-
1
-
-
0032746068
-
Thrombophilia-associated pregnancy wastage
-
Blumenfeld Z, Brenner B: Thrombophilia-associated pregnancy wastage. Fertil Steril 1999; 72:765-774.
-
(1999)
Fertil. Steril.
, vol.72
, pp. 765-774
-
-
Blumenfeld, Z.1
Brenner, B.2
-
2
-
-
0033153189
-
Hypercoagulable state mutation analysis in white patients with early first-trimester recurrent pregnancy loss
-
Kutteh WH, Park VM, Deitcher SR: Hypercoagulable state mutation analysis in white patients with early first-trimester recurrent pregnancy loss. Fertil Steril 1999; 71:1048-1053.
-
(1999)
Fertil. Steril.
, vol.71
, pp. 1048-1053
-
-
Kutteh, W.H.1
Park, V.M.2
Deitcher, S.R.3
-
3
-
-
0033973640
-
Activated protein C resistance and factor V Leiden mutation can be associated with first-as well as second-trimester recurrent pregnancy loss
-
Younis JS, Brenner B, Ohel G, Tal J, Lanir N, Ben Ami M: Activated protein C resistance and factor V Leiden mutation can be associated with first-as well as second-trimester recurrent pregnancy loss. Am J Reprod Immunol 2000; 43:31-35.
-
(2000)
Am. J. Reprod. Immunol.
, vol.43
, pp. 31-35
-
-
Younis, J.S.1
Brenner, B.2
Ohel, G.3
Tal, J.4
Lanir, N.5
Ben Ami, M.6
-
4
-
-
0034919759
-
Thrombophilic gene mutations and recurrent spontaneous abortion: Prothrombin mutation increases the risk in the first trimester
-
Pihusch R, Buchholz T, Lohse P, Rübsamen H, Rogenhofer N, Hasbargen U, Hiller E, Thaler CJ: Thrombophilic gene mutations and recurrent spontaneous abortion: Prothrombin mutation increases the risk in the first trimester. Am J Reprod Immunol 2001; 46:124-131.
-
(2001)
Am. J. Reprod. Immunol.
, vol.46
, pp. 124-131
-
-
Pihusch, R.1
Buchholz, T.2
Lohse, P.3
Rübsamen, H.4
Rogenhofer, N.5
Hasbargen, U.6
Hiller, E.7
Thaler, C.J.8
-
5
-
-
0031473789
-
Polymorphism of angiotensin converting enzyme gene is associated with circulating levels of plasminogen activator inhibitor-1
-
Kim DK, Kim JW, Kim S, Gwon HC, Ryu JC, Huh JE, Choo JA, Choi Y, Rhee CH, Lee WR: Polymorphism of angiotensin converting enzyme gene is associated with circulating levels of plasminogen activator inhibitor-1. Arterioscler Thromb Vasc Biol 1997; 17:3242-3247.
-
(1997)
Arterioscler. Thromb. Vasc. Biol.
, vol.17
, pp. 3242-3247
-
-
Kim, D.K.1
Kim, J.W.2
Kim, S.3
Gwon, H.C.4
Ryu, J.C.5
Huh, J.E.6
Choo, J.A.7
Choi, Y.8
Rhee, C.H.9
Lee, W.R.10
-
6
-
-
0027944013
-
Abnormally high circulation levels of tissue plasminogen activator and plasminogen activator inhibitor-1 in patients with a history of ischemic stroke
-
Margaglione M, Di Minno G, Grandone E, Vecchione G, Celentano E, Cappucci G, Grilli M, Simone P, Panico S, Mancini M: Abnormally high circulation levels of tissue plasminogen activator and plasminogen activator inhibitor-1 in patients with a history of ischemic stroke. Arterioscler Thromb 1994; 14:1741-1745.
-
(1994)
Arterioscler. Thromb.
, vol.14
, pp. 1741-1745
-
-
Margaglione, M.1
Di Minno, G.2
Grandone, E.3
Vecchione, G.4
Celentano, E.5
Cappucci, G.6
Grilli, M.7
Simone, P.8
Panico, S.9
Mancini, M.10
-
7
-
-
0031732774
-
4G/5G polyinorphisin of PAI-1 gene promoter and fibrinolytic capacity in patients with deep vein thrombosis
-
Sartori MT, Wiman B, Vettore S, Dazzi F, Girolami A, Patrassi GM: 4G/5G polyinorphisin of PAI-1 gene promoter and fibrinolytic capacity in patients with deep vein thrombosis. Thromb Haemost 1998; 80:956-960.
-
(1998)
Thromb. Haemost.
