Acylcarnitines in plasma and blood spots of patients with long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency

Journal of Inherited Metabolic Disease

Volumn 23, Issue 6, 2000, Pages 571-582

  Van Hove, J L K ^a   Kahler, S G ^a   Feezor, M D ^a   Ramakrishna, J P ^a   Hart, P ^a   Treem, W R ^a   Shen, J J ^a   Matern, D ^a   Millington, D S ^a  

^a DUKE UNIVERSITY MEDICAL CENTER   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

3 HYDROXYACYL COENZYME A DEHYDROGENASE; ACYLCARNITINE; CARBON; FAT; LONG CHAIN FATTY ACID; MEDIUM CHAIN TRIACYLGLYCEROL;

ARTICLE; ASSAY; BLOOD; BLOOD LEVEL; BLOOD SAMPLING; CELL LEVEL; CHILD; CLINICAL ARTICLE; CONTROLLED STUDY; DIAGNOSTIC ACCURACY; DIET THERAPY; ENZYME DEFICIENCY; ERYTHROCYTE; FEMALE; GENOTYPE; HUMAN; LOW FAT DIET; MALE; MONITORING; PLASMA;

3-HYDROXYACYL COA DEHYDROGENASES; CARNITINE; ERYTHROCYTES; FALSE NEGATIVE REACTIONS; FEMALE; GENOTYPE; HETEROZYGOTE; HOMOZYGOTE; HUMANS; MALE; MUTATION; PLASMA; SENSITIVITY AND SPECIFICITY;

EID: 0033801802     PISSN: 01418955     EISSN: None     Source Type: Journal    
DOI: 10.1023/A:1005673828469     Document Type: Article

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