(Q51637992)

8 April 2018

title

Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndrome (English)

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8 April 2018

medium chain acyl-CoA dehydrogenase deficiency

main subject

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1 reference

P F Bougnères

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8 April 2018

F Rocchiccioli

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8 April 2018

S Kølvraa

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8 April 2018

M Hadchouel

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8 April 2018

J Lalau-Keraly

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8 April 2018

J L Chaussain

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8 April 2018

S K Wadman

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8 April 2018

N Gregersen

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8 April 2018

language of work or name

English

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publication date

1 June 1985

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8 April 2018

The Journal of Pediatrics

published in

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8 April 2018

volume

106

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8 April 2018

issue

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8 April 2018

page(s)

918-921

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8 April 2018

Microdetermination of 2-ketoglutaric acid in plasma and cerebrospinal fluid by capillary gas chromatography mass spectrometry; application to pediatrics

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Ultrastructural abnormalities of liver cells in Reye's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency

7 January 2021

1 reference

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Profiles in altered metabolism. II--(omega -- 1)-hydroxyacid excretion in a case of episodic hypoglycemia

7 January 2021

1 reference

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Glucose Metabolism in Hyperinsulinemic Infants: the Effects of Fasting and Sodiumdl-β-Hydroxybutyrate on Glucose Production and Utilization Rates

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

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

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Dicarboxylic aciduria: deficient [1-14C]octanoate oxidation and medium-chain acyl-CoA dehydrogenase in fibroblasts

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Dicarboxylic aciduria due to medium chain acyl CoA dehydrogenase defect. A cause of hypoglycemia in childhood

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Medium-chain acyl-CoA dehydrogenase deficiency in children with non-ketotic hypoglycemia and low carnitine levels

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Acetoacetyl CoA thiolase deficiency: A cause of severe ketoacidosis in infancy simulating salicylism

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

beta-Hydroxy-beta-methyglutaricaciduria presenting as Reye's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Twin siblings with a Reye's-like syndrome associated with an abnormal organic aciduria, hypoglycemia, diarrhea, and vomiting with close similarities to Jamaican vomiting sickness

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Intermittent non-ketotic dicarboxylic aciduria in two siblings with hypoglycaemia: an apparent defect in beta-oxidation of fatty acids

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Systemic carnitine deficiency simulating recurrent Reye syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as Reye's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Reye's syndrome: epidemiologic and viral studies, 1963-1974

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

Aspirin as a risk factor in Reye's syndrome

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980237-7

10.1016/S0022-3476(85)80237-7

7 January 2021

Identifiers

DOI

1 reference

8 April 2018

1 reference

8 April 2018