-
1
-
-
0028314865
-
Mutations in blood coagulation factor V associated with resistance to activated protein C
-
Bertina RM, Koelman BPC, Koster T. Mutations in blood coagulation factor V associated with resistance to activated protein C. Nature 1994;369:64-7.
-
(1994)
Nature
, vol.369
, pp. 64-67
-
-
Bertina, R.M.1
Koelman, B.P.C.2
Koster, T.3
-
2
-
-
0029850530
-
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;88:3698-703.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
3
-
-
0029049553
-
A candidate risk factor for vascular disease: A common mutation in the methyltetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R et al. A candidate risk factor for vascular disease: a common mutation in the methyltetrahydrofolate reductase. Nat Genet 1995;10:111-3.
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
-
4
-
-
0041875074
-
Aetiology of preeclampsia and thrombophilic genetic mutations
-
Hayashi M. Aetiology of preeclampsia and thrombophilic genetic mutations. Clin Sci 2003;105:269-71.
-
(2003)
Clin Sci
, vol.105
, pp. 269-271
-
-
Hayashi, M.1
-
5
-
-
0037464820
-
Thrombophilia: Implications for pregnancy outcome
-
Greer IA. Thrombophilia: implications for pregnancy outcome. Thromb Res 2003;109:73-81.
-
(2003)
Thromb Res
, vol.109
, pp. 73-81
-
-
Greer, I.A.1
-
6
-
-
4444343623
-
Thrombophilia and pregnancy complications
-
Kujovich JL. Thrombophilia and pregnancy complications. Am J Obstet Gynecol 2004;191:412-24.
-
(2004)
Am J Obstet Gynecol
, vol.191
, pp. 412-424
-
-
Kujovich, J.L.1
-
7
-
-
0023392475
-
Acute atherosis in preeclampsia: Maternal determinant and fetal outcome in the presence of the lesion
-
Khong TY, Pearce JM, Robertson WB. Acute atherosis in preeclampsia: maternal determinant and fetal outcome in the presence of the lesion. Am J Obstet Gynecol 1987;157:360-3.
-
(1987)
Am J Obstet Gynecol
, vol.157
, pp. 360-363
-
-
Khong, T.Y.1
Pearce, J.M.2
Robertson, W.B.3
-
9
-
-
0030690585
-
Hyperhomocysteinemia and protein S deficiency in complicated pregnancies
-
De Vries JIP, Dekker GA, Huijgens PC et al. Hyperhomocysteinemia and protein S deficiency in complicated pregnancies. Br J Obstst Gynecol 1997;104:248-54.
-
(1997)
Br J Obstst Gynecol
, vol.104
, pp. 248-254
-
-
De Vries, J.I.P.1
Dekker, G.A.2
Huijgens, P.C.3
-
10
-
-
0033000764
-
High prevalence of hemostatic abnormalities in women with history of severe preeclampsia
-
van-Pampus MG, Dekker GA, Wolf H et al. High prevalence of hemostatic abnormalities in women with history of severe preeclampsia. Am J Obstet Gynecol 1999;180:1146-50.
-
(1999)
Am J Obstet Gynecol
, vol.180
, pp. 1146-1150
-
-
Van-Pampus, M.G.1
Dekker, G.A.2
Wolf, H.3
-
11
-
-
0035024065
-
Familial tbrombophilia and the occurrence of fetal growth restriction
-
Martinelli P, Grandone E, Collaizzo D et al. Familial tbrombophilia and the occurrence of fetal growth restriction. Haematologica 2001;86:428-31.
-
(2001)
Haematologica
, vol.86
, pp. 428-431
-
-
Martinelli, P.1
Grandone, E.2
Collaizzo, D.3
-
12
-
-
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;185:153-7.
-
(2001)
Am J Obstet Gynecol
, vol.185
, pp. 153-157
-
-
Livingston, J.C.1
Barton, J.R.2
Park, V.3
-
13
-
-
0035350680
-
Postnatal screening for thrombophilia in women with severe pregnancy complications
-
Alfirevic Z, Mousa HM, Martlew V et al. Postnatal screening for thrombophilia in women with severe pregnancy complications. Obstet Gynecol 2001;97:753-9.
