(Q41924426)

14 October 2017

title

Methylenetetrahydrofolate reductase deficiency: importance of early diagnosis (English)

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methylenetetrahydrofolate reductase deficiency

14 October 2017

main subject

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author name string

A Fattal-Valevski

1

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14 October 2017

H Bassan

2

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14 October 2017

S H Korman

3

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14 October 2017

T Lerman-Sagie

4

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14 October 2017

A Gutman

5

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14 October 2017

S Harel

6

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14 October 2017

publication date

1 August 2000

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Journal of Child Neurology

14 October 2017

published in

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14 October 2017

volume

15

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14 October 2017

issue

8

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14 October 2017

page(s)

539-543

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Congenital errors of folate metabolism

14 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Betaine for treatment of homocystinuria caused by methylenetetrahydrofolate reductase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Methylenetetrahydrofolate reductase deficiency: Prenatal diagnosis and family studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Long term treatment with betaine in methylenetetrahydrofolate reductase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Intermittent encephalopathy, reversible nerve conduction slowing, and MRI evidence of cerebral white matter disease in methylenetetrahydrofolate reductase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Morphologic Studies in a Patient with Homocystinuria due to 5,10-Methylenetetrahydrofolate Reductase Deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Symptomatic and asymptomatic methylenetetrahydrofolate reductase deficiency in two adult brothers

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Thermolabile variant of 5,10-methylenetetrahydrofolate reductase associated with low red-cell folates: implications for folate intake recommendations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Subacute combined degeneration of the cord, dementia and parkinsonism due to an inborn error of folate metabolism

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Association of demyelination with deficiency of cerebrospinal-fluid S-adenosylmethionine in inborn errors of methyl-transfer pathway

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Relation between folate status, a common mutation in methylenetetrahydrofolate reductase, and plasma homocysteine concentrations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

Clinical, fluorine-18 labeled 2-fluoro-2-deoxyglucose positron emission tomography of the brain, MR spectroscopy, and therapeutic attempts in methylenetetrahydrofolate reductase deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1177%2F088307380001500808

10.1177/088307380001500808

21 January 2018

Identifiers

DOI

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14 October 2017

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