-
1
-
-
0027080461
-
Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation
-
A.E. Czeizel and I. Dudas, Prevention of the first occurrence of neural-tube defects by periconceptional vitamin supplementation, New England Journal of Medicine 327 (1992), 1832-1835.
-
(1992)
New England Journal of Medicine
, vol.327
, pp. 1832-1835
-
-
Czeizel, A.E.1
Dudas, I.2
-
2
-
-
0028863219
-
Folate levels and neural tube defects: Implications for prevention
-
L.E. Daly, P.N. Kirke, A.M. Molloy, D.G. Weir and J.M. Scott, Folate levels and neural tube defects: Implications for prevention, Journal of the American Medical Association 274 (1995), 1698-1702.
-
(1995)
Journal of the American Medical Association
, vol.274
, pp. 1698-1702
-
-
Daly, L.E.1
Kirke, P.N.2
Molloy, A.M.3
Weir, D.G.4
Scott, J.M.5
-
3
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
P. Frosst, H.J. Blom, R. Milos, P. Goyette, C.A. Sheppard, R.G. Matthews, G.J.H. Boers, M. den Heijer, L.A.J. Kluijtmans, L.P. van den Heuvel and R. Rosen, A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase, Nature Genetics 10 (1995), 111-113.
-
(1995)
Nature Genetics
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
Boers, G.J.H.7
Den Heijer, M.8
Kluijtmans, L.A.J.9
Van Den Heuvel, L.P.10
Rosen, R.11
-
4
-
-
0026034240
-
Thermolabile methylenetetrahydrofolate reductase: An inherited risk factor for coronary artery disease
-
S.S. Kang, P.W.K. Wong, A. Susmano, J. Sora, M. Norusis and N. Ruggie, Thermolabile methylenetetrahydrofolate reductase: An inherited risk factor for coronary artery disease, American Journal of Human Genetics 48 (1991), 536-545.
-
(1991)
American Journal of Human Genetics
, vol.48
, pp. 536-545
-
-
Kang, S.S.1
Wong, P.W.K.2
Susmano, A.3
Sora, J.4
Norusis, M.5
Ruggie, N.6
-
5
-
-
0027145847
-
12 are independent risk factors for neural tube defects
-
12 are independent risk factors for neural tube defects, Quarterly Journal of Medicine 86 (1993), 703-708.
-
(1993)
Quarterly Journal of Medicine
, vol.86
, pp. 703-708
-
-
Kirke, P.N.1
Molloy, A.M.2
Daly, L.E.3
Burke, H.4
Weir, D.G.5
Scott, J.M.6
-
6
-
-
0029800387
-
Methylenetetrahydrofolate reductase mutation and neural tube defects
-
P.N. Kirke, J.L. Mills, A.S. Whitehead, A. Molloy and J.M. Scott, Methylenetetrahydrofolate reductase mutation and neural tube defects. Lancet 348 (1996), 1037-1038.
-
(1996)
Lancet
, vol.348
, pp. 1037-1038
-
-
Kirke, P.N.1
Mills, J.L.2
Whitehead, A.S.3
Molloy, A.4
Scott, J.M.5
-
7
-
-
0026509087
-
Maternal vitamin levels during pregnancies producing infants with neural tube defects
-
J.L. Mills, J. Tuomilehto, K.F. Yu, N. Colman, W.S. Blaner, P. Koskela, W.E. Rundle, M. Forman, L. Toivanen and G.G. Rhoads, Maternal vitamin levels during pregnancies producing infants with neural tube defects, Journal of Pediatrics 120 (1992), 863-871.
-
(1992)
Journal of Pediatrics
, vol.120
, pp. 863-871
-
-
Mills, J.L.1
Tuomilehto, J.2
Yu, K.F.3
Colman, N.4
Blaner, W.S.5
Koskela, P.6
Rundle, W.E.7
Forman, M.8
Toivanen, L.9
Rhoads, G.G.10
-
8
-
-
0028833677
-
Homocysteine metabolism in pregnancies complicated by neural tube defects
-
J.L. Mills, J.M. McPartlin, P.N. Kirke, Y.J. Lee, M.R. Conley, D.G. Weir and J.M. Scott, Homocysteine metabolism in pregnancies complicated by neural tube defects, Lancet 345 (1995), 149-151.
-
(1995)
Lancet
, vol.345
, pp. 149-151
-
-
Mills, J.L.1
McPartlin, J.M.2
Kirke, P.N.3
Lee, Y.J.4
Conley, M.R.5
Weir, D.G.6
Scott, J.M.7
-
9
-
-
0021889431
-
Maternal serum folate and vitamin B12 concentrations in pregnancies associated with neural tube defects
-
A.M. Molloy, P. Kirke, I. Hillary, D.G. Weir, J.M. Scott, Maternal serum folate and vitamin B12 concentrations in pregnancies associated with neural tube defects, Archives of Disease in Childhood 60 (1985), 660-665.
-
(1985)
Archives of Disease in Childhood
, vol.60
, pp. 660-665
-
-
Molloy, A.M.1
Kirke, P.2
Hillary, I.3
Weir, D.G.4
Scott, J.M.5
-
10
-
-
0030744634
-
Microbiological assay for serum, plasma and red cell folate using cryopreserved, microtiter plate method
-
A.M. Molloy and J.M. Scott, Microbiological assay for serum, plasma and red cell folate using cryopreserved, microtiter plate method, Methods in Enzymology 281 (1997), 43-53.
