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Volumn 19, Issue 1, 2013, Pages

Development of factor VIII inhibitors in two patients with moderate haemophilia A

Author keywords

[No Author keywords available]

Indexed keywords

BLOOD CLOTTING FACTOR 8; BLOOD CLOTTING FACTOR 8 INHIBITOR; RECOMBINANT BLOOD CLOTTING FACTOR 7A; RECOMBINANT BLOOD CLOTTING FACTOR 8;

EID: 84870992847     PISSN: 13518216     EISSN: 13652516     Source Type: Journal    
DOI: 10.1111/hae.12057     Document Type: Letter
Times cited : (4)

References (10)
  • 2
    • 0035077234 scopus 로고    scopus 로고
    • Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis
    • White GC 2nd, Rosendaal F, Aledort LM, Lusher JM, Rothschild C, Ingerslev J. Definitions in hemophilia. Recommendation of the scientific subcommittee on factor VIII and factor IX of the scientific and standardization committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 2001; 85: 560.
    • (2001) Thromb Haemost , vol.85 , pp. 560
    • White 2nd, G.C.1    Rosendaal, F.2    Aledort, L.M.3    Lusher, J.M.4    Rothschild, C.5    Ingerslev, J.6
  • 3
    • 0038383605 scopus 로고    scopus 로고
    • The epidemiology of inhibitors in haemophilia A: a systematic review
    • Wight J, Paisley S. The epidemiology of inhibitors in haemophilia A: a systematic review. Haemophilia 2003; 9: 418-35.
    • (2003) Haemophilia , vol.9 , pp. 418-435
    • Wight, J.1    Paisley, S.2
  • 4
    • 0030926974 scopus 로고    scopus 로고
    • The inhibitor antibody response is more complex in hemophilia A patients than in most nonhemophiliacs with factor VIII autoantibodies. Recombinate and Kogenate Study Groups
    • Prescott R, Nakai H, Saenko EL et al. The inhibitor antibody response is more complex in hemophilia A patients than in most nonhemophiliacs with factor VIII autoantibodies. Recombinate and Kogenate Study Groups. Blood 1997; 89: 3663-71.
    • (1997) Blood , vol.89 , pp. 3663-3671
    • Prescott, R.1    Nakai, H.2    Saenko, E.L.3
  • 6
    • 65849180700 scopus 로고    scopus 로고
    • Intensive peri-operative use of factor VIII and the Arg593->Cys mutation are risk factors for inhibitor development in mild/moderate hemophilia A
    • Eckhardt CL, Menke LA, van Ommen CH et al. Intensive peri-operative use of factor VIII and the Arg593->Cys mutation are risk factors for inhibitor development in mild/moderate hemophilia A. J Thromb Haemost 2009; 7: 930-7.
    • (2009) J Thromb Haemost , vol.7 , pp. 930-937
    • Eckhardt, C.L.1    Menke, L.A.2    van Ommen, C.H.3
  • 7
    • 0031958313 scopus 로고    scopus 로고
    • Factor VIII inhibitors in mild and moderate-severity haemophilia A. UK Haemophilia Centre Directors Organisation
    • Hay CR, Ludlam CA, Colvin BT et al. Factor VIII inhibitors in mild and moderate-severity haemophilia A. UK Haemophilia Centre Directors Organisation. Thromb Haemost 1998; 79: 762-6.
    • (1998) Thromb Haemost , vol.79 , pp. 762-766
    • Hay, C.R.1    Ludlam, C.A.2    Colvin, B.T.3
  • 8
    • 78649367398 scopus 로고    scopus 로고
    • In non-severe hemophilia A the risk of inhibitor after intensive factor treatment is greater in older patients: a case-control study
    • Kempton CL, Soucie JM, Miller CH et al. In non-severe hemophilia A the risk of inhibitor after intensive factor treatment is greater in older patients: a case-control study. J Thromb Haemost 2010; 8: 2224-31.
    • (2010) J Thromb Haemost , vol.8 , pp. 2224-2231
    • Kempton, C.L.1    Soucie, J.M.2    Miller, C.H.3
  • 9
    • 0034058541 scopus 로고    scopus 로고
    • Intracellular accumulation of factor VIII induced by missense mutations Arg593->Cys and Asn618->Ser explains cross-reacting material-reduced haemophilia A
    • Roelse JC, De Laaf RT, Timmermans SM, Peters M, Van Mourik JA, Voorberg J. Intracellular accumulation of factor VIII induced by missense mutations Arg593->Cys and Asn618->Ser explains cross-reacting material-reduced haemophilia A. Br J Haematol 2000; 108: 241-6.
    • (2000) Br J Haematol , vol.108 , pp. 241-246
    • Roelse, J.C.1    De Laaf, R.T.2    Timmermans, S.M.3    Peters, M.4    Van Mourik, J.A.5    Voorberg, J.6
  • 10
    • 79953106384 scopus 로고    scopus 로고
    • Factor VIII A3 domain substitution N1922S results in hemophilia A due to domain-specific misfolding and hyposecretion of functional protein
    • Summers RJ, Meeks SL, Healey JF et al. Factor VIII A3 domain substitution N1922S results in hemophilia A due to domain-specific misfolding and hyposecretion of functional protein. Blood 2011; 117: 3190-8.
    • (2011) Blood , vol.117 , pp. 3190-3198
    • Summers, R.J.1    Meeks, S.L.2    Healey, J.F.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.