(Q28376491)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

title

Fetal anticonvulsant syndrome and mutation in the maternal MTHFR gene (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

fetal anticonvulsant syndrome

2 November 2019

main subject

1 reference

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

author name string

S J Moore

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

A Osborne

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

J Howe

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

P D Turnpenny

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

language of work or name

English

0 references

publication date

1 September 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

volume

56

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

page(s)

216-220

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

Worldwide distribution of a common methylenetetrahydrofolate reductase mutation

2 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1034/J.1399-0004.1999.560306.X

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

21 April 2017

1 reference

https://api.crossref.org/works/10.1034/J.1399-0004.1999.560306.X

Congenital anomalies in children of epileptic mothers and fathers.

21 April 2017

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

21 January 2018

Fetal valproate syndrome

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

Teratogenicity of anticonvulsant drugs. I: Review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

Pattern of malformations in the children of women treated with carbamazepine during pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

Verification of the fetal valproate syndrome phenotype

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

Prenatal prediction of risk of the fetal hydantoin syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

Spina bifida in infants of women treated with carbamazepine during pregnancy

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

Interactions between folates and carbamazepine or valproate in the rat.

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects?

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

Marked accumulation of valproic acid in embryonic neuroepithelium of the mouse during early organogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

Findings in children exposed in utero to phenytoin and carbamazepine monotherapy: independent effects of epilepsy and medications

21 January 2018

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

7 January 2021

A male with fetal valproate syndrome and autism.

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

7 January 2021

The effects of carbamazepine and valproate on folate metabolism in man

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

7 January 2021

Mechanism for reduction of serum folate by antiepileptic drugs during prolonged therapy

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

7 January 2021

Is the common 677C-->T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis

1 reference

https://api.crossref.org/works/10.1034%2FJ.1399-0004.1999.560306.X

7 January 2021

10.1034/J.1399-0004.1999.560306.X

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10563481%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

1 reference