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Journal Abstract Search

365 related items for PubMed ID: 16450127

  • 1. 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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  • 5. MTHFR C677T Polymorphism and factor V Leiden mutation are not associated with recurrent spontaneous abortion of unexplained etiology in Japanese women.
    Kobashi G, Kato EH, Morikawa M, Shimada S, Ohta K, Fujimoto S, Minakami H, Yamada H.
    Semin Thromb Hemost; 2005 Jun; 31(3):266-71. PubMed ID: 16052395
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  • 7. 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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  • 8. A prospective case-control study analyzes 12 thrombophilic gene mutations in Turkish couples with recurrent pregnancy loss.
    Yenicesu GI, Cetin M, Ozdemir O, Cetin A, Ozen F, Yenicesu C, Yildiz C, Kocak N.
    Am J Reprod Immunol; 2010 Feb; 63(2):126-36. PubMed ID: 19906129
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  • 9. 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 Feb; 54(77):1438-42. PubMed ID: 17708272
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  • 10. Genetic thrombophilic mutations among couples with recurrent miscarriage.
    Jivraj S, Rai R, Underwood J, Regan L.
    Hum Reprod; 2006 May; 21(5):1161-5. PubMed ID: 16431900
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  • 11. Thrombophilia-related genetic variations in patients with pulmonary embolism in the main teaching hospital in Jordan.
    Obeidat NM, Awidi A, Sulaiman NA, Abu-Khader IB.
    Saudi Med J; 2009 Jul; 30(7):921-5. PubMed ID: 19618008
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  • 12. Molecular analysis of factor V Leiden, factor V Hong Kong, factor II G20210A, methylenetetrahydrofolate reductase C677T, and A1298C mutations related to Turkish thrombosis patients.
    Dölek B, Eraslan S, Eroğlu S, Kesim BE, Ulutin T, Yalçiner A, Laleli YR, Gözükirmizi N.
    Clin Appl Thromb Hemost; 2007 Oct; 13(4):435-8. PubMed ID: 17911197
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  • 13. 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; 13(2):166-71. PubMed ID: 17456626
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  • 15. Cerebral venous and sinus thrombosis and thrombophilic mutations in Western Iran: association with factor V Leiden.
    Rahimi Z, Mozafari H, Bigvand AH, Doulabi RM, Vaisi-Raygani A, Afshari D, Razazian N, Rezaei M.
    Clin Appl Thromb Hemost; 2010 Aug; 16(4):430-4. PubMed ID: 19703820
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  • 16. Thrombophilic genes alterations as risk factor for recurrent pregnancy loss.
    Farahmand K, Totonchi M, Hashemi M, Reyhani Sabet F, Kalantari H, Gourabi H, Mohseni Meybodi A.
    J Matern Fetal Neonatal Med; 2016 Aug; 29(8):1269-73. PubMed ID: 26135458
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  • 18. Factor V Leiden G1691A and factor II G20210A point mutations and pregnancy in North-West of Iran.
    Bagheri M, Rad IA, Nanbakhsh F.
    Arch Gynecol Obstet; 2011 Nov; 284(5):1311-5. PubMed ID: 21773779
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  • 20. [Prothrombotic gene mutations in women with recurrent abortions and intrauterine fetal death].
    Santoro R, Iannaccaro P, Sottilotta G.
    Minerva Ginecol; 2005 Aug; 57(4):447-50. PubMed ID: 16170289
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