toxin-associated haemolytic uremic syndrome: Prognostic significance of genetic background
    • International Registry of Recurrent and Familial HUS/TTP, et al.
    • Bresin E, Daina E, Noris M, International Registry of Recurrent and Familial HUS/TTP, et al. Outcome of renal transplantation in patients with non-Shiga toxin-associated haemolytic uremic syndrome: Prognostic significance of genetic background. Clin J Am Soc Nephrol 2006, 1:88-99.
    • (2006) Clin J Am Soc Nephrol , vol.1 , pp. 88-99
    • Bresin, E.1    Daina, E.2    Noris, M.3
  • 61
    • 33745767079 scopus 로고    scopus 로고
    • Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation
    • Saland JM, Emre SH, Shneider BL, et al. Favorable long-term outcome after liver-kidney transplant for recurrent hemolytic uremic syndrome associated with a factor H mutation. Am J Transplant 2006, 6:1948-1952.
    • (2006) Am J Transplant , vol.6 , pp. 1948-1952
    • Saland, J.M.1    Emre, S.H.2    Shneider, B.L.3
  • 62
    • 34248664063 scopus 로고    scopus 로고
    • A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome
    • Geelen J, van den Dries K, Roos A, et al. A missense mutation in factor I (IF) predisposes to atypical haemolytic uraemic syndrome. Pediatr Nephrol 2007, 22:371-375.
    • (2007) Pediatr Nephrol , vol.22 , pp. 371-375
    • Geelen, J.1    van den Dries, K.2    Roos, A.3
  • 63
    • 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
  • 64
    • 0027418266 scopus 로고
    • Thrombotic thrombocytopenic purpura: Evidence that infusion rather than removal of plasma induces remission of the disease
    • Ruggenenti P, Galbusera M, Cornejo RP, et al. Thrombotic thrombocytopenic purpura: Evidence that infusion rather than removal of plasma induces remission of the disease. Am J Kidney Dis 1993, 21:314-318.
    • (1993) Am J Kidney Dis , vol.21 , pp. 314-318
    • Ruggenenti, P.1    Galbusera, M.2    Cornejo, R.P.3
  • 65
    • 0035885972 scopus 로고    scopus 로고
    • Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family
    • Fujikawa K, Suzuki H, McMullen B, Chung D Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family. Blood 2001, 98:1662-1666.
    • (2001) Blood , vol.98 , pp. 1662-1666
    • Fujikawa, K.1    Suzuki, H.2    McMullen, B.3    Chung, D.4
  • 66
    • 33749872079 scopus 로고    scopus 로고
    • In-vitro and in-vivo consequences of mutations in the von Willebrand factor cleaving protease ADAMTS13 in thrombotic thrombocytopenic purpura
    • Donadelli R, Banterla F, Galbusera M, et al. In-vitro and in-vivo consequences of mutations in the von Willebrand factor cleaving protease ADAMTS13 in thrombotic thrombocytopenic purpura. Thromb Haemost 2006, 96:454-464.
    • (2006) Thromb Haemost , vol.96 , pp. 454-464
    • Donadelli, R.1    Banterla, F.2    Galbusera, M.3
  • 67
    • 0032918258 scopus 로고    scopus 로고
    • Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura
    • Furlan M, Robles R, Morselli B, et al. Recovery and half-life of von Willebrand factor-cleaving protease after plasma therapy in patients with thrombotic thrombocytopenic purpura. Thromb Haemost 1999, 81:8-13.
    • (1999) Thromb Haemost , vol.81 , pp. 8-13
    • Furlan, M.1    Robles, R.2    Morselli, B.3
  • 68
    • 0018690479 scopus 로고
    • Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology
    • Baumgartner ER, Wick H, Maurer R, et al. Congenital defect in intracellular cobalamin metabolism resulting in homocysteinuria and methylmalonic aciduria. I. Case report and histopathology. Helv Paediatr Acta 1979, 34:465-482.
