-
1
-
-
0032426841
-
Folic acid deficiency and its relationship with neural tube defects in northern Mexíco (Mexico)
-
Rodríguez M, Guerrero JF, Parra M, Segura MJ, Levario M, Sotelo EI. Folic acid deficiency and its relationship with neural tube defects in northern Mexíco (Mexico). Salud Pública México 1998: 40: 474-480.
-
(1998)
Salud Pública México
, vol.40
, pp. 474-480
-
-
Rodríguez, M.1
Guerrero, J.F.2
Parra, M.3
Segura, M.J.4
Levario, M.5
Sotelo, E.I.6
-
2
-
-
0004038829
-
-
International Centre for Birth Defects. EUROCAT. Geneva, Switzerland: World Health Organization
-
International Centre for Birth Defects. EUROCAT. World atlas of birth defects. Geneva, Switzerland: World Health Organization 1998, pp. 20.
-
(1998)
World Atlas of Birth Defects
, pp. 20
-
-
-
3
-
-
0032796617
-
The role of folate transport and metabolism in neural tube defect risk
-
Barber A, Lammer EJ, Shaw G, Greer K, Finnell R. The role of folate transport and metabolism in neural tube defect risk. Mol Genet Metab 1999: 66: 1-9.
-
(1999)
Mol. Genet. Metab.
, vol.66
, pp. 1-9
-
-
Barber, A.1
Lammer, E.J.2
Shaw, G.3
Greer, K.4
Finnell, R.5
-
4
-
-
0025863475
-
Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study
-
MCR Vitamin Study Research Group
-
MCR Vitamin Study Research Group. Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. Lancet 1991: 338: 131-137.
-
(1991)
Lancet
, vol.338
, pp. 131-137
-
-
-
5
-
-
0028803474
-
A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects
-
Whitehead AS, Gallagher P, Mills JL et al. A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects. Q J Med 1995: 88: 763-766.
-
(1995)
Q. J. Med.
, vol.88
, pp. 763-766
-
-
Whitehead, A.S.1
Gallagher, P.2
Mills, J.L.3
-
6
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
Van der Put NMJ, Steegers-Theunissen RPM, Frosst P et al. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 1995: 346: 1070-1071.
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
Van der Put, N.M.J.1
Steegers-Theunissen, R.P.M.2
Frosst, P.3
-
7
-
-
0030018760
-
5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
-
Ou CY, Stevenson RE, Brown VK et al. 5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects. Am J Med Genet 1996: 63: 610-614.
-
(1996)
Am. J. Med. Genet.
, vol.63
, pp. 610-614
-
-
Ou, C.Y.1
Stevenson, R.E.2
Brown, V.K.3
-
8
-
-
0033365197
-
The 'Thermolabile' variant of Methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother
-
Shields DC, Kirke PN, Mills JL et al. The 'Thermolabile' variant of Methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother. Am J Hum Genet 1999: 64: 1045-1055.
-
(1999)
Am. J. Hum. Genet.
, vol.64
, pp. 1045-1055
-
-
Shields, D.C.1
Kirke, P.N.2
Mills, J.L.3
-
9
-
-
0032587430
-
Association of the 677-CT mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects
-
Boduroglu K, Alikasifoglu M, Anar B, Tuncbilek E. Association of the 677-CT mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects. J Child Neurol 1999: 14: 159-161.
-
(1999)
J. Child. Neurol.
, vol.14
, pp. 159-161
-
-
Boduroglu, K.1
Alikasifoglu, M.2
Anar, B.3
Tuncbilek, E.4
-
10
-
-
0031429097
-
Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects
-
Mornet E, Muller F, Lenvoisé-Furet A et al. Screening of the C677T mutation on the methylenetetrahydrofolate reductase gene in French patients with neural tube defects. Hum Genet 1997: 100: 512-514.
-
(1997)
Hum. Genet.
, vol.100
, pp. 512-514
-
-
Mornet, E.1
Muller, F.2
Lenvoisé-Furet, A.3
-
11
-
-
0031832956
-
Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population
-
Koch MC, Stegman K, Ziegler A, Schroter B, Ermert A. Evaluation of the MTHFR C677T allele and the MTHFR gene locus in a German spina bifida population. Eur J Pediatr 1998: 157: 487-492.
-
(1998)
Eur. J. Pediatr.
