메뉴 건너뛰기




Volumn 5, Issue 4, 2003, Pages 250-253

Prothrombin gene variants in non-Caucasians with fetal loss and intrauterine growth retardation

Author keywords

[No Author keywords available]

Indexed keywords

PROTHROMBIN;

EID: 0242691713     PISSN: 15251578     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1525-1578(10)60482-5     Document Type: Article
Times cited : (28)

References (14)
  • 2
    • 0037050786 scopus 로고    scopus 로고
    • How strong is the association between maternal thrombophilia and adverse pregnancy outcome? A systematic review
    • Alfirevic Z, Roberts D, Martlew V: How strong is the association between maternal thrombophilia and adverse pregnancy outcome? A systematic review. Eur J Obstet Gynecol Reprod Biol 2002, 101:6-14
    • (2002) Eur. J. Obstet. Gynecol. Reprod. Biol. , vol.101 , pp. 6-14
    • Alfirevic, Z.1    Roberts, D.2    Martlew, V.3
  • 3
    • 0036149892 scopus 로고    scopus 로고
    • Thrombophilia is common in women with idiopathic pregnancy loss and is associated with late pregnancy wastage
    • Sarig G, Younis JS, Hoffman R, Lanir N, Blumenfeld Z, Brenner B: Thrombophilia is common in women with idiopathic pregnancy loss and is associated with late pregnancy wastage. Fertil Steril 2002, 77:342-347
    • (2002) Fertil. Steril. , vol.77 , pp. 342-347
    • Sarig, G.1    Younis, J.S.2    Hoffman, R.3    Lanir, N.4    Blumenfeld, Z.5    Brenner, B.6
  • 4
    • 0036227458 scopus 로고    scopus 로고
    • Third-trimester unexplained intrauterine fetal death is associated with inherited thrombophilia
    • Many A, Elad R, Yaron Y, Eldor A, Lessing JB, Kupferminc MJ: Third-trimester unexplained intrauterine fetal death is associated with inherited thrombophilia. Obstet Gynecol 2002, 99:684-687
    • (2002) Obstet. Gynecol. , vol.99 , pp. 684-687
    • Many, A.1    Elad, R.2    Yaron, Y.3    Eldor, A.4    Lessing, J.B.5    Kupferminc, M.J.6
  • 5
    • 0035002341 scopus 로고    scopus 로고
    • A novel point mutation in the 3′ region of the prothrombin gene at position 20221 in a Lebanese/Syrian family
    • Wylenzek M, Geisen C, Stapenhorst L, Wielckens K, Klingler KR: A novel point mutation in the 3′ region of the prothrombin gene at position 20221 in a Lebanese/Syrian family. Thromb Haemost 2001, 85:943-944
    • (2001) Thromb. Haemost. , vol.85 , pp. 943-944
    • Wylenzek, M.1    Geisen, C.2    Stapenhorst, L.3    Wielckens, K.4    Klingler, K.R.5
  • 8
    • 0023230641 scopus 로고
    • Nucleotide sequence of the gene for human prothrombin
    • Degen SJ, Davie EW: Nucleotide sequence of the gene for human prothrombin. Biochemistry 1987, 26:6165-6177
    • (1987) Biochemistry , vol.26 , pp. 6165-6177
    • Degen, S.J.1    Davie, E.W.2
  • 9
    • 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 SR, Rosendaal FR, Reitsma PH, Bertina RM: 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 1996, 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
  • 11
    • 0037019327 scopus 로고    scopus 로고
    • Clotting and hemorrhage in the placenta: A delicate balance
    • Roberts D, Schwartz RS: Clotting and hemorrhage in the placenta: a delicate balance. N Engl J Med 2002, 347:57-59
    • (2002) N. Engl. J. Med. , vol.347 , pp. 57-59
    • Roberts, D.1    Schwartz, R.S.2
  • 13
    • 0037038218 scopus 로고    scopus 로고
    • Thrombophilia polymorphisms and intrauterine growth restriction
    • Kupferminc MJ, Many A, Lessing JB: Thrombophilia polymorphisms and intrauterine growth restriction. N Engl J Med 2002, 347:1530-1531
    • (2002) N. Engl. J. Med. , vol.347 , pp. 1530-1531
    • Kupferminc, M.J.1    Many, A.2    Lessing, J.B.3
  • 14


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.