메뉴 건너뛰기




Volumn 112, Issue 3, 2005, Pages 306-311

Maternal and paternal thrombophilia: Risk factors for perinatal mortality

Author keywords

[No Author keywords available]

Indexed keywords

5,10 METHYLENETETRAHYDROFOLATE REDUCTASE (FADH2); ACTIVATED PROTEIN C; ANTITHROMBIN; BLOOD CLOTTING FACTOR 5 LEIDEN; DNA; HOMOCYSTEINE; IMMUNOGLOBULIN G ANTIBODY; IMMUNOGLOBULIN M ANTIBODY; PROTEIN S; PROTHROMBIN;

EID: 14644424565     PISSN: 14700328     EISSN: None     Source Type: Journal    
DOI: 10.1111/j.1471-0528.2004.00435.x     Document Type: Article
Times cited : (12)

References (27)
  • 2
    • 0031944566 scopus 로고    scopus 로고
    • Inherited thrombophilia and pregnancy
    • Girling J, de Swiet M. Inherited thrombophilia and pregnancy. Curr Opin Obstet Gynecol 1998;10(2):135-144.
    • (1998) Curr Opin Obstet Gynecol , vol.10 , Issue.2 , pp. 135-144
    • Girling, J.1    De Swiet, M.2
  • 4
    • 0027330937 scopus 로고
    • Hyperhomocysteinaemia: A risk factor in women with unexplained recurrent early pregnancy loss
    • Wouters MGAJ, Boers GHJ, Blom HJ, et al. Hyperhomocysteinaemia: a risk factor in women with unexplained recurrent early pregnancy loss. Fertil Steril 1993;60:820-825.
    • (1993) Fertil Steril , vol.60 , pp. 820-825
    • Wouters, M.G.A.J.1    Boers, G.H.J.2    Blom, H.J.3
  • 6
    • 0032767244 scopus 로고    scopus 로고
    • Thrombophilic polymorphisms are common in women with fetal loss without apparent cause
    • Brenner B, Sarig G, Weiner Z, Younis J, Blumenfeld Z, Lanir N. Thrombophilic polymorphisms are common in women with fetal loss without apparent cause. Thromb Haemost 1999;82(1):6-9.
    • (1999) Thromb Haemost , vol.82 , Issue.1 , pp. 6-9
    • Brenner, B.1    Sarig, G.2    Weiner, Z.3    Younis, J.4    Blumenfeld, Z.5    Lanir, N.6
  • 7
    • 0033955432 scopus 로고    scopus 로고
    • Factor V Leiden and Prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages
    • Foka ZJ, Lambropoulos AF, Saravelos H, et al. Factor V Leiden and Prothrombin G20210A mutations, but not methylenetetrahydrofolate reductase C677T, are associated with recurrent miscarriages. Hum Reprod 2000;15(2):458-462.
    • (2000) Hum Reprod , vol.15 , Issue.2 , pp. 458-462
    • Foka, Z.J.1    Lambropoulos, A.F.2    Saravelos, H.3
  • 8
    • 0031767657 scopus 로고    scopus 로고
    • Thrombophilia: A mechanism of disease in women with adverse pregnancy outcome and thrombotic lesions in the placenta
    • Arias F, Romero R, Joist H, Kraus FT. Thrombophilia: a mechanism of disease in women with adverse pregnancy outcome and thrombotic lesions in the placenta. J Matern-Fetal Med 1998;7(6):277-286.
    • (1998) J Matern-Fetal Med , vol.7 , Issue.6 , pp. 277-286
    • Arias, F.1    Romero, R.2    Joist, H.3    Kraus, F.T.4
  • 9
    • 0005517354 scopus 로고    scopus 로고
    • Case-control study of the frequency of thrombophilic disorders in couples with late foetal loss and no thrombotic antecedent - The Nimes Obstetricians and Haematologists Study5 (NOHA5)
    • Gris JC, Quere I, Monpeyroux F, et al. Case-control study of the frequency of thrombophilic disorders in couples with late foetal loss and no thrombotic antecedent-the Nimes Obstetricians and Haematologists Study5 (NOHA5). Thromb Haemost 1999;81(6):891-899.
    • (1999) Thromb Haemost , vol.81 , Issue.6 , pp. 891-899
    • Gris, J.C.1    Quere, I.2    Monpeyroux, F.3
