Literature DB >> 7430959

Determination of orotic acid in children's urine.

C Bachmann, J P Colombo.   

Abstract

A reliable method is described for the determination of urinary orotic acid. The orotic acid is separated quickly and easily from the urine by anion exchange chromatography. Reference values are reported for children. The method is suitable for the differentiation of those inherited metabolic defects that lead to hyperammonemia.

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Year:  1980        PMID： 7430959     DOI： 10.1515/cclm.1980.18.5.293

Source DB:  PubMed          Journal:  J Clin Chem Clin Biochem        ISSN： 0340-076X


  6 in total

1.  Late-onset form of partial N-acetylglutamate synthetase deficiency.

Authors:  O N Elpeleg; J P Colombo; N Amir; C Bachmann; H Hurvitz
Journal:  Eur J Pediatr       Date:  1990-06       Impact factor: 3.183

2.  DNA analysis of ornithine transcarbamylase deficiency.

Authors:  U Wendel; E Wilichowski; J Schmidtke; C Bachmann
Journal:  Eur J Pediatr       Date:  1988-05       Impact factor: 3.183

3.  Neonatal pyruvate dehydrogenase deficiency with lipoate responsive lactic acidaemia and hyperammonaemia.

Authors:  D J Byrd; H P Krohn; L Winkler; C Steinborn; M Hadam; J Brodehl; D H Hunneman
Journal:  Eur J Pediatr       Date:  1989-04       Impact factor: 3.183

4.  Ornithine transcarbamylase deficiency in a male: strict correlation between metabolic control and plasma arginine concentration.

Authors:  U Wendel; J Wieland; H J Bremer; C Bachmann
Journal:  Eur J Pediatr       Date:  1989-01       Impact factor: 3.183

5.  Ornithine transcarbamylase (OTC) deficiency in a female patient with a de nova deletion of the paternal X chromosome.

Authors:  R Slomski; I Braulke; C Behrend; E Schröder; J P Colombo; J Reiss
Journal:  Hum Genet       Date:  1992-08       Impact factor: 4.132

6.  Arginine, an indispensable amino acid for patients with inborn errors of urea synthesis.

Authors:  S W Brusilow
Journal:  J Clin Invest       Date:  1984-12       Impact factor: 14.808
  6 in total

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