, vol.80
, pp. 956-960
-
-
Sartori, M.T.1
Wiman, B.2
Vettore, S.3
Dazzi, F.4
Girolami, A.5
Patrassi, G.M.6
-
8
-
-
0035175459
-
Genetic hypofibrinolysis in complicated pregnancies
-
Glueck CJ, Kupferminc MJ, Fontaine RN, Wang P, Weksler BB, Eldor A: Genetic hypofibrinolysis in complicated pregnancies. Obstet Gynecol 2001; 97:44-48.
-
(2001)
Obstet. Gynecol.
, vol.97
, pp. 44-48
-
-
Glueck, C.J.1
Kupferminc, M.J.2
Fontaine, R.N.3
Wang, P.4
Weksler, B.B.5
Eldor, A.6
-
9
-
-
0242606846
-
Polymorphisms in the ACE and PAI-1 genes are associated with recurrent spontaneous miscarriages
-
Buchholz T, Lohse P, Rogenhofer N, Kosian E, Pihusch R, Thaler CJ: Polymorphisms in the ACE and PAI-1 genes are associated with recurrent spontaneous miscarriages. Hum Reprod 2003; 18:2473-2477.
-
(2003)
Hum. Reprod.
, vol.18
, pp. 2473-2477
-
-
Buchholz, T.1
Lohse, P.2
Rogenhofer, N.3
Kosian, E.4
Pihusch, R.5
Thaler, C.J.6
-
10
-
-
0022586197
-
The renin-angiotensin system in pregnancy and parturition
-
Alhenc-Gelas F, Tache A, Saint-Andre JP, Milliez J, Sureau C, Corvol P, Menard J: The renin-angiotensin system in pregnancy and parturition. Adv Nephrol Necker Hosp 1986; 15:25-33.
-
(1986)
Adv. Nephrol. Necker Hosp.
, vol.15
, pp. 25-33
-
-
Alhenc-Gelas, F.1
Tache, A.2
Saint-Andre, J.P.3
Milliez, J.4
Sureau, C.5
Corvol, P.6
Menard, J.7
-
11
-
-
0034100147
-
Molecular and cellular mechanisms of angiotensin II-mediated cardiovascular and renal diseases
-
Kim S, Iwao H: Molecular and cellular mechanisms of angiotensin II-mediated cardiovascular and renal diseases. Pharmacol Rev 2000; 52:11-34.
-
(2000)
Pharmacol. Rev.
, vol.52
, pp. 11-34
-
-
Kim, S.1
Iwao, H.2
-
12
-
-
0035138962
-
Angiotensin II type 1 receptor gene polymorphisms in humans: Physiology and pathophysiology of the genotypes
-
Duncan JA, Scholey JW, Miller JA: Angiotensin II type 1 receptor gene polymorphisms in humans: physiology and pathophysiology of the genotypes. Curr Opin Nephrol Hypertens 2001; 10:111-116.
-
(2001)
Curr. Opin. Nephrol. Hypertens.
, vol.10
, pp. 111-116
-
-
Duncan, J.A.1
Scholey, J.W.2
Miller, J.A.3
-
13
-
-
0037277016
-
Renin-angiotensin system gene polymorphisms: Assessment of the risk of coronary heart disease
-
Buraczynska M, Pijanowski Z, Spasiewicz D, Nowicka T, Sodolski T, Widomska-Czekajska T, Ksiazek A: Renin-angiotensin system gene polymorphisms: assessment of the risk of coronary heart disease. Kardiol Pol 2003; 58:1-9.
-
(2003)
Kardiol. Pol.
, vol.58
, pp. 1-9
-
-
Buraczynska, M.1
Pijanowski, Z.2
Spasiewicz, D.3
Nowicka, T.4
Sodolski, T.5
Widomska-Czekajska, T.6
Ksiazek, A.7
-
14
-
-
0033766424
-
Angiotensin-converting enzyme DD genotype, angiotensin type 1 receptor CC genotype, and hyperhomocysteinemia increase first-trimester fetal-loss susceptibility
-
Fatini C, Gensini F, Battaglini B, Prisco D, Cellai AP, Fedi S, Marcucci R, Brunelli T, Mello G, Parretti E, Pepe G, Abbate R: Angiotensin-converting enzyme DD genotype, angiotensin type 1 receptor CC genotype, and hyperhomocysteinemia increase first-trimester fetal-loss susceptibility. Blood Coagul Fibrinolysis 2000; 11:657-662.
-
(2000)
Blood Coagul. Fibrinolysis
, vol.11
, pp. 657-662
-
-
Fatini, C.1
Gensini, F.2
Battaglini, B.3
Prisco, D.4
Cellai, A.P.5
Fedi, S.6
Marcucci, R.7
Brunelli, T.8
Mello, G.9
Parretti, E.10
Pepe, G.11
Abbate, R.12
-
15
-
-
0041926722
-
Interaction between the polymorphisms of the renin-angiotensin system in preeclampsia
-
Bouba I, Makrydimas G, Kalaitzidis R, Lolis DE, Siamopoulos KC, Georgiou I: Interaction between the polymorphisms of the renin-angiotensin system in preeclampsia. Eur J Obstet Gynecol Reprod Biol 2003; 110:811.