, vol.157
, pp. 487-492
-
-
Koch, M.C.1
Stegman, K.2
Ziegler, A.3
Schroter, B.4
Ermert, A.5
-
12
-
-
0034190659
-
5,10 Methylenetetrahydrofolate reductase gene variants and congenital anomalies: A Huge Review
-
Botto LD, Yang Q. 5,10 Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a Huge Review. Am J Epidemiol 2000: 151: 862-877.
-
(2000)
Am. J. Epidemiol.
, vol.151
, pp. 862-877
-
-
Botto, L.D.1
Yang, Q.2
-
13
-
-
0034958324
-
Folate levels and N5,N1O-Methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: A case-control study
-
Martínez de Villarreal L, Delgado-Enciso I, Váldez-Leal R et al. Folate levels and N5,N1O-Methylenetetrahydrofolate reductase genotype (MTHFR) in mothers of offspring with neural tube defects: a case-control study. Arch Medical Res 2001: 32: 277-282.
-
(2001)
Arch. Medical Res.
, vol.32
, pp. 277-282
-
-
Martínez de Villarreal, L.1
Delgado-Enciso, I.2
Váldez-Leal, R.3
-
14
-
-
0033807422
-
The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations
-
Davalos IP, Olivares N, Castillo MT et al. The C677T polymorphism of the methylenetetrahydrofolate reductase gene in Mexican mestizo neural-tube defect parents, control mestizo and native populations. Ann Génét 2000: 43: 89-92.
-
(2000)
Ann. Génét.
, vol.43
, pp. 89-92
-
-
Davalos, I.P.1
Olivares, N.2
Castillo, M.T.3
-
15
-
-
0343503018
-
High prevalence of the thermolabile Methylenetetrahydrofolate reductase variant in Mexico: A country with a very high prevalence of neural tube defects
-
Ryvemce Collaborative Group VE
-
Mutchinik OM, López Luna MA, Waxman L, Babinsky J, Ryvemce Collaborative Group VE. High prevalence of the thermolabile Methylenetetrahydrofolate reductase variant in Mexico: a country with a very high prevalence of neural tube defects. Mol Genet Metab 1999: 68: 461-467.
-
(1999)
Mol. Genet. Metab.
, vol.68
, pp. 461-467
-
-
Mutchinik, O.M.1
López Luna, M.A.2
Waxman, L.3
Babinsky, J.4
-
16
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nature Genet 1995: 10: 111-113.
-
(1995)
Nature Genet.
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
-
17
-
-
0034116765
-
Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas Hispanic population
-
Barber R, Shalat S, Hendrincks K et al. Investigation of folate pathway gene polymorphisms and the incidence of neural tube defects in a Texas Hispanic population. Mol Genet Metab 2000: 70: 45-52.
-
(2000)
Mol. Genet. Metab.
, vol.70
, pp. 45-52
-
-
Barber, R.1
Shalat, S.2
Hendrincks, K.3
-
18
-
-
0034613964
-
Methyelenetetrahydrofolate reductase and spina bifida: Evaluation of level of defect and maternal genotypic risk in Hispanics
-
Volcik K, Blanton Tyerman S et al. Methyelenetetrahydrofolate reductase and spina bifida: Evaluation of level of defect and maternal genotypic risk in Hispanics. Am J Med Genet 2000: 95: 21-27.
-
(2000)
Am. J. Med. Genet.
, vol.95
, pp. 21-27
-
-
Volcik, K.1
Blanton Tyerman, S.2
-
19
-
-
0032125774
-
Maternal vitamin use, genetic variation of infant methylentetrahydrofolate reductase, and risk for spina bífida
-
Shaw GM, Rozen R, Finnell RH, Wasserman C, Lammer E. Maternal vitamin use, genetic variation of infant methylentetrahydrofolate reductase, and risk for spina bífida. Am J Epidemiol 1998: 148: 30-37.
-
(1998)
Am. J. Epidemiol.
, vol.148
, pp. 30-37
-
-
Shaw, G.M.1
Rozen, R.2
Finnell, R.H.3
Wasserman, C.4
Lammer, E.5
-
20
-
-
0343471524
-
Genetic risk factor for unexplained recurrent early pregnancy loss
-
Nelen WL, Steegers EA, Eskes TK, Blom HJ. Genetic risk factor for unexplained recurrent early pregnancy loss. Lancet 1997: 350: 861.
-
(1997)
Lancet
, vol.350
, pp. 861
-
-
Nelen, W.L.1
Steegers, E.A.2
Eskes, T.K.3
Blom, H.J.4
-
21
-
-
0033794925
-
Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: An examination of C677T and A1298C mutations
-
Isotalo PA, Wells GA, Donelly JG. Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: An examination of C677T and A1298C mutations. Am J Hum Genet 2000: 67: 986-990.
