(Q43446495)

English

Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency

scientific article published in June 1987

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

Sudden infant death syndrome and multiple acyl-coenzyme A dehydrogenase deficiency, ethylmalonic-adipic aciduria, or systemic carnitine deficiency (English)

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

sudden infant death syndrome

1 reference

based on heuristic

inferred from title

author name string

J P Harpey

1

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

C Charpentier

2

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

M Coudé

3

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

P Divry

4

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

M Paturneau-Jouas

5

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

language of work or name

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publication date

1 June 1987

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Europe PubMed Central

PubMed publication ID

23 November 2017

The Journal of Pediatrics

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Europe PubMed Central

PubMed publication ID

23 November 2017

110

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Europe PubMed Central

PubMed publication ID

23 November 2017

6

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

881-884

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

Multiple acyl-CoA dehydrogenase deficiency occurring in pregnancy and caused by a defect in riboflavin metabolism in the mother. Study of a kindred with seven deaths in infancy: Value of riboflavin therapy in preventing this syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980401-8

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980401-8

7 January 2021

Systemic carnitine deficiency presenting as familial endocardial fibroelastosis: a treatable cardiomyopathy

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980401-8

7 January 2021

Recognition of medium-chain acyl-CoA dehydrogenase deficiency in asymptomatic siblings of children dying of sudden infant death or Reye-like syndromes

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980401-8

7 January 2021

Riboflavin-responsive ethylmalonic-adipic aciduria

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980401-8

7 January 2021

Defects of metabolism of fatty acids in the sudden infant death syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2887%2980401-8

7 January 2021

based on heuristic

inferred from DOI database lookup

Identifiers

10.1016/S0022-3476(87)80401-8

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

23 November 2017

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