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Journal Abstract Search

675 related items for PubMed ID: 18066962

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  • 6. 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, Wunsiedler U, Beckmann MW, Fischer T.
    Clin Sci (Lond); 2003 Sep; 105(3):279-85. PubMed ID: 12725641
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  • 8. Maternal and fetal inherited thrombophilias are not related to the development of severe preeclampsia.
    Livingston JC, Barton JR, Park V, Haddad B, Phillips O, Sibai BM.
    Am J Obstet Gynecol; 2001 Jul; 185(1):153-7. PubMed ID: 11483920
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  • 11. [Frequency of antiphospholipid antibodies and factor V (G1691A), prothrombin (G20210A) gene polimorphism among women with pregnancy complications].
    Rajewski M, Skrzypczak J.
    Pol Arch Med Wewn; 2006 May; 115(5):417-25. PubMed ID: 17195354
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  • 12. 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, Kunzmann E, Hommel G.
    Thromb Res; 2000 Nov 15; 100(4):363-5. PubMed ID: 11187029
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  • 13. Fetal genotype for specific inherited thrombophilias is not associated with severe preeclampsia.
    Stanley-Christian H, Ghidini A, Sacher R, Shemirani M.
    J Soc Gynecol Investig; 2005 Apr 15; 12(3):198-201. PubMed ID: 15784506
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  • 15. Maternal and perinatal outcome in pregnancies complicated with hypertensive disorder of pregnancy: a seven year experience of a tertiary care center.
    Yücesoy G, Ozkan S, Bodur H, Tan T, Calişkan E, Vural B, Corakçi A.
    Arch Gynecol Obstet; 2005 Nov 15; 273(1):43-9. PubMed ID: 15834580
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  • 16. ProC Global assay in the evaluation of women with history of severe preeclampsia or HELLP syndrome.
    Heilmann L, von Tempelhoff GF, Pollow K.
    Clin Appl Thromb Hemost; 2002 Oct 15; 8(4):319-24. PubMed ID: 12518722
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  • 17. Antiphospholipid antibody profile based obstetric outcomes of primary antiphospholipid syndrome: the PREGNANTS study.
    Saccone G, Berghella V, Maruotti GM, Ghi T, Rizzo G, Simonazzi G, Rizzo N, Facchinetti F, Dall'Asta A, Visentin S, Sarno L, Xodo S, Bernabini D, Monari F, Roman A, Eke AC, Hoxha A, Ruffatti A, Schuit E, Martinelli P, PREGNANTS (PREGNancy in women with ANTiphospholipid Syndrome) working group.
    Am J Obstet Gynecol; 2017 May 15; 216(5):525.e1-525.e12. PubMed ID: 28153662
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  • 18. Lower birth-weight in neonates of mothers carrying factor V G1691A and factor II A(20210) mutations.
    Grandone E, Margaglione M, Colaizzo D, Pavone G, Paladini D, Martinelli P, Di Minno G.
    Haematologica; 2002 Feb 15; 87(2):177-81. PubMed ID: 11836168
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  • 20. Primary upper-extremity deep vein thrombosis: high prevalence of thrombophilic defects.
    Hendler MF, Meschengieser SS, Blanco AN, Alberto MF, Salviú MJ, Gennari L, Lazzari MA.
    Am J Hematol; 2004 Aug 15; 76(4):330-7. PubMed ID: 15282664
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