-
1
-
-
65649125690
-
The global impact of pre-eclampsia and eclampsia
-
Duley L. The global impact of pre-eclampsia and eclampsia. Semin Perinatol. 2009;33(3): 130-137.
-
(2009)
Semin Perinatol
, vol.33
, Issue.3
, pp. 130-137
-
-
Duley, L.1
-
2
-
-
33645737208
-
Who analysis of causes of maternal death: A systematic review
-
Khan KS,Wojdyla D, Say L, et al. WHO analysis of causes of maternal death: a systematic review. Lancet. 2006;367(9516): 1066-1074.
-
(2006)
Lancet
, vol.367
, Issue.9516
, pp. 1066-1074
-
-
Khan, K.S.1
Wojdyla, D.2
Say, L.3
-
5
-
-
34249698202
-
Expectant management of severe preeclampsia remote from term: Patient selection, treatment, and delivery indications
-
Sibai BM, Barton JR. Expectant management of severe preeclampsia remote from term: patient selection, treatment, and delivery indications. Am J Obstet Gynecol. 2007;196(6): 514.e1-514.e9.
-
(2007)
Am J Obstet Gynecol
, vol.196
, Issue.6
-
-
Sibai, B.M.1
Barton, J.R.2
-
6
-
-
84876571215
-
Prevention of perinatal death and adverse perinatal outcome using low-dose aspirin: A meta-Analysis
-
Roberge S, Nicolaides KH, Demers S, et al. Prevention of perinatal death and adverse perinatal outcome using low-dose aspirin: a meta-Analysis. Ultrasound Obstet Gynecol. 2013; 41(5): 491-499.
-
(2013)
Ultrasound Obstet Gynecol
, vol.41
, Issue.5
, pp. 491-499
-
-
Roberge, S.1
Nicolaides, K.H.2
Demers, S.3
-
7
-
-
34247501729
-
Prioritisation of tests for the prediction of preeclampsia complications: A delphi survey
-
Thangaratinam S, Ismail K, Sharp S, et al. Prioritisation of tests for the prediction of preeclampsia complications: a Delphi survey. Hypertens Pregnancy. 2007;26(1): 131-138.
-
(2007)
Hypertens Pregnancy
, vol.26
, Issue.1
, pp. 131-138
-
-
Thangaratinam, S.1
Ismail, K.2
Sharp, S.3
-
8
-
-
64949129865
-
Estimation of proteinuria as a predictor of complications of pre-eclampsia: A systematic review
-
Thangaratinam S, Coomarasamy A, O'Mahony F, et al. Estimation of proteinuria as a predictor of complications of pre-eclampsia: a systematic review. BMC Med. 2009;7: 10.
-
(2009)
BMC Med
, vol.7
, pp. 10
-
-
Thangaratinam, S.1
Coomarasamy, A.2
O'Mahony, F.3
-
9
-
-
79956190637
-
How accurate are maternal symptoms in predicting impending complications in women with preeclampsia? A systematic review and meta-Analysis
-
Thangaratinam S, Gallos ID, Meah N, et al. How accurate are maternal symptoms in predicting impending complications in women with preeclampsia? A systematic review and meta-Analysis. Acta Obstet Gynecol Scand. 2011;90(6): 564-573.
-
(2011)
Acta Obstet Gynecol Scand
, vol.90
, Issue.6
, pp. 564-573
-
-
Thangaratinam, S.1
Gallos, I.D.2
Meah, N.3
-
10
-
-
79956208933
-
Accuracy of liver function tests for predicting adverse maternal and fetal outcomes in women with preeclampsia: A systematic review
-
Thangaratinam S, Koopmans CM, Iyengar S, et al. Accuracy of liver function tests for predicting adverse maternal and fetal outcomes in women with preeclampsia: a systematic review. Acta Obstet Gynecol Scand. 2011;90(6): 574-585.
-
(2011)
Acta Obstet Gynecol Scand
, vol.90
, Issue.6
, pp. 574-585
-
-
Thangaratinam, S.1
Koopmans, C.M.2
Iyengar, S.3
-
11
-
-
15044344544
-
Risk factors for pre-eclampsia at antenatal booking: Systematic review of controlled studies
-
Duckitt K, Harrington D. Risk factors for pre-eclampsia at antenatal booking: systematic review of controlled studies. BMJ. 2005;330(7491): 565.
-
(2005)
BMJ
, vol.330
, Issue.7491
, pp. 565
-
-
Duckitt, K.1
Harrington, D.2
-
12
-
-
84907357880
-
Genetics of preeclampsia-current concepts
-
Seremak-Mrzoikiewicz A. Genetics of preeclampsia-current concepts. Arch Perinat Med. 2008;14(4): 9-11.
-
(2008)
Arch Perinat Med
, vol.14
, Issue.4
, pp. 9-11
-
-
Seremak-Mrzoikiewicz, A.1
-
13
-
-
0026633369
-
Maternal mortality associated with hypertensive disorders of pregnancy in africa, asia, latin america and the caribbean
-
Duley L. Maternal mortality associated with hypertensive disorders of pregnancy in Africa, Asia, Latin America and the Caribbean. Br J Obstet Gynaecol. 1992;99(7): 547-553.
-
(1992)
Br J Obstet Gynaecol
, vol.99
, Issue.7
, pp. 547-553
-
-
Duley, L.1
-
14
-
-
13244271259
-
Genetic thrombophilias and preeclampsia: A meta-Analysis
-
Lin J, August P. Genetic thrombophilias and preeclampsia: a meta-Analysis. Obstet Gynecol. 2005;105(1): 182-192.
-
(2005)
Obstet Gynecol
, vol.105
, Issue.1
, pp. 182-192
-
-
Lin, J.1
August, P.2
-
15
-
-
32544441595
-
Thrombophilia in pregnancy: A systematic review
-
Robertson L, Wu O, Langhorne P, et al. Thrombophilia in pregnancy: a systematic review. Br J Haematol. 2006;132(2): 171-196.
-
(2006)
Br J Haematol
, vol.132
, Issue.2
, pp. 171-196
-
-
Robertson, L.1
Wu, O.2
Langhorne, P.3
-
16
-
-
84872156900
-
Genetic association studies in pre-eclampsia: Systematic meta-Analyses and field synopsis
-
Staines-Urias E, Paez MC, Doyle P, et al. Genetic association studies in pre-eclampsia: systematic meta-Analyses and field synopsis. Int J Epidemiol. 2012;41(6): 1764-1775.
-
(2012)
Int J Epidemiol
, vol.41
, Issue.6
, pp. 1764-1775
-
-
Staines-Urias, E.1
Paez, M.C.2
Doyle, P.3
-
17
-
-
0037050786
-
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(1): 6-14.
