Vitamin B12-responsive megaloblastic anemia, homocystinuria, and transient methylmalonic aciduria in cb1E disease (Q67971957)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3193313%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

title

Vitamin B12-responsive megaloblastic anemia, homocystinuria, and transient methylmalonic aciduria in cb1E disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3193313%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

1 reference

1 reference

1 reference

M Tuchman

1

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20 September 2019

P Kelly

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3193313%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

D Watkins

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3193313%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

D S Rosenblatt

series ordinal

4

1 reference

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20 September 2019

language of work or name

English

0 references

publication date

1 December 1988

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The Journal of Pediatrics

20 September 2019

published in

1 reference

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20 September 2019

volume

113

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20 September 2019

issue

6

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20 September 2019

page(s)

1052-1056

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Inherited defects of vitamin B12 metabolism

20 September 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980582-1

Homocystinuria and megaloblastic anemia responsive to vitamin B12 therapy. An inborn error of metabolism due to a defect in cobalamin metabolism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980582-1

Prenatal vitamin B12 therapy of a fetus with methylcobalamin deficiency (cobalamin E disease).

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980582-1

Vitamin B12 responsive homocystinuria and megaloblastic anemia: heterogeneity in methylcobalamin deficiency.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980582-1

Genetic heterogeneity among patients with methylcobalamin deficiency. Definition of two complementation groups, cblE and cblG.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980582-1

Altered vitamin B12 metabolism in fibroblasts from a patient with megaloblastic anemia and homocystinuria due to a new defect in methionine biosynthesis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980582-1

Cobalamin Binding and Cobalamin-Dependent Enzyme Activity in Normal and Mutant Human Fibroblasts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2888%2980582-1

10.1016/S0022-3476(88)80582-1

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:3193313%20AND%20SRC:MED&resulttype=core&format=json

20 September 2019

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