-
1
-
-
0023182692
-
Risk of unexplained stillbirth at different gestational ages
-
Yudkin PL, Wood L, Redman CW. Risk of unexplained stillbirth at different gestational ages. Lancet 1987;1:1192-1194.
-
(1987)
Lancet
, vol.1
, pp. 1192-1194
-
-
Yudkin, P.L.1
Wood, L.2
Redman, C.W.3
-
2
-
-
0027724570
-
Recurrent stillbirth: Significance and characteristics
-
Samueloff A, Xenakis EM, Berkus MD, Huff, RW, Langer O. Recurrent stillbirth: Significance and characteristics. J Reprod Med 1993;38:883-886.
-
(1993)
J Reprod Med
, vol.38
, pp. 883-886
-
-
Samueloff, A.1
Xenakis, E.M.2
Berkus, M.D.3
Huff, R.W.4
Langer, O.5
-
4
-
-
0033531184
-
Increased frequency of genetic thrombophilia in women with complications of pregnancy
-
Kupferminc M, Eldor A, Steinman N, Many A, Bar-Am A, Jaffa A, Fait G, Lessing JB. 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
-
-
Kupferminc, M.1
Eldor, A.2
Steinman, N.3
Many, A.4
Bar-Am, A.5
Jaffa, A.6
Fait, G.7
Lessing, J.B.8
-
5
-
-
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;101:6-14.
-
(2002)
Eur J Obstet Gynecol Reprod Biol
, vol.101
, pp. 6-14
-
-
Alfirevic, Z.1
Roberts, D.2
Martlew, V.3
-
6
-
-
16044369784
-
Increased fetal loss in women with heritable thrombophilia
-
Preston FE, Rosendaal FR, Walker ID, Briet E, Berntorp E, Conard J, Fontcuberta J, Makris M, Mariani G, Noteboom W et al. Increased fetal loss in women with heritable thrombophilia. Lancet 1996;348:913-916.
-
(1996)
Lancet
, vol.348
, pp. 913-916
-
-
Preston, F.E.1
Rosendaal, F.R.2
Walker, I.D.3
Briet, E.4
Berntorp, E.5
Conard, J.6
Fontcuberta, J.7
Makris, M.8
Mariani, G.9
Noteboom, W.10
-
7
-
-
0034610031
-
Mutations in coagulation factors in women with unexplained fetal loss
-
Martinelli I, Taioli E, Cetin I, Marinoni, A, Gerosja S, Villa MV, Bozza M, Mannucci PM. Mutations in coagulation factors in women with unexplained fetal loss. N Engl J Med 2000;343:1015-1018.
-
(2000)
N Engl J Med
, vol.343
, pp. 1015-1018
-
-
Martinelli, I.1
Taioli, E.2
Cetin, I.3
Marinoni, A.4
Gerosja, S.5
Villa, M.V.6
Bozza, M.7
Mannucci, P.M.8
-
9
-
-
0031981017
-
Geographic distribution of the 20210 G to A prothrombin variant
-
Rosendaal FR, Doggen CJ, Zivelin A, Arruda VR, Aiach M, Siscovick DS, Hillarp A, Watzke HH, Bernardi F, Cuming AM et al. Geographic distribution of the 20210 G to A prothrombin variant. Thromb Haemost 1998;79:706-708.
-
(1998)
Thromb Haemost
, vol.79
, pp. 706-708
-
-
Rosendaal, F.R.1
Doggen, C.J.2
Zivelin, A.3
Arruda, V.R.4
Aiach, M.5
Siscovick, D.S.6
Hillarp, A.7
Watzke, H.H.8
Bernardi, F.9
Cuming, A.M.10
-
10
-
-
0032827489
-
The risk of fetal loss in family members of probands with factor V Leiden mutation
-
Tormene D, Simioni P, Prandoni P, Luni S, Innella B, Sabbion P, Girolami A. The risk of fetal loss in family members of probands with factor V Leiden mutation. Thromb Haemost 1999;82:1237-1239.
-
(1999)
Thromb Haemost
, vol.82
, pp. 1237-1239
-
-
Tormene, D.1
Simioni, P.2
Prandoni, P.3
Luni, S.4
Innella, B.5
Sabbion, P.6
Girolami, A.7
-
11
-
-
0033522394
-
Increased risk for fetal loss in carriers of factor V Leiden mutation
-
Meinardi JR, Middeldorp S, de Kam PJ, Koopman MM, van Pampus EC, Hamulyak K, Prins MH, Buller HR, van der Meer J. Increased risk for fetal loss in carriers of factor V Leiden mutation. Ann Intern Med 1999;130:9736-9739.
-
(1999)
Ann Intern Med
, vol.130
, pp. 9736-9739
-
-
Meinardi, J.R.1
Middeldorp, S.2
De Kam, P.J.3
Koopman, M.M.4
Van Pampus, E.C.5
Hamulyak, K.6
Prins, M.H.7
Buller, H.R.8
Van Der Meer, J.9
-
12
-
-
0030928377
-
Factor V Leiden is associated with repeated and recurrent unexplained fetal losses
-
Grandone E, Margaglione M, Colaizzo D, d'Addedda M, Cappucci G, Vecchione G, Scianname N, Pavone G, DiMinno G. Factor V Leiden is associated with repeated and recurrent unexplained fetal losses. Thromb Haemost 1997;77:822-824.
