Quantitative Determination of Plasma C8–C26 Total Fatty Acids for the Biochemical Diagnosis of Nutritional and Metabolic Disorders
- 1 May 2001
- journal article
- research article
- Published by Elsevier in Molecular Genetics and Metabolism
- Vol. 73 (1), 38-45
- https://doi.org/10.1006/mgme.2001.3170
Abstract
No abstract availableKeywords
This publication has 23 references indexed in Scilit:
- Improved Stable Isotope Dilution-Gas Chromatography-Mass Spectrometry Method for Serum or Plasma Free 3-Hydroxy-Fatty Acids and Its Utility for the Study of Disorders of Mitochondrial Fatty Acid β-OxidationClinical Chemistry, 2000
- Inborn Errors of Mitochondrial Fatty Acid OxidationCritical Reviews in Clinical Laboratory Sciences, 2000
- Peroxisomal disorders: clinical, biochemical, and molecular aspects.Neurochemical Research, 1999
- Plasma very long chain fatty acids in 3,000 peroxisome disease patients and 29,000 controlsAnnals of Neurology, 1999
- Clinical and biochemical features of fatty acid oxidation disordersCurrent Opinion in Pediatrics, 1998
- Long-Chain Polyunsaturated Fatty AcidsNeonatology, 1998
- Diagnosing Essential Fatty Acid DeficiencyCirculation, 1998
- Simultaneous analysis of plasma free fatty acids and their 3-hydroxy analogs in fatty acid β-oxidation disordersClinical Chemistry, 1998
- Altered fatty acid metabolism in patients with angiographically documented coronary artery diseaseMetabolism, 1994
- Abnormal profiles of polyunsaturated fatty acids in the brain, liver, kidney and retina of patients with peroxisomal disordersBrain Research, 1992