(Q70499022)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6434841%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

title

Fatty acyl-CoA dehydrogenase deficiency: enzyme measurement and studies on alternative metabolism (English)

1 reference

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11 October 2019

author name string

N Gregersen

series ordinal

1

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11 October 2019

publication date

1 January 1984

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6434841%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

11 October 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6434841%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

volume

7 Suppl 1

1 reference

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11 October 2019

page(s)

28-32

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https://scigraph.springernature.com/pub.10.1007/bf03047370

11 October 2019

exact match

0 references

cites work

Non-ketotic C6-C10-dicarboxylic aciduria: biochemical investigations of two cases

1 reference

12 December 2020

45 Acyl-CoA dehydrogenases from pig liver mitochondria

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12 December 2020

Dicarboxylic aciduria: The response to fasting

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12 December 2020

Cyanide-insensitive and clofibrate enhanced beta-oxidation of dodecanedioic acid in rat liver. An indication of peroxisomal beta-oxidation of N-dicarboxylic acids

1 reference

12 December 2020

Glutaric aciduria type II: in vitro studies on substrate oxidation, acyl-CoA dehydrogenases, and electron-transferring flavoprotein in cultured skin fibroblasts

1 reference

12 December 2020

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

1 reference

12 December 2020

Separation and properties of five distinct acyl-CoA dehydrogenases from rat liver mitochondria. Identification of a new 2-methyl branched chain acyl-CoA dehydrogenase

1 reference

12 December 2020

Purification and Properties of Rat Liver Acyl-CoA Dehydrogenases and Electron Transfer Flavoprotein1

1 reference

12 December 2020

Novel tritium release assays for isovaleryl-CoA and butyryl-CoA dehydrogenases

1 reference

12 December 2020

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

1 reference

12 December 2020

The biological origin of ketotic dicarboxylic aciduria. II. In vivo and in vitro investigations of the beta-oxidation of C8-C16-dicarboxylic acids in unstarved, starved and diabetic rats

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

Rat liver peroxisomes catalyze the beta oxidation of fatty acids

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12 December 2020

The absolute configuration of urinary 5-hydroxyhexanoic acid - a product of fatty acid (omega-1)-oxidation - in patients with non-ketotic dicarboxylic aciduria

1 reference

12 December 2020

The biological origin of ketotic dicarboxylic aciduria. In vivo and in vitro investigations of the omega-oxidation of C6-C16-monocarboxylic acids in unstarved, starved and diabetic rats

1 reference

12 December 2020

Fatty acid oxidation by human liver peroxisomes

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12 December 2020

Mammalian metabolism of glutaric acid

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12 December 2020

Episodic hypoglycemia with psi-hydroxy fatty acid excretion

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12 December 2020

A new iron-sulfur flavoprotein of the respiratory chain. A component of the fatty acid beta oxidation pathway

1 reference

12 December 2020

Purification and characterization of isovaleryl coenzyme A dehydrogenase from rat liver mitochondria

1 reference

12 December 2020

Demonstration of a specific mitochondrial isovaleryl-CoA dehydrogenase deficiency in fibroblasts from patients with isovaleric acidemia

1 reference

12 December 2020

Suberylglycine excretion in the urine from a patient with dicarboxylic aciduria

1 reference

12 December 2020

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

1 reference

12 December 2020

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

1 reference

12 December 2020

On the biologic origin of C6-C10-dicarboxylic and C6-C10-omega-1-hydroxy monocarboxylic acids in human and rat with acyl-CoA dehydrogenation deficiencies: in vitro studies on the omega- and omega-1-oxidation of medium-chain (C6-C12) fatty acids in h

1 reference

12 December 2020

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

1 reference

12 December 2020

The purification and some properties of electron transfer flavoprotein and general fatty acyl coenzyme A dehydrogenase from pig liver mitochondria

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF03047370

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:6434841%20AND%20SRC:MED&resulttype=core&format=json

11 October 2019

1 reference