-
(1997)
Thromb Haemost
, vol.77
, pp. 822-824
-
-
Grandone, E.1
Margaglione, M.2
Colaizzo, D.3
D'Addedda, M.4
Cappucci, G.5
Vecchione, G.6
Scianname, N.7
Pavone, G.8
DiMinno, G.9
-
13
-
-
0033768987
-
High prevalence of the prothrombin gene mutation in women with intrauterine growth retardation, abruptio placentae and second trimester loss
-
Kupferminc MJ, Peri H, Zwang E, Yaron Y, Wolman I, Eldor A. 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
Yaron, Y.4
Wolman, I.5
Eldor, A.6
-
14
-
-
0025708282
-
Recurrent miscarriage. I. Definition and epidemiology
-
Stirrat GM. Recurrent miscarriage. I. Definition and epidemiology. Lancet 1990;336:673-675.
-
(1990)
Lancet
, vol.336
, pp. 673-675
-
-
Stirrat, G.M.1
-
15
-
-
0029933176
-
Coexistence of hereditary homocystinuria and Factor V Leiden-effect on thrombosis
-
Mandel H, Brenner B, Berant M, Rosenberg N, Lanir N, Jakobs C, Fowler B, Seligsohn U. Coexistence of hereditary homocystinuria and Factor V Leiden-effect on thrombosis. N Eng J Med 1996;334:763-768.
-
(1996)
N Eng J Med
, vol.334
, pp. 763-768
-
-
Mandel, H.1
Brenner, B.2
Berant, M.3
Rosenberg, N.4
Lanir, N.5
Jakobs, C.6
Fowler, B.7
Seligsohn, U.8
-
16
-
-
0029850530
-
A 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 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.
-
(1996)
Blood
, vol.88
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
17
-
-
0032767244
-
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;82:6-9.
-
(1999)
Thromb Haemost
, vol.82
, pp. 6-9
-
-
Brenner, B.1
Sarig, G.2
Weiner, Z.3
Younis, J.4
Blumenfeld, Z.5
Lanir, N.6
-
18
-
-
0036227458
-
Third trimester unexplained intrauterine fetal death is associated with inherited thrombophilia
-
Many A, Elad R, Yaron Y, Eldor A, Lessing JB, Kupferminc MJ. Third trimester unexplained intrauterine fetal death is associated with inherited thrombophilia. Obstet Gynecol 2002;99:684-687.
-
(2002)
Obstet Gynecol
, vol.99
, pp. 684-687
-
-
Many, A.1
Elad, R.2
Yaron, Y.3
Eldor, A.4
Lessing, J.B.5
Kupferminc, M.J.6
-
19
-
-
0031007628
-
Frequency of factor V Leiden (Arg506Gln) in Turkey
-
Ozbek U, Tangun Y. Frequency of factor V Leiden (Arg506Gln) in Turkey. Br J Haematol 1997;97:504-505.
-
(1997)
Br J Haematol
, vol.97
, pp. 504-505
-
-
Ozbek, U.1
Tangun, Y.2
-
20
-
-
0032837985
-
High prevalence of activated protein C resistance due to factor V Leiden mutation in cases of intrauterine fetal death
-
Rothbart H, Ohel G, Younis J, Lanir N, Brenner B. High prevalence of activated protein C resistance due to factor V Leiden mutation in cases of intrauterine fetal death. J Matern Fetal Med 1999;8:228-230.
-
(1999)
J Matern Fetal Med
, vol.8
, pp. 228-230
-
-
Rothbart, H.1
Ohel, G.2
Younis, J.3
Lanir, N.4
Brenner, B.5
-
21
-
-
0037443934
-
Thrombophilic disorders and fetal loss: A meta-analysis
-
Rey E, Kahn SR, David M, Shreir I. Thrombophilic disorders and fetal loss: A meta-analysis. Lancet 2003;361:901-908.
-
(2003)
Lancet
, vol.361
, pp. 901-908
-
-
Rey, E.1
Kahn, S.R.2
David, M.3
Shreir, I.4
-
22
-
-
1842637313
-
The association between adverse pregnancy outcomes and maternal factor V Leiden genotype: A meta-analysis
-
Dudding TE, Attia J. The association between adverse pregnancy outcomes and maternal factor V Leiden genotype: A meta-analysis. Thromb Haemost 2004;91:700-711.
-
(2004)
Thromb Haemost
, vol.91
, pp. 700-711
-
-
Dudding, T.E.1
Attia, J.2
-
23
-
-
30344482303
-
Immunofluorescent study of placental bed vessels in preeclampsia
-
Kitzmiller JL, Benirschke K. Immunofluorescent study of placental bed vessels in preeclampsia. Am J Obstet Gynecol 1964;89:225-232.
-
(1964)
Am J Obstet Gynecol
, vol.89
, pp. 225-232
-
-
Kitzmiller, J.L.1
Benirschke, K.2
-
24
-
-
84906418745
-
The histopathology of placental insufficiency
-
Fox H. The histopathology of placental insufficiency. J Clin Path 1976;10:1-8.
-
(1976)
J Clin Path
, vol.10
, pp. 1-8
-
-
Fox, H.1
-
25
-
-
0017706598
-
Placental infarction leading to fetal or neonatal death
-
Naeye RL. Placental infarction leading to fetal or neonatal death. Obstet Gynecol 1977;50:583-588.
-
(1977)
Obstet Gynecol
, vol.50
, pp. 583-588
-
-
Naeye, R.L.1
|