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Items: 1 to 20 of 192

1.
2.

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;11 Suppl 1:S14-7.

PMID:
11813127
3.

Spina bifida and other neural tube defects.

Northrup H, Volcik KA.

Curr Probl Pediatr. 2000 Nov-Dec;30(10):313-32. Review.

PMID:
11147289
4.

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;46(3):105-9.

PMID:
11310576
5.

Folate, homocysteine and neural tube defects: an overview.

van der Put NM, van Straaten HW, Trijbels FJ, Blom HJ.

Exp Biol Med (Maywood). 2001 Apr;226(4):243-70. Review.

PMID:
11368417
6.

Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects.

Christensen B, Arbour L, Tran P, Leclerc D, Sabbaghian N, Platt R, Gilfix BM, Rosenblatt DS, Gravel RA, Forbes P, Rozen R.

Am J Med Genet. 1999 May 21;84(2):151-7.

PMID:
10323741
7.

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.

Whitehead AS, Gallagher P, Mills JL, Kirke PN, Burke H, Molloy AM, Weir DG, Shields DC, Scott JM.

QJM. 1995 Nov;88(11):763-6.

PMID:
8542260
8.

C677T polymorphism of the methylenetetrahydrofolate reductase gene does not affect folic acid, vitamin B12, and homocysteine serum levels in Turkish children with neural tube defects.

Erdogan MO, Yildiz SH, Solak M, Eser O, Cosar E, Eser B, Koken R, Buyukbas S.

Genet Mol Res. 2010 Jun 22;9(2):1197-203. doi: 10.4238/vol9-2gmr816.

9.

Neural tube defects and a disturbed folate dependent homocysteine metabolism.

van der Put NM, Blom HJ.

Eur J Obstet Gynecol Reprod Biol. 2000 Sep;92(1):57-61. Review.

PMID:
10986435
10.

Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas hispanic population.

Barber R, Shalat S, Hendricks K, Joggerst B, Larsen R, Suarez L, Finnell R.

Mol Genet Metab. 2000 May;70(1):45-52.

PMID:
10833330
11.

[Methylene tetrahydrofolate reductase mutations as genetic risk factors for neural tube defects (NTF)].

Mierzejewska E.

Med Wieku Rozwoj. 1999 Oct-Dec;3(4):521-7. Review. Polish.

PMID:
10910677
12.

Folate levels and N(5),N(10)-methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case-control study.

Martínez de Villarreal LE, Delgado-Enciso I, Valdéz-Leal R, Ortíz-López R, Rojas-Martínez A, Limón-Benavides C, Sánchez-Peña MA, Ancer-Rodríguez J, Barrera-Saldaña HA, Villarreal-Pérez JZ.

Arch Med Res. 2001 Jul-Aug;32(4):277-82.

PMID:
11440783
13.

Abnormal folate metabolism and genetic polymorphism of the folate pathway in a child with Down syndrome and neural tube defect.

Al-Gazali LI, Padmanabhan R, Melnyk S, Yi P, Pogribny IP, Pogribna M, Bakir M, Hamid ZA, Abdulrazzaq Y, Dawodu A, James SJ.

Am J Med Genet. 2001 Oct 1;103(2):128-32.

PMID:
11568918
14.

[Genetic risk factors of neural tube defects].

Sliwerska E, Szpecht-Potocka A.

Med Wieku Rozwoj. 2002 Oct-Dec;6(4):349-70. Review. Polish.

PMID:
12810987
15.

Analysis of select folate pathway genes, PAX3, and human T in a Midwestern neural tube defect population.

Trembath D, Sherbondy AL, Vandyke DC, Shaw GM, Todoroff K, Lammer EJ, Finnell RH, Marker S, Lerner G, Murray JC.

Teratology. 1999 May;59(5):331-41.

PMID:
10332959
17.

Neural tube defects, vitamins and homocysteine.

Eskes TK.

Eur J Pediatr. 1998 Apr;157 Suppl 2:S139-41. Review.

PMID:
9587043
18.

Maternal one-carbon metabolism, MTHFR and TCN2 genotypes and neural tube defects in India.

Godbole K, Gayathri P, Ghule S, Sasirekha BV, Kanitkar-Damle A, Memane N, Suresh S, Sheth J, Chandak GR, Yajnik CS.

Birth Defects Res A Clin Mol Teratol. 2011 Sep;91(9):848-56. doi: 10.1002/bdra.20841. Epub 2011 Jul 18.

PMID:
21770021
19.

Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor.

Molloy AM, Mills JL, Kirke PN, Ramsbottom D, McPartlin JM, Burke H, Conley M, Whitehead AS, Weir DG, Scott JM.

Am J Med Genet. 1998 Jun 30;78(2):155-9.

PMID:
9674907
20.

The curly-tail (ct) mouse, an animal model of neural tube defects, displays altered homocysteine metabolism without folate responsiveness or a defect in Mthfr.

Tran P, Hiou-Tim F, Frosst P, Lussier-Cacan S, Bagley P, Selhub J, Bottiglieri T, Rozen R.

Mol Genet Metab. 2002 Aug;76(4):297-304.

PMID:
12208134

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