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Journal Abstract Search

318 related items for PubMed ID: 18387982

  • 1.
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  • 2. Evaluation of the interactions of common genetic mutations in stroke subtypes.
    Szolnoki Z, Somogyvári F, Kondacs A, Szabó M, Fodor L.
    J Neurol; 2002 Oct; 249(10):1391-7. PubMed ID: 12382154
    [Abstract] [Full Text] [Related]

  • 3. Deletion polymorphism in the angiotensin-converting enzyme gene as a thrombophilic risk factor after hip arthroplasty.
    Philipp CS, Dilley A, Saidi P, Evatt B, Austin H, Zawadsky J, Harwood D, Ellingsen D, Barnhart E, Phillips DJ, Hooper WC.
    Thromb Haemost; 1998 Dec; 80(6):869-73. PubMed ID: 9869151
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  • 6. 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
    [Abstract] [Full Text] [Related]

  • 7. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.
    Eid SS, Rihani G.
    Clin Lab Sci; 2004 Feb; 17(4):200-2. PubMed ID: 15559724
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  • 8. Endothelial nitric oxide synthase gene interactions and the risk of ischaemic stroke.
    Szolnoki Z, Havasi V, Bene J, Komlósi K, Szöke D, Somogyvári F, Kondacs A, Szabó M, Fodor L, Bodor A, Gáti I, Wittman I, Melegh B.
    Acta Neurol Scand; 2005 Jan; 111(1):29-33. PubMed ID: 15595935
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  • 9. [Genetics of blood coagulation in young stroke patients].
    Pongrácz E, Tordai A, Csornai M, Nagy Z.
    Ideggyogy Sz; 2002 Mar 20; 55(3-4):111-7. PubMed ID: 12122980
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  • 11. Evaluation of the angiotensin-converting enzyme insertion/deletion polymorphism and the risk of ischaemic stroke.
    Tuncer N, Tuglular S, Kiliç G, Sazci A, Us O, Kara I.
    J Clin Neurosci; 2006 Feb 20; 13(2):224-7. PubMed ID: 16446094
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  • 12. 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; 20(4):252-6. PubMed ID: 19349859
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  • 13. [Polymorphisms of ACE-1 and MTHFR genes and genetic susceptibility of ischemic stroke].
    Li C, Zhang C, Qiu S, Lu X, Zeng Y, Wu H, Chen W, Luo W, Liu J.
    Zhonghua Yi Xue Za Zhi; 2002 Aug 10; 82(15):1046-9. PubMed ID: 12194796
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  • 14. Angiotensin-converting enzyme insertion/deletion polymorphism and the risk of ischemic stroke in a South Indian population.
    Munshi A, Sultana S, Kaul S, Reddy BP, Alladi S, Jyothy A.
    J Neurol Sci; 2008 Sep 15; 272(1-2):132-5. PubMed ID: 18586276
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  • 15. Common genetic markers and prediction of recurrent events after ischemic stroke in young adults.
    Pezzini A, Grassi M, Del Zotto E, Lodigiani C, Ferrazzi P, Spalloni A, Patella R, Giossi A, Volonghi I, Iacoviello L, Magoni M, Rota LL, Rasura M, Padovani A.
    Neurology; 2009 Sep 01; 73(9):717-23. PubMed ID: 19720979
    [Abstract] [Full Text] [Related]

  • 16. 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 Sep 01; 54(77):1438-42. PubMed ID: 17708272
    [Abstract] [Full Text] [Related]

  • 17. Inherited thrombophilia in infertile women: implication in unexplained infertility.
    Casadei L, Puca F, Privitera L, Zamaro V, Emidi E.
    Fertil Steril; 2010 Jul 01; 94(2):755-7. PubMed ID: 19939360
    [Abstract] [Full Text] [Related]

  • 18. The C677T polymorphism of the methylenetetrahydrofolate reductase gene is associated with idiopathic ischemic stroke in the young Mexican-Mestizo population.
    Isordia-Salas I, Barinagarrementería-Aldatz F, Leaños-Miranda A, Borrayo-Sánchez G, Vela-Ojeda J, García-Chávez J, Ibarra-González I, Majluf-Cruz A.
    Cerebrovasc Dis; 2010 Jul 01; 29(5):454-9. PubMed ID: 20203488
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  • 19. Factor V Leiden and prothrombin gene G 20210 A variant in children with ischemic stroke.
    Zenz W, Bodó Z, Plotho J, Streif W, Male C, Bernert G, Rauter L, Ebetsberger G, Kaltenbrunner K, Kurnik P, Lischka A, Paky F, Ploier R, Höfler G, Mannhalter C, Muntean W.
    Thromb Haemost; 1998 Nov 01; 80(5):763-6. PubMed ID: 9843168
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  • 20. ACE I/D polymorphism in different etiologies of ischemic stroke.
    Pera J, Slowik A, Dziedzic T, Wloch D, Szczudlik A.
    Acta Neurol Scand; 2006 Nov 01; 114(5):320-2. PubMed ID: 17022779
    [Abstract] [Full Text] [Related]

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