  • 10
    • 0034610031 scopus 로고    scopus 로고
    • Mutations in coagulation factors in women with unexplained late fetal loss
    • Martinelli I, Taioli E, Cetin I, et al. Mutations in coagulation factors in women with unexplained late fetal loss. N Engl J Med 2000;343(14): 1015-1018.
    • (2000) N Engl J Med , vol.343 , Issue.14 , pp. 1015-1018
    • Martinelli, I.1    Taioli, E.2    Cetin, I.3
  • 11
    • 0033531184 scopus 로고    scopus 로고
    • Increased frequency of genetic thrombophilia in women with complications of pregnancy
    • Kupfermine MJ, Eldor A, Steinman N, et al. Increased frequency of genetic thrombophilia in women with complications of pregnancy. N Engl J Med 1999;340:9-13.
    • (1999) N Engl J Med , vol.340 , pp. 9-13
    • Kupfermine, M.J.1    Eldor, A.2    Steinman, N.3
  • 12
    • 16044369784 scopus 로고    scopus 로고
    • Increased fetal loss in women with heritable thrombophilia
    • Preston FE, Rosendaal FR, Walker ID, et al. Increased fetal loss in women with heritable thrombophilia. Lancet 1996;348(9032):913-916.
    • (1996) Lancet , vol.348 , Issue.9032 , pp. 913-916
    • Preston, F.E.1    Rosendaal, F.R.2    Walker, I.D.3
  • 13
    • 0032474219 scopus 로고    scopus 로고
    • Fetal and maternal contributions to risk of pre-eclampsia: Population based study
    • Lie RT, Rasmussen S, Brunborg H, Gjessing HK, Lie-Nielsen E, Irgens LM. Fetal and maternal contributions to risk of pre-eclampsia: population based study. BMJ 1998;316(7141):1343-1347.
    • (1998) BMJ , vol.316 , Issue.7141 , pp. 1343-1347
    • Lie, R.T.1    Rasmussen, S.2    Brunborg, H.3    Gjessing, H.K.4    Lie-Nielsen, E.5    Irgens, L.M.6
  • 16
    • 0031049804 scopus 로고    scopus 로고
    • Discrepancy between results of registration of perinatal cause of death by the CBS (Central Bureau of Statistics) and by personal studies in the Delft-Westland-Oostland region
    • Galan-Roosen AE, Kuijpers JC, Oei YB, van Velzen D, Mackenbach JP. Discrepancy between results of registration of perinatal cause of death by the CBS (Central Bureau of Statistics) and by personal studies in the Delft-Westland-Oostland region. Ned Tijdschr Geneeskd 1997;141(5):237-240.
    • (1997) Ned Tijdschr Geneeskd , vol.141 , Issue.5 , pp. 237-240
    • Galan-Roosen, A.E.1    Kuijpers, J.C.2    Oei, Y.B.3    Van Velzen, D.4    Mackenbach, J.P.5
  • 17
    • 0033950364 scopus 로고    scopus 로고
    • Automated, simultaneous detection of the factor V Leiden and prothrombin (G20210A) variants using multiplex PCR and a line probe assay
    • Leyte A, Smits PH, van Straalen JP, van Doom LJ, Quint WG. Automated, simultaneous detection of the factor V Leiden and prothrombin (G20210A) variants using multiplex PCR and a line probe assay. Thromb Haemost 2000;83(2):354-355.
    • (2000) Thromb Haemost , vol.83 , Issue.2 , pp. 354-355
    • Leyte, A.1    Smits, P.H.2    Van Straalen, J.P.3    Van Doom, L.J.4    Quint, W.G.5
  • 18
    • 84960989652 scopus 로고
    • On estimating the relation between blood group and disease
    • Woolf B. On estimating the relation between blood group and disease. Ann Hum Genet 1955;19:251-253.
    • (1955) Ann Hum Genet , vol.19 , pp. 251-253
    • Woolf, B.1
  • 19
    • 0035932518 scopus 로고    scopus 로고
    • Paternal and maternal components of the predisposition to preeclampsia
