The determination of urinary phenylacetylglutamine as phenylacetic acid. Studies on its origin in normal subjects and children with cystic fibrosis

Clin Chim Acta. 1971 Nov;35(1):121-31. doi: 10.1016/0009-8981(71)90302-0.
No abstract available

MeSH terms

  • Administration, Oral
  • Capsules
  • Child
  • Child, Preschool
  • Chromatography, Gas
  • Chromatography, Ion Exchange
  • Circadian Rhythm
  • Cystic Fibrosis / urine*
  • Diet
  • Female
  • Glutamine / urine*
  • Humans
  • Hydrolysis
  • Infant
  • Infant, Newborn
  • Lactates / urine
  • Male
  • Phenethylamines / administration & dosage
  • Phenethylamines / urine
  • Phenylacetates / administration & dosage
  • Phenylacetates / urine*
  • Phenylalanine / administration & dosage
  • Phenylalanine / urine
  • Phenylpyruvic Acids / urine
  • Time Factors
  • Tyramine / administration & dosage
  • Tyrosine / administration & dosage

Substances

  • Capsules
  • Lactates
  • Phenethylamines
  • Phenylacetates
  • Phenylpyruvic Acids
  • Glutamine
  • Tyrosine
  • Phenylalanine
  • Tyramine