Urinary excretion of l-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of l-carnitine.
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Acylcarnitines: reflecting or inflicting insulin resistance?Neuropsychiatric manifestations of defect in mitochondrial beta oxidation response to riboflavinIdentification of 3-methylglutarylcarnitine. A new diagnostic metabolite of 3-hydroxy-3-methylglutaryl-coenzyme A lyase deficiencyTranslating the basic knowledge of mitochondrial functions to metabolic therapy: role of L-carnitineDifferential HMG-CoA lyase expression in human tissues provides clues about 3-hydroxy-3-methylglutaric aciduria.Acute management of propionic acidemia.Plasma and hepatic carnitine and coenzyme A pools in a patient with fatal, valproate induced hepatotoxicity.Network analysis of a Pkd1-mouse model of autosomal dominant polycystic kidney disease identifies HNF4α as a disease modifier.In HepG2 cells, coexisting carnitine deficiency masks important indicators of marginal biotin deficiency.¹H-NMR and MS based metabolomics study of the intervention effect of curcumin on hyperlipidemia mice induced by high-fat diet.Influences of bone and mineral metabolism in epilepsy.Inborn errors of ketogenesis and ketone body utilization.Metabolic acidosis in newborn infants.Discovery of early-stage biomarkers for diabetic kidney disease using ms-based metabolomics (FinnDiane study).Inhibition of oxidative metabolism by propionic acid and its reversal by carnitine in isolated rat hepatocytes.Technical standards and guidelines for the diagnosis of biotinidase deficiency.Quantification of plasma carnitine and acylcarnitines by high-performance liquid chromatography-tandem mass spectrometry using online solid-phase extraction.Clinical variability of isovaleric acidemia in a genetically homogeneous population.L-Carnitine and Acetyl-L-carnitine Roles and Neuroprotection in Developing Brain.Development of a newborn screening follow-up algorithm for the diagnosis of isobutyryl-CoA dehydrogenase deficiency.Disorders of branched chain amino acid metabolism.
P2860
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P2860
Urinary excretion of l-carnitine and acylcarnitines by patients with disorders of organic acid metabolism: evidence for secondary insufficiency of l-carnitine.
description
1984 nî lūn-bûn
@nan
1984年の論文
@ja
1984年論文
@yue
1984年論文
@zh-hant
1984年論文
@zh-hk
1984年論文
@zh-mo
1984年論文
@zh-tw
1984年论文
@wuu
1984年论文
@zh
1984年论文
@zh-cn
name
Urinary excretion of l-carniti ...... insufficiency of l-carnitine.
@en
Urinary excretion of l-carniti ...... insufficiency of l-carnitine.
@nl
type
label
Urinary excretion of l-carniti ...... insufficiency of l-carnitine.
@en
Urinary excretion of l-carniti ...... insufficiency of l-carnitine.
@nl
prefLabel
Urinary excretion of l-carniti ...... insufficiency of l-carnitine.
@en
Urinary excretion of l-carniti ...... insufficiency of l-carnitine.
@nl
P2093
P1433
P1476
Urinary excretion of l-carniti ...... insufficiency of l-carnitine.
@en
P2093
P304
P356
10.1203/00006450-198412000-00021
P407
P577
1984-12-01T00:00:00Z
P5875
P6179
1019109269