-
(2001)
Obstet Gynecol
, vol.97
, pp. 753-759
-
-
Alfirevic, Z.1
Mousa, H.M.2
Martlew, V.3
-
14
-
-
0036357995
-
Thrombophilia and immunologic disorders in pregnancies as risk factors for small gestational age infants
-
Verspyck E, Le Cam-Duchez V, Goffinet F et al. Thrombophilia and immunologic disorders in pregnancies as risk factors for small gestational age infants. Br J Obstet Gynecol 2002;109:28-33.
-
(2002)
Br J Obstet Gynecol
, vol.109
, pp. 28-33
-
-
Verspyck, E.1
Le Cam-Duchez, V.2
Goffinet, F.3
-
15
-
-
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 Eng J Med 1999;340:9-13.
-
(1999)
N Eng J Med
, vol.340
, pp. 9-13
-
-
Kupferminc, M.J.1
Eldor, A.2
Steinman, N.3
-
16
-
-
0343049152
-
Usefulness of screening for congenital or acquired hemostatic abnormalities in women with previous complicated pregnancies
-
Mello G, Parretti E, Martini E et al. Usefulness of screening for congenital or acquired hemostatic abnormalities in women with previous complicated pregnancies. Haemostasis 1999;29:197-203.
-
(1999)
Haemostasis
, vol.29
, pp. 197-203
-
-
Mello, G.1
Parretti, E.2
Martini, E.3
-
17
-
-
0034668897
-
Incidence of the factor V Leiden mutation, coagulation inhibitor deficiency, and elevated antiphospholipid-antibodies in patients with preeclampsia or HELLP syndrome
-
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. Thromb Res 2000;100:363-5.
-
(2000)
Thromb Res
, vol.100
, pp. 363-365
-
-
Von Tempelhoff, G.F.1
Heilmann, L.2
Spanuth, E.3
-
18
-
-
0030743692
-
Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia
-
Grandone E, Margaglione M, Colaizzo D et al. Factor V Leiden, C>T MTHFR polymorphism and genetic susceptibility to preeclampsia. Thromb Haemost 1997;77:1052-4.
-
(1997)
Thromb Haemost
, vol.77
, pp. 1052-1054
-
-
Grandone, E.1
Margaglione, M.2
Colaizzo, D.3
-
20
-
-
0033932801
-
Maternal and neonatal outcome of preeclamptic pregnancies:The potential roles of factor V Leiden mutation and 5, 10 methylentetrahydrofolate reductase
-
Rigo 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 methylentetrahydrofolate reductase. Hypertens Pregnancy 2000;19: 163-72.
-
(2000)
Hypertens Pregnancy
, vol.19
, pp. 163-172
-
-
Rigo Jr., J.1
Nagy, B.2
Fintor, L.3
-
21
-
-
0033431657
-
The factor V Leiden mutation is not a common cause of pregnancy-induced hypertension in Japan
-
Kobashi G, Yamada H, Asano T et al. The factor V Leiden mutation is not a common cause of pregnancy-induced hypertension in Japan. Semin Thromb Hemost 1999;25:487-9.
-
(1999)
Semin Thromb Hemost
, vol.25
, pp. 487-489
-
-
Kobashi, G.1
Yamada, H.2
Asano, T.3
-
22
-
-
0031034899
-
Preeclampsia is associated with reduced response to activated protein C
-
Lindoff C, Ingemarsson I, Martinsson G et al. Preeclampsia is associated with reduced response to activated protein C. Am J Obstet Gynecol 1997; 176:457-60.
-
(1997)
Am J Obstet Gynecol
, vol.176
, pp. 457-460
-
-
Lindoff, C.1
Ingemarsson, I.2
Martinsson, G.3
-
23
-
-
0036483204
-
Is there an increased maternal-infant prevalence of factor V Leiden in association with severe preeclampsia?
-
Currie L, Peek M, McNiven M et al. Is there an increased maternal-infant prevalence of factor V Leiden in association with severe preeclampsia? BJOG 2002;109:191-6.
-
(2002)
BJOG
, vol.109
, pp. 191-196
-
-
Currie, L.1
Peek, M.2
McNiven, M.3
-
24
-
-
0032972632
-
Prothrombotic genetic risk factors and the occurrence of gestational hypertension with or without proteinuria
-
Grandone E, Margaglione M, Colaizzo D et al. Prothrombotic genetic risk factors and the occurrence of gestational hypertension with or without proteinuria. Thromb Haemost 1999;81:349-52.
