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Journal Abstract Search

1079 related items for PubMed ID: 23827456

  • 1. Methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and variations of homocysteine concentrations in patients with Behcet's disease.
    Messedi M, Frigui M, Chaabouni Kh, Turki M, Neifer M, Lahiyani A, Messaouad M, Bahloul Z, Ayedi F, Jamoussi K.
    Gene; 2013 Sep 15; 527(1):306-10. PubMed ID: 23827456
    [Abstract] [Full Text] [Related]

  • 2. 5,10-Methylenetetrahydrofolate reductase (MTHFR) C677T and A1298C polymorphisms: genotype frequency and association with homocysteine and folate levels in middle-southern Italian adults.
    Zappacosta B, Graziano M, Persichilli S, Di Castelnuovo A, Mastroiacovo P, Iacoviello L.
    Cell Biochem Funct; 2014 Jan 15; 32(1):1-4. PubMed ID: 24277487
    [Abstract] [Full Text] [Related]

  • 3. Methylenetetrahydrofolate reductase (C677T and A1298C) polymorphisms, hyperhomocysteinemia, and ischemic stroke in Tunisian patients.
    Fekih-Mrissa N, Mrad M, Klai S, Mansour M, Nsiri B, Gritli N, Mrissa R.
    J Stroke Cerebrovasc Dis; 2013 May 15; 22(4):465-9. PubMed ID: 23642756
    [Abstract] [Full Text] [Related]

  • 4. 5,10-Methylenetetrahydrofolate reductase C677T gene polymorphism in Behcet's patients with or without ocular involvement.
    Ozkul Y, Evereklioglu C, Borlu M, Taheri S, Calis M, Dündar M, Ilhan O.
    Br J Ophthalmol; 2005 Dec 15; 89(12):1634-7. PubMed ID: 16299146
    [Abstract] [Full Text] [Related]

  • 5. MTHFR C677T and A1298C gene polymorphisms and their relation to homocysteine level in Egyptian children with congenital heart diseases.
    Zidan HE, Rezk NA, Mohammed D.
    Gene; 2013 Oct 15; 529(1):119-24. PubMed ID: 23933414
    [Abstract] [Full Text] [Related]

  • 6. Methylenetetrahydrofolate reductase (MTHFR) gene C677T, A1298C and G1793A polymorphisms: association with risk for clear cell renal cell carcinoma and tumour behaviour in men.
    Safarinejad MR, Shafiei N, Safarinejad S.
    Clin Oncol (R Coll Radiol); 2012 May 15; 24(4):269-81. PubMed ID: 21489764
    [Abstract] [Full Text] [Related]

  • 7. Association of hyperhomocysteinemia with genetic variants in key enzymes of homocysteine metabolism and methotrexate toxicity in rheumatoid arthritis patients.
    Chaabane S, Messedi M, Akrout R, Ben Hamad M, Turki M, Marzouk S, Keskes L, Bahloul Z, Rebai A, Ayedi F, Maalej A.
    Inflamm Res; 2018 Aug 15; 67(8):703-710. PubMed ID: 29796841
    [Abstract] [Full Text] [Related]

  • 8. Evaluation of the relationship between C677T variants of methylenetetrahydrofolate reductase gene and hyperhomocysteinemia in children receiving antiepileptic drug therapy.
    Vurucu S, Demirkaya E, Kul M, Unay B, Gul D, Akin R, Gokçay E.
    Prog Neuropsychopharmacol Biol Psychiatry; 2008 Apr 01; 32(3):844-8. PubMed ID: 18234410
    [Abstract] [Full Text] [Related]

  • 9. Association of MTHFR and RFC1 gene polymorphism with hyperhomocysteinemia and its modulation by vitamin B12 and folic acid in an Indian population.
    Sukla KK, Raman R.
    Eur J Clin Nutr; 2012 Jan 01; 66(1):111-8. PubMed ID: 21878957
    [Abstract] [Full Text] [Related]