-
(2002)
Eur J Obstet Gynecol Reprod Biol
, vol.101
, Issue.1
, pp. 6-14
-
-
Alfirevic, Z.1
Roberts, D.2
Martlew, V.3
-
18
-
-
77955027422
-
The association of factor v leiden and prothrombin gene mutation and placenta-mediated pregnancy complications: A systematic review and meta-Analysis of prospective cohort studies
-
Rodger MA, Betancourt MT, Clark P, et al. The association of factor V Leiden and prothrombin gene mutation and placenta-mediated pregnancy complications: a systematic review and meta-Analysis of prospective cohort studies. PLoS Med. 2010;7(6): e1000292.
-
(2010)
PLoS Med
, vol.7
, Issue.6
-
-
Rodger, M.A.1
Betancourt, M.T.2
Clark, P.3
-
22
-
-
84872351368
-
The definition of severe and early onset preeclampsia. Statements from the international society for the study of hypertension in pregnancy (isshp)
-
Tranquilli AL, Brown MA, Zeeman GG, et al. The definition of severe and early onset preeclampsia. Statements from the International Society for the Study of Hypertension in Pregnancy (ISSHP). Pregnancy Hypertens. 2013;14: 44-47.
-
(2013)
Pregnancy Hypertens
, vol.14
, pp. 44-47
-
-
Tranquilli, A.L.1
Brown, M.A.2
Zeeman, G.G.3
-
23
-
-
38649091333
-
A navigator for human genome epidemiology
-
Yu W, Gwinn M, Clyne M, et al. A navigator for human genome epidemiology. Nat Genet. 2008;40(2): 124-125.
-
(2008)
Nat Genet
, vol.40
, Issue.2
, pp. 124-125
-
-
Yu, W.1
Gwinn, M.2
Clyne, M.3
-
24
-
-
61449255938
-
Strengthening the reporting of genetic association studies (strega): An extension of the strobe statement
-
Little J, Higgins J, Ioannidis J, et al. STrengthening the REporting of Genetic Association studies (STREGA): an extension of the STROBE statement. PLoS Med. 2009;6(2): e1000022.
-
(2009)
PLoS Med
, vol.6
, Issue.2
-
-
Little, J.1
Higgins, J.2
Ioannidis, J.3
-
25
-
-
79956320492
-
A comparison of clinical officers with medical doctors on outcomes of caesarean section in the developing world: Meta-Analysis of controlled studies
-
Wilson A, Lissauer D, Thangaratinam S, et al. A comparison of clinical officers with medical doctors on outcomes of caesarean section in the developing world: meta-Analysis of controlled studies. BMJ. 2011;342: d2600.
-
(2011)
BMJ
, vol.342
-
-
Wilson, A.1
Lissauer, D.2
Thangaratinam, S.3
-
27
-
-
2442650305
-
Detection of genotyping errors by hardy-weinberg equilibrium testing
-
Hosking L, Lumsden S, Lewis K, et al. Detection of genotyping errors by Hardy-Weinberg equilibrium testing. Eur J Hum Genet. 2004;12(5): 395-399.
-
(2004)
Eur J Hum Genet
, vol.12
, Issue.5
, pp. 395-399
-
-
Hosking, L.1
Lumsden, S.2
Lewis, K.3
-
28
-
-
38949094880
-
Assessment of cumulative evidence on genetic associations: Interim guidelines
-
Ioannidis JP, Boffetta P, Little J, et al. Assessment of cumulative evidence on genetic associations: interim guidelines. Int J Epidemiol. 2008;37(1): 120-132.
-
(2008)
Int J Epidemiol
, vol.37
, Issue.1
, pp. 120-132
-
-
Ioannidis, J.P.1
Boffetta, P.2
Little, J.3
-
29
-
-
67749106283
-
Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases
-
Khoury MJ, Bertram L, Boffetta P, et al. Genome-wide association studies, field synopses, and the development of the knowledge base on genetic variation and human diseases. Am J Epidemiol. 2009;170(3): 269-279.
-
(2009)
Am J Epidemiol
, vol.170
, Issue.3
, pp. 269-279
-
-
Khoury, M.J.1
Bertram, L.2
Boffetta, P.3
-
30
-
-
33748090675
-
A modified test for small-study effects in meta-Analyses of controlled trials with binary endpoints
-
Harbord RM, Egger M, Sterne JA. A modified test for small-study effects in meta-Analyses of controlled trials with binary endpoints. Stat Med. 2006;25(20): 3443-3457.
-
(2006)
Stat Med
, vol.25
, Issue.20
, pp. 3443-3457
-
-
Harbord, R.M.1
Egger, M.2
Sterne, J.A.3
-
31
-
-
84888431150
-
-
Copenhagen, Denmark: The Nordic Cochrane Centre, The Cochrane Collaboration
-
Review Manager (RevMan) computer program. Version 5.2. Copenhagen, Denmark: The Nordic Cochrane Centre, The Cochrane Collaboration; 2012.
-
(2012)
Review Manager (RevMan) Computer Program. Version 5.2
-
-
-
32
-
-
84977525922
-
-
Stata Corporation. College Station, TX: Stata Corporation
-
Stata Corporation. Stata statistical software, release 12. College Station, TX: Stata Corporation; 2013.
-
(2013)
Stata Statistical Software, Release 12
-
-
-
33
-
-
79960004464
-
Genetic polymorphisms of killer cell immunoglobulin-like receptor 3dl2 in preeclampsia
-
Wang XL, Wang Q, Sun CJ, et al. Genetic polymorphisms of killer cell immunoglobulin-like receptor 3DL2 in preeclampsia. J Perinat Med. 2011;39(3): 273-278.
-
(2011)
J Perinat Med
, vol.39
, Issue.3
, pp. 273-278
-
-
Wang, X.L.1
Wang, Q.2
Sun, C.J.3
-
34
-
-
77951245020
-
Leptin gene (tttc)(n) microsatellite polymorphism as well as leptin receptor r223q and ppargamma2 p12a substitutions are not associated with hypertensive disorders in pregnancy
-
Wiedemann A, Vocke F, Fitzgerald JS, et al. Leptin gene (TTTC)(n) microsatellite polymorphism as well as leptin receptor R223Q and PPARgamma2 P12A substitutions are not associated with hypertensive disorders in pregnancy. Am J Reprod Immunol. 2010;63(4): 310-317.
