메뉴 건너뛰기




Volumn 6, Issue 2, 2010, Pages 74-81

Genotipurile trombofilice mutante materne şi fetale ca factori de risc pentru preeclampsie

Author keywords

Genetic thrombophilias; PCR RFLP methods; Preeclampsia

Indexed keywords

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

EID: 79955795213     PISSN: 18414435     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article
Times cited : (2)

References (40)
  • 1
    • 0023038667 scopus 로고
    • Functional and immunologic protein S levels are decreased during pregnancy
    • Comp P.C., Thurnau G.R., Welsh J., et al. Functional and immunologic protein S levels are decreased during pregnancy. Blood 1986; 68: 881-885
    • (1986) Blood , vol.68 , pp. 881-885
    • Comp, P.C.1    Thurnau, G.R.2    Welsh, J.3
  • 2
    • 0029019014 scopus 로고
    • Development of resistance to activated protein C during pregnancy
    • Cumming A.M., Tait R.C., Fildes S. Development of resistance to activated protein C during pregnancy. Br J Haematol 1995; 90: 725-727
    • (1995) Br J Haematol , vol.90 , pp. 725-727
    • Cumming, A.M.1    Tait, R.C.2    Fildes, S.3
  • 5
  • 6
  • 8
    • 0035814640 scopus 로고    scopus 로고
    • Pathogenesis and genetics of preeclampsia
    • Roberts J.M., Cooper D.W. Pathogenesis and genetics of preeclampsia. Lancet 2001; 357: 53-56
    • (2001) Lancet , vol.357 , pp. 53-56
    • Roberts, J.M.1    Cooper, D.W.2
  • 10
    • 0028810738 scopus 로고
    • World distribution of factor V Leiden
    • Rees D.C., Cox M., Clegg J.B. World distribution of factor V Leiden. Lancet 1995; 346: 1133-1134
    • (1995) Lancet , vol.346 , pp. 1133-1134
    • Rees, D.C.1    Cox, M.2    Clegg, J.B.3
  • 11
    • 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., et al. 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 (Pubitemid 26383091)
    • (1996) Blood , vol.88 , Issue.10 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 12
    • 0029049553 scopus 로고
    • A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
    • Frosst P., Blom H.J., Milos R. et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet. 1995; 10: 111-113
    • (1995) Nat Genet , vol.10 , pp. 111-113
    • Frosst, P.1    Blom, H.J.2    Milos, R.3
  • 13
    • 0032497941 scopus 로고    scopus 로고
    • Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: The result of a meta- analysis
    • Brattstrom L. Common methylenetetrahydrofolate reductase gene mutation leads to hyperhomocysteinemia but not to vascular disease: the result of a meta-analysis. Circulation 1998; 98: 2520-2526 (Pubitemid 29001189)
    • (1998) Circulation , vol.98 , Issue.23 , pp. 2520-2526
    • Brattstrom, L.1    Wilcken, D.E.L.2    Ohrvik, J.3    Brudin, L.4
  • 14
    • 0034190659 scopus 로고    scopus 로고
    • 5, 10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: A HuGE review
    • Botto L.D., Yang Q. 5, 10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGE review. Am. J. Epidemiol. 2000; 151: 862-877
    • (2000) Am. J. Epidemiol. , vol.151 , pp. 862-877
    • Botto, L.D.1    Yang, Q.2
  • 15
    • 0028844492 scopus 로고
    • Mutated methylenetetrahydrofolate reductase as a risk factor for sfina bifida
    • van der Put N.M., Steegers-Theunissen R.P., Frosst P. et al. Mutated methylenetetrahydrofolate reductase as a risk factor for sfina bifida. Lancet 1995; 346: 1071-1071
    • (1995) Lancet , vol.346 , pp. 1071-1071
    • Van Der Put, N.M.1    Steegers-Theunissen, R.P.2    Frosst, P.3
  • 17
    • 0031687887 scopus 로고    scopus 로고
    • A second genetic polymorphism in methylenetetrahydrofolate reductase (MTHFR) associated with decreased enzyme activity
    • DOI 10.1006/mgme.1998.2714
    • Wisberg I., Tran P., Christensen B., et al. A second genetic polymorphism in the methylene tetrahydropholate reductase (MTHFR) associated with decreased enzyme activity. Mol Genet Metab 1998; 64: 169-172 (Pubitemid 28453294)
