Literature DB >> 994457

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

P Koepp.   

Abstract

Urinary phenylalanine metabolites after phenylalanine load of 4 healthy controls, 15 patients with classical phenylketonuria and 8 patients with hyperphenylalaninemic variants are measured quantitatively by gas chromatography. Statistically significant differences are found for a number of metabolites, e.g. phenylpyruvate, phenyllactate, ortho-hydroxy-phenylacetate, para-hydroxy-phenylpyruvate and para-hydroxy-phenyllactate. The results are discussed with respect to discrimination of phenylketonuria patients and patients with hyperphenylalaninemic variants and in respect to pathophysiological aspects.

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Year:  1976        PMID: 994457     DOI: 10.1007/bf01469250

Source DB:  PubMed          Journal:  Klin Wochenschr        ISSN: 0023-2173


  49 in total

1.  [Severe metabolic diseases in neonates. Diagnosis and treatment (author's transl)].

Authors:  P Koepp; R Grüttner
Journal:  Klin Padiatr       Date:  1975-01       Impact factor: 1.349

2.  TYROSINE HYDROXYLASE. THE INITIAL STEP IN NOREPINEPHRINE BIOSYNTHESIS.

Authors:  T NAGATSU; M LEVITT; S UDENFRIEND
Journal:  J Biol Chem       Date:  1964-09       Impact factor: 5.157

3.  The influence of phenylalanine intake on the chemistry and behaviour of a phenyl-ketonuric child.

Authors:  H BICKEL; J GERRARD; E M HICKMANS
Journal:  Acta Paediatr       Date:  1954-01       Impact factor: 2.299

4.  Phenylalanine and tyrosine utilization in normal and phenylalanine-deficient young mice.

Authors:  C R GRAU; R STEELE
Journal:  J Nutr       Date:  1954-05-10       Impact factor: 4.798

5.  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

6.  Phenylketonemia in phenylketonuria.

Authors:  M W Partington; S K Vickery
Journal:  Neuropadiatrie       Date:  1974-05

7.  Neonatal screening for phenylketonuria. I. Effectiveness.

Authors:  N A Holtzman; A G Meek; E D Mellits
Journal:  JAMA       Date:  1974-08-05       Impact factor: 56.272

8.  The source of aromatic ketoacids in tyrosinaemia and phenylketonuria.

Authors:  J H Fellman; N R Buist; N G Kennaway; R E Swanson
Journal:  Clin Chim Acta       Date:  1972-06       Impact factor: 3.786

9.  Influence of age on ortho-hydroxyphenylacetic acid excretion in phenylketonuria and its genetic variants.

Authors:  F Rey; C Pellié; M Sivy; F Blandin-Savoja; J Rey; J Frézal
Journal:  Pediatr Res       Date:  1974-05       Impact factor: 3.756

10.  [Phenylalanine hydroxylase activity in the liver as a parameter for distinguishing various forms of hyperphenylalaninemias (author's transl)].

Authors:  U Grimm; A Knapp; K Schlenzka; H Reddemann
Journal:  Clin Chim Acta       Date:  1975-01-06       Impact factor: 3.786

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  2 in total

1.  Standardized loading test with protein for the differentiation of phenylketonuria from hyperphenylalaninaemia.

Authors:  P Lutz; H Schmidt; G Frey; H Bickel
Journal:  J Inherit Metab Dis       Date:  1982       Impact factor: 4.982

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

Authors:  P Koepp; M Scholtyssek; C Plettner
Journal:  Eur J Pediatr       Date:  1978-04-20       Impact factor: 3.183

  2 in total

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