-
(2003)
Eur. J. Obstet. Gynecol. Reprod. Biol.
, vol.110
, pp. 811
-
-
Bouba, I.1
Makrydimas, G.2
Kalaitzidis, R.3
Lolis, D.E.4
Siamopoulos, K.C.5
Georgiou, I.6
-
16
-
-
0025321355
-
Biosynthesis and metabolism of endothelium-derived nitric oxide
-
Ignarro LJ: Biosynthesis and metabolism of endothelium-derived nitric oxide. Annu Rev Pharmacol Toxicol 1990; 30:535-560.
-
(1990)
Annu. Rev. Pharmacol. Toxicol.
, vol.30
, pp. 535-560
-
-
Ignarro, L.J.1
-
17
-
-
0033804809
-
Endothelial nitric oxide synthase gene sequence variations and vascular disease
-
Wang XL, Wang J: Endothelial nitric oxide synthase gene sequence variations and vascular disease. Mol Genet Metab 2000; 70:241-251.
-
(2000)
Mol. Genet. Metab.
, vol.70
, pp. 241-251
-
-
Wang, X.L.1
Wang, J.2
-
18
-
-
0032929550
-
Expression and functional analysis of endothelial nitric oxide synthase (eNOS) in human placenta
-
Rossmanith WG, Hoffmeister U, Wolfahrt S, Kleine B, McLean M, Jacobs RA, Grossman AB: Expression and functional analysis of endothelial nitric oxide synthase (eNOS) in human placenta. Mol Hum Reprod 1999; 5:487-494.
-
(1999)
Mol. Hum. Reprod.
, vol.5
, pp. 487-494
-
-
Rossmanith, W.G.1
Hoffmeister, U.2
Wolfahrt, S.3
Kleine, B.4
McLean, M.5
Jacobs, R.A.6
Grossman, A.B.7
-
19
-
-
0036847113
-
Human chorionic gonadotropin (hCG) is an angiogenetic factor for uterine endothelial cells in vitro
-
Zygmunt M, Herr F, Keller-Schönwein S, Rao CV, Lang U, Preissner KT: Human chorionic gonadotropin (hCG) is an angiogenetic factor for uterine endothelial cells in vitro. J Clin Endocrinol Metab 2002; 87:5290-5296.
-
(2002)
J. Clin. Endocrinol. Metab.
, vol.87
, pp. 5290-5296
-
-
Zygmunt, M.1
Herr, F.2
Keller-Schönwein, S.3
Rao, C.V.4
Lang, U.5
Preissner, K.T.6
-
20
-
-
0035192272
-
Variation at the angiotensin-converting enzyme and endothelial nitric oxide synthase genes is associated with the risk of esophageal varices among patients with alcoholic cirrhosis
-
Coto E, Rodrigo L, Alvarez R, Fuentes D, Rodriguez M, Menendez LG, Ciriza C, Gonzalez P, Alvarez V: Variation at the angiotensin-converting enzyme and endothelial nitric oxide synthase genes is associated with the risk of esophageal varices among patients with alcoholic cirrhosis. J Cardiovasc Pharmacol 2001; 38:833-839.
-
(2001)
J. Cardiovasc. Pharmacol.
, vol.38
, pp. 833-839
-
-
Coto, E.1
Rodrigo, L.2
Alvarez, R.3
Fuentes, D.4
Rodriguez, M.5
Menendez, L.G.6
Ciriza, C.7
Gonzalez, P.8
Alvarez, V.9
-
21
-
-
0034889174
-
Endothelial nitric oxide synthase gene polymorphism in women with idiopathic recurrent miscarriage
-
Tempfer C, Unfried G, Zeillinger R, Hefler L, Nagele F, Huber JC: Endothelial nitric oxide synthase gene polymorphism in women with idiopathic recurrent miscarriage. Hum Reprod 2001; 16:1644-1647.
-
(2001)
Hum. Reprod.
, vol.16
, pp. 1644-1647
-
-
Tempfer, C.1
Unfried, G.2
Zeillinger, R.3
Hefler, L.4
Nagele, F.5
Huber, J.C.6
-
22
-
-
0036146840
-
Polymorphisms of the angiotensinogen gene, the endothelial nitric oxide synthase gene, and the interleukin-1 beta gene promoter in women with idiopathic recurrent miscarriage
-
Hefler LA, Tempfer CB, Bashford MT, Unfried G, Zeillinger R, Schneeberger C, Koelbl H, Nagele F, Huber JC: Polymorphisms of the angiotensinogen gene, the endothelial nitric oxide synthase gene, and the interleukin-1 beta gene promoter in women with idiopathic recurrent miscarriage. Mol Hum Reprod 2002; 8:95-100.
