Homocysteine metabolism in pregnancies complicated by neural tube defects (Q74059719)

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8 November 2019

editorial

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title

Homocysteine metabolism in pregnancies complicated by neural tube defects (English)

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8 November 2019

2

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8 November 2019

author name string

P N Kirke

series ordinal

1

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8 November 2019

J M Scott

series ordinal

3

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8 November 2019

publication date

1 November 1997

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8 November 2019

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8 November 2019

volume

13

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8 November 2019

issue

11-12

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8 November 2019

page(s)

994-995

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Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. MRC Vitamin Study Research Group

8 November 2019

cites work

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7 January 2021

Prevention of the First Occurrence of Neural-Tube Defects by Periconceptional Vitamin Supplementation

1 reference

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7 January 2021

Folate levels and neural tube defects. Implications for prevention

1 reference

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7 January 2021

Folic acid absorption in women with a history of pregnancy with neural tube defect.

1 reference

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7 January 2021

Homocysteine metabolism in pregnancies complicated by neural-tube defects

1 reference

https://api.crossref.org/works/10.1016%2FS0899-9007%2897%2982079-5

7 January 2021

Maternal hyperhomocysteinemia: a risk factor for neural-tube defects?

1 reference

https://api.crossref.org/works/10.1016%2FS0899-9007%2897%2982079-5

7 January 2021

Neural tube defects and elevated homocysteine levels in amniotic fluid

1 reference

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7 January 2021

A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase

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7 January 2021

Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida

1 reference

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7 January 2021

Methylenetetrahydrofolate reductase mutation and neural tube defects

1 reference

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7 January 2021

Decreased methylene tetrahydrofolate reductase activity due to the 677C-->T mutation in families with spina bifida offspring

1 reference

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7 January 2021

Is mutated MTHFR a risk factor for neural tube defects?

1 reference

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7 January 2021

10.1016/S0899-9007(97)82079-5

Identifiers

DOI

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8 November 2019

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