Abstract
A simple paper chromatographic method was found to be effective for the study of phenylketonuria and tyrosyluria. It proved to be much more reliable than conventional tests for the detection of abnormal amounts of ketoacids in urine and was suitable and convenient for following the effects of dietary variations on the excretion of these compounds. Information obtained about ketones other than those of primary importance to the conditions studied included confirmation of the excretion of p-hydroxyphenylpyruvic acid in phenylketonuria. A modification of the method applicable to histidinaemia was devised.
Full text
PDF




Images in this article
Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- Harries J. T., Seakins J. W., Ersser R. S., Lloyd J. K. Recovery after dietary treatment of an infant with features of tyrosinosis. Arch Dis Child. 1969 Apr;44(234):258–267. doi: 10.1136/adc.44.234.258. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SCHREIER K., FLAIG H. Uber die Ausscheidung von Indolbrenztraubensäure im Urin von Gesunden und Patienten mit Föllingscher Krankheit. Klin Wochenschr. 1956 Nov 15;34(43-44):1213–1213. doi: 10.1007/BF01467863. [DOI] [PubMed] [Google Scholar]
- ZANNONI V. G., LA DU B. N. The tyrosine oxidation system of liver. IV. Studies on the inhibition of p-hydroxyphenylpyruvic acid oxidase by excess substrate. J Biol Chem. 1959 Nov;234:2925–2931. [PubMed] [Google Scholar]


