(Q42228864)

19 October 2017

title

Octanoic acidemia and octanoylcarnitine excretion with dicarboxylic aciduria due to defective oxidation of medium-chain fatty acids (English)

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19 October 2017

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Duran M

1

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19 October 2017

Mitchell G

2

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19 October 2017

de Klerk JB

3

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19 October 2017

de Jager JP

4

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19 October 2017

Hofkamp M

5

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19 October 2017

Bruinvis L

6

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19 October 2017

Ketting D

7

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19 October 2017

Saudubray JM

8

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19 October 2017

Wadman SK

9

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19 October 2017

language of work or name

English

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publication date

1 September 1985

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The Journal of Pediatrics

19 October 2017

published in

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19 October 2017

volume

107

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19 October 2017

issue

3

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19 October 2017

page(s)

397-404

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

19 October 2017

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980514-X

Systemic carnitine deficiency--a treatable inherited lipid-storage disease presenting as 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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Lethal hypoglycemia in a child with a deficiency of 3-hydroxy-3-methylglutarylcoenzyme A lyase

7 January 2021

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Jamaican vomiting sickness. Biochemical investigation of two cases

7 January 2021

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Gas chromatography of urinary N-phenylacetylglutamine

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980514-X

Oxidation of fatty acids in cultured fibroblasts: a model system for the detection and study of defects in oxidation

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980514-X

Regional Cerebral Na+K+ ATPase Activity following Octanoate Administration

7 January 2021

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https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980514-X

Effects of octanoate on rat brain and liver mitochondria.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980514-X

General (medium-chain) acyl-CoA dehydrogenase deficiency (non-ketotic dicarboxylic aciduria): quantitative urinary excretion pattern of 23 biologically significant organic acids in three cases

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980514-X

Episodic hypoglycemia with psi-hydroxy fatty acid excretion

7 January 2021

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Suberylglycine excretion in the urine from a patient with dicarboxylic aciduria

7 January 2021

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Mechanism of free fatty acid-induced arrhythmias

7 January 2021

1 reference

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In vitro fibroblast studies in a patient with C6-C10-dicarboxylic aciduria: evidence for a defect in general acyl-CoA dehydrogenase

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

https://api.crossref.org/works/10.1016%2FS0022-3476%2885%2980514-X

The cerebrohepatorenal (Zellweger) syndrome. Increased levels and impaired degradation of very-long-chain fatty acids and their use in prenatal diagnosis

7 January 2021

1 reference

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Adrenoleukodystrophy: impaired oxidation of very long chain fatty acids in white blood cells, cultured skin fibroblasts, and amniocytes

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

1 reference

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10.1016/S0022-3476(85)80514-X

7 January 2021

Identifiers

DOI

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19 October 2017

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