-
(2010)
Am J Reprod Immunol
, vol.63
, Issue.4
, pp. 310-317
-
-
Wiedemann, A.1
Vocke, F.2
Fitzgerald, J.S.3
-
35
-
-
39049115688
-
Relationship between dopamine-beta-hydroxylase gene polymorphism and hypertensive disorder complicating pregnancy [in chinese]
-
Zhu H, Zhao YH, Zhang WY, et al. Relationship between dopamine-beta-hydroxylase gene polymorphism and hypertensive disorder complicating pregnancy [in Chinese]. Zhonghua Fu Chan Ke Za Zhi. 2006;41(6): 384-386.
-
(2006)
Zhonghua Fu Chan Ke Za Zhi
, vol.41
, Issue.6
, pp. 384-386
-
-
Zhu, H.1
Zhao, Y.H.2
Zhang, W.Y.3
-
36
-
-
77957693476
-
Relationships among adiponectin gene polymorphisms, proteinuria and increased blood pressure in the context of placental diseases
-
Youpeng B, Wei X, Wei L, et al. Relationships among adiponectin gene polymorphisms, proteinuria and increased blood pressure in the context of placental diseases. Hypertens Res. 2010;33(10): 1066-1070.
-
(2010)
Hypertens Res
, vol.33
, Issue.10
, pp. 1066-1070
-
-
Youpeng, B.1
Wei, X.2
Wei, L.3
-
37
-
-
23044517241
-
The g20210a prothrombin-gene mutation and the plasminogen activator inhibitor (pai-1) 5g/5g genotype are associated with early onset of severe preeclampsia
-
Gerhardt A, GoeckeTW, BeckmannMW, et al. The G20210A prothrombin-gene mutation and the plasminogen activator inhibitor (PAI-1) 5G/5G genotype are associated with early onset of severe preeclampsia. J Thromb Haemost. 2005;3(4): 686-691.
-
(2005)
J Thromb Haemost
, vol.3
, Issue.4
, pp. 686-691
-
-
Gerhardt, A.1
Goecke, T.W.2
Beckmann, M.W.3
-
38
-
-
0036483204
-
Is there an increased maternal-infant prevalence of factor v leiden in association with severe pre-eclampsia?
-
Currie L, Peek M, McNiven M, et al. Is there an increased maternal-infant prevalence of factor V Leiden in association with severe pre-eclampsia? BJOG. 2002;109(2): 191-196.
-
(2002)
BJOG
, vol.109
, Issue.2
, pp. 191-196
-
-
Currie, L.1
Peek, M.2
McNiven, M.3
-
39
-
-
84877252808
-
Association between pre-eclampsia and inherited thrombophilias
-
Deveer R, Engin-Ustun Y, Akbaba E, et al. Association between pre-eclampsia and inherited thrombophilias. Fetal Pediatr Pathol. 2013;32(3): 213-217.
-
(2013)
Fetal Pediatr Pathol
, vol.32
, Issue.3
, pp. 213-217
-
-
Deveer, R.1
Engin-Ustun, Y.2
Akbaba, E.3
-
40
-
-
0029999583
-
The factor v leiden mutation may predispose women to severe preeclampsia
-
Dizon-Townson DS, Nelson LM, Easton K, et al. The factor V Leiden mutation may predispose women to severe preeclampsia. Am J Obstet Gynecol. 1996;175(4 Pt 1): 902-905.
-
(1996)
Am J Obstet Gynecol
, vol.175
, Issue.4 PART 1
, pp. 902-905
-
-
Dizon-Townson, D.S.1
Nelson, L.M.2
Easton, K.3
-
41
-
-
77951236101
-
Transforming growth factor-beta 1 gene polymorphisms in korean patients with pre-eclampsia
-
Kim SY, Lim JH, Park SY, et al. Transforming growth factor-beta 1 gene polymorphisms in Korean patients with pre-eclampsia. Am J Reprod Immunol. 2010;63(4): 291-298.
-
(2010)
Am J Reprod Immunol
, vol.63
, Issue.4
, pp. 291-298
-
-
Kim, S.Y.1
Lim, J.H.2
Park, S.Y.3
-
42
-
-
0034924655
-
Maternal and fetal inherited thrombophilias are not related to the development of severe preeclampsia
-
Livingston JC, Barton JR, Park V, et al. Maternal and fetal inherited thrombophilias are not related to the development of severe preeclampsia. Am J Obstet Gynecol. 2001;185(1): 153-157.
-
(2001)
Am J Obstet Gynecol
, vol.185
, Issue.1
, pp. 153-157
-
-
Livingston, J.C.1
Barton, J.R.2
Park, V.3
-
43
-
-
67249114711
-
Blood group ab and factor v leiden as risk factors for pre-eclampsia: A population-based nested case-control study
-
Hiltunen LM, Laivuori H, Rautanen A, et al. Blood group AB and factor V Leiden as risk factors for pre-eclampsia: a population-based nested case-control study. Thromb Res. 2009;124(2): 167-173.
-
(2009)
Thromb Res
, vol.124
, Issue.2
, pp. 167-173
-
-
Hiltunen, L.M.1
Laivuori, H.2
Rautanen, A.3
-
44
-
-
34147187301
-
Mannose-binding lectin (mbl) codon 54 gene polymorphism protects against development of pre-eclampsia hellp syndrome and pre-eclampsia-Associated intrauterine growth restriction
-
Sziller I, Babula O, Hupuczi P, et al. Mannose-binding lectin (MBL) codon 54 gene polymorphism protects against development of pre-eclampsia, HELLP syndrome and pre-eclampsia-Associated intrauterine growth restriction. Mol Hum Reprod. 2007;13(4): 281-285.
-
(2007)
Mol Hum Reprod
, vol.13
, Issue.4
, pp. 281-285
-
-
Sziller, I.1
Babula, O.2
Hupuczi, P.3
-
45
-
-
77949472807
-
Leptin receptor (lepr) snp polymorphisms in hellp syndrome patients determined by quantitative real-Time pcr and melting curve analysis
-
Várkonyi T, Lázár L, Molvarec A, et al. Leptin receptor (LEPR) SNP polymorphisms in HELLP syndrome patients determined by quantitative real-Time PCR and melting curve analysis. BMC Med Genet. 2010;11: 25.
-
(2010)
BMC Med Genet
, vol.11
, pp. 25
-
-
Várkonyi, T.1
Lázár, L.2
Molvarec, A.3
-
46
-
-
0032740843
-
Preeclampsia and genetic risk factors for thrombosis: A case-control study
-
De Groot CJ, Bloemenkamp KW, Duvekot EJ, et al. Preeclampsia and genetic risk factors for thrombosis: a case-control study. Am J Obstet Gynecol. 1999;181(4): 975-980.