-
(1999)
Thromb Haemost
, vol.81
, pp. 349-352
-
-
Grandone, E.1
Margaglione, M.2
Colaizzo, D.3
-
25
-
-
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;96:45-9.
-
(2000)
Obstet Gynecol
, vol.96
, pp. 45-49
-
-
Kupferminc, M.J.1
Fait, G.2
Many, A.3
-
26
-
-
0036271250
-
The methylentetrahidrofolat reductase 677 C->T polymorphism and preeclampsia in two populations
-
Prasmusinto D, Skrablin S, Hofstaetter C et al. The methylentetrahidrofolat reductase 677 C->T polymorphism and preeclampsia in two populations. Obstet Gynecol 2002;99:1085-92.
-
(2002)
Obstet Gynecol
, vol.99
, pp. 1085-1092
-
-
Prasmusinto, D.1
Skrablin, S.2
Hofstaetter, C.3
-
27
-
-
0034679870
-
Absence of association between a common mutation in the methylentetrahidrofolat reductase gene and preeclampsia in Japanese women
-
Kobashi G, Yamada H, Asano T et al. Absence of association between a common mutation in the methylentetrahidrofolat reductase gene and preeclampsia in Japanese women. Am J Med Genet 2000;93:122-5.
-
(2000)
Am J Med Genet
, vol.93
, pp. 122-125
-
-
Kobashi, G.1
Yamada, H.2
Asano, T.3
-
28
-
-
0033623927
-
677 C->T polymorphism of the methylentetrahidrofolat reductase gene and preeclampsia
-
Laivuori H, Kaaja R, Ylikorkola O et al. 677 C->T polymorphism of the methylentetrahidrofolat reductase gene and preeclampsia. Obstet Gynecol 2000;96:277-80.
-
(2000)
Obstet Gynecol
, vol.96
, pp. 277-280
-
-
Laivuori, H.1
Kaaja, R.2
Ylikorkola, O.3
-
29
-
-
0035212604
-
C677T methylentetrahidrofolat reductase polymorphism is not a risk factor for preeclamsia/eclampsia among Australian women
-
Kaiser T, Brennecke SAP, Moses EK. C677T methylentetrahidrofolat reductase polymorphism is not a risk factor for preeclamsia/eclampsia among Australian women. Hum Hered 2001;51:20-2.
-
(2001)
Hum Hered
, vol.51
, pp. 20-22
-
-
Kaiser, T.1
Brennecke, S.A.P.2
Moses, E.K.3
-
30
-
-
0032767244
-
Thrombophilic polymorphism are common in women with fetal loss without apparent cause
-
Brenner B, Sarig G, Weiner Z et al. Thrombophilic polymorphism are common in women with fetal loss without apparent cause. Thromb Haemost 1999;82:6-9.
-
(1999)
Thromb Haemost
, vol.82
, pp. 6-9
-
-
Brenner, B.1
Sarig, G.2
Weiner, Z.3
-
31
-
-
0033955432
-
Factor V Leiden and G20210A prothrombin mutations, but not methylentetrahidrofolat reductase C677T, are associated with recurrent miscarriages
-
Foka ZJ, Lambropoulos AF, Saravelos H et al. Factor V Leiden and G20210A prothrombin mutations, but not methylentetrahidrofolat reductase C677T, are associated with recurrent miscarriages. Hum Reprod 2000; 15:458-62.
-
(2000)
Hum Reprod
, vol.15
, pp. 458-462
-
-
Foka, Z.J.1
Lambropoulos, A.F.2
Saravelos, H.3
-
32
-
-
0035690634
-
Factor V Leiden and G20210A prothrombin mutations are risk factors for very early recurrent miscarriage
-
Reznikoff-Etievan MF, Cayol V, Carbonne B et al. Factor V Leiden and G20210A prothrombin mutations are risk factors for very early recurrent miscarriage. BJOG 2001;108:1251-4.
-
(2001)
BJOG
, vol.108
, pp. 1251-1254
-
-
Reznikoff-Etievan, M.F.1
Cayol, V.2
Carbonne, B.3
-
33
-
-
0032827489
-
The risk of fetal loss in family members of probands with factor V Leiden mutation
-
Tormene D, Simioni P, Prandoni P et al. The risk of fetal loss in family members of probands with factor V Leiden mutation. Thromb Haemost 1999;82:1237-9.
