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Journal Abstract Search

159 related items for PubMed ID: 11239192

  • 1. Mild hyperhomocyst(e)inemia: a possible risk factor for cervical artery dissection.
    Gallai V, Caso V, Paciaroni M, Cardaioli G, Arning E, Bottiglieri T, Parnetti L.
    Stroke; 2001 Mar; 32(3):714-8. PubMed ID: 11239192
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  • 3. 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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  • 4. 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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  • 9. 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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  • 12. 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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  • 14. 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 Jul 11; 47(6):324-9. PubMed ID: 11721146
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  • 15. Plasma homocysteine, methylenetetrahydrofolate reductase genotypes, and age at onset of symptoms of myocardial ischemia.
    Mager A, Battler A, Birnbaum Y, Magal N, Shohat M.
    Am J Cardiol; 2002 Apr 15; 89(8):919-23. PubMed ID: 11950428
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  • 16. 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 15; 134(1):57-61. PubMed ID: 12095808
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  • 17. Genetic polymorphism of 5,10-methylenetetrahydrofolate reductase (MTHFR) as a risk factor for coronary artery disease.
    Morita H, Taguchi J, Kurihara H, Kitaoka M, Kaneda H, Kurihara Y, Maemura K, Shindo T, Minamino T, Ohno M, Yamaoki K, Ogasawara K, Aizawa T, Suzuki S, Yazaki Y.
    Circulation; 1997 Apr 15; 95(8):2032-6. PubMed ID: 9133512
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  • 18. Low vitamin B6 but not homocyst(e)ine is associated with increased risk of stroke and transient ischemic attack in the era of folic acid grain fortification.
    Kelly PJ, Shih VE, Kistler JP, Barron M, Lee H, Mandell R, Furie KL.
    Stroke; 2003 Jun 15; 34(6):e51-4. PubMed ID: 12738890
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  • 19. 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 15; 112(2):171-7. PubMed ID: 12522558
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