(Q59504449)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9762600%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

title

Lactic acidosis in long-chain fatty acid beta-oxidation disorders (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9762600%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1 reference

1

1 reference

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5 December 2019

author name string

J P Ruiter

2

1 reference

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5 December 2019

L IJlst

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9762600%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

I T de Almeida

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9762600%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

R J Wanders

5

1 reference

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5 December 2019

publication date

1 August 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9762600%20AND%20SRC:MED&resulttype=core&format=json

Journal of Inherited Metabolic Disease

5 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9762600%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

volume

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9762600%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

issue

6

1 reference

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5 December 2019

page(s)

645-654

1 reference

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https://scigraph.springernature.com/pub.10.1023/a:1005480516801

5 December 2019

exact match

0 references

cites work

Combined enzyme defect of mitochondrial fatty acid oxidation

1 reference

12 December 2020

3-Hydroxydicarboxylic aciduria due to long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency associated with sudden neonatal death: protective effect of medium-chain triglyceride treatment

1 reference

12 December 2020

Two alpha subunit donor splice site mutations cause human trifunctional protein deficiency

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12 December 2020

Inhibition by fatty acyl esters of adenine nucleotide translocation in rat-liver mitochondria

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12 December 2020

Clinical diagnosis of long-chain acyl-coenzyme A-dehydrogenase deficiency: use of stress and fat-loading tests.

1 reference

12 December 2020

Inhibition of oxidative phosphorylation by palmitoyl-CoA in digitonin permeabilized fibroblasts: implications for long-chain fatty acid β-oxidation disorders

1 reference

12 December 2020

Acute fatty liver of pregnancy and long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

1 reference

12 December 2020

Effects of Palmitoyl CoA on Citrate and Malate Transport by Rat Liver Mitochondria

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12 December 2020

Long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Purification of human very-long-chain acyl-coenzyme A dehydrogenase and characterization of its deficiency in seven patients

1 reference

12 December 2020

Prenatal diagnosis of systemic disorders of the respiratory chain in cultured amniocytes and chorionic villus fibroblasts by studying the formation of lactate and pyruvate from glucose

1 reference

12 December 2020

Measurement of protein using bicinchoninic acid

1 reference

12 December 2020

An appraisal of the functional significance of the inhibitory effect of long chain acyl-CoAs on mitochondrial transports

1 reference

12 December 2020

Inhibition of the mitochondrial adenine nucleotide transport system by oleyl CoA.

1 reference

12 December 2020

SYSTEMS USED FOR THE TRANSPORT OF SUBSTRATES INTO MITOCHONDRIA

1 reference

12 December 2020

Medium-chain acyl-coenzyme A dehydrogenase deficiency: clinical course in 120 affected children.

1 reference

12 December 2020

Metabolite Transport in Mitochondria

1 reference

12 December 2020

Analysis of fatty acid oxidation intermediates in cultured fibroblasts to detect mitochondrial oxidation disorders

1 reference

12 December 2020

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency with the G1528C mutation: clinical presentation of thirteen patients.

1 reference

12 December 2020

Detection of respiratory chain dysfunction by measuring lactate and pyruvate production in cultured fibroblasts

1 reference

12 December 2020

Mitochondrial very long chain acyl-CoA dehydrogenase deficiency--a new disorder of fatty acid oxidation

1 reference

12 December 2020

Inhibitory effect of 3-hydroxyacyl-CoAs and other long-chain fatty acidβ-oxidation intermediates on mitochondrial oxidative phosphorylation

1 reference

12 December 2020

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency--diagnosis, plasma carnitine fractions and management in a further patient

1 reference

12 December 2020

Peripheral sensory-motor polyneuropathy, pigmentary retinopathy, and fatal cardiomyopathy in long-chain 3-hydroxy-acyl-CoA dehydrogenase deficiency

1 reference

12 December 2020

Hypoglycemia, hypotonia, and cardiomyopathy: the evolving clinical picture of long-chain acyl-CoA dehydrogenase deficiency

1 reference

12 December 2020