-
(1999)
Am J Obstet Gynecol
, vol.181
, Issue.4
, pp. 975-980
-
-
De Groot, C.J.1
Bloemenkamp, K.W.2
Duvekot, E.J.3
-
47
-
-
38449120804
-
Ser128arg e-selectin and thr715pro p-selectin polymorphisms and severe preeclampsia
-
Derzbach L, Balogh A, Bokodi G, et al. Ser128Arg E-selectin and Thr715Pro P-selectin polymorphisms and severe preeclampsia. J Reprod Med. 2007;52(9): 815-818.
-
(2007)
J Reprod Med
, vol.52
, Issue.9
, pp. 815-818
-
-
Derzbach, L.1
Balogh, A.2
Bokodi, G.3
-
48
-
-
33947709164
-
Association between estrogen receptor alpha (esr1) gene polymorphisms and severe preeclampsia
-
Molvarec A, Vér A, Fekete A, et al. Association between estrogen receptor alpha (ESR1) gene polymorphisms and severe preeclampsia. Hypertens Res. 2007;30(3): 205-211.
-
(2007)
Hypertens Res
, vol.30
, Issue.3
, pp. 205-211
-
-
Molvarec, A.1
Vér, A.2
Fekete, A.3
-
49
-
-
42749086229
-
Association between tumor necrosis factor (tnf)-Alpha g-308a gene polymorphism and preeclampsia complicated by severe fetal growth restriction
-
Molvarec A, Jermendy A, Nagy B, et al. Association between tumor necrosis factor (TNF)-Alpha G-308A gene polymorphism and preeclampsia complicated by severe fetal growth restriction. Clin Chim Acta. 2008;392(1-2): 52-57.
-
(2008)
Clin Chim Acta
, vol.392
, Issue.1-2
, pp. 52-57
-
-
Molvarec, A.1
Jermendy, A.2
Nagy, B.3
-
50
-
-
59249083026
-
Association of extracellular superoxide dismutase (sod3) ala40thr gene polymorphism with pre-eclampsia complicated by severe fetal growth restriction
-
Rosta K, Molvarec A, Enzsöly A, et al. Association of extracellular superoxide dismutase (SOD3) Ala40Thr gene polymorphism with pre-eclampsia complicated by severe fetal growth restriction. Eur J Obstet Gynecol Reprod Biol. 2009; 142(2): 134-138.
-
(2009)
Eur J Obstet Gynecol Reprod Biol
, vol.142
, Issue.2
, pp. 134-138
-
-
Rosta, K.1
Molvarec, A.2
Enzsöly, A.3
-
51
-
-
0035350680
-
Postnatal screening for thrombophilia in women with severe pregnancy complications
-
Alfirevic Z, Mousa HA, Martlew V, et al. Postnatal screening for thrombophilia in women with severe pregnancy complications. Obstet Gynecol. 2001;97(5 Pt 1): 753-759.
-
(2001)
Obstet Gynecol
, vol.97
, Issue.5 PART 1
, pp. 753-759
-
-
Alfirevic, Z.1
Mousa, H.A.2
Martlew, V.3
-
52
-
-
79952423162
-
Immunoregulatory gene polymorphisms in women with preeclampsia
-
Pendeloski KP, Sass N, Torloni MR, et al. Immunoregulatory gene polymorphisms in women with preeclampsia. Hypertens Res. 2011;34(3): 384-388.
-
(2011)
Hypertens Res
, vol.34
, Issue.3
, pp. 384-388
-
-
Pendeloski, K.P.1
Sass, N.2
Torloni, M.R.3
-
53
-
-
84863902802
-
Preeclampsia in north indian women: The contribution of genetic polymorphisms
-
Aggarwal S, Dimri N, Tandon I, et al. Preeclampsia in North Indian women: the contribution of genetic polymorphisms. J Obstet Gynaecol Res. 2011;37(10): 1335-1341.
-
(2011)
J Obstet Gynaecol Res
, vol.37
, Issue.10
, pp. 1335-1341
-
-
Aggarwal, S.1
Dimri, N.2
Tandon, I.3
-
54
-
-
25844523220
-
Association of angiotensin-converting enzyme gene polymorphism with pregnancy-induced hypertension
-
Kaur R, Jain V, Khuller M, et al. Association of angiotensin-converting enzyme gene polymorphism with pregnancy-induced hypertension. Acta Obstet Gynecol Scand. 2005;84(10): 929-933.
-
(2005)
Acta Obstet Gynecol Scand
, vol.84
, Issue.10
, pp. 929-933
-
-
Kaur, R.1
Jain, V.2
Khuller, M.3
-
55
-
-
70350732618
-
Angiotensin-converting enzyme and adducin-1 polymorphisms in women with preeclampsia and gestational hypertension
-
Mandô C, Antonazzo P, Tabano S, et al. Angiotensin-converting enzyme and adducin-1 polymorphisms in women with preeclampsia and gestational hypertension. Reprod Sci. 2009;16(9): 819-826.
-
(2009)
Reprod Sci
, vol.16
, Issue.9
, pp. 819-826
-
-
Mandô, C.1
Antonazzo, P.2
Tabano, S.3
-
56
-
-
2542439029
-
Hypertension-related gene polymorphisms in pre-eclampsia, eclampsia and gestational hypertension in black south african women
-
Roberts CB, Rom L, Moodley J, et al. Hypertension-related gene polymorphisms in pre-eclampsia, eclampsia and gestational hypertension in black South African women. J Hypertens. 2004;22(5): 945-948.
-
(2004)
J Hypertens
, vol.22
, Issue.5
, pp. 945-948
-
-
Roberts, C.B.1
Rom, L.2
Moodley, J.3
-
57
-
-
0036653362
-
Angiotensinogen gene m235t variant and pre-eclampsia in romanian pregnant women
-
Procopciuc L, Jebeleanu G, Surcel I, et al. Angiotensinogen gene M235T variant and pre-eclampsia in Romanian pregnant women. J Cell Mol Med. 2002;6(3): 383-388.
-
(2002)
J Cell Mol Med
, vol.6
, Issue.3
, pp. 383-388
-
-
Procopciuc, L.1
Jebeleanu, G.2
Surcel, I.3
-
58
-
-
2342428666
-
Polymorphisms of thrombophilic and vasoactive genes and severe preeclampsia: A pilot study
-
Tempfer CB, Jirecek S, Riener EK, et al. Polymorphisms of thrombophilic and vasoactive genes and severe preeclampsia: a pilot study. J Soc Gynecol Investig. 2004;11(4): 227-231.
