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474 related items for PubMed ID: 12095808

  • 1. 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
    [Abstract] [Full Text] [Related]

  • 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
    [Abstract] [Full Text] [Related]

  • 4. 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; 83(4):563-70. PubMed ID: 10780318
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  • 5. Methylenetetrahydrofolate reductase gene polymorphism, hyperhomocysteinemia and occlusive retinal vascular disease in type 2 diabetic and non-diabetic subjects.
    Wirta V, Saransaari P, Wirta O, Rantalaiho V, Oja SS, Pasternack A, Koivula T, Lehtimäki T.
    Clin Nephrol; 2002 Sep; 58(3):171-8. PubMed ID: 12356186
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  • 6. 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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  • 7. The C677T mutation in methylenetetrahydrofolate reductase gene, plasma homocysteine concentration and the risk of coronary artery disease.
    Kadziela J, Janas J, Dzielińska Z, Szperl M, Gaździk D, Chotkowska E, Piotrowski W, Ruzyłło W.
    Kardiol Pol; 2003 Jul 11; 59(7):17-26; discussion 26. PubMed ID: 14560345
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  • 9. Hyperhomocyst(e)inaemia, but not MTHFR C677T mutation, as a risk factor for non-arteritic ischaemic optic neuropathy.
    Weger M, Stanger O, Deutschmann H, Simon M, Renner W, Schmut O, Semmelrock J, Haas A.
    Br J Ophthalmol; 2001 Jul 11; 85(7):803-6. PubMed ID: 11423453
    [Abstract] [Full Text] [Related]

  • 10. Hyperhomocysteinemia and the MTHFR C677T mutation in central retinal vein occlusion.
    Larsson J, Hultberg B, Hillarp A.
    Acta Ophthalmol Scand; 2000 Jun 11; 78(3):340-3. PubMed ID: 10893069
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  • 11. Hyperhomocysteinemia and the MTHFR C677T mutation in Budd-Chiari syndrome.
    Li XM, Wei YF, Hao HL, Hao YB, He LS, Li JD, Mei B, Wang SY, Wang C, Wang JX, Zhu JZ, Liang JQ.
    Am J Hematol; 2002 Sep 11; 71(1):11-4. PubMed ID: 12221667
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  • 13. 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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  • 14. The effect of methylenetetrahydrofolate reductase C677T common variant on hypertensive risk is not solely explained by increased plasma homocysteine values.
    Rodríguez-Esparragón F, Hernández-Perera O, Rodríguez-Pérez JC, Anábitarte A, Díaz-Cremades JM, Losada A, Fiuza D, Hernández E, Yunis C, Ferrario CM.
    Clin Exp Hypertens; 2003 May 11; 25(4):209-20. PubMed ID: 12797595
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  • 15. The 677T genotype of the common MTHFR thermolabile variant and fasting homocysteine in childhood venous thrombosis.
    Koch HG, Nabel P, Junker R, Auberger K, Schobess R, Homberger A, Linnebank M, Nowak-Göttl U.
    Eur J Pediatr; 1999 Dec 11; 158 Suppl 3():S113-6. PubMed ID: 10650848
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  • 17. 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 11; 92(1):120-6. PubMed ID: 12187094
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  • 18. High prevalence of mild hyperhomocysteinemia in patients with abdominal aortic aneurysm.
    Brunelli T, Prisco D, Fedi S, Rogolino A, Farsi A, Marcucci R, Giusti B, Pratesi C, Pulli R, Gensini GF, Abbate R, Pepe G.
    J Vasc Surg; 2000 Sep 11; 32(3):531-6. PubMed ID: 10957660
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  • 19. Role of a common mutation in the homocysteine regulatory enzyme methylenetetrahydrofolate reductase in ischemic stroke.
    Press RD, Beamer N, Evans A, DeLoughery TG, Coull BM.
    Diagn Mol Pathol; 1999 Mar 11; 8(1):54-8. PubMed ID: 10408794
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  • 20. Plasma homocysteine concentration, C677T MTHFR genotype, and 844ins68bp CBS genotype in young adults with spontaneous cervical artery dissection and atherothrombotic stroke.
    Pezzini A, Del Zotto E, Archetti S, Negrini R, Bani P, Albertini A, Grassi M, Assanelli D, Gasparotti R, Vignolo LA, Magoni M, Padovani A.
    Stroke; 2002 Mar 11; 33(3):664-9. PubMed ID: 11872884
    [Abstract] [Full Text] [Related]

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