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Journal Abstract Search

69 related items for PubMed ID: 19776610

  • 21.
    ; . PubMed ID:
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  • 22. ACE and MTHFR gene polymorphisms in unexplained recurrent pregnancy loss.
    Vettriselvi V, Vijayalakshmi K, Paul SF, Venkatachalam P.
    J Obstet Gynaecol Res; 2008 Jun; 34(3):301-6. PubMed ID: 18588608
    [Abstract] [Full Text] [Related]

  • 23. Combined thrombophilic mutations in women with unexplained recurrent miscarriage.
    Sotiriadis A, Vartholomatos G, Pavlou M, Kolaitis N, Dova L, Stefos T, Paraskevaidis E, Kalantaridou SN.
    Am J Reprod Immunol; 2007 Feb; 57(2):133-41. PubMed ID: 17217367
    [Abstract] [Full Text] [Related]

  • 24.
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  • 25. Multiple thrombophilic gene mutations rather than specific gene mutations are risk factors for recurrent miscarriage.
    Coulam CB, Jeyendran RS, Fishel LA, Roussev R.
    Am J Reprod Immunol; 2006 May; 55(5):360-8. PubMed ID: 16635210
    [Abstract] [Full Text] [Related]

  • 26. Genetic risk factors for arterial ischemic stroke in children: a possible MTHFR and eNOS gene-gene interplay?
    Djordjevic V, Stankovic M, Brankovic-Sreckovic V, Rakicevic L, Radojkovic D.
    J Child Neurol; 2009 Jul; 24(7):823-7. PubMed ID: 19372095
    [Abstract] [Full Text] [Related]

  • 27. Thrombophilic polymorphisms in Israel.
    Zoossmann-Diskin A, Gazit E, Peleg L, Shohat M, Turner D.
    Blood Cells Mol Dis; 2008 Jul; 41(2):230-3. PubMed ID: 18583164
    [Abstract] [Full Text] [Related]

  • 28. 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
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  • 29.
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  • 30.
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  • 31. AB0 blood group and risk of venous or arterial thrombosis in carriers of factor V Leiden or prothrombin G20210A polymorphisms.
    Miñano A, Ordóñez A, España F, González-Porras JR, Lecumberri R, Fontcuberta J, Llamas P, Marín F, Estellés A, Alberca I, Vicente V, Corral J.
    Haematologica; 2008 May; 93(5):729-34. PubMed ID: 18387978
    [Abstract] [Full Text] [Related]

  • 32. No association of factor V Leiden, prothrombin G20210A, and MTHFR C677T gene polymorphisms with kidney allograft survival: a multicenter study.
    Meyer M, Laux G, Scherer S, Tran TH, Opelz G, Mytilineos J.
    Transplantation; 2007 Apr 27; 83(8):1055-8. PubMed ID: 17452895
    [Abstract] [Full Text] [Related]

  • 33. [Genetic variant C677T in the MTHFR in women with recurrent early fetal loss].
    Ivanov P, Kovacheva K, Komsa-Penkova R, Konova E, Simeonova M, Popov I, Gecheva S, Bozhinova S, Tanchev S, Tsafarov M.
    Akush Ginekol (Sofiia); 2007 Apr 27; 46(4):19-22. PubMed ID: 17974190
    [Abstract] [Full Text] [Related]

  • 34. [Polymorphism of genes coding for angiotensin I converting enzyme and methylenetetrahydrofolate reductase in patients with ischemic heart disease].
    Goracy I.
    Ann Acad Med Stetin; 2000 Apr 27; 46():97-108. PubMed ID: 11712321
    [Abstract] [Full Text] [Related]

  • 35. Factor V Leiden G1691A, prothrombin G20210A, and MTHFR C677T mutations in Turkish inflammatory bowel disease patients.
    Yasa MH, Bolaman Z, Yukselen V, Kadikoylu G, Karaoglul AO, Batun S.
    Hepatogastroenterology; 2007 Apr 27; 54(77):1438-42. PubMed ID: 17708272
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  • 36. The frequency of factor V Leiden and concomitance of factor V Leiden with prothrombin G20210A mutation and methylene tetrahydrofolate reductase C677T gene mutation in healthy population of Denizli, Aegean region of Turkey.
    Kabukcu S, Keskin N, Keskin A, Atalay E.
    Clin Appl Thromb Hemost; 2007 Apr 27; 13(2):166-71. PubMed ID: 17456626
    [Abstract] [Full Text] [Related]

  • 37. Thrombosis of sinus sagitalis during puerperium caused by thrombophilic gene mutation.
    Titlic M, Pavelin S, Tonkic A, Jukic I, Buca A, Andelinovic S.
    J Thromb Thrombolysis; 2008 Jun 27; 25(3):270-2. PubMed ID: 17574520
    [Abstract] [Full Text] [Related]

  • 38. [Genetic thrombophilia and markers of endothelial activation in patients with preeclampsia].
    Rojas JC, Luna M, Rangel-Nava H, Baños D, Collados MT.
    Ginecol Obstet Mex; 2010 Aug 27; 78(8):401-9. PubMed ID: 20939248
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  • 39.
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  • 40. High prevalence of combined thrombophilic abnormalities in patients with inflammatory bowel disease.
    Magro F, Dinis-Ribeiro M, Araújo FM, Pereira P, Fraga MC, Cunha-Ribeiro LM, Tomé-Ribeiro A.
    Eur J Gastroenterol Hepatol; 2003 Nov 27; 15(11):1157-63. PubMed ID: 14560147
    [Abstract] [Full Text] [Related]

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