-
(2004)
J Soc Gynecol Investig
, vol.11
, Issue.4
, pp. 227-231
-
-
Tempfer, C.B.1
Jirecek, S.2
Riener, E.K.3
-
59
-
-
0036774978
-
Factor v leiden and prothrombin g20210a mutations in pregnancies with adverse outcome
-
Agorastos T, Karavida A, Lambropoulos A, et al. Factor V Leiden and prothrombin G20210A mutations in pregnancies with adverse outcome. J Matern Fetal Neonatal Med. 2002; 12(4): 267-273.
-
(2002)
J Matern Fetal Neonatal Med
, vol.12
, Issue.4
, pp. 267-273
-
-
Agorastos, T.1
Karavida, A.2
Lambropoulos, A.3
-
60
-
-
0036901330
-
Factor v leiden and factor ii g20210a in preeclampsia and hellp syndrome
-
Benedetto C, Marozio L, Salton L, et al. Factor V Leiden and factor II G20210A in preeclampsia and HELLP syndrome. Acta Obstet Gynecol Scand. 2002;81(12): 1095-1100.
-
(2002)
Acta Obstet Gynecol Scand
, vol.81
, Issue.12
, pp. 1095-1100
-
-
Benedetto, C.1
Marozio, L.2
Salton, L.3
-
61
-
-
0035340294
-
Genetic susceptibility to preeclampsia: Roles of cytosine-To-Thymine substitution at nucleotide 677 of the gene for methylenetetrahydrofolate reductase, 68-base pair insertion at nucleotide 844 of the gene for cystathionine beta-synthase, and factor v leiden mutation
-
Kim Y, Williamson R, Murray J, et al. Genetic susceptibility to preeclampsia: roles of cytosine-To-Thymine substitution at nucleotide 677 of the gene for methylenetetrahydrofolate reductase, 68-base pair insertion at nucleotide 844 of the gene for cystathionine beta-synthase, and factor V Leiden mutation. Am J Obstet Gynecol. 2001;184(6): 1211-1217.
-
(2001)
Am J Obstet Gynecol
, vol.184
, Issue.6
, pp. 1211-1217
-
-
Kim, Y.1
Williamson, R.2
Murray, J.3
-
62
-
-
0033531184
-
Increased frequency of genetic thrombophilia in women with complications of pregnancy
-
Kupferminc MJ, Eldor A, Steinman N, et al. Increased frequency of genetic thrombophilia in women with complications of pregnancy. N Engl J Med. 1999;340(1): 9-13.
-
(1999)
N Engl J Med
, vol.340
, Issue.1
, pp. 9-13
-
-
Kupferminc, M.J.1
Eldor, A.2
Steinman, N.3
-
63
-
-
0034079143
-
Severe preeclampsia and high frequency of genetic thrombophilic mutations
-
Kupferminc MJ, Fait G, Many A, et al. Severe preeclampsia and high frequency of genetic thrombophilic mutations. Obstet Gynecol. 2000;96(1): 45-49.
-
(2000)
Obstet Gynecol
, vol.96
, Issue.1
, pp. 45-49
-
-
Kupferminc, M.J.1
Fait, G.2
Many, A.3
-
64
-
-
84858860242
-
Thrombophilic mutations and susceptibility to preeclampsia in western iran
-
Malek-Khosravi S, Rahimi Z, Rahimi Z, et al. Thrombophilic mutations and susceptibility to preeclampsia in Western Iran. J Thromb Thrombolysis. 2012;33(1): 109-115.
-
(2012)
J Thromb Thrombolysis
, vol.33
, Issue.1
, pp. 109-115
-
-
Malek-Khosravi, S.1
Rahimi, Z.2
Rahimi, Z.3
-
65
-
-
45849144786
-
Maternal factor v leiden mutation is associated with hellp syndrome in caucasian women
-
Muetze S, Leeners B, Ortlepp JR, et al. Maternal factor V Leiden mutation is associated with HELLP syndrome in Caucasian women. Acta Obstet Gynecol Scand. 2008;87(6): 635-642.
-
(2008)
Acta Obstet Gynecol Scand
, vol.87
, Issue.6
, pp. 635-642
-
-
Muetze, S.1
Leeners, B.2
Ortlepp, J.R.3
-
66
-
-
2642617790
-
Detection of factor v leiden mutation in severe pre-eclamptic hungarian women
-
Nagy B, Tóth T, Rigó J Jr, et al. Detection of factor V Leiden mutation in severe pre-eclamptic Hungarian women. Clin Genet. 1998;53(6): 478-481.
-
(1998)
Clin Genet
, vol.53
, Issue.6
, pp. 478-481
-
-
Nagy, B.1
Tóth, T.2
Rigó Jr., J.3
-
67
-
-
0033932801
-
Maternal and neonatal outcome of preeclamptic pregnancies: The potential roles of factor v leiden mutation and 5,10 methylenetetrahydrofolate reductase
-
Rigó J Jr, Nagy B, Fintor L, et al. Maternal and neonatal outcome of preeclamptic pregnancies: the potential roles of factor V Leiden mutation and 5,10 methylenetetrahydrofolate reductase. Hypertens Pregnancy. 2000;19(2): 163-172.
-
(2000)
Hypertens Pregnancy
, vol.19
, Issue.2
, pp. 163-172
-
-
Rigó Jr., J.1
Nagy, B.2
Fintor, L.3
-
68
-
-
0042877163
-
Association of maternal and/or fetal factor v leiden and g20210a prothrombin mutation with hellp syndrome and intrauterine growth restriction
-
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 (Lond). 2003;105(3): 279-285.
-
(2003)
Clin Sci (Lond)
, vol.105
, Issue.3
, pp. 279-285
-
-
Schlembach, D.1
Beinder, E.2
Zingsem, J.3
-
69
-
-
77953870122
-
The significance of genetic polymorphisms of factor v leiden and prothrombin in the preeclamptic polish women
-
Seremak-Mrozikiewicz A, Drews K, Wender-Ozegowska E, et al. The significance of genetic polymorphisms of factor V Leiden and prothrombin in the preeclamptic Polish women. J Thromb Thrombolysis. 2010;30(1): 97-104.
-
(2010)
J Thromb Thrombolysis
, vol.30
, Issue.1
, pp. 97-104
-
-
Seremak-Mrozikiewicz, A.1
Drews, K.2
Wender-Ozegowska, E.3
-
70
-
-
0035663185
-
Prothrombin 20210 g: A mutation and factor v leiden mutation in women with a history of severe preeclampsia and (h)ellp syndrome
-
van Pampus MG, Wolf H, Koopman MM, et al. Prothrombin 20210 G: a mutation and factor V Leiden mutation in women with a history of severe preeclampsia and (H)ELLP syndrome. Hypertens Pregnancy. 2001;20(3): 291-298.