-
(1999)
Thromb Haemost
, vol.82
, pp. 1237-1239
-
-
Tormene, D.1
Simioni, P.2
Prandoni, P.3
-
34
-
-
16044369784
-
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;348:913-6.
-
(1996)
Lancet
, vol.348
, pp. 913-916
-
-
Preston, F.E.1
Rosendaal, F.R.2
Walker, I.D.3
-
35
-
-
0033522394
-
Increased risk for fetal loss in carriers of the factor V Leiden mutation
-
Meinardi JR, Middeldorp S, de Kam PJ et al. Increased risk for fetal loss in carriers of the factor V Leiden mutation. Ann Intern Med 1999;130:736-9.
-
(1999)
Ann Intern Med
, vol.130
, pp. 736-739
-
-
Meinardi, J.R.1
Middeldorp, S.2
De Kam, P.J.3
-
36
-
-
0036129677
-
The C677T polymorphism of the methylenetetrahidrofolat reductase gene and idiopathic recurrent miscarriage
-
Unfried G, Griesmacher A, Weismuller W et al. The C677T polymorphism of the methylenetetrahidrofolat reductase gene and idiopathic recurrent miscarriage. Obstet Gynecol 2002;99:614-9.
-
(2002)
Obstet Gynecol
, vol.99
, pp. 614-619
-
-
Unfried, G.1
Griesmacher, A.2
Weismuller, W.3
-
37
-
-
0034023381
-
Hyperhomocysteinemia and other risk factors in women with placental vasculopathy
-
van der Molen EF, Verbruggen B, Novakova I et al. Hyperhomocysteinemia and other risk factors in women with placental vasculopathy. BJOG 2000;107:785-91.
-
(2000)
BJOG
, vol.107
, pp. 785-791
-
-
Van Der Molen, E.F.1
Verbruggen, B.2
Novakova, I.3
-
38
-
-
0005517354
-
Case-control study of the frequency of thrombophilic disorders in couples with late fetal loss and no thrombotic accident - The Nimes Obstetricians and Haematologists Study 5 (NOHA5)
-
Gris JC, Quere I, Monpeyroux F et al. Case-control study of the frequency of thrombophilic disorders in couples with late fetal loss and no thrombotic accident-the Nimes Obstetricians and Haematologists Study 5 (NOHA5). Thromb Haemost 1999;81:891-9.
-
(1999)
Thromb Haemost
, vol.81
, pp. 891-899
-
-
Gris, J.C.1
Quere, I.2
Monpeyroux, F.3
-
39
-
-
0038300096
-
Combined thrombophilic polymorphisms in women with idiopathic recurrent miscarriage
-
Hohlagschwandtner M, Unfried G, Heinze G et al. Combined thrombophilic polymorphisms in women with idiopathic recurrent miscarriage. Fertil Steril 2003;79:1141-8.
-
(2003)
Fertil Steril
, vol.79
, pp. 1141-1148
-
-
Hohlagschwandtner, M.1
Unfried, G.2
Heinze, G.3
-
40
-
-
0032891393
-
The C677T MTHFR gene mutation is not predictive of risk for recurrent fetal loss
-
Holmes ZR, Regan L, Chilcot I, Cohen H. The C677T MTHFR gene mutation is not predictive of risk for recurrent fetal loss. Br J Haematol 1999;105:98-101.
-
(1999)
Br J Haematol
, vol.105
, pp. 98-101
-
-
Holmes, Z.R.1
Regan, L.2
Chilcot, I.3
Cohen, H.4
-
41
-
-
0037443934
-
Thrombophilic disorders and fetal loss: A meta-analysis
-
Rey E, Kahn SR, David M, Shrier I. Thrombophilic disorders and fetal loss: a meta-analysis. Lancet 2003;361:901-8.
-
(2003)
Lancet
, vol.361
, pp. 901-908
-
-
Rey, E.1
Kahn, S.R.2
David, M.3
Shrier, I.4
-
42
-
-
0036854180
-
Acquired and inherited thrombophilia in women with unexplained fetal losses
-
Alonso A, Soto I, Urgelles MF et al. Acquired and inherited thrombophilia in women with unexplained fetal losses. Am J Obstet Gynecol 2002;187: 1337-42.
