Quantitative liquid chromatography coupled with tandem mass spectrometry analysis of urinary acylglycines: Application to the diagnosis of inborn errors of metabolism
Author:
Publisher
Elsevier BV
Subject
Cell Biology,Molecular Biology,Biochemistry,Biophysics
Reference14 articles.
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3. The acyl-CoA dehydrogenation deficiencies: recent advances in the enzyme characterization and understanding of the metabolic and pathophysiological disturbances in patients with acyl-CoA dehydrogenation deficiencies;Gregersen;Scand. J. Clin. Lab. Invest.,1985
4. Stable isotope dilution analysis of n-hexanoylglycine, 3-phenylpropionylglycine, and suberylglycine in human urine using chemical ionization gas chromatography/mass spectrometry selected ion monitoring;Rinaldo;Biomed. Environ. Mass Spectrom.,1989
5. Medium-chain acyl-CoA dehydrogenase deficiency: diagnosis by stable-isotope dilution measurement of urinary n-hexanoylglycine and 3-phenylpropionylglycine;Rinaldo;N. Engl. J. Med.,1988
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