-
(1997)
Methods in Enzymology
, vol.281
, pp. 43-53
-
-
Molloy, A.M.1
Scott, J.M.2
-
11
-
-
0030955502
-
Association of thermolabile variant of 5,10-methylenetetrahydrofolate reductase with low red-cell folates: Implications for folate intake recommendations
-
A.M. Molloy, S. Daly, J.L. Mills, P.N. Kirke, A.S. Whitehead, D. Ramsbottom, M.R. Conley, D.G. Weir and J.M. Scott, Association of thermolabile variant of 5,10-methylenetetrahydrofolate reductase with low red-cell folates: Implications for folate intake recommendations, Lancet 349 (1997), 1591-1593.
-
(1997)
Lancet
, vol.349
, pp. 1591-1593
-
-
Molloy, A.M.1
Daly, S.2
Mills, J.L.3
Kirke, P.N.4
Whitehead, A.S.5
Ramsbottom, D.6
Conley, M.R.7
Weir, D.G.8
Scott, J.M.9
-
12
-
-
0032581051
-
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
-
A.M. Molloy, J.L. Mills, P.N. Kirke, D. Ramsbottom, J.M. McPartlin, H. Burke, M. Conley, A.S. Whitehead, D.G. Weir, J.M. Scott, 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, American Journal of Medical Genetics 78 (1998), 155-159.
-
(1998)
American Journal of Medical Genetics
, vol.78
, pp. 155-159
-
-
Molloy, A.M.1
Mills, J.L.2
Kirke, P.N.3
Ramsbottom, D.4
McPartlin, J.M.5
Burke, H.6
Conley, M.7
Whitehead, A.S.8
Weir, D.G.9
Scott, J.M.10
-
13
-
-
0025863475
-
Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study
-
MRC Vitamin Study Research Group, Prevention of neural tube defects: results of the Medical Research Council Vitamin Study, Lancet 338 (1991), 131-137.
-
(1991)
Lancet
, vol.338
, pp. 131-137
-
-
-
14
-
-
0030018760
-
5,10-methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
-
C.Y. Ou, R.E. Stevenson, V.K. Brown, C.E. Schwartz, W.P. Allen, M.J. Khoury, R. Rozen, G.P. Oakley, Jr. and M.J. Adams, Jr., 5,10-methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects, American Journal of Medical Genetics 63 (1996), 610-614.
-
(1996)
American Journal of Medical Genetics
, vol.63
, pp. 610-614
-
-
Ou, C.Y.1
Stevenson, R.E.2
Brown, V.K.3
Schwartz, C.E.4
Allen, W.P.5
Khoury, M.J.6
Rozen, R.7
Oakley Jr., G.P.8
Adams Jr., M.J.9
-
15
-
-
0031961002
-
Worldwide distribution of a common methylenetetrahydrofolate reductase mutation
-
J.A. Schneider, D.C. Rees, Y-T. Liu and J.B. Clegg, Worldwide distribution of a common methylenetetrahydrofolate reductase mutation, American Journal of Human Genetics 62 (1998), 1258-1260.
-
(1998)
American Journal of Human Genetics
, vol.62
, pp. 1258-1260
-
-
Schneider, J.A.1
Rees, D.C.2
Liu, Y.-T.3
Clegg, J.B.4
-
16
-
-
0029758391
-
Homocysteine and cardiovascular disease
-
J. Scott and D Weir, Homocysteine and cardiovascular disease (editorial), Quarterly Journal of Medicine 89 (1996), 561-563.
-
(1996)
Quarterly Journal of Medicine
, vol.89
, pp. 561-563
-
-
Scott, J.1
Weir, D.2
-
17
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
N.M.J. van der Put, R.P.M. Steegers-Theunissen, P. Frosst, F.J.M. Trijbels, T.K.A.B. Eskes, L.P. van den Heuvel, E.C.M. Mariman, M. den Heyer, R. Rozen and H.J. Blom, Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida, Lancet 346 (1995), 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
Trijbels, F.J.M.4
Eskes, T.K.A.B.5
Van Den Heuvel, L.P.6
Mariman, E.C.M.7
Den Heyer, M.8
Rozen, R.9
Blom, H.J.10
-
18
-
-
0028803474
-
A genetic defect in 5,10-methylenetetrahydrofolate reductase in neural tube defects
-
A.S. Whitehead, P. Gallagher, J.L. Mills, P.N. Kirke, H. Burke, A.M. Molloy, D.G. Weir, D.C. Shields and J.M. Scott, A genetic defect in 5,10-methylenetetrahydrofolate reductase in neural tube defects, Quarterly Journal of Medicine 88 (1995), 763-766.
-
(1995)
Quarterly Journal of Medicine
, vol.88
, pp. 763-766
-
-
Whitehead, A.S.1
Gallagher, P.2
Mills, J.L.3
Kirke, P.N.4
Burke, H.5
Molloy, A.M.6
Weir, D.G.7
Shields, D.C.8
Scott, J.M.9
|