These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


PUBMED FOR HANDHELDS

Journal Abstract Search


407 related items for PubMed ID: 11483920

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 2. 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; 12(3):198-201. PubMed ID: 15784506
    [Abstract] [Full Text] [Related]

  • 3. Lack of association of severe preeclampsia with maternal and fetal mutant alleles for tumor necrosis factor alpha and lymphotoxin alpha genes and plasma tumor necrosis factor alpha levels.
    Livingston JC, Park V, Barton JR, Elfering S, Haddad B, Mabie WC, Quasney M, Sibai BM.
    Am J Obstet Gynecol; 2001 May; 184(6):1273-7. PubMed ID: 11349201
    [Abstract] [Full Text] [Related]

  • 4. 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, Kovács M, Várkonyi T, Hupuczi P, Prohászka Z, Rigó J.
    Clin Chim Acta; 2008 Jun; 392(1-2):52-7. PubMed ID: 18396154
    [Abstract] [Full Text] [Related]

  • 5. Genetic susceptibility to preeclampsia: roles of cytosineto-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 YJ, Williamson RA, Murray JC, Andrews J, Pietscher JJ, Peraud PJ, Merrill DC.
    Am J Obstet Gynecol; 2001 May; 184(6):1211-7. PubMed ID: 11349190
    [Abstract] [Full Text] [Related]

  • 6. Relationship between polymorphisms in thrombophilic genes and preeclampsia in a Brazilian population.
    Dalmáz CA, Santos KG, Botton MR, Tedoldi CL, Roisenberg I.
    Blood Cells Mol Dis; 2006 May; 37(2):107-10. PubMed ID: 16963292
    [Abstract] [Full Text] [Related]

  • 7. Genetic thrombophilias and preeclampsia: a meta-analysis.
    Lin J, August P.
    Obstet Gynecol; 2005 Jan; 105(1):182-92. PubMed ID: 15625161
    [Abstract] [Full Text] [Related]

  • 8. 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
    [Abstract] [Full Text] [Related]

  • 9. [Impact of inherited thrombophilia on the development of some pregnancy complications].
    Koleva R, Dimitrova V, Chernev T, Savov A, Karag'ozova Zh, Mazneŭkova V, Kremenski I.
    Akush Ginekol (Sofiia); 2005 Sep; 44(5):18-26. PubMed ID: 16313049
    [Abstract] [Full Text] [Related]

  • 10. Maternal and fetal thrombophilia in intrauterine growth restriction in the presence or absence of maternal hypertensive disease.
    Pileri P, Franchi F, Cetin I, Mandò C, Antonazzo P, Ibrahim B, Rossi F, Biguzzi E.
    Reprod Sci; 2010 Sep; 17(9):844-8. PubMed ID: 20601540
    [Abstract] [Full Text] [Related]

  • 11. Absence of association of thrombophilia polymorphisms with intrauterine growth restriction.
    Infante-Rivard C, Rivard GE, Yotov WV, Génin E, Guiguet M, Weinberg C, Gauthier R, Feoli-Fonseca JC.
    N Engl J Med; 2002 Jul 04; 347(1):19-25. PubMed ID: 12097536
    [Abstract] [Full Text] [Related]

  • 12. Inherited thrombophilias and adverse pregnancy outcomes: a case-control study in an Australian population.
    Said JM, Higgins JR, Moses EK, Walker SP, Monagle PT, Brennecke SP.
    Acta Obstet Gynecol Scand; 2012 Feb 04; 91(2):250-5. PubMed ID: 21985600
    [Abstract] [Full Text] [Related]

  • 13. [Genetic thrombophilic defects (Factor V Leiden, prothrombin G20210A, MTHFR C677T) in women with recurrent fetal loss].
    Kovacheva K, Ivanov P, Konova E, Simeonova M, Komsa-Penkova R.
    Akush Ginekol (Sofiia); 2007 Feb 04; 46(7):10-6. PubMed ID: 18333414
    [Abstract] [Full Text] [Related]

  • 14. Double inherited thrombophilias and adverse pregnancy outcomes: fashion or science?
    Larciprete G, Rossi F, Deaibess T, Brienza L, Barbati G, Romanini E, Gioia S, Cirese E.
    J Obstet Gynaecol Res; 2010 Oct 04; 36(5):996-1002. PubMed ID: 20868443
    [Abstract] [Full Text] [Related]

  • 15. Association between inherited thrombophilias, antiphospholipid antibodies, and lipoprotein A levels and venous thromboembolism in pregnancy.
    Ogunyemi D, Cuellar F, Ku W, Arkel Y.
    Am J Perinatol; 2003 Jan 04; 20(1):17-24. PubMed ID: 12638077
    [Abstract] [Full Text] [Related]

  • 16. Fetal inherited thrombophilias influence the severity of preeclampsia, IUGR and placental abruption.
    Anteby EY, Musalam B, Milwidsky A, Blumenfeld A, Gilis S, Valsky D, Hamani Y.
    Eur J Obstet Gynecol Reprod Biol; 2004 Mar 15; 113(1):31-5. PubMed ID: 15036707
    [Abstract] [Full Text] [Related]

  • 17. Increased frequency of genetic thrombophilia in women with complications of pregnancy.
    Kupferminc MJ, Eldor A, Steinman N, Many A, Bar-Am A, Jaffa A, Fait G, Lessing JB.
    N Engl J Med; 1999 Jan 07; 340(1):9-13. PubMed ID: 9878639
    [Abstract] [Full Text] [Related]

  • 18.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]

  • 19. [Prevalence of factor V Leiden, hyperhomocysteinemia, prothrombin G20210A, and methylene tetrahydrofolate reductase C677T mutations in obstetrical complications].
    Verdy E, Berkane N, Magdelaine A, Soubrier F, Uzan S.
    Ann Biol Clin (Paris); 1999 Jan 07; 57(5):539-44. PubMed ID: 10518055
    [Abstract] [Full Text] [Related]

  • 20.
    ; . PubMed ID:
    [No Abstract] [Full Text] [Related]


    Page: [Next] [New Search]
    of 21.