-
(2001)
Hypertens Pregnancy
, vol.20
, Issue.3
, pp. 291-298
-
-
Van Pampus, M.G.1
Wolf, H.2
Koopman, M.M.3
-
71
-
-
0034668897
-
Incidence of the factor v leiden-mutation, coagulation inhibitor deficiency, and elevated antiphospholipid-Antibodies in patients with preeclampsia or hellp-syndrome. Hemolysis, elevated liver-enzymes, low platelets
-
von Tempelhoff GF, Heilmann L, Spanuth E, et al. Incidence of the factor V Leiden-mutation, coagulation inhibitor deficiency, and elevated antiphospholipid-Antibodies in patients with preeclampsia or HELLP-syndrome. Hemolysis, elevated liver-enzymes, low platelets. Thromb Res. 2000; 100(4): 363-365.
-
(2000)
Thromb Res
, vol.100
, Issue.4
, pp. 363-365
-
-
Von Tempelhoff, G.F.1
Heilmann, L.2
Spanuth, E.3
-
72
-
-
70349488035
-
Leptin gene (tttc)(n) microsatellite polymorphism in pre-eclampsia and hellp syndrome
-
Nagy B, Varkonyi T, Molvarec A, et al. Leptin gene (TTTC)(n) microsatellite polymorphism in pre-eclampsia and HELLP syndrome. Clin Chem Lab Med. 2009;47(9): 1033-1037.
-
(2009)
Clin Chem Lab Med
, vol.47
, Issue.9
, pp. 1033-1037
-
-
Nagy, B.1
Varkonyi, T.2
Molvarec, A.3
-
73
-
-
33750456996
-
Leptin receptor gene polymorphisms in severely pre-eclamptic women
-
Rigó J, Szendei G, Rosta K, et al. Leptin receptor gene polymorphisms in severely pre-eclamptic women. Gynecol Endocrinol. 2006;22(9): 521-525.
-
(2006)
Gynecol Endocrinol
, vol.22
, Issue.9
, pp. 521-525
-
-
Rigó, J.1
Szendei, G.2
Rosta, K.3
-
74
-
-
80155187789
-
Association of leptin level and leptin receptor gene polymorphisms with susceptibility to severe pre-eclampsia [in chinese]
-
Guan LX, Gao L, Gao Y, et al. Association of leptin level and leptin receptor gene polymorphisms with susceptibility to severe pre-eclampsia [in Chinese]. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2011;28(5): 562-567.
-
(2011)
Zhonghua Yi Xue Yi Chuan Xue Za Zhi
, vol.28
, Issue.5
, pp. 562-567
-
-
Guan, L.X.1
Gao, L.2
Gao, Y.3
-
75
-
-
0034679870
-
Absence of association between a common mutation in the methylenetetrahydrofolate reductase gene and preeclampsia in japanese women
-
Kobashi G, Yamada H, Asano T, et al. Absence of association between a common mutation in the methylenetetrahydrofolate reductase gene and preeclampsia in Japanese women. Am J Med Genet. 2000;93(2): 122-125.
-
(2000)
Am J Med Genet
, vol.93
, Issue.2
, pp. 122-125
-
-
Kobashi, G.1
Yamada, H.2
Asano, T.3
-
76
-
-
67650529836
-
Cytokine gene polymorphisms in preeclampsia and eclampsia
-
de Lima TH, Sass N, Mattar R, et al. Cytokine gene polymorphisms in preeclampsia and eclampsia. Hypertens Res. 2009;32(7): 565-569.
-
(2009)
Hypertens Res
, vol.32
, Issue.7
, pp. 565-569
-
-
De Lima, T.H.1
Sass, N.2
Mattar, R.3
-
77
-
-
2342576718
-
Association of the tnf2 allele with eclampsia
-
Kaiser T, Grehan M, Brennecke S, et al. Association of the TNF2 allele with eclampsia. Gynecol Obstet Invest. 2004; 57(4): 204-209.
-
(2004)
Gynecol Obstet Invest
, vol.57
, Issue.4
, pp. 204-209
-
-
Kaiser, T.1
Grehan, M.2
Brennecke, S.3
-
78
-
-
34447304062
-
Polymorphisms in the tumor necrosis factor-Alpha gene in turkish women with pre-eclampsia and eclampsia
-
Pazarbasi A, Kasap M, Güzel AI, et al. Polymorphisms in the tumor necrosis factor-Alpha gene in Turkish women with pre-eclampsia and eclampsia. Acta Med Okayama. 2007; 61(3): 153-160.
-
(2007)
Acta Med Okayama
, vol.61
, Issue.3
, pp. 153-160
-
-
Pazarbasi, A.1
Kasap, M.2
Güzel, A.I.3
-
80
-
-
60249089098
-
The two stage model of preeclampsia: Variations on the theme
-
Roberts JM, Hubel CA. The two stage model of preeclampsia: variations on the theme. Placenta. 2009;30(suppl A): S32-S37.
-
(2009)
Placenta
, vol.30
, Issue.SUPPL. A
-
-
Roberts, J.M.1
Hubel, C.A.2
-
81
-
-
0029866102
-
Surface blebs on apoptotic cells are sites of enhanced procoagulant activity: Implications for coagulation events and antigenic spread in systemic lupus erythematosus
-
Casciola-Rosen L, Rosen A, Petri M, et al. Surface blebs on apoptotic cells are sites of enhanced procoagulant activity: implications for coagulation events and antigenic spread in systemic lupus erythematosus. Proc Natl Acad Sci U S A. 1996;93(4): 1624-1629.
-
(1996)
Proc Natl Acad Sci U S A
, vol.93
, Issue.4
, pp. 1624-1629
-
-
Casciola-Rosen, L.1
Rosen, A.2
Petri, M.3
-
83
-
-
0033812095
-
Longitudinal analysis of maternal plasma leptin concentrations during normal pregnancy and pre-eclampsia
-
Anim-Nyame N, Sooranna SR, Steer PJ, et al. Longitudinal analysis of maternal plasma leptin concentrations during normal pregnancy and pre-eclampsia. Hum Reprod. 2000; 15(9): 2033-2036.
-
(2000)
Hum Reprod
, vol.15
, Issue.9
, pp. 2033-2036
-
-
Anim-Nyame, N.1
Sooranna, S.R.2
Steer, P.J.3
-
84
-
-
80052583870
-
Serum leptin levels in relation to circulating cytokines, chemokines, adhesion molecules and angiogenic factors in normal pregnancy and preeclampsia
-
Molvarec A, Szarka A,Walentin S, et al. Serum leptin levels in relation to circulating cytokines, chemokines, adhesion molecules and angiogenic factors in normal pregnancy and preeclampsia. Reprod Biol Endocrinol. 2011;9: 124.
