Literature DB >> 668711

Urinary excretion of aromatic acids in hyperphenylalaninemic states: response to a protein challenge.

P Koepp, M Scholtyssek, C Plettner.   

Abstract

A protein challenge (3g/kg) was given to 15 hyperphenylalaninemic patients for 4 days and urinary excretion of aromatic phenylalanine metabolites (e.g. phenylpyruvic acid; mandelic acid; ortho-hydroxy-phenylacetic acid) was studied by quantitative gas chromatographic analysis. Two groups of patients, different in their serum phenylalanine pattern, could be distinguished from the pattern of urinary aromatic acid excretion. In the first group, the aromatic acid excretion declined towards the end of the challenge whereas aromatic acid excretion increased throughout the challenge in the second group. The differences could be ascertained by statistical analysis.

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Year:  1978        PMID: 668711     DOI: 10.1007/BF00493543

Source DB:  PubMed          Journal:  Eur J Pediatr        ISSN: 0340-6199            Impact factor:   3.183


  7 in total

1.  Detection of heterozygotes for phenylketonuria and hyperphenylaianinemia by gas-chromatographic analysis of aromatic acid excretion in urine.

Authors:  P Koepp; B Hoffman
Journal:  Clin Chim Acta       Date:  1975-02-08       Impact factor: 3.786

2.  The effects of phenylketonuric and other metabolites on sulfated galactocerebroside synthesis in vivo and in culture.

Authors:  T J Sprinkle; O M Rennert
Journal:  J Neurochem       Date:  1976-03       Impact factor: 5.372

3.  Phenylalaninaemia. Differential diagnosis.

Authors:  M E Blaskovics; G E Schaeffler; S Hack
Journal:  Arch Dis Child       Date:  1974-11       Impact factor: 3.791

Review 4.  The implications of multiple forms of phenylalanine hydroxylase in phenylketonuria and related diseases of phenylalanine metabolism.

Authors:  J A Barranger
Journal:  Biochem Med       Date:  1976-02

5.  Aromatic acids in urine of healthy infants, persistent hyperphenylalaninemia, and phenylketonuria, before and after phenylalanine load.

Authors:  S Rampini; J A Völlmin; H R Bosshard; M Müller; H C Curtius
Journal:  Pediatr Res       Date:  1974-07       Impact factor: 3.756

6.  Aromatic acid excretion in classical phenylketonuria and hyperphenylalaninemic variants.

Authors:  P Koepp; B Hoffmann
Journal:  Helv Paediatr Acta       Date:  1974-11

7.  [Urinary phenylalanine metabolites in hyperphenylalaninemia (author's transl)].

Authors:  P Koepp
Journal:  Klin Wochenschr       Date:  1976-11-01
  7 in total
  2 in total

1.  Absent phenylalanine hydroxylase activity without phenylketonuria.

Authors:  M Yudkoff; S Segal
Journal:  Eur J Pediatr       Date:  1980-06       Impact factor: 3.183

2.  Absence of a significant renal threshold for two aromatic acids in phenylketonuric children over two years of age.

Authors:  U Langenbeck; A Behbehani; A Mench-Hoinowski; M Petersen
Journal:  Eur J Pediatr       Date:  1980-08       Impact factor: 3.183

  2 in total

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