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163 related items for PubMed ID: 10893069

  • 1. 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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  • 2. Hyperhomocyst(e)inemia and MTHFR C677T genotypes in patients with central retinal vein occlusion.
    Weger M, Stanger O, Deutschmann H, Temmel W, Renner W, Schmut O, Semmelrock J, Haas A.
    Graefes Arch Clin Exp Ophthalmol; 2002 Apr; 240(4):286-90. PubMed ID: 11981642
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  • 3. Hyperhomocyst(e)inemia, but not methylenetetrahydrofolate reductase C677T mutation, as a risk factor in branch retinal vein occlusion.
    Weger M, Stanger O, Deutschmann H, Temmel W, Renner W, Schmut O, Quehenberger F, Semmelrock J, Haas A.
    Ophthalmology; 2002 Jun; 109(6):1105-9. PubMed ID: 12045051
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  • 4. The role of hyperhomocysteinemia and methylenetetrahydrofolate reductase (MTHFR) C677T mutation in patients with retinal artery occlusion.
    Weger M, Stanger O, Deutschmann H, Leitner FJ, Renner W, Schmut O, Semmelrock J, Haas A.
    Am J Ophthalmol; 2002 Jul; 134(1):57-61. PubMed ID: 12095808
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  • 5. MTHFR C677T mutation in central retinal vein occlusion: a case-control study in Chinese population.
    Gao W, Wang YS, Zhang P, Wang HY.
    Thromb Res; 2008 Jul; 121(5):699-703. PubMed ID: 17719079
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  • 6. The common mutations C677T and A1298C in the human methylenetetrahydrofolate reductase gene are associated with hyperhomocysteinemia and cardiovascular disease in hemodialysis patients.
    Haviv YS, Shpichinetsky V, Goldschmidt N, Atta IA, Ben-Yehuda A, Friedman G.
    Nephron; 2002 Sep; 92(1):120-6. PubMed ID: 12187094
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  • 7. Genetic determinants of fasting and post-methionine hyperhomocysteinemia in patients with retinal vein occlusion.
    Marcucci R, Giusti B, Betti I, Evangelisti L, Fedi S, Sodi A, Cappelli S, Menchini U, Abbate R, Prisco D.
    Thromb Res; 2003 Apr 15; 110(1):7-12. PubMed ID: 12877902
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  • 9. The role of vitamin B12 in fasting hyperhomocysteinemia and its interaction with the homozygous C677T mutation of the methylenetetrahydrofolate reductase (MTHFR) gene. A case-control study of patients with early-onset thrombotic events.
    D'Angelo A, Coppola A, Madonna P, Fermo I, Pagano A, Mazzola G, Galli L, Cerbone AM.
    Thromb Haemost; 2000 Apr 15; 83(4):563-70. PubMed ID: 10780318
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  • 10. Hyperhomocysteinemia and C677T MTHFR genotype in patients with retinal vein thrombosis.
    Sottilotta G, Siboni SM, Latella C, Oriana V, Romeo E, Santoro R, Consonni D, Trapani Lombardo V.
    Clin Appl Thromb Hemost; 2010 Oct 15; 16(5):549-53. PubMed ID: 19825913
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  • 11. Mutations C677T and A1298C of the 5,10-methylenetetrahydrofolate reductase gene and fasting plasma homocysteine levels are not associated with the increased risk of venous thromboembolic disease.
    Domagala TB, Adamek L, Nizankowska E, Sanak M, Szczeklik A.
    Blood Coagul Fibrinolysis; 2002 Jul 15; 13(5):423-31. PubMed ID: 12138370
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  • 12. Hyperhomocysteinemia but not the C677T mutation of methylenetetrahydrofolate reductase is an independent risk determinant of carotid wall thickening. The Perth Carotid Ultrasound Disease Assessment Study (CUDAS).
    McQuillan BM, Beilby JP, Nidorf M, Thompson PL, Hung J.
    Circulation; 1999 May 11; 99(18):2383-8. PubMed ID: 10318658
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  • 13. Association of retinal vein occlusion, homocysteine, and the thrombophilic mutations in a Turkish population: A case-control study.
    Koylu MT, Kucukevcilioglu M, Erdurman FC, Durukan AH, Sobacı G, Torun D, Tunca Y, Ayyildiz O.
    Ophthalmic Genet; 2017 May 11; 38(4):352-356. PubMed ID: 28085519
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  • 14. 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 11; 84(9):824-8. PubMed ID: 10477457
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  • 15. Hyperhomocysteinemia and BRVO.
    Yanamandra K, Thurmon TF, Bocchini JA, Kooragayala LM.
    Ophthalmology; 2003 Oct 11; 110(10):2069; author reply 2069. PubMed ID: 14522804
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  • 18. Hyperhomocysteinemia and the methylenetetrahydrofolate reductase 677C-T mutation in patients under 50 years of age affected by central retinal vein occlusion.
    Di Crecchio L, Parodi MB, Sanguinetti G, Iacono P, Ravalico G.
    Ophthalmology; 2004 May 11; 111(5):940-5. PubMed ID: 15121372
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  • 19. Plasma homocysteine levels, methylene tetrahydrofolate reductase A1298C gene polymorphism and risk of retinal vein thrombosis.
    Ghaznavi H, Soheili Z, Samiei S, Soltanpour MS.
    Blood Coagul Fibrinolysis; 2016 Sep 11; 27(6):679-83. PubMed ID: 26650461
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  • 20. Plasma folate, vitamin B(12), and total homocysteine and homozygosity for the C677T mutation of the 5,10-methylene tetrahydrofolate reductase gene in patients with Alzheimer's dementia. A case-control study.
    Postiglione A, Milan G, Ruocco A, Gallotta G, Guiotto G, Di Minno G.
    Gerontology; 2001 Sep 11; 47(6):324-9. PubMed ID: 11721146
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