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Journal Abstract Search

178 related items for PubMed ID: 9863598

  • 1. The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy.
    de Franchis R, Buoninconti A, Mandato C, Pepe A, Sperandeo MP, Del Gado R, Capra V, Salvaggio E, Andria G, Mastroiacovo P.
    J Med Genet; 1998 Dec; 35(12):1009-13. PubMed ID: 9863598
    [Abstract] [Full Text] [Related]

  • 2. Maternal vitamin use, genetic variation of infant methylenetetrahydrofolate reductase, and risk for spina bifida.
    Shaw GM, Rozen R, Finnell RH, Wasserman CR, Lammer EJ.
    Am J Epidemiol; 1998 Jul 01; 148(1):30-7. PubMed ID: 9663401
    [Abstract] [Full Text] [Related]

  • 3. C677T mutation in methylenetetrahydrofolate reductase gene and neural tube defects: should Japanese women undergo gene screening before pregnancy?
    Kondo A, Fukuda H, Matsuo T, Shinozaki K, Okai I.
    Congenit Anom (Kyoto); 2014 Feb 01; 54(1):30-4. PubMed ID: 24588777
    [Abstract] [Full Text] [Related]

  • 4. Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects.
    Volcik KA, Shaw GM, Lammer EJ, Zhu H, Finnell RH.
    Birth Defects Res A Clin Mol Teratol; 2003 Mar 01; 67(3):154-7. PubMed ID: 12797455
    [Abstract] [Full Text] [Related]

  • 5. Methylenetetrahydrofolate reductase and spina bifida: evaluation of level of defect and maternal genotypic risk in Hispanics.
    Volcik KA, Blanton SH, Tyerman GH, Jong ST, Rott EJ, Page TZ, Romaine NK, Northrup H.
    Am J Med Genet; 2000 Nov 06; 95(1):21-7. PubMed ID: 11074490
    [Abstract] [Full Text] [Related]

  • 6. Altered folate metabolism and disposition in mothers affected by a spina bifida pregnancy: influence of 677c --> t methylenetetrahydrofolate reductase and 2756a --> g methionine synthase genotypes.
    Lucock M, Daskalakis I, Briggs D, Yates Z, Levene M.
    Mol Genet Metab; 2000 May 06; 70(1):27-44. PubMed ID: 10833329
    [Abstract] [Full Text] [Related]

  • 7. Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring.
    van der Put NM, van den Heuvel LP, Steegers-Theunissen RP, Trijbels FJ, Eskes TK, Mariman EC, den Heyer M, Blom HJ.
    J Mol Med (Berl); 1996 Nov 06; 74(11):691-4. PubMed ID: 8956155
    [Abstract] [Full Text] [Related]

  • 8. Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida.
    Shaw GM, Lammer EJ, Zhu H, Baker MW, Neri E, Finnell RH.
    Am J Med Genet; 2002 Feb 15; 108(1):1-6. PubMed ID: 11857541
    [Abstract] [Full Text] [Related]

  • 9. Spina bifida and folate-related genes: a study of gene-gene interactions.
    de Franchis R, Botto LD, Sebastio G, Ricci R, Iolascon A, Capra V, Andria G, Mastroiacovo P.
    Genet Med; 2002 Feb 15; 4(3):126-30. PubMed ID: 12180146
    [Abstract] [Full Text] [Related]

  • 10. Elevated plasma total homocysteine and C677T mutation of the methylenetetrahydrofolate reductase gene in patients with spina bifida.
    Bjørke-Monsen AL, Ueland PM, Schneede J, Vollset SE, Refsum H.
    QJM; 1997 Sep 15; 90(9):593-6. PubMed ID: 9349452
    [Abstract] [Full Text] [Related]

  • 11. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida.
    van der Put NM, Steegers-Theunissen RP, Frosst P, Trijbels FJ, Eskes TK, van den Heuvel LP, Mariman EC, den Heyer M, Rozen R, Blom HJ.
    Lancet; 1995 Oct 21; 346(8982):1070-1. PubMed ID: 7564788
    [Abstract] [Full Text] [Related]

  • 12. Spina bifida and other neural tube defects.
    Northrup H, Volcik KA.
    Curr Probl Pediatr; 2000 Oct 21; 30(10):313-32. PubMed ID: 11147289
    [Abstract] [Full Text] [Related]

  • 13. Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population.
    Koch MC, Stegmann K, Ziegler A, Schröter B, Ermert A.
    Eur J Pediatr; 1998 Jun 21; 157(6):487-92. PubMed ID: 9667406
    [Abstract] [Full Text] [Related]

  • 14. A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida.
    Wilson A, Platt R, Wu Q, Leclerc D, Christensen B, Yang H, Gravel RA, Rozen R.
    Mol Genet Metab; 1999 Aug 21; 67(4):317-23. PubMed ID: 10444342
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  • 16. Methylenetetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida.
    Perez AB, D'Almeida V, Vergani N, de Oliveira AC, de Lima FT, Brunoni D.
    Am J Med Genet A; 2003 May 15; 119A(1):20-5. PubMed ID: 12707953
    [Abstract] [Full Text] [Related]

  • 17. Polymorphisms of the 5,10-methylenetetrahydrofolate and the methionine synthase reductase genes as independent risk factors for spina bifida.
    Pietrzyk JJ, Bik-Multanowski M, Sanak M, Twardowska M.
    J Appl Genet; 2003 May 15; 44(1):111-3. PubMed ID: 12590188
    [Abstract] [Full Text] [Related]

  • 18. Spina bifida, folate metabolism, and dietary folate intake in a Northern Canadian aboriginal population.
    Arbour L, Christensen B, Delormier T, Platt R, Gilfix B, Forbes P, Kovitch I, Morel J, Rozen R.
    Int J Circumpolar Health; 2002 Nov 15; 61(4):341-51. PubMed ID: 12546192
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