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Journal Abstract Search

343 related items for PubMed ID: 12382154

  • 1. 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]

  • 2. 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
    [Abstract] [Full Text] [Related]

  • 3. Prevalence of thrombophilic mutations and ACE I/D polymorphism in Turkish ischemic stroke patients.
    Celiker G, Can U, Verdi H, Yazici AC, Ozbek N, Atac FB.
    Clin Appl Thromb Hemost; 2009 Jan; 15(4):415-20. PubMed ID: 18387982
    [Abstract] [Full Text] [Related]

  • 4. Prevalence of prothrombin G20210A, factor V G1691A (Leiden), and methylenetetrahydrofolate reductase (MTHFR) C677T in seven different populations determined by multiplex allele-specific PCR.
    Hessner MJ, Luhm RA, Pearson SL, Endean DJ, Friedman KD, Montgomery RR.
    Thromb Haemost; 1999 May; 81(5):733-8. PubMed ID: 10365746
    [Abstract] [Full Text] [Related]

  • 5. Genetic risk factors for arterial ischemic stroke in children: a possible MTHFR and eNOS gene-gene interplay?
    Djordjevic V, Stankovic M, Brankovic-Sreckovic V, Rakicevic L, Radojkovic D.
    J Child Neurol; 2009 Jul; 24(7):823-7. PubMed ID: 19372095
    [Abstract] [Full Text] [Related]

  • 6. [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
    [Abstract] [Full Text] [Related]

  • 7. Effects of factor V gene G1691A, methylenetetrahydrofolate reductase gene C677T, and prothombin gene G20210A mutations on deep venous thrombogenesis in Behçet's disease.
    Toydemir PB, Elhan AH, Tükün A, Toydemir R, Gürler A, Tüzüner A, Bökesoy I.
    J Rheumatol; 2000 Dec 10; 27(12):2849-54. PubMed ID: 11128675
    [Abstract] [Full Text] [Related]

  • 8. [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
    [Abstract] [Full Text] [Related]

  • 9. MTHFR C677T, FII G20210A, FV Leiden G1691A, NOS3 intron 4 VNTR, and APOE epsilon4 gene polymorphisms are not associated with spontaneous cervical artery dissection.
    Jara-Prado A, Alonso ME, Martínez Ruano L, Guerrero Camacho J, Leyva A, López M, Gutierrez-Castrellon P, Arauz A.
    Int J Stroke; 2010 Apr 20; 5(2):80-5. PubMed ID: 20446941
    [Abstract] [Full Text] [Related]

  • 10. [C677T mutation in methylentetrahydrofolatereductase gene in patients with venous thromboses from the central region of Russia correlates with a high risk of pulmonary artery thromboembolism].
    Avdonin PV, Kirienko AI, Kozhevnikova LM, Shostak NA, Babadaeva NM, Leont'ev SG, Petukhov EB, Kubatiev AA, Savel'ev VS.
    Ter Arkh; 2006 Apr 20; 78(6):70-6. PubMed ID: 16881367
    [Abstract] [Full Text] [Related]

  • 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 Apr 20; 54(77):1438-42. PubMed ID: 17708272
    [Abstract] [Full Text] [Related]

  • 12. 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 20; 80(6):869-73. PubMed ID: 9869151
    [Abstract] [Full Text] [Related]

  • 13. [Polymorphism of genes coding for angiotensin I converting enzyme and methylenetetrahydrofolate reductase in patients with ischemic heart disease].
    Goracy I.
    Ann Acad Med Stetin; 2000 Dec 20; 46():97-108. PubMed ID: 11712321
    [Abstract] [Full Text] [Related]

  • 14. Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies.
    Kim RJ, Becker RC.
    Am Heart J; 2003 Dec 20; 146(6):948-57. PubMed ID: 14660985
    [Abstract] [Full Text] [Related]

  • 15. 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 20; 41(5):808-15. PubMed ID: 15886665
    [Abstract] [Full Text] [Related]

  • 16. Methylenetetrahydrofolate reductase gene polymorphism and ischemic stroke: sex difference in Japanese.
    Wu Y, Tomon M, Sumino K.
    Kobe J Med Sci; 2001 Dec 20; 47(6):255-62. PubMed ID: 11870335
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Lower contribution of factor V Leiden or G202104 mutations to ischemic stroke in patients with clinical risk factors: pair-matched case-control study.
    Eterović D, Titlić M, Culić V, Zadro R, Primorac D.
    Clin Appl Thromb Hemost; 2007 Apr 01; 13(2):188-93. PubMed ID: 17456629
    [Abstract] [Full Text] [Related]

  • 19. [Interactions between the MTHFR C677T and MTHFR A1298C mutations in ischaemic stroke].
    Szolnoki Z, Somogyvári F, Szabó M, Kondacs A, Fodor L, Melegh B.
    Ideggyogy Sz; 2006 Mar 20; 59(3-4):107-12. PubMed ID: 16634455
    [Abstract] [Full Text] [Related]

  • 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 20; 114(5):320-2. PubMed ID: 17022779
    [Abstract] [Full Text] [Related]

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