-
(2011)
Reprod Biol Endocrinol
, vol.9
, pp. 124
-
-
Molvarec, A.1
Szarka, A.2
Walentin, S.3
-
85
-
-
0036020034
-
Leptin and preeclampsia
-
Poston L. Leptin and preeclampsia. Semin Reprod Med. 2002; 20(2): 131-138.
-
(2002)
Semin Reprod Med
, vol.20
, Issue.2
, pp. 131-138
-
-
Poston, L.1
-
86
-
-
0038334588
-
Interactions between leptin and the human sympathetic nervous system
-
Eikelis N, Schlaich M, Aggarwal A, et al. Interactions between leptin and the human sympathetic nervous system. Hypertension. 2003;41(5): 1072-1079.
-
(2003)
Hypertension
, vol.41
, Issue.5
, pp. 1072-1079
-
-
Eikelis, N.1
Schlaich, M.2
Aggarwal, A.3
-
87
-
-
0344132050
-
A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13
-
Arngrímsson R, Sigurõardóttir S, Frigge ML, et al. A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13. Hum Mol Genet. 1999; 8(9): 1799-1805.
-
(1999)
Hum Mol Genet
, vol.8
, Issue.9
, pp. 1799-1805
-
-
Arngrímsson, R.1
Sigurõardóttir, S.2
Frigge, M.L.3
-
88
-
-
16944366181
-
A genomewide linkage study of preeclampsia/eclampsia reveals evidence for a candidate region on 4q
-
Harrison GA, Humphrey KE, Jones N, et al. A genomewide linkage study of preeclampsia/eclampsia reveals evidence for a candidate region on 4q. Am J Hum Genet. 1997;60(5): 1158-1167.
-
(1997)
Am J Hum Genet
, vol.60
, Issue.5
, pp. 1158-1167
-
-
Harrison, G.A.1
Humphrey, K.E.2
Jones, N.3
-
90
-
-
0037219649
-
Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in finnish families
-
Laivuori H, Lahermo P, Ollikainen V, et al. Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families. Am J Hum Genet. 2003;72(1): 168-177.
-
(2003)
Am J Hum Genet
, vol.72
, Issue.1
, pp. 168-177
-
-
Laivuori, H.1
Lahermo, P.2
Ollikainen, V.3
-
91
-
-
0033659638
-
A genome scan in families from australia and new zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2
-
Moses E, Lade J, Guo G, et al. A genome scan in families from Australia and New Zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2. Am J Hum Genet. 2000;67(6): 1581-1585.
-
(2000)
Am J Hum Genet
, vol.67
, Issue.6
, pp. 1581-1585
-
-
Moses, E.1
Lade, J.2
Guo, G.3
-
92
-
-
84863399988
-
Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta b gene
-
Johnson MP, Brennecke SP, East CE, et al. Genome-wide association scan identifies a risk locus for preeclampsia on 2q14, near the inhibin, beta B gene. PLoS One. 2012;7(3): e33666.
-
(2012)
PLoS One
, vol.7
, Issue.3
-
-
Johnson, M.P.1
Brennecke, S.P.2
East, C.E.3
-
93
-
-
84863010013
-
Genome-wide association study identifies a maternal copy-number deletion in psg11 enriched among preeclampsia patients
-
Zhao L, Triche EW, Walsh KM, et al. Genome-wide association study identifies a maternal copy-number deletion in PSG11 enriched among preeclampsia patients. BMC Pregnancy Childbirth. 2012;12: 61.
-
(2012)
BMC Pregnancy Childbirth
, vol.12
, pp. 61
-
-
Zhao, L.1
Triche, E.W.2
Walsh, K.M.3
-
94
-
-
0034149941
-
Oxygen and placental development during the first trimester: Implications for the pathophysiology of pre-eclampsia
-
Caniggia I, Winter J, Lye SJ, et al. Oxygen and placental development during the first trimester: implications for the pathophysiology of pre-eclampsia. Placenta. 2000;21(suppl A): S25-S30.
-
(2000)
Placenta
, vol.21
, Issue.SUPPL. A
-
-
Caniggia, I.1
Winter, J.2
Lye, S.J.3
-
95
-
-
0037395928
-
Inhibin, activin, follistatin, activin receptors and beta-glycan gene expression in the placental tissue of patients with pre-eclampsia
-
Casagrandi D, Bearfield C, Geary J, et al. Inhibin, activin, follistatin, activin receptors and beta-glycan gene expression in the placental tissue of patients with pre-eclampsia. Mol Hum Reprod. 2003;9(4): 199-203.
-
(2003)
Mol Hum Reprod
, vol.9
, Issue.4
, pp. 199-203
-
-
Casagrandi, D.1
Bearfield, C.2
Geary, J.3
-
96
-
-
0031750218
-
Inhibin-A and pro-Alpha c are elevated in preeclamptic pregnancy and correlate with human chorionic gonadotropin
-
Fraser RF 2nd, McAsey ME, Coney P. Inhibin-A and pro-Alpha C are elevated in preeclamptic pregnancy and correlate with human chorionic gonadotropin. Am J Reprod Immunol. 1998;40(1): 37-42.
-
(1998)
Am J Reprod Immunol
, vol.40
, Issue.1
, pp. 37-42
-
-
Fraser II, R.F.1
McAsey, M.E.2
Coney, P.3
-
97
-
-
0030895475
-
Activin a and inhibin a as possible endocrine markers for pre-eclampsia
-
Muttukrishna S, Knight PG, Groome NP, et al. Activin A and inhibin A as possible endocrine markers for pre-eclampsia. Lancet. 1997;349(9061): 1285-1288.
-
(1997)
Lancet
, vol.349
, Issue.9061
, pp. 1285-1288
-
-
Muttukrishna, S.1
Knight, P.G.2
Groome, N.P.3
-
98
-
-
0033797919
-
Serum inhibin a and activin a are elevated prior to the onset of pre-eclampsia
-
Muttukrishna S, North RA, Morris J, et al. Serum inhibin A and activin A are elevated prior to the onset of pre-eclampsia. Hum Reprod. 2000;15(7): 1640-1645.
-
(2000)
Hum Reprod
, vol.15
, Issue.7
, pp. 1640-1645
-
-
Muttukrishna, S.1
North, R.A.2
Morris, J.3
-
99
-
-
0029076455
-
Hypertension in pregnancy: Changes in activin a maternal serum concentration
-
Petraglia F, Aguzzoli L, Gallinelli A, et al. Hypertension in pregnancy: changes in activin A maternal serum concentration. Placenta. 1995;16(5): 447-454.
