(Q28328120)

English

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

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scholarly article

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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 (English)

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long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

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1 reference

based on heuristic

inferred from title

author name string

M Duran

1

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R J Wanders

2

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J P de Jager

3

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L Dorland

4

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L Bruinvis

5

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D Ketting

6

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L Ijlst

7

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F J van Sprang

8

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language of work or name

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publication date

January 1991

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European Journal of Pediatrics

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150

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190-5

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3

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The existence of an inner-membrane-bound, long acyl-chain-specific 3-hydroxyacyl-CoA dehydrogenase in mammalian mitochondria

1 reference

https://api.crossref.org/works/10.1007%2FBF01963564

21 January 2018

Hepatic and Muscular Presentations of Carnitine Palmitoyl Transferase Deficiency: Two Distinct Entities

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

An improved and simplified radioisotopic assay for the determination of free and esterified carnitine

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Familial hypoketotic hypoglycaemia associated with peripheral neuropathy, pigmentary retinopathy and C6–C14 hydroxydicarboxylic aciduria. A new defect in fatty acid oxidation?

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sudden child death and 'healthy' affected family members with medium-chain acyl-coenzyme A dehydrogenase deficiency.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

3-Hydroxyoctanoic aciduria: identification of a new organic acid in the urine of a patient with non-ketotic hypoglycemia

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defects of metabolism of fatty acids in the sudden infant death syndrome

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cis-4-decenoic acid in plasma: a characteristic metabolite in medium-chain acyl-CoA dehydrogenase deficiency

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary carnitine deficiency due to a failure of carnitine transport in kidney, muscle, and fibroblasts

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Peroxisomal fatty acid beta-oxidation in relation to the accumulation of very long chain fatty acids in cultured skin fibroblasts from patients with Zellweger syndrome and other peroxisomal disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hypoglycemia, hepatic dysfunction, muscle weakness, cardiomyopathy, free carnitine deficiency and long-chain acylcarnitine excess responsive to medium chain triglyceride diet.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1,6-Anhydro-beta-D-glucopyranose (beta-glucosan), a constituent of human urine

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Investigation of inborn errors of metabolism in unexpected infant deaths

1 reference

https://pubmed.ncbi.nlm.nih.gov/2044590

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01963564

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Dimensions Publication ID

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release_hdm42evneva3dgkbfnr2ncwmuu

1 reference

https://api.fatcat.wiki/v0/release/hdm42evneva3dgkbfnr2ncwmuu

24 November 2022

based on heuristic

mapped directly with Wikidata item

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Springer Nature article ID

10.1007/bf01963564

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