    • (1998) Molecular Genetics and Metabolism , vol.64 , Issue.3 , pp. 169-172
    • Weisberg, I.1    Tran, P.2    Christensen, B.3    Sibani, S.4    Rozen, R.5
  • 18
    • 0035944725 scopus 로고    scopus 로고
    • Long term mortality of mothers and fathers after pre-eclampsia: Population based cohort study
    • Irgens H., Reisaeter L., Irgens L.M., et al. Long term mortality of mothers and fathers after pre-eclampsia: population based cohort study. British Medical Journal, 2001
    • (2001) British Medical Journal
    • Irgens, H.1    Reisaeter, L.2    Irgens, L.M.3
  • 19
    • 0028910906 scopus 로고
    • Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke and venous thrombosis in apparently healthy men
    • Ridker P.M., Hennekens C.H., Lindpaintner K. Mutation in the gene coding for coagulation factor V and the risk of myocardial infarction, stroke and venous thrombosis in apparently healthy men. N Engl J Med 1995; 332: 912-917
    • (1995) N Engl J Med , vol.332 , pp. 912-917
    • Ridker, P.M.1    Hennekens, C.H.2    Lindpaintner, K.3
  • 20
    • 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
    • Poor S.R., Rosendaal F.R., Reitsma P.H., et al. A common genetic variation in the 3′ untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venosu thrombosis. Blood 1996; 88: 3698-703 (Pubitemid 26383091)
    • (1996) Blood , vol.88 , Issue.10 , pp. 3698-3703
    • Poort, S.R.1    Rosendaal, F.R.2    Reitsma, P.H.3    Bertina, R.M.4
  • 21
    • 0033614946 scopus 로고    scopus 로고
    • Increased frequency of genetic thrombophilic in women with complications of pregancy
    • Kupferminc M., Eldor A. Stainman N., et al. Increased frequency of genetic thrombophilic in women with complications of pregancy. N Engl J Med 1999; 341(5): 384
    • (1999) N Engl J Med , vol.341 , Issue.5 , pp. 384
    • Kupferminc, M.1    Eldor, A.2    Stainman, N.3
  • 24
    • 0036901330 scopus 로고    scopus 로고
    • Factor V Leiden and factor II G20210A in pre-eclampsia and HELLP syndrome
    • Benedetto C., Marozio L., Salton L., et al. Factor V Leiden and factor II G20210A in pre-eclampsia and HELLP syndrome. Acta Obstet Gynecol Scand 2001; 81: 1095-1100
    • (2001) Acta Obstet Gynecol Scand , vol.81 , pp. 1095-1100
    • Benedetto, C.1    Marozio, L.2    Salton, L.3
  • 27
    • 79955836408 scopus 로고    scopus 로고
    • Prevention of recurrent preeclampsia in women with thrombophilia
    • Abstracts from XXII ISTH Congress
    • Makatsariya A.D., Bitsadze V.O., Baimuradova S.M., et al. Prevention of recurrent preeclampsia in women with thrombophilia. Journal of Thrombosis and Haemostasis, vol 7 Suppl 2, Abstracts from XXII ISTH Congress, 2009
    • (2009) Journal of Thrombosis and Haemostasis , vol.7 , Issue.SUPPL. 2
    • Makatsariya, A.D.1    Bitsadze, V.O.2    Baimuradova, S.M.3
  • 28
    • 31944434778 scopus 로고    scopus 로고
    • Thrombophilic is significantly associated with severe preeclampsia. Results of large scale, case- controlled study
    • Mello G., Parretti E., Marozio L., et al. Thrombophilic is significantly associated with severe preeclampsia. Results of large scale, case- controlled study. Hypertension 2005; 46: 1270-1274
    • (2005) Hypertension , vol.46 , pp. 1270-1274
    • Mello, G.1    Parretti, E.2    Marozio, L.3
  • 30
    • 60749128922 scopus 로고    scopus 로고
    • Genetic thrombophilic variants and the risk for preeclampsia among American Indians
    • Best L., Dorsam S., Nadeau M., et al. Genetic thrombophilic variants and the risk for preeclampsia among American Indians. Hypertension and pregnancy 2009; 28(1): 85-94
    • (2009) Hypertension and Pregnancy , vol.28 , Issue.1 , pp. 85-94
    • Best, L.1    Dorsam, S.2    Nadeau, M.3
  • 32
    • 12444320081 scopus 로고    scopus 로고
