Medium-chain acyl-CoA dehydrogenase deficiency in two siblings with a Reye-like syndrome. (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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P F Bougnères

1

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F Rocchiccioli

2

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S Kølvraa

3

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M Hadchouel

4

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J Lalau-Keraly

5

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J L Chaussain

6

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S K Wadman

7

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N Gregersen

8

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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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volume

106

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issue

6

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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

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Ultrastructural abnormalities of liver cells in Reye's syndrome

7 January 2021

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Fasting hypoglycemia resulting from hepatic carnitine palmitoyl transferase deficiency.

7 January 2021

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

7 January 2021

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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

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

7 January 2021

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

7 January 2021

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

7 January 2021

1 reference

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

7 January 2021

1 reference

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

7 January 2021

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

7 January 2021

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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

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

7 January 2021

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Systemic carnitine deficiency simulating recurrent Reye syndrome.

7 January 2021

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

7 January 2021

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

7 January 2021

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Aspirin as a risk factor in Reye's syndrome

7 January 2021

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10.1016/S0022-3476(85)80237-7

7 January 2021

Identifiers

DOI

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8 April 2018

1 reference

8 April 2018