Literature DB >> 14860747

[Urinary excretion of p-oxyphenylpyruvic acid, pyruvic acid, phenol and diacetic acid following intake of p-oxyphenylpyruvic acid in the normal state and in liver disease].

K FELIX, G LEONHARDI, I von GLASENAPP.   

Abstract

Entities:  

Keywords:  LIVER DISEASE; PYRUVIC ACID; URINE

Mesh：

Substances：

Year:  1951        PMID： 14860747

Source DB:  PubMed          Journal:  Hoppe Seylers Z Physiol Chem        ISSN： 0018-4888


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  5 in total

Review 1.  INHERITED ENZYME DEFECTS: A REVIEW.

Authors:  T HARGREAVES
Journal:  J Clin Pathol       Date:  1963-07       Impact factor: 3.411

2.  Tests for phenylketonuria: results of a one-year programme for its detection in infancy and among mental defectives.

Authors:  N K GIBBS; L I WOOLF
Journal:  Br Med J       Date:  1959-09-26

3.  Some investigations on the metabolism of phenylalanine and tyrosine in children with vitamin C deficiency.

Authors:  T H HUISMAN; J H JONXIS
Journal:  Arch Dis Child       Date:  1957-04       Impact factor: 3.791

4.  An inborn defect in the metabolism of tyrosine in infants on a normal diet.

Authors:  H R Bloxam; M G Day; N K Gibbs; L I Woolf
Journal:  Biochem J       Date:  1960-11       Impact factor: 3.857

5.  [Tyrosine metabolism and liver function].

Authors:  G LEONHARDI
Journal:  Klin Wochenschr       Date:  1952-02-15
  5 in total

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