-
(2000)
Am. J. Hum. Genet.
, vol.67
, pp. 986-990
-
-
Isotalo, P.A.1
Wells, G.A.2
Donelly, J.G.3
-
22
-
-
0034759422
-
Examinations of Methylenetetrahydrofolate reductase C677T and A1298C mutations - And in utero viability
-
Volcik KA, Blanton SH, Northrup H. Examinations of Methylenetetrahydrofolate reductase C677T and A1298C mutations - and in utero viability. Am J Hum Genet 2001: 69: 1150-1152.
-
(2001)
Am. J. Hum. Genet.
, vol.69
, pp. 1150-1152
-
-
Volcik, K.A.1
Blanton, S.H.2
Northrup, H.3
-
24
-
-
0029886679
-
Methylenetetrahydrofolate reductase and neural tube defects
-
Papapetrou C, Lynch SA, Burn J, Edwards YH. Methylenetetrahydrofolate reductase and neural tube defects. Lancet 1996: 348: 58.
-
(1996)
Lancet
, vol.348
, pp. 58
-
-
Papapetrou, C.1
Lynch, S.A.2
Burn, J.3
Edwards, Y.H.4
-
25
-
-
0030955502
-
Thermolabile variant of 5,10-methylenetetrahydrofolate reductase associated with low red-cell folates: Implications for folate intake recommendations
-
Molloy A, Daly S, Mills J et al. Thermolabile variant of 5,10-methylenetetrahydrofolate reductase associated with low red-cell folates: implications for folate intake recommendations. Lancet 1997: 349: 1591-1593.
-
(1997)
Lancet
, vol.349
, pp. 1591-1593
-
-
Molloy, A.1
Daly, S.2
Mills, J.3
-
26
-
-
0032845492
-
Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects
-
NTD Collaborative Group
-
Speer M, Nye J, McLone D et al. Possible interaction of genotypes at cystathionine beta-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects. NTD Collaborative Group. Clin Genet 1999: 6: 142-144.
-
(1999)
Clin. Genet.
, vol.6
, pp. 142-144
-
-
Speer, M.1
Nye, J.2
McLone, D.3
-
27
-
-
0031817447
-
Exploring gene-gene interactions in the etiology of neural tube defects
-
Botto LD, Mastroiacovo P. Exploring gene-gene interactions in the etiology of neural tube defects. Clin Genet 1998: 53: 456-459.
-
(1998)
Clin. Genet.
, vol.53
, pp. 456-459
-
-
Botto, L.D.1
Mastroiacovo, P.2
-
28
-
-
0031971515
-
A second common mutation in the methylenentetrahydrofolate reductase gene: An additional risk factor for neural tube defects?
-
van der Put M, Gabreëls F, Stevens EM et al. A second common mutation in the methylenentetrahydrofolate reductase gene: an additional risk factor for neural tube defects? Am J Hum Genet 1998: 62: 1044-1051.
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 1044-1051
-
-
van der Put, M.1
Gabreëls, F.2
Stevens, E.M.3
-
29
-
-
18344389032
-
Genetic admixture in three Mexican Mestizo populations based on D1S80 and HLA-DQA1 loci
-
Cerda-Flores R, Villalobos-Torres M, Barrera-Saldaña H et al. Genetic admixture in three Mexican Mestizo populations based on D1S80 and HLA-DQA1 loci. Am J Hum Biol 2002: 14: 257-263.
-
(2002)
Am. J. Hum. Biol.
, vol.14
, pp. 257-263
-
-
Cerda-Flores, R.1
Villalobos-Torres, M.2
Barrera-Saldaña, H.3
-
30
-
-
0028890671
-
Thermolabile 5, 10-Methylenetetrahydrofolate reductase as a cause of mild hyperhomocisteinemia
-
Engbersen A, Franken D, Boers G, Stevens E, Trijbels F, Blom H. Thermolabile 5, 10-Methylenetetrahydrofolate reductase as a cause of mild hyperhomocisteinemia. Am J Hum Genet 1995: 56: 142-150.
-
(1995)
Am. J. Hum. Genet.
, vol.56
, pp. 142-150
-
-
Engbersen, A.1
Franken, D.2
Boers, G.3
Stevens, E.4
Trijbels, F.5
Blom, H.6
|