-
(1995)
Placenta
, vol.16
, Issue.5
, pp. 447-454
-
-
Petraglia, F.1
Aguzzoli, L.2
Gallinelli, A.3
-
100
-
-
33744985816
-
Soluble endoglin contributes to the pathogenesis of preeclampsia
-
Venkatesha S, Toporsian M, Lam C, et al. Soluble endoglin contributes to the pathogenesis of preeclampsia. Nat Med. 2006;12(6): 642-649.
-
(2006)
Nat Med
, vol.12
, Issue.6
, pp. 642-649
-
-
Venkatesha, S.1
Toporsian, M.2
Lam, C.3
-
101
-
-
67649227647
-
Preeclampsia: The role of angiogenic factors in its pathogenesis
-
Wang A, Rana S, Karumanchi SA. Preeclampsia: the role of angiogenic factors in its pathogenesis. Physiology (Bethesda). 2009;24: 147-158.
-
(2009)
Physiology (Bethesda)
, vol.24
, pp. 147-158
-
-
Wang, A.1
Rana, S.2
Karumanchi, S.A.3
-
102
-
-
84861751153
-
A functional variant in angpt1 and the risk of pregnancies with hypertensive disorders and small-for-gestational-Age infants
-
Andraweera PH, Dekker GA, Thompson SD, et al. A functional variant in ANGPT1 and the risk of pregnancies with hypertensive disorders and small-for-gestational-Age infants. Mol Hum Reprod. 2012;18(6): 325-332.
-
(2012)
Mol Hum Reprod
, vol.18
, Issue.6
, pp. 325-332
-
-
Andraweera, P.H.1
Dekker, G.A.2
Thompson, S.D.3
-
103
-
-
84874356849
-
Single nucleotide polymorphisms in g protein signaling pathway genes in preeclampsia
-
Kvehaugen AS, Melien O, Holmen OL, et al. Single nucleotide polymorphisms in G protein signaling pathway genes in preeclampsia. Hypertension. 2013;61(3): 655-661.
-
(2013)
Hypertension
, vol.61
, Issue.3
, pp. 655-661
-
-
Kvehaugen, A.S.1
Melien, O.2
Holmen, O.L.3
-
104
-
-
33746906743
-
Lack of association between the cyp11b2 gene polymorphism and preeclampsia, eclampsia, and the hellp syndrome in turkish women
-
Percin FE, Cetin M, Pinarbasi E, et al. Lack of association between the CYP11B2 gene polymorphism and preeclampsia, eclampsia, and the HELLP syndrome in Turkish women. Eur J Obstet Gynecol Reprod Biol. 2006; 127(2): 213-217.
-
(2006)
Eur J Obstet Gynecol Reprod Biol
, vol.127
, Issue.2
, pp. 213-217
-
-
Percin, F.E.1
Cetin, M.2
Pinarbasi, E.3
-
105
-
-
84867050188
-
Apolipoprotein e genotypes, lipid peroxidation, and antioxidant status among mild and severe preeclamptic women from western iran: Protective role of apolipoprotein e2 allele in severe preeclampsia
-
Ahmadi R, Rahimi Z, Vaisi-Raygani A, et al. Apolipoprotein E genotypes, lipid peroxidation, and antioxidant status among mild and severe preeclamptic women from western Iran: protective role of apolipoprotein e2 allele in severe preeclampsia. Hypertens Pregnancy. 2012;31(4): 405-418.
-
(2012)
Hypertens Pregnancy
, vol.31
, Issue.4
, pp. 405-418
-
-
Ahmadi, R.1
Rahimi, Z.2
Vaisi-Raygani, A.3
-
106
-
-
77957245709
-
Genetic polymorphism of catechol-o-methyltransferase and cytochrome p450c17a in preeclampsia
-
Lim JH, Kim SY, Kim do J, et al. Genetic polymorphism of catechol-O-methyltransferase and cytochrome P450c17a in preeclampsia. Pharmacogenet Genomics. 2010;20(10): 605-610.
-
(2010)
Pharmacogenet Genomics
, vol.20
, Issue.10
, pp. 605-610
-
-
Lim, J.H.1
Kim, S.Y.2
Kim Do, J.3
-
107
-
-
84859776532
-
The effect of the d1-c785t polymorphism in the type 1 iodothyronine deiodinase gene on the circulating thyroid hormone levels in romanian women with preeclampsia. Association with the degree of severity and pregnancy outcome of preeclampsia
-
Procopciuc LM, Hazi GM, Caracostea G, et al. The effect of the D1-C785T polymorphism in the type 1 iodothyronine deiodinase gene on the circulating thyroid hormone levels in Romanian women with preeclampsia. Association with the degree of severity and pregnancy outcome of preeclampsia. Gynecol Endocrinol. 2012;28(5): 386-390.
-
(2012)
Gynecol Endocrinol
, vol.28
, Issue.5
, pp. 386-390
-
-
Procopciuc, L.M.1
Hazi, G.M.2
Caracostea, G.3
-
108
-
-
84860819057
-
Intercellular adhesion molecule-1 k469e polymorphism: Is it associated with preeclampsia in the korean population?
-
Kwon HS, Sohn IS, Hwang HS, et al. Intercellular adhesion molecule-1 K469E polymorphism: Is it associated with preeclampsia in the Korean population? J Reprod Med. 2012; 57(3-4): 148-152.
-
(2012)
J Reprod Med
, vol.57
, Issue.3-4
, pp. 148-152
-
-
Kwon, H.S.1
Sohn, I.S.2
Hwang, H.S.3
-
109
-
-
67650514322
-
Search for an association between v249i and t280m cx3cr1 genetic polymorphisms, endothelial injury and preeclampsia: The eclaxir study
-
Stepanian A, Benchenni S, Beillat-Lucas T, et al. Search for an association between V249I and T280M CX3CR1 genetic polymorphisms, endothelial injury and preeclampsia: the ECLAXIR Study. PLoS One. 2009;4(7): e6192.
-
(2009)
PLoS One
, vol.4
, Issue.7
-
-
Stepanian, A.1
Benchenni, S.2
Beillat-Lucas, T.3
-
110
-
-
0036082104
-
The c242t-polymorphism of the nadph/nadh oxidase gene p22phox subunit is not associated with pre-eclampsia
-
Raijmakers MT, Roes EM., Steegers EA, et al. The C242T-polymorphism of the NADPH/NADH oxidase gene p22phox subunit is not associated with pre-eclampsia. J Hum Hypertens. 2002;16(6): 423-425.
-
(2002)
J Hum Hypertens
, vol.16
, Issue.6
, pp. 423-425
-
-
Raijmakers, M.T.1
Roes, E.M.2
Steegers, E.A.3
|