(Q71872911)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609446%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Pearson syndrome: altered tricarboxylic acid and urea-cycle metabolites, adrenal insufficiency and corneal opacities (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609446%20AND%20SRC:MED&resulttype=core&format=json

https://api.crossref.org/works/10.1007/BF00711675

21 October 2019

Pearson syndrome: Altered tricarboxylic acid and urea‐cycle metabolites, adrenal insufficiency and corneal opacities (English)

1 reference

15 June 2024

1 reference

adrenal insufficiency

1 reference

8

A. Rötig

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7609446

15 June 2024

author name string

A. Ribes

1

1 reference

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15 June 2024

E. Riudor

2

1 reference

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15 June 2024

R. Valcárel

3

1 reference

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15 June 2024

A. Salvá

4

1 reference

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15 June 2024

F. Castelló

5

1 reference

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15 June 2024

S. Murillo

6

1 reference

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15 June 2024

C. Dominguez

7

1 reference

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15 June 2024

C. Jakobs

9

1 reference

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15 June 2024

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=7609446

15 June 2024

publication date

1 January 1993

1 reference

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full work available at URL

21 October 2019

https://onlinelibrary.wiley.com/doi/pdf/10.1007/BF00711675

1 reference

https://api.crossref.org/works/10.1007/BF00711675

Journal of Inherited Metabolic Disease

15 June 2024

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609446%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

16

1 reference

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21 October 2019

issue

3

1 reference

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21 October 2019

page(s)

537-540

1 reference

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https://scigraph.springernature.com/pub.10.1007/bf00711675

21 October 2019

exact match

0 references

cites work

Pearson's marrow-pancreas syndrome. A multisystem mitochondrial disorder in infancy

1 reference

12 December 2020

Significance of bound glutarate in the diagnosis of glutaric aciduria type I

1 reference

12 December 2020

Citrate therapy in argininosuccinate lyase deficiency

1 reference

12 December 2020

Organic aciduria in Pearson syndrome

1 reference

12 December 2020

Mitochondrial DNA deletion in an 8-year-old boy with Pearson syndrome

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00711675

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609446%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference