Literature DB >> 7439195

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

U Langenbeck, A Behbehani, A Mench-Hoinowski, M Petersen.   

Abstract

There is a steady and nonlinear relationship between the levels of both phenylpyruvic acid (PPA) and o-hydroxyphenylacetic acid (oOPAA) in urine and the plasma levels of phenylalanine (phe) in children more than two years of age with phenylketonuria (PKU). If phe levels in blood rise above 0.35 mM (5.8 mg/100 ml) both aromatic acids are found regularly in urine. Typically, urinary concentrations of PPA are about 5 times higher than those of oOPAA. This report is based on the analysis of 94 samples from 51 children, on or off diet.

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Year:  1980        PMID: 7439195     DOI: 10.1007/bf01846027

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


  16 in total

1.  The renal clearance of phenylpyruvate.

Authors:  C L VINK
Journal:  Clin Chim Acta       Date:  1961-11       Impact factor: 3.786

2.  Observation of behavioral and personality characteristics of phenylketonurics according to their dietary duration: early treatment and normal intelligence.

Authors:  P Chang; R O Fisch
Journal:  Psychol Rep       Date:  1976-12

3.  Urinary creatinine is unsuitable as reference value for collagen metabolite output.

Authors:  N Blumenkrantz; G Asboe-Hansen
Journal:  Clin Biochem       Date:  1977-06       Impact factor: 3.281

4.  Phenylketonemia in phenylketonuria.

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

5.  Phenylalaninaemia. Differential diagnosis.

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

6.  Clearance of endogenous phenylpyruvate in phenylketonurics.

Authors:  E Zelnícek; O Podhradská
Journal:  Clin Chim Acta       Date:  1969-07       Impact factor: 3.786

7.  O-trimethylsilylquinoxalinol derivatives of aromatic alpha-keto acids. Mass spectra and quantitative gas chromatography.

Authors:  U Langenbeck; A Mench-Hoinowski; K P Dieckmann; H U Möhring; M Petersen
Journal:  J Chromatogr       Date:  1978-03-01

8.  Phenylalaninaemia or classical phenylketonuria (PKU)?

Authors:  H Bickel
Journal:  Neuropadiatrie       Date:  1970-04

9.  Computer analysis of the EEG as an aid in the evaluation of dietetic treatment in phenylketonuria.

Authors:  D N Donker; D Reits; F J Van Sprang; W S van Leeuwen; S K Wadman
Journal:  Electroencephalogr Clin Neurophysiol       Date:  1979-02

10.  Permanent chemical phenylketonuria and a normal phenylalanine tolerance in two sisters with a normal mental development.

Authors:  S K Wadman; D Ketting; P K De Bree; C Van der Heiden; M T Grimberg; H Kruijswijk
Journal:  Clin Chim Acta       Date:  1975-12-01       Impact factor: 3.786

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  6 in total

1.  Plasma concentrations of phenyllactic acid in phenylketonuria.

Authors:  P C Clemens; M H Schünemann; G F Hoffmann; A Kohlschütter
Journal:  J Inherit Metab Dis       Date:  1990       Impact factor: 4.982

2.  Development of Metabolic Phenotype in Phenylketonuria: Evaluation of the Blaskovics Protein Loading Test at 5 Years of Age.

Authors:  P Burgard; E Mönch; J Zschocke; U Wendel; U Langenbeck
Journal:  JIMD Rep       Date:  2015-12-19

3.  A synopsis of the unconjugated acidic transamination metabolites of phenylalanine in phenylketonuria.

Authors:  U Langenbeck; A Behbehani; A Mench-Hoinowski
Journal:  J Inherit Metab Dis       Date:  1992       Impact factor: 4.982

4.  Renal transport of aromatic acids in patients with phenylketonuria.

Authors:  U Langenbeck; A Behbehani; H Luthe
Journal:  J Inherit Metab Dis       Date:  1981       Impact factor: 4.982

5.  Examination of urine metabolites in the newborn period and during protein loading tests at 6 months of age--Part 1.

Authors:  E Mönch; J Kneer; C Jakobs; M Arnold; H Diehl; U Batzler
Journal:  Eur J Pediatr       Date:  1990       Impact factor: 3.183

6.  Routine neonatal screening for phenylketonuria in the United Kingdom 1964-78. Medical Research Council Steering Committee for the MRC/DHSS Phenylketonuria Register.

Authors: 
Journal:  Br Med J (Clin Res Ed)       Date:  1981-05-23
  6 in total

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