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Volumn 195, Issue 4, 2006, Pages 1114-1118

Prevalence of factor V Leiden, prothrombin and methylene tetrahydrofolate reductase mutations in women with adverse pregnancy outcomes in Lebanon

Author keywords

Obstetric complication; Pregnancy outcome; Thrombophilia

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); BLOOD CLOTTING FACTOR 5 LEIDEN; PROTHROMBIN;

EID: 33748780670     PISSN: 00029378     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.ajog.2006.06.082     Document Type: Article
Times cited : (23)

References (23)
  • 1
    • 14644435132 scopus 로고    scopus 로고
    • A systematic review of the association between factor V Leiden or prothrombin gene variant and intrauterine growth restriction
    • Howley H.E., Walker M., and Rodger M.A. A systematic review of the association between factor V Leiden or prothrombin gene variant and intrauterine growth restriction. Am J Obstet Gynecol 192 (2005) 694-708
    • (2005) Am J Obstet Gynecol , vol.192 , pp. 694-708
    • Howley, H.E.1    Walker, M.2    Rodger, M.A.3
  • 2
    • 4444343623 scopus 로고    scopus 로고
    • Thrombophilia and pregnancy complications
    • Kujovich J.L. Thrombophilia and pregnancy complications. Am J Obstet Gynecol 191 (2004) 412-424
    • (2004) Am J Obstet Gynecol , vol.191 , pp. 412-424
    • Kujovich, J.L.1
  • 4
    • 23944441722 scopus 로고    scopus 로고
    • The relationship of the factor V Leiden mutation and pregnancy outcomes for mother and fetus
    • Dizon-Townson D., Miller C., Sibai B., Spong C.Y., Thom E., Wendel Jr. G., et al. The relationship of the factor V Leiden mutation and pregnancy outcomes for mother and fetus. Obstet Gynecol 106 (2005) 517-524
    • (2005) Obstet Gynecol , vol.106 , pp. 517-524
    • Dizon-Townson, D.1    Miller, C.2    Sibai, B.3    Spong, C.Y.4    Thom, E.5    Wendel Jr., G.6
  • 6
    • 13244271259 scopus 로고    scopus 로고
    • Genetic thrombophilias and preeclampsia: a meta-analysis
    • Lin J., and August P. Genetic thrombophilias and preeclampsia: a meta-analysis. Obstet Gynecol 105 (2005) 182-192
    • (2005) Obstet Gynecol , vol.105 , pp. 182-192
    • Lin, J.1    August, P.2
  • 7
    • 0033531184 scopus 로고    scopus 로고
    • Increased frequency of genetic thrombophilia in women with complications of pregnancy
    • Kupferminc M.J., Eldor A., Steinman N., Many A., Bar-Am A., Jaffa A., et al. Increased frequency of genetic thrombophilia in women with complications of pregnancy. N Engl J Med 340 (1999) 9-13
    • (1999) N Engl J Med , vol.340 , pp. 9-13
    • Kupferminc, M.J.1    Eldor, A.2    Steinman, N.3    Many, A.4    Bar-Am, A.5    Jaffa, A.6
  • 8
    • 0036157110 scopus 로고    scopus 로고
    • Inherited thrombophilias in pregnant patients: detection and treatment paradigm
    • Lockwood C.J. Inherited thrombophilias in pregnant patients: detection and treatment paradigm. Obstet Gynecol 99 (2002) 333-341
    • (2002) Obstet Gynecol , vol.99 , pp. 333-341
    • Lockwood, C.J.1
  • 9
    • 0033843870 scopus 로고    scopus 로고
    • The prevalence factor V R506Q mutation-Leiden among apparently healthy Lebanese
    • Irani-Hakime N., Tamim H., Kreidy R., and Almawi W.Y. The prevalence factor V R506Q mutation-Leiden among apparently healthy Lebanese. Am J Hematol 65 (2000) 45-49
    • (2000) Am J Hematol , vol.65 , pp. 45-49
    • Irani-Hakime, N.1    Tamim, H.2    Kreidy, R.3    Almawi, W.Y.4
  • 10
    • 0037954204 scopus 로고    scopus 로고
    • High prevalence of prothrombin G20210A mutation among patients with deep venous thrombosis in Lebanon
    • Taher A., Khalil I., Abou-Merhi R., Shamseddine A., and Bazarbachi A. High prevalence of prothrombin G20210A mutation among patients with deep venous thrombosis in Lebanon. Thromb Haemost 89 (2003) 945-946
    • (2003) Thromb Haemost , vol.89 , pp. 945-946
    • Taher, A.1    Khalil, I.2    Abou-Merhi, R.3    Shamseddine, A.4    Bazarbachi, A.5
  • 11
    • 2342642866 scopus 로고    scopus 로고
    • Differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene among the Lebanese population
    • Almawi W.Y., Finan R.R., Tamim H., Daccache J.L., and Irani-Hakime N. Differences in the frequency of the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene among the Lebanese population. Am J Hematol 76 (2004) 85-87
    • (2004) Am J Hematol , vol.76 , pp. 85-87
    • Almawi, W.Y.1    Finan, R.R.2    Tamim, H.3    Daccache, J.L.4    Irani-Hakime, N.5
  • 12
    • 12344298603 scopus 로고    scopus 로고