-
(2002)
Mol. Hum. Reprod.
, vol.8
, pp. 95-100
-
-
Hefler, L.A.1
Tempfer, C.B.2
Bashford, M.T.3
Unfried, G.4
Zeillinger, R.5
Schneeberger, C.6
Koelbl, H.7
Nagele, F.8
Huber, J.C.9
-
23
-
-
0035029541
-
Factor XII but not protein C, protein S, antithrombin III, or factor XIII is a predictor of recurrent miscarriage
-
Ogasawara MS, Aoki K, Katano K, Ozaki Y, Suzumori K: Factor XII but not protein C, protein S, antithrombin III, or factor XIII is a predictor of recurrent miscarriage. Fertil Steril 2001; 75:916-919.
-
(2001)
Fertil. Steril.
, vol.75
, pp. 916-919
-
-
Ogasawara, M.S.1
Aoki, K.2
Katano, K.3
Ozaki, Y.4
Suzumori, K.5
-
24
-
-
0032907662
-
Haemostatic and metabolic abnormalities in women with unexplained recurrent abortion
-
Coumans AB, Huijgens PC, Jakobs C, Schats R, de Vries JI, van Pampus MG, Dekker GA: Haemostatic and metabolic abnormalities in women with unexplained recurrent abortion. Hum Reprod 1999; 14:211-214.
-
(1999)
Hum. Reprod.
, vol.14
, pp. 211-214
-
-
Coumans, A.B.1
Huijgens, P.C.2
Jakobs, C.3
Schats, R.4
de Vries, J.I.5
van Pampus, M.G.6
Dekker, G.A.7
-
25
-
-
0032212736
-
Angiotensin-converting enzyme and angiotensin II receptor 1 polymorphisms: Association with early coronary disease
-
Alvarez R, Reguero JR, Batalla A, Iglesias-Cubero G, Cortina A, Alvarez V, Coto E: Angiotensin-converting enzyme and angiotensin II receptor 1 polymorphisms: association with early coronary disease. Cardiovasc Res 1998; 40:375-379.
-
(1998)
Cardiovasc. Res.
, vol.40
, pp. 375-379
-
-
Alvarez, R.1
Reguero, J.R.2
Batalla, A.3
Iglesias-Cubero, G.4
Cortina, A.5
Alvarez, V.6
Coto, E.7
-
26
-
-
0031704975
-
Endothelial nitric oxide synthase gene polymorphism and acute myocardial infarction
-
Hibi K, Ishigami T, Tamura K, Mizushima S, Nyui N, Fujita T, Ochiai H, Kosuge M, Watanabe Y, Yoshii Y, Kihara M, Kimura K, Ishii M, Umemura S: Endothelial nitric oxide synthase gene polymorphism and acute myocardial infarction. Hypertension 1998; 32:521-526.
-
(1998)
Hypertension
, vol.32
, pp. 521-526
-
-
Hibi, K.1
Ishigami, T.2
Tamura, K.3
Mizushima, S.4
Nyui, N.5
Fujita, T.6
Ochiai, H.7
Kosuge, M.8
Watanabe, Y.9
Yoshii, Y.10
Kihara, M.11
Kimura, K.12
Ishii, M.13
Umemura, S.14
-
28
-
-
0041879912
-
Angiotensinogen and angiotensin II type 1 receptor gene polymorphism in patients with autosomal dominant polycystic kidney disease: Effect on hypertension and ESRD
-
Lee KB, Kim UK: Angiotensinogen and angiotensin II type 1 receptor gene polymorphism in patients with autosomal dominant polycystic kidney disease: effect on hypertension and ESRD. Yonsei Med 2003; 44:641-647.
-
(2003)
Yonsei Med.
, vol.44
, pp. 641-647
-
-
Lee, K.B.1
Kim, U.K.2
-
30
-
-
0035226262
-
Development of early uteroplacental circulation
-
Jaffe R: Development of early uteroplacental circulation. Early Pregnancy 2001; 5:34-35.
-
(2001)
Early Pregnancy
, vol.5
, pp. 34-35
-
-
Jaffe, R.1
-
31
-
-
0030575910
-
Hypertension induced in pregnant mice by placental renin and maternal angiotensinogen
-
Takimoto E, Ishida J, Sugiyama F, Horiguchi H, Murakami K, Fukamizu A. Hypertension induced in pregnant mice by placental renin and maternal angiotensinogen. Science 1996; 274:995-998.
-
(1996)
Science
, vol.274
, pp. 995-998
-
-
Takimoto, E.1
Ishida, J.2
Sugiyama, F.3
Horiguchi, H.4
Murakami, K.5
Fukamizu, A.6
|