    • (1979) Helv Paediatr Acta , vol.34 , pp. 465-482
    • Baumgartner, E.R.1    Wick, H.2    Maurer, R.3
  • 69
    • 4243238319 scopus 로고    scopus 로고
    • Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy
    • Van Hove JL, Van Damme-Lombaerts R, Grunewald S, et al. Cobalamin disorder Cbl-C presenting with late-onset thrombotic microangiopathy. Am J Med Genet 2002, 111:195-201.
    • (2002) Am J Med Genet , vol.111 , pp. 195-201
    • Van Hove, J.L.1    Van Damme-Lombaerts, R.2    Grunewald, S.3
  • 70
    • 0037062233 scopus 로고    scopus 로고
    • Combined kidney and liver transplantation for familial haemolytic uraemic syndrome
    • Remuzzi G, Ruggenenti P, Codazzi D, et al. Combined kidney and liver transplantation for familial haemolytic uraemic syndrome. Lancet 2002, 359:1671-1672.
    • (2002) Lancet , vol.359 , pp. 1671-1672
    • Remuzzi, G.1    Ruggenenti, P.2    Codazzi, D.3
  • 71
    • 0034663327 scopus 로고    scopus 로고
    • How I treat patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome
    • George JN How I treat patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Blood 2000, 96:1223-1229.
    • (2000) Blood , vol.96 , pp. 1223-1229
    • George, J.N.1
  • 72
    • 0034059721 scopus 로고    scopus 로고
    • A new biological agent for treatment of Shiga toxigenic Escherichia coli infections and dysentery in humans
    • Paton AW, Morona R, Paton JC A new biological agent for treatment of Shiga toxigenic Escherichia coli infections and dysentery in humans. Nat Med 2000, 6:265-270.
    • (2000) Nat Med , vol.6 , pp. 265-270
    • Paton, A.W.1    Morona, R.2    Paton, J.C.3
  • 73
    • 2442573691 scopus 로고    scopus 로고
    • Refinement of a therapeutic Shiga toxin-binding probiotic for human trials
    • Pinyon RA, Paton JC, Paton AW, et al. Refinement of a therapeutic Shiga toxin-binding probiotic for human trials. J Infect Dis 2004, 189:1547-1555.
    • (2004) J Infect Dis , vol.189 , pp. 1547-1555
    • Pinyon, R.A.1    Paton, J.C.2    Paton, A.W.3
  • 74
    • 2942545832 scopus 로고    scopus 로고
    • The effect of probiotic treatment with Clostridium butyricum on enterohemorrhagic Escherichia coli O157:H7 infection in mice
    • Takahashi M, Taguchi H, Yamaguchi H, et al. The effect of probiotic treatment with Clostridium butyricum on enterohemorrhagic Escherichia coli O157:H7 infection in mice. FEMS Immunol Med Microbiol 2004, 41:219-226.
    • (2004) FEMS Immunol Med Microbiol , vol.41 , pp. 219-226
    • Takahashi, M.1    Taguchi, H.2    Yamaguchi, H.3
  • 75
    • 33646493151 scopus 로고    scopus 로고
    • A plant-based oral vaccine to protect against systemic intoxication by Shiga toxin type 2
    • Wen SX, Teel LD, Judge NA, O-Brien AD A plant-based oral vaccine to protect against systemic intoxication by Shiga toxin type 2. Proc Natl Acad Sci U S A 2006, 103:7082-7087.
    • (2006) Proc Natl Acad Sci U S A , vol.103 , pp. 7082-7087
    • Wen, S.X.1    Teel, L.D.2    Judge, N.A.3    O-Brien, A.D.4
  • 76
    • 0037442497 scopus 로고    scopus 로고
    • Assessment in mice of the therapeutic potential of tailored, multivalent Shiga toxin carbohydrate ligands
    • Mulvey GL, Marcato P, Kitov PI, et al. Assessment in mice of the therapeutic potential of tailored, multivalent Shiga toxin carbohydrate ligands. J Infect Dis 2003, 187:640-649.
