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Journal Abstract Search

209 related items for PubMed ID: 18583164

  • 1. Thrombophilic polymorphisms in Israel.
    Zoossmann-Diskin A, Gazit E, Peleg L, Shohat M, Turner D.
    Blood Cells Mol Dis; 2008; 41(2):230-3. PubMed ID: 18583164
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  • 2. Factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase polymorphism C677T are not associated with coronary artery disease and type 2 diabetes mellitus in western Iran.
    Rahimi Z, Nomani H, Mozafari H, Vaisi-Raygani A, Madani H, Malek-Khosravi S, Parsian A.
    Blood Coagul Fibrinolysis; 2009 Jun; 20(4):252-6. PubMed ID: 19349859
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  • 4. Thrombophilic polymorphisms - factor V Leiden G1691A, prothrombin G20210A and MTHFR C677T - in Tunisian patients with cerebral venous thrombosis.
    Ben Salem-Berrabah O, Fekih-Mrissa N, N'siri B, Ben Hamida A, Benammar-Elgaaied A, Gritli N, Mrissa R.
    J Clin Neurosci; 2012 Sep; 19(9):1326-7. PubMed ID: 22721898
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  • 5. Primer-engineered multiplex PCR-RFLP for detection of MTHFR C677T, prothrombin G20210A and factor V Leiden mutations.
    Koksal V, Baris I, Etlik O.
    Exp Mol Pathol; 2007 Aug; 83(1):1-3. PubMed ID: 17275807
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  • 6. 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 Aug; 54(77):1438-42. PubMed ID: 17708272
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  • 7. The 19-bp deletion of dihydrofolate reductase (DHFR), methylenetetrahydrofolate reductase (MTHFR) C677T, Factor V Leiden, prothrombin G20210A polymorphisms in cancer patients with and without thrombosis.
    Eroglu A, Egin Y, Cam R, Akar N.
    Ann Hematol; 2009 Jan; 88(1):73-6. PubMed ID: 18682947
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  • 8. Frequency of three prothrombotic polymorphisms among Syrian population: factor V G1691A, prothrombin G20210A and methylenetetrahydrofolate reductase C677T.
    Jarjour RA, Ammar S, Majdalawi R.
    Ann Hum Biol; 2017 Feb; 44(1):70-73. PubMed ID: 26560857
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  • 12. Spectrum and prevalence of prothrombotic single nucleotide polymorphism profiles in the Greek Cypriot population.
    Xenophontos SL, Hadjivassiliou M, Ayrton N, Karagrigoriou A, Pantzaris M, Nicolaides AN, Cariolou MA.
    Int Angiol; 2002 Dec; 21(4):322-9. PubMed ID: 12518110
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  • 13. Inherited thrombophilias and pre-eclampsia in Brazilian women.
    Dusse LM, Carvalho Md, Bragança WF, Paiva SG, Godoi LC, Guimarães DA, Fernandes AP.
    Eur J Obstet Gynecol Reprod Biol; 2007 Sep; 134(1):20-3. PubMed ID: 17097210
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  • 16. 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
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  • 19. Thrombophilic mutations in Iranian patients with infertility and recurrent spontaneous abortion.
    Behjati R, Modarressi MH, Jeddi-Tehrani M, Dokoohaki P, Ghasemi J, Zarnani AH, Aarabi M, Memariani T, Ghaffari M, Akhondi MA.
    Ann Hematol; 2006 Apr; 85(4):268-71. PubMed ID: 16450127
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