(Q71872943)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

title

Ethylmalonic aciduria associated with progressive neurological disease and partial cytochrome c oxidase deficiency (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609451%20AND%20SRC:MED&resulttype=core&format=json

https://api.crossref.org/works/10.1007/BF00711680

21 October 2019

Ethylmalonic aciduria associated with progressive neurological disease and partial cytochromec oxidase deficiency (English)

1 reference

15 June 2024

author name string

W. Lehnert

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7609451

15 June 2024

W. Ruitenbeek

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7609451

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=7609451

15 June 2024

publication date

1 January 1993

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609451%20AND%20SRC:MED&resulttype=core&format=json

full work available at URL

21 October 2019

https://onlinelibrary.wiley.com/doi/pdf/10.1007/BF00711680

1 reference

https://api.crossref.org/works/10.1007/BF00711680

Journal of Inherited Metabolic Disease

15 June 2024

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

volume

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

issue

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

page(s)

557-559

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609451%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1007/bf00711680

21 October 2019

exact match

0 references

cites work

Short-chain acyl-CoA dehydrogenase deficiency associated with a lipid-storage myopathy and secondary carnitine deficiency.

1 reference

12 December 2020

New clinical phenotype of branched-chain acyl-CoA oxidation defect

1 reference

12 December 2020

The urinary excretion of ethylmalonic acid: What level requires further attention?

1 reference

12 December 2020

Cytochrome C oxidase deficiency and Long‐Chain acyl coenzyme A dehydrogenase deficiency with Leigh's subacute necrotizing encephalomyelopathy

1 reference

12 December 2020

Ethylmalonic-adipic aciduria. In vivo and in vitro studies indicating deficiency of activities of multiple acyl-CoA dehydrogenases

1 reference

12 December 2020

Disorders of the mitochondrial respiratory chain: clinical manifestations and diagnostic approach

1 reference

12 December 2020

Progressive fatal pancytopenia, psychomotor retardation and muscle carnitine deficiency in a child with ethylmalonic aciduria and ethylmalonic acidaemia

1 reference

12 December 2020

Muscle cytochromec oxidase deficiency accompanied by a urinary organic acid pattern mimicking multiple acyl‐CoA dehydrogenase deficiency

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00711680

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7609451%20AND%20SRC:MED&resulttype=core&format=json

21 October 2019

1 reference