    • (2003) J Infect Dis , vol.187 , pp. 640-649
    • Mulvey, G.L.1    Marcato, P.2    Kitov, P.I.3
  • 77
    • 0035863536 scopus 로고    scopus 로고
    • Intervention with Shiga toxin (Stx) antibody after infection by Stx-producing Escherichia coli
    • Matise I, Cornick NA, Booher SL, et al. Intervention with Shiga toxin (Stx) antibody after infection by Stx-producing Escherichia coli. J Infect Dis 2001, 183:347-350.
    • (2001) J Infect Dis , vol.183 , pp. 347-350
    • Matise, I.1    Cornick, N.A.2    Booher, S.L.3
  • 78
    • 0021304014 scopus 로고
    • [Treatment of childhood hemolyticuremic syndrome with urokinase. Cooperative controlled trial]
    • Loirat C, Beaufils F, Sonsino E, et al. [Treatment of childhood hemolyticuremic syndrome with urokinase. Cooperative controlled trial]. Arch Fr Pediatr 1984, 41:15-19.
    • (1984) Arch Fr Pediatr , vol.41 , pp. 15-19
    • Loirat, C.1    Beaufils, F.2    Sonsino, E.3
  • 79
    • 0023692638 scopus 로고    scopus 로고
    • Heparin plus dipyridamole in childhood hemolyticuremic syndrome: A prospective, randomized study
    • Van Damme-Lombaerts R, Proesmans W, Van Damme B, et al. Heparin plus dipyridamole in childhood hemolyticuremic syndrome: A prospective, randomized study. J Pediatr 1998, 113:913-918.
    • (1998) J Pediatr , vol.113 , pp. 913-918
    • Van Damme-Lombaerts, R.1    Proesmans, W.2    Van Damme, B.3
  • 80
    • 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
  • 81
    • 0027321238 scopus 로고
    • Plasma exchange in children with hemolyticuremic syndrome at risk of poor outcome
    • Gianviti A, Perna A, Caringella A, et al. Plasma exchange in children with hemolyticuremic syndrome at risk of poor outcome. Am J Kidney Dis 1993, 22:264-266.
    • (1993) Am J Kidney Dis , vol.22 , pp. 264-266
    • Gianviti, A.1    Perna, A.2    Caringella, A.3
  • 82
    • 0022651344 scopus 로고
    • Thrombotic thrombocytopenic purpura (TTP) treatment: Italian cooperative retrospective study on 29 cases
    • Italian Cooperative Group for the Study of Thrombotic Thrombocytopenic Purpura
    • Italian Cooperative Group for the Study of Thrombotic Thrombocytopenic Purpura Thrombotic thrombocytopenic purpura (TTP) treatment: Italian cooperative retrospective study on 29 cases. Haematologica 1986, 71:39-43.
    • (1986) Haematologica , vol.71 , pp. 39-43
  • 83
    • 0027074789 scopus 로고
    • Adult hemolytic uremic syndrome with renal microangiopathy. Outcome according to therapeutic protocol in 53 cases. French Cooperative Study Group for Adult HUS
    • Adult hemolytic uremic syndrome with renal microangiopathy. Outcome according to therapeutic protocol in 53 cases. French Cooperative Study Group for Adult HUS. Ann Med Interne (Paris) 1992, 143(Suppl 1):27-32.
    • (1992) Ann Med Interne (Paris) , vol.143 , Issue.SUPPL.1 , pp. 27-32
  • 84
    • 0026420717 scopus 로고
    • [Treatment of thrombotic thrombopenic purpura. Results of a multicenter randomized clinical study]
    • Henon P [Treatment of thrombotic thrombopenic purpura. Results of a multicenter randomized clinical study]. Presse Med 1991, 20:1761-1767.
    • (1991) Presse Med , vol.20 , pp. 1761-1767
    • Henon, P.1
  • 85
    • 33746508999 scopus 로고    scopus 로고
    • A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders
    • European Paediatric Research Group for HUS
    • Besbas N, Karpman D, Landau D, European Paediatric Research Group for HUS, et al. A classification of hemolytic uremic syndrome and thrombotic thrombocytopenic purpura and related disorders. Kidney Int 2006, 70:423-431.