    • Esplin MS, Fausett MB, Fraser A, et al. Paternal and maternal components of the predisposition to preeclampsia. N Engl J Med 2001;344(12):867-872.
    • (2001) N Engl J Med , vol.344 , Issue.12 , pp. 867-872
    • Esplin, M.S.1    Fausett, M.B.2    Fraser, A.3
  • 21
    • 0030963627 scopus 로고    scopus 로고
    • Fetal carriers of the factor V Leiden mutation are prone to miscarriage and placental infarction
    • Dizon-Townson DS, Meline L, Nelson LM, Varner M, Ward K. Fetal carriers of the factor V Leiden mutation are prone to miscarriage and placental infarction. Am J Obstet Gynecol 1997;177:402-405.
    • (1997) Am J Obstet Gynecol , vol.177 , pp. 402-405
    • Dizon-Townson, D.S.1    Meline, L.2    Nelson, L.M.3    Varner, M.4    Ward, K.5
  • 22
    • 0030767010 scopus 로고    scopus 로고
    • Leiden mutation: An unrecognized cause of hemiplegic cerebral palsy, neonatal stroke, and placental thrombosis
    • Thorarensen O, Ryan S, Hunter J, Younkin DP, Factor V. Leiden mutation: an unrecognized cause of hemiplegic cerebral palsy, neonatal stroke, and placental thrombosis. Ann Neurol 1997;42(3):372-375.
    • (1997) Ann Neurol , vol.42 , Issue.3 , pp. 372-375
    • Thorarensen, O.1    Ryan, S.2    Hunter, J.3    Younkin, D.P.4    Factor, V.5
  • 23
    • 0029876985 scopus 로고    scopus 로고
    • Inherited thrombophilia: Pathogenesis, clinical syndromes, and management
    • De Stefano V, Finazzi G, Mannucci PM. Inherited thrombophilia: pathogenesis, clinical syndromes, and management. Blood 1996;87(9):3531-3544.
    • (1996) Blood , vol.87 , Issue.9 , pp. 3531-3544
    • De Stefano, V.1    Finazzi, G.2    Mannucci, P.M.3
  • 24
    • 0034130511 scopus 로고    scopus 로고
    • Heritability of elevated factor VIII antigen levels in factor V Leiden families with thrombophilia
    • Kamphuisen PW, Lensen R, Houwing-Duistermaat JJ, et al. Heritability of elevated factor VIII antigen levels in factor V Leiden families with thrombophilia. Br J Haematol 2000;109(3):519-522.
    • (2000) Br J Haematol , vol.109 , Issue.3 , pp. 519-522
    • Kamphuisen, P.W.1    Lensen, R.2    Houwing-Duistermaat, J.J.3
  • 25
    • 0033901546 scopus 로고    scopus 로고
    • Thrombophilia in pregnancy
    • Walker ID. Thrombophilia in pregnancy. J Clin Pathol 2000;53(8): 573-580.
    • (2000) J Clin Pathol , vol.53 , Issue.8 , pp. 573-580
    • Walker, I.D.1
  • 26
    • 0033518980 scopus 로고    scopus 로고
    • Periconceptional folic acid intake in the northern Netherlands
    • De Walle HE, de Jong-van den Berg LT, Cornel MC. Periconceptional folic acid intake in the northern Netherlands. Lancet 1999;353(9159):1187.
    • (1999) Lancet , vol.353 , Issue.9159 , pp. 1187
    • De Walle, H.E.1    De Jong-Van Den Berg, L.T.2    Cornel, M.C.3
  • 27
    • 0031022366 scopus 로고    scopus 로고
    • Randomised controlled trial of aspirin and aspirin plus heparin in pregnant women with recurrent miscarriage associated with phospholipid antibodies (or antiphospholipid antibodies)
    • Rai R, Cohen H, Dave M, Regan L. Randomised controlled trial of aspirin and aspirin plus heparin in pregnant women with recurrent miscarriage associated with phospholipid antibodies (or antiphospholipid antibodies). BMJ 1997;314(7076):253-257.
    • (1997) BMJ , vol.314 , Issue.7076 , pp. 253-257
    • Rai, R.1    Cohen, H.2    Dave, M.3    Regan, L.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.