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Journal Abstract Search

177 related items for PubMed ID: 18937358

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  • 4. Hispanic origin and neural tube defects in Houston/Harris County, Texas. II. Risk factors.
    Canfield MA, Annegers JF, Brender JD, Cooper SP, Greenberg F.
    Am J Epidemiol; 1996 Jan 01; 143(1):12-24. PubMed ID: 8533743
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  • 5. Associations of ethnicity and SES with IQ and achievement in spina bifida meningomyelocele.
    Swartwout MD, Garnaat SL, Myszka KA, Fletcher JM, Dennis M.
    J Pediatr Psychol; 2010 Oct 01; 35(9):927-36. PubMed ID: 20150339
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  • 8. Phosphatidylethanolamine N-methyltransferase (PEMT) gene polymorphisms and risk of spina bifida.
    Zhang J, Zhu H, Yang W, Shaw GM, Lammer EJ, Finnell RH.
    Am J Med Genet A; 2006 Apr 01; 140(7):785-9. PubMed ID: 16523512
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  • 11. Spina Bifida Research Resource: study design and participant characteristics.
    Mitchell LE.
    Birth Defects Res A Clin Mol Teratol; 2008 Oct 01; 82(10):684-91. PubMed ID: 18553493
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  • 13. Association of folate receptor (FOLR1, FOLR2, FOLR3) and reduced folate carrier (SLC19A1) genes with meningomyelocele.
    O'Byrne MR, Au KS, Morrison AC, Lin JI, Fletcher JM, Ostermaier KK, Tyerman GH, Doebel S, Northrup H.
    Birth Defects Res A Clin Mol Teratol; 2010 Aug 01; 88(8):689-94. PubMed ID: 20683905
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  • 14. [Methylenetetrahydrofolate reductase polymorphisms as risk factors for myelomeningocele].
    Pardo R, Suazo J, Castillo S, Vargas M, Zalavari A, Santos JL, Blanco R, Rotter K, Solar M, Tapia E.
    Rev Med Chil; 2014 May 01; 142(5):587-92. PubMed ID: 25427015
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  • 15. 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
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  • 16. Genetic and lifestyle variables associated with homocysteine concentrations and the distribution of folate derivatives in healthy premenopausal women.
    Summers CM, Mitchell LE, Stanislawska-Sachadyn A, Baido SF, Blair IA, Von Feldt JM, Whitehead AS.
    Birth Defects Res A Clin Mol Teratol; 2010 Aug 06; 88(8):679-88. PubMed ID: 20544798
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  • 18. The methionine synthase reductase 66A>G polymorphism is a maternal risk factor for spina bifida.
    van der Linden IJ, den Heijer M, Afman LA, Gellekink H, Vermeulen SH, Kluijtmans LA, Blom HJ.
    J Mol Med (Berl); 2006 Dec 06; 84(12):1047-54. PubMed ID: 17024475
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  • 19. Racial and ethnic differences in epilepsy classification among probands in the Epilepsy Phenome/Genome Project (EPGP).
    Friedman D, Fahlstrom R, EPGP Investigators.
    Epilepsy Res; 2013 Dec 06; 107(3):306-10. PubMed ID: 24139856
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  • 20. Association between CFL1 gene polymorphisms and spina bifida risk in a California population.
    Zhu H, Enaw JO, Ma C, Shaw GM, Lammer EJ, Finnell RH.
    BMC Med Genet; 2007 Mar 12; 8():12. PubMed ID: 17352815
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