Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (Q72376095)

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26 October 2019

title

Secondary 3-hydroxydicarboxylic aciduria mimicking long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency (English)

1 reference

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long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

26 October 2019

main subject

1 reference

M J Bennett

1

1 reference

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26 October 2019

M J Weinberger

series ordinal

2

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26 October 2019

W G Sherwood

series ordinal

3

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:7807934%20AND%20SRC:MED&resulttype=core&format=json

26 October 2019

A B Burlina

series ordinal

4

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26 October 2019

publication date

1 January 1994

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Journal of Inherited Metabolic Disease

26 October 2019

published in

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26 October 2019

volume

17

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26 October 2019

issue

3

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26 October 2019

page(s)

283-286

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https://scigraph.springernature.com/pub.10.1007/bf00711808

26 October 2019

exact match

0 references

cites work

Human liver long-chain 3-hydroxyacyl-coenzyme A dehydrogenase is a multifunctional membrane-bound beta-oxidation enzyme of mitochondria

1 reference

12 December 2020

The L-3-hydroxyacyl-CoA dehydrogenase deficiency.

1 reference

12 December 2020

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency: identification of a new inborn error of mitochondrial fatty acid beta-oxidation

1 reference

12 December 2020

Secondary inhibition of multiple NAD‐requiring dehydrogenases in respiratory chain complex I deficiency: Possible metabolic markers for the primary defect

1 reference

12 December 2020

Ethylmalonic aciduria associated with progressive neurological disease and partial cytochromec oxidase deficiency

1 reference

12 December 2020

Clinical and biochemical presentations in 20 cases of hydroxydicarboxylic aciduria.

1 reference

12 December 2020

Muscle cytochromec oxidase deficiency accompanied by a urinary organic acid pattern mimicking multiple acyl‐CoA dehydrogenase deficiency

1 reference

12 December 2020

Sudden infant death and long-chain 3-hydroxyacyl-CoA dehydrogenase

1 reference

12 December 2020

Marked elevation of urinary 3-hydroxydecanedioic acid in a malnourished infant with glycogen storage disease, mimicking long-chain L-3-hydroxyacyl-CoA dehydrogenase deficiency.

1 reference

12 December 2020

A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts

1 reference

12 December 2020

Differential diagnosis of hydroxydicarboxylic aciduria based on release of3H2O from [9,10‐3H]myristic and [9,10‐3H]palmitic acids by intact cultured fibroblasts

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF00711808

1 reference

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26 October 2019

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