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Journal Abstract Search

159 related items for PubMed ID: 9667406

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  • 2. 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; 67(3):154-7. PubMed ID: 12797455
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  • 7. 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; 54(1):30-4. PubMed ID: 24588777
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  • 8. 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
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  • 9. Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects(NTD).
    Stegmann K, Ziegler A, Ngo ET, Kohlschmidt N, Schröter B, Ermert A, Koch MC.
    Am J Med Genet; 1999 Nov 05; 87(1):23-9. PubMed ID: 10528242
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  • 10. 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
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  • 11. Effect of MTHFR 677C>T on plasma total homocysteine levels in renal graft recipients.
    Födinger M, Wölfl G, Fischer G, Rasoul-Rockenschaub S, Schmid R, Hörl WH, Sunder-Plassmann G.
    Kidney Int; 1999 Mar 01; 55(3):1072-80. PubMed ID: 10027946
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  • 12. Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population.
    Richter B, Stegmann K, Röper B, Böddeker I, Ngo ET, Koch MC.
    J Hum Genet; 2001 Mar 01; 46(3):105-9. PubMed ID: 11310576
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  • 13. 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 01; 35(12):1009-13. PubMed ID: 9863598
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  • 14. 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
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  • 15. The relation between erythrocyte volume and folate levels is influenced by a common mutation in the methylenetetrahydrofolate reductase (MTHFR) gene (C677T).
    Lalouschek W, Aull S, Serles W, Wolfsberger M, Deecke L, Pabinger-Fasching I, Mannhalter C.
    J Investig Med; 2000 Jan 15; 48(1):14-20. PubMed ID: 10695265
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  • 16. 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 Jan 15; 47(6):324-9. PubMed ID: 11721146
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  • 17. Polymorphisms in genes involved in folate metabolism as risk factors for NTDs.
    De Marco P, Calevo MG, Moroni A, Arata L, Merello E, Cama A, Finnell RH, Andreussi L, Capra V.
    Eur J Pediatr Surg; 2001 Dec 15; 11 Suppl 1():S14-7. PubMed ID: 11813127
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  • 18. Spina bifida and other neural tube defects.
    Northrup H, Volcik KA.
    Curr Probl Pediatr; 2000 Dec 15; 30(10):313-32. PubMed ID: 11147289
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  • 19. 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 Dec 15; 4(3):126-30. PubMed ID: 12180146
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  • 20. 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 15; 67(4):317-23. PubMed ID: 10444342
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