    • The polymorphism of platelet membrane integrin alpha2beta1 (alpha2807TT) is associated with premature onset of fetal loss
    • Gerhardt A., Scharf R.E., Mikat-Drozdzynski B., Krussel J.S., Bender H.G., and Zotz R.B. The polymorphism of platelet membrane integrin alpha2beta1 (alpha2807TT) is associated with premature onset of fetal loss. Thromb Haemost 93 (2005) 124-129
    • (2005) Thromb Haemost , vol.93 , pp. 124-129
    • Gerhardt, A.1    Scharf, R.E.2    Mikat-Drozdzynski, B.3    Krussel, J.S.4    Bender, H.G.5    Zotz, R.B.6
  • 13
    • 10044245813 scopus 로고    scopus 로고
    • The common prothrombotic factors in nulliparous women do not compromise blood flow in the feto-maternal circulation and are not associated with preeclampsia or intrauterine growth restriction
    • Salomon O., Seligsohn U., Steinberg D.M., Zalel Y., Lerner A., Rosenberg N., et al. The common prothrombotic factors in nulliparous women do not compromise blood flow in the feto-maternal circulation and are not associated with preeclampsia or intrauterine growth restriction. Am J Obstet Gynecol 191 (2004) 2002-2009
    • (2004) Am J Obstet Gynecol , vol.191 , pp. 2002-2009
    • Salomon, O.1    Seligsohn, U.2    Steinberg, D.M.3    Zalel, Y.4    Lerner, A.5    Rosenberg, N.6
  • 14
    • 21844458934 scopus 로고    scopus 로고
    • MTHFR C677T Polymorphism and factor V Leiden mutation are not associated with recurrent spontaneous abortion of unexplained etiology in Japanese women
    • Kobashi G., Kato E.H., Morikawa M., Shimada S., Ohta K., Fujimoto S., et al. MTHFR C677T Polymorphism and factor V Leiden mutation are not associated with recurrent spontaneous abortion of unexplained etiology in Japanese women. Semin Thromb Hemost 31 (2005) 266-271
    • (2005) Semin Thromb Hemost , vol.31 , pp. 266-271
    • Kobashi, G.1    Kato, E.H.2    Morikawa, M.3    Shimada, S.4    Ohta, K.5    Fujimoto, S.6
  • 15
    • 15244344074 scopus 로고    scopus 로고
    • Fetal genotype for specific inherited thrombophilias is not associated with severe preeclampsia
    • Stanley-Christian H., Ghidini A., Sacher R., and Shemirani M. Fetal genotype for specific inherited thrombophilias is not associated with severe preeclampsia. J Soc Gynecol Investig 12 (2005) 198-201
    • (2005) J Soc Gynecol Investig , vol.12 , pp. 198-201
    • Stanley-Christian, H.1    Ghidini, A.2    Sacher, R.3    Shemirani, M.4
  • 16
    • 14644446017 scopus 로고    scopus 로고
    • Absence of association of inherited thrombophilia with unexplained third-trimester intrauterine fetal death
    • Gonen R., Lavi N., Attias D., Schliamser L., Borochowitz Z., Toubi E., et al. Absence of association of inherited thrombophilia with unexplained third-trimester intrauterine fetal death. Am J Obstet Gynecol 192 (2005) 742-746
    • (2005) Am J Obstet Gynecol , vol.192 , pp. 742-746
    • Gonen, R.1    Lavi, N.2    Attias, D.3    Schliamser, L.4    Borochowitz, Z.5    Toubi, E.6
  • 18
    • 0036893569 scopus 로고    scopus 로고
    • Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population
    • Finan R.R., Tamim H., Ameen G., Sharida H.E., Rashid M., and Almawi W.Y. Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population. Am J Hematol 71 (2002) 300-305
    • (2002) Am J Hematol , vol.71 , pp. 300-305
    • Finan, R.R.1    Tamim, H.2    Ameen, G.3    Sharida, H.E.4    Rashid, M.5    Almawi, W.Y.6
  • 19
    • 0037443934 scopus 로고    scopus 로고
    • Thrombophilic disorders and fetal loss: a meta-analysis
    • Rey E., Kahn S.R., David M., and Shrier I. Thrombophilic disorders and fetal loss: a meta-analysis. Lancet 361 (2003) 901-908
    • (2003) Lancet , vol.361 , pp. 901-908
    • Rey, E.1    Kahn, S.R.2    David, M.3    Shrier, I.4
  • 20
    • 0024284028 scopus 로고
    • A simple salting out procedure for extracting DNA from human nucleated cells
    • Miller S.A., Dykes D.D., and Polesky H.F. A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16 (1988) 1215-1218
    • (1988) Nucleic Acids Res , vol.16 , pp. 1215-1218
    • Miller, S.A.1    Dykes, D.D.2    Polesky, H.F.3
  • 22
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: a common mutation in the methylenetetrahydrofolate reductase
    • Frosst P., Blom H.J., Milos R., Goyette P., Sheppard C.A., Matthews R.G., et al. A candidate genetic risk factor for vascular disease: a common mutation in the methylenetetrahydrofolate reductase. Nat Genet 10 (1995) 111-113
    • (1995) Nat Genet , vol.10 , pp. 111-113
    • Frosst, P.1    Blom, H.J.2    Milos, R.3    Goyette, P.4    Sheppard, C.A.5    Matthews, R.G.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.