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Volumn 50, Issue 5, 2008, Pages 947-948

Congenital thrombotic thrombocytopenic purpura: Lessons for recognition and management of rare syndromes

Author keywords

[No Author keywords available]

Indexed keywords

VON WILLEBRAND FACTOR CLEAVING PROTEINASE;

EID: 41849099697     PISSN: 15455009     EISSN: 15455017     Source Type: Journal    
DOI: 10.1002/pbc.21481     Document Type: Short Survey
Times cited : (14)

References (10)
  • 1
    • 0042413393 scopus 로고    scopus 로고
    • Effect of awareness of a randomized controlled trial on use of experimental therapy
    • Clark WF, Garg AX, Blake PG, et al. Effect of awareness of a randomized controlled trial on use of experimental therapy. JAMA 2003;290:1351-1355.
    • (2003) JAMA , vol.290 , pp. 1351-1355
    • Clark, W.F.1    Garg, A.X.2    Blake, P.G.3
  • 2
    • 33646360865 scopus 로고    scopus 로고
    • Thrombotic thrombocytopenic purpura
    • George JN. Thrombotic thrombocytopenic purpura. New Eng J Med 2006;354:1927-1935.
    • (2006) New Eng J Med , vol.354 , pp. 1927-1935
    • George, J.N.1
  • 3
    • 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
  • 4
    • 72849154313 scopus 로고
    • Studies on thrombopoiesis. I. A factor in normal plasma required for platelet production: Chronic thrombocytopenia due to its deficiency
    • Schulman I, Pierce M, Lukens A, et al. Studies on thrombopoiesis. I. A factor in normal 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
  • 5
    • 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. New Eng J Med 1978;298:1350-1352.
    • (1978) New Eng J Med , vol.298 , pp. 1350-1352
    • Upshaw Jr., J.D.1
  • 6
    • 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. New Eng J Med 1982; 307:1432-1435.
    • (1982) New Eng J Med , vol.307 , pp. 1432-1435
    • Moake, J.L.1    Rudy, C.K.2    Troll, J.H.3
  • 7
    • 8844248794 scopus 로고    scopus 로고
    • Defective processing of unusually large von Willebrand factor multimers and thrombotic thrombocytopenic purpura
    • Moake JL. Defective processing of unusually large von Willebrand factor multimers and thrombotic thrombocytopenic purpura. J Thromb Haemost 2004;2:1515-1521.
    • (2004) J Thromb Haemost , vol.2 , pp. 1515-1521
    • Moake, J.L.1
  • 8
    • 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
  • 9
    • 0034917642 scopus 로고    scopus 로고
    • Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome: The role of von Willebrand factor-cleaving protease
    • Furlan M, Lammle B. Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome: The role of von Willebrand factor-cleaving protease. Best Pract Res Clin Haematol 2001;14:437-454.
    • (2001) Best Pract Res Clin Haematol , vol.14 , pp. 437-454
    • Furlan, M.1    Lammle, B.2
  • 10
    • 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


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.