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Pubmed for Handhelds

PUBMED FOR HANDHELDS

Journal Abstract Search

179 related items for PubMed ID: 21170721

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  • 6. Sudden hearing loss followed by deep vein thrombosis and pulmonary embolism in a patient with factor V Leiden mutation.
    Lovato A, Tormene D, Staffieri C, Breda S, Staffieri A, Marioni G.
    Int J Audiol; 2014 Sep; 53(9):625-8. PubMed ID: 24735015
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  • 7. 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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  • 8. A case control study on the contribution of factor V-Leiden, prothrombin G20210A, and MTHFR C677T mutations to the genetic susceptibility of deep venous thrombosis.
    Almawi WY, Tamim H, Kreidy R, Timson G, Rahal E, Nabulsi M, Finan RR, Irani-Hakime N.
    J Thromb Thrombolysis; 2005 Jun; 19(3):189-96. PubMed ID: 16082606
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  • 9. Prevalence of factor V G1691A (factor V-Leiden) and prothrombin G20210A gene mutations in a recurrent miscarriage population.
    Finan RR, Tamim H, Ameen G, Sharida HE, Rashid M, Almawi WY.
    Am J Hematol; 2002 Dec; 71(4):300-5. PubMed ID: 12447960
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  • 10. 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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  • 11. 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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  • 12. Factor V Leiden and prothrombin gene G20210A mutations in Italian patients with Behçet's disease and deep vein thrombosis.
    Silingardi M, Salvarani C, Boiardi L, Accardo P, Iorio A, Olivieri I, Cantini F, Salvi F, La Corte R, Triolo G, Ciccia F, Ghirarduzzi A, Filippini D, Paolazzi G, Iori I.
    Arthritis Rheum; 2004 Apr 15; 51(2):177-83. PubMed ID: 15077257
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  • 13. [Factor V Leiden (G1691A) and prothrombin-G20210A alleles among patients with deep venous thrombosis and in the general population from Spain].
    Francès F, Portolès O, Gabriel F, Corella D, Sorlí JV, Sabater A, Alfonso JL, Guillén M.
    Rev Med Chil; 2006 Jan 15; 134(1):13-20. PubMed ID: 16532157
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  • 14. [Factor V Leiden and prothrombin G20210A among Chilean patients with venous and arterial thrombosis].
    Palomo I, Pereira J, Alarcón M, Pinochet C, Vélez MT, Hidalgo P, Skagerberg K, Poblete F.
    Rev Med Chil; 2005 Dec 15; 133(12):1425-33. PubMed ID: 16446869
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  • 16. Factor V Leiden mutation and PAI-1 gene 4G/5G genotype in thrombotic patients with Behcet's disease.
    Gurgey A, Balta G, Boyvat A.
    Blood Coagul Fibrinolysis; 2003 Feb 15; 14(2):121-4. PubMed ID: 12632020
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  • 18. Prevalence of factor V Leiden (G1691A) and prothrombin (G20210A) among Kurdish population from Western Iran.
    Rahimi Z, Vaisi-Raygani A, Mozafari H, Kharrazi H, Rezaei M, Nagel RL.
    J Thromb Thrombolysis; 2008 Jun 15; 25(3):280-3. PubMed ID: 17700999
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  • 19. Prothrombotic gene mutations in patients with sudden sensorineural hearing loss and cardiovascular thrombotic disease.
    Capaccio P, Cuccarini V, Ottaviani F, Fracchiolla NS, Bossi A, Pignataro L.
    Ann Otol Rhinol Laryngol; 2009 Mar 15; 118(3):205-10. PubMed ID: 19374152
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