(Q67521827)

English

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis

scientific article published on 01 January 1992

In more languages

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357231%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

Bifunctional enzyme deficiency: identification of a new type of peroxisomal disorder in a patient with an impairment in peroxisomal beta-oxidation of unknown aetiology by means of complementation analysis (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357231%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

author name string

R. J. Wanders

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1357231

17 September 2022

C. W. van Roermund

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1357231

17 September 2022

S. Brul

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1357231

17 September 2022

R. B. Schutgens

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1357231

17 September 2022

J. M. Tager

5

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A1357231

17 September 2022

language of work or name

1 reference

National Center for Biotechnology Information

PubMed publication ID

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=1357231

17 September 2022

publication date

1 January 1992

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357231%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357231%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

15

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357231%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357231%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

385-388

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:1357231%20AND%20SRC:MED&resulttype=core&format=json

14 September 2019

https://scigraph.springernature.com/pub.10.1007/bf02435983

0 references

Peroxisomal beta-oxidation defect with detectable peroxisomes: a case with neonatal onset and progressive course

1 reference

https://pubmed.ncbi.nlm.nih.gov/1357231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The inborn errors of peroxisomal beta-oxidation: a review

1 reference

https://pubmed.ncbi.nlm.nih.gov/1357231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Neonatal seizures and retardation in a girl with biochemical features of X-linked adrenoleukodystrophy: a possible new peroxisomal disease entity

1 reference

https://pubmed.ncbi.nlm.nih.gov/1357231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal disorders: complementation analysis using beta-oxidation of very long chain fatty acids

1 reference

https://pubmed.ncbi.nlm.nih.gov/1357231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal disorders in neurology

1 reference

https://pubmed.ncbi.nlm.nih.gov/1357231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Genetic heterogeneity in the cerebrohepatorenal (Zellweger) syndrome and other inherited disorders with a generalized impairment of peroxisomal functions. A study using complementation analysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/1357231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Bile acid analyses in "pseudo-Zellweger" syndrome; clues to the defect in peroxisomal beta-oxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/1357231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Atypical riboflavin-responsive glutaric aciduria, and deficient peroxisomal glutaryl-CoA oxidase activity: a new peroxisomal disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/1357231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

First prenatal diagnosis of acyl-CoA oxidase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/1357231

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

Sitelinks

Wikipedia(0 entries)

Wikibooks(0 entries)

Wikinews(0 entries)

Wikiquote(0 entries)

Wikisource(0 entries)

Wikiversity(0 entries)

Wikivoyage(0 entries)

Wiktionary(0 entries)

Multilingual sites(0 entries)

Retrieved from "https://www.wikidata.org/w/index.php?title=Q67521827&oldid=1889722936"