Results 121 to 130 of about 954 (132)

A narrative review of metabolomics approaches in identifying biomarkers of doxorubicin-induced cardiotoxicity. [PDF]

open access: yesMetabolomics
Singh A   +7 more
europepmc   +1 more source

Serum concentrations of lipids, ketones and acylcarnitines during the postprandial and fasting state: the Postprandial Metabolism (PoMet) study in healthy young adults. [PDF]

open access: yesBr J Nutr
Anfinsen ÅM   +9 more
europepmc   +1 more source
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Quantitation of Butyrylcarnitine, Isobutyrylcarnitine, and Glutarylcarnitine in Urine Using Ultra-Performance Liquid Chromatography-Tandem Mass Spectrometry (UPLC-MS/MS)

2022
Acylcarnitines are formed when an acyl group is transferred from coenzyme A to a molecule of L-carnitine. In organic acidemias, and in fatty acid oxidation disorders, specific acylcarnitine species accumulate in a pattern that is characteristic for each disease.
Judith A, Hobert   +2 more
openaire   +2 more sources

Stability of malonylcarnitine and glutarylcarnitine in stored blood spots

Journal of Inherited Metabolic Disease, 2004
AbstractSummary: Malonylcarnitine and glutarylcarnitine are important diagnostic metabolites in the screening of dried blood spots by tandem mass spectrometry. The stability of these compounds in spiked blood spots stored at room temperature was studied. Both showed biphasic curves.
D W, Johnson, M-U, Trinh
openaire   +2 more sources

Identification of glutarylcarnitine in glutaric aciduria type 1 by carboxylic acid analyzer with an ODS reverse-phase column

Clinica Chimica Acta, 1987
A technique for the identification of glutarylcarnitine in urine from a patient with glutaric aciduria type 1 is described. The patient's urine sample was partially purified using an anion exchange column and analyzed by a carboxylic acid analyzer fitted with an ODS reverse-phase column.
K, Kidouchi   +5 more
openaire   +2 more sources

The urinary excretion of glutarylcarnitine is an informative tool in the biochemical diagnosis of glutaric acidemia type I

Molecular Genetics and Metabolism, 2005
Glutaric acidemia type I (GA-1) is a progressive neurodegenerative inborn error of metabolism that typically manifests acutely in infants during an intercurrent illness. The diagnosis is established biochemically by the detection of glutaric acid and 3-hydroxy glutaric acid in urine and glutarylcarnitine in plasma.
S, Tortorelli   +5 more
openaire   +2 more sources

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