A narrative review of metabolomics approaches in identifying biomarkers of doxorubicin-induced cardiotoxicity. [PDF]
Singh A +7 more
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Serum concentrations of lipids, ketones and acylcarnitines during the postprandial and fasting state: the Postprandial Metabolism (PoMet) study in healthy young adults. [PDF]
Anfinsen ÅM +9 more
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Interaction of metabolic and inflammatory dysregulation on central degeneration and cognitive function in behavioral variant Frontotemporal dementia. [PDF]
Hou JH +10 more
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Retrospective analysis of reference intervals for dried blood spot based ms/ms newborn screening programs in Chinese preterm neonates: a nationwide study. [PDF]
He F, Xie T, Huang X, Zhang J, Tang T.
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Plasma metabolomics of immune-related adverse events for patients with lung cancer treated with PD-1/PD-L1 inhibitors. [PDF]
Chen J +8 more
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Lysine <i>α</i>-ketoglutarate reductase as a therapeutic target for saccharopine pathway related diseases. [PDF]
Valderrama GV, Moreira GA, Arruda P.
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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
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Stability of malonylcarnitine and glutarylcarnitine in stored blood spots
Journal of Inherited Metabolic Disease, 2004AbstractSummary: 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
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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
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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
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