    • Polymorphisms of methylenetetrahydropholate reductase in women with pre-eclampsia 12th international Society for the study of hypertension in pregnancy
    • Hauge B., Wiltshire E., Nelson P., et al. Polymorphisms of methylenetetrahydropholate reductase in women with pre-eclampsia 12th international Society for the study of hypertension in pregnancy. Hypertens Pregnancy 2000; 19: 23
    • (2000) Hypertens Pregnancy , vol.19 , pp. 23
    • Hauge, B.1    Wiltshire, E.2    Nelson, P.3
  • 33
    • 0033768987 scopus 로고    scopus 로고
    • High prevalence of the prothrombin gene mutation in women with intrauterine growth retardation, abruptio placentae and second trimester loss
    • Kupferminc M.J., Peri H., Zwang E., et al. High prevalence of the prothrombin gene mutation in women with intrauterine growth retardation, abruptio placentae and second trimester loss. Acta Obstet Gynecol Scand 2000; 79: 963-967
    • (2000) Acta Obstet Gynecol Scand , vol.79 , pp. 963-967
    • Kupferminc, M.J.1    Peri, H.2    Zwang, E.3
  • 34
    • 0034668897 scopus 로고    scopus 로고
    • Incidence of factor V Leiden mutation, coagulation inhibitors deficiency, and elevated antiphospholipid antibodies in patients with preeclampsia or HELLP syndrome
    • von Tempelhoff G.F., Heilmann L., Spanuth E., et al. Incidence of factor V Leiden mutation, coagulation inhibitors deficiency, and elevated antiphospholipid antibodies in patients with preeclampsia or HELLP syndrome. Thromb Res 2000; 100: 363-365
    • (2000) Thromb Res , vol.100 , pp. 363-365
    • Von Tempelhoff, G.F.1    Heilmann, L.2    Spanuth, E.3
  • 36
    • 13244271259 scopus 로고    scopus 로고
    • Genetic thrombophilias and preeclampsia. A meta-analysis
    • Lin J., August P. Genetic thrombophilias and preeclampsia. A meta-analysis. Obstet Gynecol. 2005; 105: 182-192
    • (2005) Obstet Gynecol , vol.105 , pp. 182-192
    • Lin, J.1    August, P.2
  • 37
    • 0042877163 scopus 로고    scopus 로고
    • Association of maternal and/or fetal factor V Leiden and G20210A prothrombin mutation with HELLP syndrome and intrauterine growth restriction
    • DOI 10.1042/CS20030073
    • Schlembach D., Beinder E., Zingsem J., et al. Association of maternal and/or fetal factor V Leiden and G20210A prothrombin mutation with HELLP syndrome and intrauterine growth restriction. Clin.Sci 2003; 105: 279-285 (Pubitemid 37088566)
    • (2003) Clinical Science , vol.105 , Issue.3 , pp. 279-285
    • Schlembach, D.1    Beinder, E.2    Zingsem, J.3    Wunsiedler, U.4    Beckmann, M.W.5    Fischer, T.6
  • 38
    • 0041875074 scopus 로고    scopus 로고
    • Aetiology of pre-eclampsia and thrombophilic genetic mutations
    • DOI 10.1042/CS20030181
    • Hayashi M. Aetiology of pre-eclampsia and thrombophilic genetic mutations. Clinical Science 2003; 105: 269-271 (Pubitemid 37088564)
    • (2003) Clinical Science , vol.105 , Issue.3 , pp. 269-271
    • Hayashi, M.1
  • 39
    • 3142714601 scopus 로고    scopus 로고
    • Maternal and fetal variants of genetic thrombophilias and the risk of preeclampsia
    • DOI 10.1097/01.ede.0000112217.33111.23
    • Vefring H., Lie R.T., Degard R., et al. Maternal and fetal variants of genetic trombophilia and the risk of preeclampsia. Epidemiology 2004; 15 (83): 317-22 (Pubitemid 40416951)
    • (2004) Epidemiology , vol.15 , Issue.3 , pp. 317-322
    • Vefring, H.1    Lie, R.T.2    Odegard, R.3    Mansoor, M.A.4    Nilsen, S.T.5
  • 40
    • 3042770797 scopus 로고    scopus 로고
    • Placental pathology in fetal thrombophilia
    • DOI 10.1016/j.humpath.2004.02.010, PII S0046817704001388
    • Ariel I. Placental pathology in fetal thrombophilia. Hum Pathol 2004; 35 (5): 729-33 (Pubitemid 38881083)
    • (2004) Human Pathology , vol.35 , Issue.6 , pp. 729-733
    • Ariel, I.1    Anteby, E.2    Hamani, Y.3    Redline, R.W.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.