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343 related items for PubMed ID: 24588777
1. 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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
3. Polymorphisms of 5,10-methylenetetrahydrofolate reductase and cystathionine beta-synthase genes as a risk factor for neural tube defects in Sétif, Algeria. Houcher B, Bourouba R, Djabi F, Yilmaz E, Eğin Y, Akar N. Pediatr Neurosurg; 2009 Mar; 45(6):472-7. PubMed ID: 20160465 [Abstract] [Full Text] [Related]
4. 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]
5. Association of neural tube defects in children of mothers with MTHFR 677TT genotype and abnormal carbohydrate metabolism risk: a case-control study. Cadenas-Benitez NM, Yanes-Sosa F, Gonzalez-Meneses A, Cerrillos L, Acosta D, Praena-Fernandez JM, Neth O, Gomez de Terreros I, Ybot-González P. Genet Mol Res; 2014 Mar 26; 13(1):2200-7. PubMed ID: 24737468 [Abstract] [Full Text] [Related]
7. 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]
8. 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]
12. Distribution of alleles of the methylenetetrahydrofolate reductase (MTHFR) C677T gene polymorphism in familial spina bifida. Johnson WG, Stenroos ES, Heath SC, Chen Y, Carroll R, McKoy VV, Chatkupt S, Lehner T. Am J Med Genet; 1999 Dec 22; 87(5):407-12. PubMed ID: 10594879 [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 22; 157(6):487-92. PubMed ID: 9667406 [Abstract] [Full Text] [Related]
20. Interaction between maternal 5,10-methylenetetrahydrofolate reductase C677T and methionine synthase A2756G gene variants to increase the risk of fetal neural tube defects in a Shanxi Han population. Liu ZZ, Zhang JT, Liu D, Hao YH, Chang BM, Xie J, Li PZ. Chin Med J (Engl); 2013 Mar 22; 126(5):865-9. PubMed ID: 23489792 [Abstract] [Full Text] [Related] Page: [Next] [New Search]