    • (2006) Kidney Int , vol.70 , pp. 423-431
    • Besbas, N.1    Karpman, D.2    Landau, D.3
  • 86
    • 2442701758 scopus 로고    scopus 로고
    • Thrombotic microangiopathic haemolytic anaemia and antiphospholipid antibodies
    • Espinosa G, Bucciarelli S, Cervera R, et al. Thrombotic microangiopathic haemolytic anaemia and antiphospholipid antibodies. Ann Rheum Dis 2004, 63:730-736.
    • (2004) Ann Rheum Dis , vol.63 , pp. 730-736
    • Espinosa, G.1    Bucciarelli, S.2    Cervera, R.3
  • 87
    • 33646360865 scopus 로고    scopus 로고
    • Clinical practice. Thrombotic thrombocytopenic purpura
    • George JN Clinical practice. Thrombotic thrombocytopenic purpura. N Engl J Med 2006, 354:1927-1935.
    • (2006) N Engl J Med , vol.354 , pp. 1927-1935
    • George, J.N.1
  • 88
    • 6444228597 scopus 로고    scopus 로고
    • Potential therapeutic agents for the prevention and treatment of haemolytic uraemic syndrome in Shiga toxin producing Escherichia coli infection
    • MacConnachie AA, Todd WTA Potential therapeutic agents for the prevention and treatment of haemolytic uraemic syndrome in Shiga toxin producing Escherichia coli infection. Curr Opin Infect Dis 2004, 17:479-482.
    • (2004) Curr Opin Infect Dis , vol.17 , pp. 479-482
    • MacConnachie, A.A.1    Todd, W.T.A.2
  • 89
    • 18044374090 scopus 로고    scopus 로고
    • Controversies with the diagnosis and management of HELLP syndrome
    • O-Brian JM, Barton JR Controversies with the diagnosis and management of HELLP syndrome. Clin Obstet Gynecol 2005, 48:460-477.
    • (2005) Clin Obstet Gynecol , vol.48 , pp. 460-477
    • O-Brian, J.M.1    Barton, J.R.2
  • 90
    • 33751035523 scopus 로고    scopus 로고
    • Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome
    • Richards A, Liszewski KM, Kavanagh D, et al. Implications of the initial mutations in membrane cofactor protein (MCP; CD46) leading to atypical hemolytic uremic syndrome. Mol Immunol 2007, 44:111-122.
    • (2007) Mol Immunol , vol.44 , pp. 111-122
    • Richards, A.1    Liszewski, K.M.2    Kavanagh, D.3
  • 91
    • 17144365102 scopus 로고    scopus 로고
    • Hemolytic uremic syndrome; pathogenesis, treatment, and outcome
    • Siegler R, Oakes R Hemolytic uremic syndrome; pathogenesis, treatment, and outcome. Curr Opin Pediatr 2005, 17:200-2004.
    • (2005) Curr Opin Pediatr , vol.17 , pp. 200-2004
    • Siegler, R.1    Oakes, R.2
  • 92
    • 33745683637 scopus 로고    scopus 로고
    • The molecular biology of thrombotic microangiopathy
    • Tsai HM The molecular biology of thrombotic microangiopathy. Kidney Int 2006, 70:16-23.
    • (2006) Kidney Int , vol.70 , pp. 16-23
    • Tsai, H.M.1
  • 93
    • 30344470197 scopus 로고    scopus 로고
    • Drug-induced thrombotic microangiopathy
    • Zakarija A, Bennet C Drug-induced thrombotic microangiopathy. Semin Thromb Hemost 2005, 31:681-690.
    • (2005) Semin Thromb Hemost , vol.31 , pp. 681-690
    • Zakarija, A.1    Bennet, C.2
  • 94
    • 33746926773 scopus 로고    scopus 로고
    • Complement dysfunction in hemolytic uremic syndrome
    • Zipfel PF, Skerka C Complement dysfunction in hemolytic uremic syndrome. Curr Opin Rheumatol 2006, 18:548-555.
    • (2006) Curr Opin Rheumatol , vol.18 , pp. 548-555
    • Zipfel, P.F.1    Skerka, C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.