  • 10. MTHFR C677T and A1298C gene polymorphisms and hyperhomocysteinemia as risk factors of diabetic nephropathy in type 2 diabetes patients.
    Mtiraoui N, Ezzidi I, Chaieb M, Marmouche H, Aouni Z, Chaieb A, Mahjoub T, Vaxillaire M, Almawi WY.
    Diabetes Res Clin Pract; 2007 Jan 01; 75(1):99-106. PubMed ID: 16828193
    [Abstract] [Full Text] [Related]

  • 11. [Hyperhomocysteinemia and deep-vein thrombosis].
    Qiu L, Yan SK, Song YH.
    Zhongguo Yi Xue Ke Xue Yuan Xue Bao; 2003 Dec 01; 25(6):706-9. PubMed ID: 14714317
    [Abstract] [Full Text] [Related]

  • 12. Polymorphism C776G in the transcobalamin II gene and homocysteine, folate and vitamin B12 concentrations. Association with MTHFR C677T and A1298C and MTRR A66G polymorphisms in healthy children.
    Aléssio AC, Höehr NF, Siqueira LH, Bydlowski SP, Annichino-Bizzacchi JM.
    Thromb Res; 2007 Dec 01; 119(5):571-7. PubMed ID: 16820193
    [Abstract] [Full Text] [Related]

  • 13. 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 01; 59(7):17-26; discussion 26. PubMed ID: 14560345
    [Abstract] [Full Text] [Related]

  • 14. 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 01; 131(2):395-401. PubMed ID: 16452733
    [Abstract] [Full Text] [Related]

  • 15. Methylenetetrahydrofolate reductase gene polymorphism and serum homocysteine levels in nonalcoholic fatty liver disease.
    Franco Brochado MJ, Domenici FA, Candolo Martinelli Ade L, Zucoloto S, de Carvalho da Cunha SF, Vannucchi H.
    Ann Nutr Metab; 2013 Feb 01; 63(3):193-9. PubMed ID: 24051448
    [Abstract] [Full Text] [Related]

  • 16. Effect of folate, vitamin B6, and vitamin B12 intake and MTHFR C677T polymorphism on homocysteine concentrations of renal transplant recipients.
    Biselli PM, Sanches de Alvarenga MP, Abbud-Filho M, Ferreira-Baptista MA, Galbiatti AL, Goto MT, Cardoso MA, Eberlin MN, Haddad R, Goloni-Bertollo EM, Pavarino-Bertelli EC.
    Transplant Proc; 2007 Dec 01; 39(10):3163-5. PubMed ID: 18089344
    [Abstract] [Full Text] [Related]

  • 17. Methylenetetrahydrofolate reductase genotype, vitamin B12, and folate influence plasma homocysteine in hemodialysis patients.
    Nakamura T, Saionji K, Hiejima Y, Hirayama H, Tago K, Takano H, Tajiri M, Hayashi K, Kawabata M, Funamizu M, Makita Y, Hata A.
    Am J Kidney Dis; 2002 May 01; 39(5):1032-9. PubMed ID: 11979347
    [Abstract] [Full Text] [Related]

  • 18. Association of COMT, MTHFR, and SLC19A1(RFC-1) polymorphisms with homocysteine blood levels and cognitive impairment in Parkinson's disease.
    Białecka M, Kurzawski M, Roszmann A, Robowski P, Sitek EJ, Honczarenko K, Gorzkowska A, Budrewicz S, Mak M, Jarosz M, Gołąb-Janowska M, Koziorowska-Gawron E, Droździk M, Sławek J.
    Pharmacogenet Genomics; 2012 Oct 01; 22(10):716-24. PubMed ID: 22890010
    [Abstract] [Full Text] [Related]

  • 19. 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 Oct 01; 122(5):648-56. PubMed ID: 18384842
    [Abstract] [Full Text] [Related]

  • 20. Methylenetetrahydrofolate reductase gene C677T and A1298C polymorphisms, plasma homocysteine, folate, and vitamin B12 levels and the extent of coronary artery disease.
    Kölling K, Ndrepepa G, Koch W, Braun S, Mehilli J, Schömig A, Kastrati A.
    Am J Cardiol; 2004 May 15; 93(10):1201-6. PubMed ID: 15135689
    [Abstract] [Full Text] [Related]

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