(Q73298362)

English

Quantitative measurement of total and free 3-hydroxy fatty acids in serum or plasma samples: short-chain 3-hydroxy fatty acids are not esterified

scientific article published on 01 November 2000

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11117435%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

Quantitative measurement of total and free 3-hydroxy fatty acids in serum or plasma samples: short-chain 3-hydroxy fatty acids are not esterified (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11117435%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

author name string

P M Jones

1

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2 November 2019

A B Burlina

2

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11117435%20AND%20SRC:MED&resulttype=core&format=json

2 November 2019

M J Bennett

3

1 reference

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2 November 2019

publication date

1 November 2000

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2 November 2019

Journal of Inherited Metabolic Disease

1 reference

Europe PubMed Central

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2 November 2019

23

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2 November 2019

7

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2 November 2019

745-750

1 reference

Europe PubMed Central

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2 November 2019

https://scigraph.springernature.com/pub.10.1023/a:1005643201489

0 references

1 reference

https://pubmed.ncbi.nlm.nih.gov/11117435

12 December 2020

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/11117435

12 December 2020

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3-, 6- and 7-Hydroxyoctanoic Acids are Metabolites of Medium-Chain Triglycerides and Excreted in Urine as Glucuronides

2 references

https://pubmed.ncbi.nlm.nih.gov/11117435

12 December 2020

based on heuristic

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7 January 2021

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The laboratory diagnosis of inborn errors of mitochondrial fatty acid oxidation

1 reference

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The molecular basis of pediatric long chain 3-hydroxyacyl-CoA dehydrogenase deficiency associated with maternal acute fatty liver of pregnancy

1 reference

https://pubmed.ncbi.nlm.nih.gov/11117435

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Medium chain 3-ketoacyl-coenzyme A thiolase deficiency: a new disorder of mitochondrial fatty acid beta-oxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11117435

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Fatal hepatic short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: clinical, biochemical, and pathological studies on three subjects with this recently identified disorder of mitochondrial beta-oxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11117435

12 December 2020

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Diagnosing disorders of fatty acid oxidation

1 reference

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12 December 2020

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Mammalian mitochondrial beta-oxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11117435

12 December 2020

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Mitochondrial short-chain L-3-hydroxyacyl-coenzyme A dehydrogenase deficiency: a new defect of fatty acid oxidation.

1 reference

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12 December 2020

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

1 reference

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Molecular basis of human mitochondrial very-long-chain acyl-CoA dehydrogenase deficiency causing cardiomyopathy and sudden death in childhood

1 reference

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12 December 2020

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Fatty acid oxidation disorders: A new class of metabolic diseases

1 reference

https://pubmed.ncbi.nlm.nih.gov/11117435

12 December 2020

based on heuristic

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Improved stable isotope dilution-gas chromatography-mass spectrometry method for serum or plasma free 3-hydroxy-fatty acids and its utility for the study of disorders of mitochondrial fatty acid beta-oxidation

1 reference

https://pubmed.ncbi.nlm.nih.gov/11117435

12 December 2020

based on heuristic

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