Quantitative liquid chromatography coupled with tandem mass spectrometry analysis of urinary acylglycines: Application to the diagnosis of inborn errors of metabolism

Author:

Ombrone Daniela,Salvatore Francesco,Ruoppolo Margherita

Publisher

Elsevier BV

Subject

Cell Biology,Molecular Biology,Biochemistry,Biophysics

Reference14 articles.

1. N-Acylglycine amidation: Implications for the biosynthesis of fatty acid primary amides;Wilcox;Biochemistry,1999

2. The specificity of glycine-N-acylase and acylglycine excretion in organic acidemias;Bartlett;Biochem. Med.,1974

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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