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Journal Abstract Search

171 related items for PubMed ID: 21070369

  • 21. Mesenteric venous thrombosis with bowel infarction and hyperhomocysteinemia due to homozygous methylenetetrahydrofolate reductase C677T genotype.
    Hotoleanu C, Andercou O, Andercou A.
    Vasc Endovascular Surg; 2008; 42(5):477-81. PubMed ID: 19000982
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  • 23. Retinal vein occlusion, homocysteine, and methylene tetrahydrofolate reductase genotype.
    McGimpsey SJ, Woodside JV, Bamford L, Gilchrist SE, Graydon R, McKeeman GC, Young IS, Hughes AE, Patterson CC, O'Reilly D, McGibbon D, Chakravarthy U.
    Invest Ophthalmol Vis Sci; 2005 Dec; 46(12):4712-6. PubMed ID: 16303969
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  • 24. C677T substitution in the methylenetetrahydrofolate reductase gene as a risk factor for venous thrombosis and arterial disease in selected patients.
    Gemmati D, Serino ML, Trivellato C, Fiorini S, Scapoli GL.
    Haematologica; 1999 Sep; 84(9):824-8. PubMed ID: 10477457
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  • 26. Hyperhomocysteinemia and the MTHFR C677T polymorphism promote steatosis and fibrosis in chronic hepatitis C patients.
    Adinolfi LE, Ingrosso D, Cesaro G, Cimmino A, D'Antò M, Capasso R, Zappia V, Ruggiero G.
    Hepatology; 2005 May; 41(5):995-1003. PubMed ID: 15834927
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  • 29. Serum total homocysteine levels and the prevalence of folic acid deficiency and C677T mutation at the MTHFR gene in an indigenous population of Amazonia: the relationship of homocysteine with other cardiovascular risk factors.
    Tavares EF, Vieira-Filho JP, Andriolo A, Perez AB, Vergani N, Sañudo A, Gimeno SG, Franco LJ.
    Ethn Dis; 2004 May; 14(1):49-56. PubMed ID: 15002923
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  • 32. Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion.
    Larsson J, Hultberg B, Hillarp A.
    Acta Ophthalmol Scand; 2000 Jun; 78(3):340-3. PubMed ID: 10893069
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  • 33. Heterozygous prothrombin 20210G/A mutation, associated with hyperhomocysteinemia, and homozygous methylenetetrahydrofolate reductase 677C/T mutation, in a patient with portal and mesenteric venous thrombosis.
    Elhajj II, Salem ZM, Birjawi GA, Taher AT, Soweid AM.
    Hematol J; 2004 Jun; 5(6):540-2. PubMed ID: 15570301
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  • 35. 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 Jun; 122(5):648-56. PubMed ID: 18384842
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  • 36. Hyperhomocysteinemia and MTHFR C677T homozygosity in a vegetarian male with sinovenous thrombosis of the brain.
    Bharatkumar VP, Nagaraja D, Shankar SK, Christopher R.
    J Clin Neurosci; 2009 Oct; 16(10):1380-1. PubMed ID: 19592255
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  • 38. Segmental renal artery thrombosis secondary to methylene tetrahydrofolate reductase mutation: an unusual presentation.
    Mendonca S, Gupta D, Gupta A.
    Iran J Kidney Dis; 2012 Nov; 6(6):464-6. PubMed ID: 23146986
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  • 39. Interaction between hyperhomocysteinemia and inherited thrombophilic factors in venous thromboembolism.
    De Stefano V, Casorelli I, Rossi E, Zappacosta B, Leone G.
    Semin Thromb Hemost; 2000 Nov; 26(3):305-11. PubMed ID: 11011848
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  • 40. No interaction between factor V Leiden and hyperhomocysteinemia or MTHFR 677TT genotype in venous thrombosis. Results of a meta-analysis of published studies and a large case-only study.
    Keijzer MB, Borm GF, Blom HJ, Bos GM, Rosendaal FR, den Heijer M.
    Thromb Haemost; 2007 Jan; 97(1):32-7. PubMed ID: 17200768
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