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Volumn 103, Issue 4, 1998, Pages 1045-1050

Prothrombin antigen levels in symptomatic and asymptomatic carriers of the 20210A prothrombin variant

Author keywords

20210A variant; Antigen level; Prothrombin; Thrombophilia

Indexed keywords

PROTHROMBIN;

EID: 0032440472     PISSN: 00071048     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1365-2141.1998.01112.x     Document Type: Article
Times cited : (63)

References (16)
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  • 3
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    • Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3′-untranslated region of the prothrombin gene
    • Brown, K., Luddington, R., Williamson, D., Baker, P. & Baglin, T. (1997) Risk of venous thromboembolism associated with a G to A transition at position 20210 in the 3′-untranslated region of the prothrombin gene. British Journal of Haematology, 98, 907-909.
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    • Brown, K.1    Luddington, R.2    Williamson, D.3    Baker, P.4    Baglin, T.5
  • 4
    • 0031911455 scopus 로고    scopus 로고
    • Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene
    • Bucciarelli, P., Franchi, F., Alatri, A., Bettini, P. & Moia, M. (1998) Budd-Chiari syndrome in a patient heterozygous for the G20210A mutation of the prothrombin gene. Thrombosis and Haemostasis, 79, 445-446.
    • (1998) Thrombosis and Haemostasis , vol.79 , pp. 445-446
    • Bucciarelli, P.1    Franchi, F.2    Alatri, A.3    Bettini, P.4    Moia, M.5
  • 8
    • 0030845360 scopus 로고    scopus 로고
    • The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis
    • Hillarp, A., Zoller, B., Svensson, P.J. & Dahlback, B. (1997) The 20210 A allele of the prothrombin gene is a common risk factor among Swedish outpatients with verified deep venous thrombosis. Thrombosis and Haemostasis, 78, 990-992.
    • (1997) Thrombosis and Haemostasis , vol.78 , pp. 990-992
    • Hillarp, A.1    Zoller, B.2    Svensson, P.J.3    Dahlback, B.4
  • 9
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    • A patient homozygous for a mutation in the prothrombin gene 3′-untranslated region associated with massive thrombosis
    • Howard, T.E., Marusa, M., Channell, C. & Duncan, A. (1997) A patient homozygous for a mutation in the prothrombin gene 3′-untranslated region associated with massive thrombosis. Blood Coagulation and Fibrinolysis, 8, 316-319.
    • (1997) Blood Coagulation and Fibrinolysis , vol.8 , pp. 316-319
    • Howard, T.E.1    Marusa, M.2    Channell, C.3    Duncan, A.4
  • 12
    • 0029850530 scopus 로고    scopus 로고
    • A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
    • Poort, S.R., Rosendaal, F.R., Reitsma, P.H. & Bertina, R.M. (1996) A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood, 88, 3698-3703.
    • (1996) Blood , vol.88 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 14
    • 0029795615 scopus 로고    scopus 로고
    • Compound heterozygous protein C deficiency resulting in the presence of only the beta form of protein C in plasma
    • Simioni, P., Kalafatis, M., Millar, D.S., Henderson, S.C., Luni, S., Cooper, D.N. & Girolami, A. (1996a) Compound heterozygous protein C deficiency resulting in the presence of only the beta form of protein C in plasma. Blood, 88, 2101-2108.
    • (1996) Blood , vol.88 , pp. 2101-2108
    • Simioni, P.1    Kalafatis, M.2    Millar, D.S.3    Henderson, S.C.4    Luni, S.5    Cooper, D.N.6    Girolami, A.7
  • 16
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    • Pseudo-homozygous activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: Report of two cases belonging to two unrelated kindreds
    • Simioni, P., Scudeller, A., Radossi, P., Gavasso, S., Girolami, B., Tormene, D. & Girolami, A. (1996c) Pseudo-homozygous activated protein C resistance due to double heterozygous factor V defects (factor V Leiden mutation and type I quantitative factor V defect) associated with thrombosis: report of two cases belonging to two unrelated kindreds. Thrombosis and Haemostasis, 75, 422-426.
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* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.