(Q56241354)

English

Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6–C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?

scientific article published on 01 January 1988

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6-C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation? (English)

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

0 references

1 reference

based on heuristic

inferred from title

peripheral neuropathy

1 reference

based on heuristic

inferred from title

Jean-Paul Bonnefont

2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

Anastella Pelet

5

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

author name string

B T Poll-The

1

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

H Ogier

3

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

C Charpentier

4

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

J M Le Fur

6

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

C Jakobs

7

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

R M Kok

8

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

M Duran

9

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

P Divry

10

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

publication date

1 January 1988

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 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:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

11 Suppl 2

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

S2

0 references

183-185

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

https://scigraph.springernature.com/pub.10.1007/bf01804230

0 references

Peroxisomal disorders: a newly recognised group of genetic diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/2846959

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The acyl-CoA dehydrogenation deficiencies. Recent advances in the enzymic characterization and understanding of the metabolic and pathophysiological disturbances in patients with acyl-CoA dehydrogenation deficiencies

1 reference

https://pubmed.ncbi.nlm.nih.gov/2846959

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Formation of cholic acid from 3 alpha, 7 alpha, 12 alpha-trihydroxy-5 beta-cholestanoic acid by rat liver peroxisomes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2846959

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01804230

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:2846959%20AND%20SRC:MED&resulttype=core&format=json

6 October 2019

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