-
(2002)
Am J Obstet Gynecol
, vol.187
, pp. 1337-1342
-
-
Alonso, A.1
Soto, I.2
Urgelles, M.F.3
-
43
-
-
0036910040
-
Mid-trimester severe intrauterine growth restriction is associated with a high prevalence of thrombophilia
-
Kupferminc MJ, Many A, Bar-Am A et al. Mid-trimester severe intrauterine growth restriction is associated with a high prevalence of thrombophilia. BJOG 2002;109:1373-6.
-
(2002)
BJOG
, vol.109
, pp. 1373-1376
-
-
Kupferminc, M.J.1
Many, A.2
Bar-Am, A.3
-
44
-
-
0037019341
-
Absence of association of thrombophilia polymorphisms with intrauterine growth restriction
-
Infante-Rivard C, Rivard GE, Yotov WV et al. Absence of association of thrombophilia polymorphisms with intrauterine growth restriction. N Eng J Med 2002;347:19-25.
-
(2002)
N Eng J Med
, vol.347
, pp. 19-25
-
-
Infante-Rivard, C.1
Rivard, G.E.2
Yotov, W.V.3
-
45
-
-
0033964464
-
Prospective evaluation of the risk conferred by factor V Leiden and thermolabile methylentetrahidrofolat polymorphism in pregnancy
-
Murphy RP, Donoghue C, Nallen RJ et al. Prospective evaluation of the risk conferred by factor V Leiden and thermolabile methylentetrahidrofolat polymorphism in pregnancy. Arterioscler Thromb Vasc Biol 2000;20:266-70.
-
(2000)
Arterioscler Thromb Vasc Biol
, vol.20
, pp. 266-270
-
-
Murphy, R.P.1
Donoghue, C.2
Nallen, R.J.3
-
46
-
-
0032441447
-
Resistance to activated protein C and the Leiden mutation: High prevalence in patients with abruptio placentae
-
Wiener-Megnagi Z, Ben-Shlomo I, Goldberg Y, Shalev E. Resistance to activated protein C and the Leiden mutation: high prevalence in patients with abruptio placentae. Am J Obstet Gynecol 1998;179:1567-70.
-
(1998)
Am J Obstet Gynecol
, vol.179
, pp. 1567-1570
-
-
Wiener-Megnagi, Z.1
Ben-Shlomo, I.2
Goldberg, Y.3
Shalev, E.4
-
47
-
-
0037483677
-
Thrombophilic mutations are a main risk factor for placental abruption
-
Facchinetti F, Marozio L, Grandone E et al. Thrombophilic mutations are a main risk factor for placental abruption. Haematologica 2003;88:785-8.
-
(2003)
Haematologica
, vol.88
, pp. 785-788
-
-
Facchinetti, F.1
Marozio, L.2
Grandone, E.3
-
48
-
-
11244255194
-
Genotype and allele frequencies of the polymorphic methylenetetrahidrofolat reductase gene in Turkey
-
Sazci A, Ergul E, Kaya G, Kara I. Genotype and allele frequencies of the polymorphic methylenetetrahidrofolat reductase gene in Turkey. Cell Biochem Funct 2005;23:51-4.
-
(2005)
Cell Biochem Funct
, vol.23
, pp. 51-54
-
-
Sazci, A.1
Ergul, E.2
Kaya, G.3
Kara, I.4
-
49
-
-
0033646197
-
Prothrombin G20210A mutation: Is it associated with preeclampsia?
-
Higgins JR, Kaiser T, Moses EK et al. Prothrombin G20210A mutation: is it associated with preeclampsia? Gynecol Obstet Invest 2000;50:254-7.
-
(2000)
Gynecol Obstet Invest
, vol.50
, pp. 254-257
-
-
Higgins, J.R.1
Kaiser, T.2
Moses, E.K.3
-
50
-
-
4344685226
-
Prothrombin G20210A gene mutation with LightCycler polymerase chain reaction in venous thrombosis and healthy populations in southeast of Turkey
-
Ayyildiz O, Kalkanli S, Batun S et al. Prothrombin G20210A gene mutation with LightCycler polymerase chain reaction in venous thrombosis and healthy populations in southeast of Turkey. Heart Vessels 2004;19:164-6.
-
(2004)
Heart Vessels
, vol.19
, pp. 164-166
-
-
Ayyildiz, O.1
Kalkanli, S.2
Batun, S.3
|