(Q70459531)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418873%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

title

Lipoamide dehydrogenase deficiency with primary lactic acidosis: favorable response to treatment with oral lipoic acid (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418873%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

1 reference

2

1 reference

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11 October 2019

author name string

R Matalon

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418873%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

K Michals

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418873%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

R D Hart

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418873%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

J K Parks

5

1 reference

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11 October 2019

S I Goodman

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418873%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

language of work or name

English

0 references

publication date

1 January 1984

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418873%20AND%20SRC:MED&resulttype=core&format=json

The Journal of Pediatrics

11 October 2019

published in

1 reference

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11 October 2019

volume

104

1 reference

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11 October 2019

issue

1

1 reference

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11 October 2019

page(s)

65-69

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418873%20AND%20SRC:MED&resulttype=core&format=json

Deficiency of Dihydrolipoyl Dehydrogenase (a Component of the Pyruvate and α-Ketoglutarate Dehydrogenase Complexes): A Cause of Congenital Chronic Lactic Acidosis in Infancy

11 October 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980591-0

A Defect in Branched-Chain Amino Acid Metabolism in a Patient with Congenital Lactic Acidosis due to Dihydrolipoyl Dehydrogenase Deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980591-0

Hurler's syndrome: biosynthesis of acid mucopolysaccharides in tissue culture

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980591-0

Friedreich ataxia. II. Normal kinetics of lipoamide dehydrogenase

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980591-0

The genetic heterogeneity of lactic acidosis: occurrence of recognizable inborn errors of metabolism in pediatric population with lactic acidosis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980591-0

Lactic acidemia, neurologic deterioration and carbohydrate dependence in a girl with dihydrolipoyl dehydrogenase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980591-0

Sensitivity to carbohydrate in a patient with familial intermittent lactic acidosis and pyruvate dehydrogenase deficiency

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2884%2980591-0

10.1016/S0022-3476(84)80591-0

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6418873%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

1 reference