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Journal Abstract Search

298 related items for PubMed ID: 16572609

  • 1. Lack of association between inherited thrombophilic risk factors and idiopathic sudden sensorineural hearing loss in Italian patients.
    Cadoni G, Scipione S, Rocca B, Agostino S, La Greca C, Bonvissuto D, Paludetti G.
    Ann Otol Rhinol Laryngol; 2006 Mar; 115(3):195-200. PubMed ID: 16572609
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  • 2. Primary thrombophilia in Mexico. II. Factor V G1691A (Leiden), prothrombin G20210A, and methylenetetrahydrofolate reductase C677T polymorphism in thrombophilic Mexican mestizos.
    Ruiz-Argüelles GJ, Garcés-Eisele J, Reyes-Núñez V, Ramírez-Cisneros FJ.
    Am J Hematol; 2001 Jan; 66(1):28-31. PubMed ID: 11426488
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  • 3. Genetic and acquired prothrombotic risk factors and sudden hearing loss.
    Capaccio P, Ottaviani F, Cuccarini V, Bottero A, Schindler A, Cesana BM, Censuales S, Pignataro L.
    Laryngoscope; 2007 Mar; 117(3):547-51. PubMed ID: 17334320
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  • 4. Factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations are not associated with chronic limb ischemia: the Linz Peripheral Arterial Disease (LIPAD) study.
    Mueller T, Marschon R, Dieplinger B, Haidinger D, Gegenhuber A, Poelz W, Webersinke G, Haltmayer M.
    J Vasc Surg; 2005 May; 41(5):808-15. PubMed ID: 15886665
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  • 5. 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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  • 10. Role of genetic and acquired prothrombotic risk factors in genesis of sudden sensorineural hearing loss.
    Fusconi M, Chistolini A, Angelosanto N, Pignoloni P, Tombolini M, De Virgilio A, Pagliarella M, de Vincentiis M.
    Audiol Neurootol; 2011 Jun; 16(3):185-90. PubMed ID: 20798492
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  • 12. Impact of methionine synthase gene and methylenetetrahydrofolate reductase gene polymorphisms on the risk of sudden sensorineural hearing loss.
    Gross M, Friedman G, Eliashar R, Koren-Morag N, Goldschmidt N, Atta IA, Ben-Yehuda A.
    Audiol Neurootol; 2006 Jun; 11(5):287-93. PubMed ID: 16778415
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  • 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 Jun; 46(7):10-6. PubMed ID: 18333414
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  • 14. -455G/A beta-fibrinogen gene polymorphism, factor V Leiden, prothrombin G20210A mutation and MTHFR C677T, and placental vascular complications.
    Camilleri RS, Peebles D, Portmann C, Everington T, Cohen H.
    Blood Coagul Fibrinolysis; 2004 Mar; 15(2):139-47. PubMed ID: 15091001
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  • 17. Prevalence of genetic risk factors related with thrombophilia and hypofibrinolysis in patients with osteonecrosis of the femoral head in Poland.
    Gagala J, Buraczynska M, Mazurkiewicz T, Ksiazek A.
    BMC Musculoskelet Disord; 2013 Sep 11; 14():264. PubMed ID: 24025446
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  • 18. Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study.
    Koylu MT, Kucukevcilioglu M, Erdurman FC, Durukan AH, Sobacı G, Torun D, Tunca Y, Ayyildiz O.
    Ophthalmic Genet; 2017 Sep 11; 38(4):352-356. PubMed ID: 28085519
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