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Journal Abstract Search

369 related items for PubMed ID: 19520684

  • 21. Methylenetetrahydrofolate reductase gene, homocysteine and coronary artery disease: the A1298C polymorphism does matter. Inferences from a case study (Madeira, Portugal).
    Freitas AI, Mendonça I, Guerra G, Brión M, Reis RP, Carracedo A, Brehm A.
    Thromb Res; 2008; 122(5):648-56. PubMed ID: 18384842
    [Abstract] [Full Text] [Related]

  • 22. Methylenetetrahydrofolate reductase C677T and A1298C polymorphism and changes in homocysteine concentrations in women with idiopathic recurrent pregnancy losses.
    Mtiraoui N, Zammiti W, Ghazouani L, Braham NJ, Saidi S, Finan RR, Almawi WY, Mahjoub T.
    Reproduction; 2006 Feb; 131(2):395-401. PubMed ID: 16452733
    [Abstract] [Full Text] [Related]

  • 23. Dietary factors and biomarkers involved in the methylenetetrahydrofolate reductase genotype-colorectal adenoma pathway.
    Martínez ME, Thompson P, Jacobs ET, Giovannucci E, Jiang R, Klimecki W, Alberts DS.
    Gastroenterology; 2006 Dec; 131(6):1706-16. PubMed ID: 17087956
    [Abstract] [Full Text] [Related]

  • 24. Methylenetetrahydrofolate reductase C677T polymorphism in Iraqi patients with ischemic stroke.
    Al-Allawi NA, Avo AS, Jubrael JM.
    Neurol India; 2009 Dec; 57(5):631-5. PubMed ID: 19934565
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  • 26. 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 Dec; 54(77):1438-42. PubMed ID: 17708272
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  • 28. [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 Dec; 78(6):70-6. PubMed ID: 16881367
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  • 29. The 19-bp deletion of dihydrofolate reductase (DHFR), methylenetetrahydrofolate reductase (MTHFR) C677T, Factor V Leiden, prothrombin G20210A polymorphisms in cancer patients with and without thrombosis.
    Eroglu A, Egin Y, Cam R, Akar N.
    Ann Hematol; 2009 Jan; 88(1):73-6. PubMed ID: 18682947
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  • 30. Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in 200 healthy Jordanians.
    Eid SS, Rihani G.
    Clin Lab Sci; 2004 Jan; 17(4):200-2. PubMed ID: 15559724
    [Abstract] [Full Text] [Related]

  • 31. Hyperhomocysteinaemia, methylenetetrahydrofolate reductase polymorphism and risk of coronary artery disease.
    Kerkeni M, Addad F, Chauffert M, Myara A, Gerhardt M, Chevenne D, Trivin F, Farhat MB, Miled A, Maaroufi K.
    Ann Clin Biochem; 2006 May; 43(Pt 3):200-6. PubMed ID: 16704755
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  • 32. Methylenetetrahydrofolate reductase gene C677T polymorphism, homocysteine, vitamin B12, and DNA damage in coronary artery disease.
    Andreassi MG, Botto N, Cocci F, Battaglia D, Antonioli E, Masetti S, Manfredi S, Colombo MG, Biagini A, Clerico A.
    Hum Genet; 2003 Feb; 112(2):171-7. PubMed ID: 12522558
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  • 33. 677TT polymorphism of methylenetetrahydrofolate reductase in combination with low serum vitamin B12 is associated with coronary in-stent restenosis.
    Chung SL, Chiou KR, Charng MJ.
    Catheter Cardiovasc Interv; 2006 Mar; 67(3):349-55. PubMed ID: 16489563
    [Abstract] [Full Text] [Related]

  • 34. Association of the C677T and A1298C polymorphisms of methylenetetrahydrofolate reductase gene with schizophrenia: association is significant in men but not in women.
    Sazci A, Ergul E, Kucukali I, Kara I, Kaya G.
    Prog Neuropsychopharmacol Biol Psychiatry; 2005 Sep; 29(7):1113-23. PubMed ID: 16084002
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  • 35. 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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  • 36. Absence of association of thrombophilia polymorphisms with intrauterine growth restriction.
    Infante-Rivard C, Rivard GE, Yotov WV, Génin E, Guiguet M, Weinberg C, Gauthier R, Feoli-Fonseca JC.
    N Engl J Med; 2002 Jul 04; 347(1):19-25. PubMed ID: 12097536
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  • 37. Folate, homocysteine, interleukin-6, and tumor necrosis factor alfa levels, but not the methylenetetrahydrofolate reductase C677T polymorphism, are risk factors for schizophrenia.
    García-Miss Mdel R, Pérez-Mutul J, López-Canul B, Solís-Rodríguez F, Puga-Machado L, Oxté-Cabrera A, Gurubel-Maldonado J, Arankowsky-Sandoval G.
    J Psychiatr Res; 2010 May 04; 44(7):441-6. PubMed ID: 19939410
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  • 38. The early-onset preeclampsia is associated with MTHFR and FVL polymorphisms.
    Salimi S, Saravani M, Yaghmaei M, Fazlali Z, Mokhtari M, Naghavi A, Farajian-Mashhadi F.
    Arch Gynecol Obstet; 2015 Jun 04; 291(6):1303-12. PubMed ID: 25480409
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  • 40. The prevalence of factor V Leiden (G1691A), prothrombin G20210A and methylenetetrahydrofolate reductase C677T mutations in Jordanian patients with beta-thalassemia major.
    Al-Sweedan SA, Jaradat S, Iraqi M, Beshtawi M.
    Blood Coagul Fibrinolysis; 2009 Dec 04; 20(8):675-8. PubMed ID: 19710606
    [Abstract] [Full Text] [Related]

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