Phenylalanine and its metabolites were determined in serum and urine of phenylketonuric subjects and in subjects with milder hyperphenylalaninemia in whom blood phenylalanine concentrations were usually <200 mg/liter. Metabolite concentrations were related to serum phenylalanine, and in hyperphenylalaninemic subjects were between those for treated and untreated phenylketonuric subjects. Phenyilactic and phenylpyru-vic acids were excreted by all of the mild hyperphenyl-alaninemic subjects except for the youngest (one-year-old twins) and the only subject with a serum phenylala-nine of <100 mg/liter. Serum and urinary metabolites of heterozygotes of both conditions were similar before and after a phenylalanine load. The similar pattern o...
The absence of a convenient, direct enzymatic assay for detecting phenylketonuria (PKU) heterozygote...
Despite extensive clinical and biochemical re-search, the relationship of the metabolic error in phe...
Phenylketonuria (PKU) is caused by deficient activity of phenylalanine hydroxylase (PAH), responsibl...
Gas-liquid chromatographic methods have been developed for the analysis of: urinary phenylalanine me...
and phenylethylamine, were measured in the urine of PKU patients. In general correlation was found b...
W measured therate of elimination of phenylalanine by constant intravenous infusion of L-phenylalani...
Phenylketonuria (PKU), an autosomal-recessive inborn error of phenylalanine (Phe) metabolism is the ...
Spectrophotofluorometricmicromethodsfor the determination of phenylalanineand tyrosine on 25,J. of s...
peer reviewedPhenylketonuria is an inherited metabolic disease, of autosomal recessive transmission,...
A gas Chromatographie method for the quantitative determination of aromatic acids in human urine is ...
In this pilot study, we show that plasma phenylalanine concentration can be predicted from urine con...
phenylalanine in routine care of phenylketonuric children. Fluorimetry, paper and column chromatogra...
A positive ferric chloride reaction was found at routine examination of the urine of a 14 year old m...
The occurrence of γ-glutamylphenylalanine in the urine of patients with phenylketonuria could be dem...
Phenylalanine (Phe) is the most reliable indicator for the diagnosis of phenylketonuria (PKU). The p...
The absence of a convenient, direct enzymatic assay for detecting phenylketonuria (PKU) heterozygote...
Despite extensive clinical and biochemical re-search, the relationship of the metabolic error in phe...
Phenylketonuria (PKU) is caused by deficient activity of phenylalanine hydroxylase (PAH), responsibl...
Gas-liquid chromatographic methods have been developed for the analysis of: urinary phenylalanine me...
and phenylethylamine, were measured in the urine of PKU patients. In general correlation was found b...
W measured therate of elimination of phenylalanine by constant intravenous infusion of L-phenylalani...
Phenylketonuria (PKU), an autosomal-recessive inborn error of phenylalanine (Phe) metabolism is the ...
Spectrophotofluorometricmicromethodsfor the determination of phenylalanineand tyrosine on 25,J. of s...
peer reviewedPhenylketonuria is an inherited metabolic disease, of autosomal recessive transmission,...
A gas Chromatographie method for the quantitative determination of aromatic acids in human urine is ...
In this pilot study, we show that plasma phenylalanine concentration can be predicted from urine con...
phenylalanine in routine care of phenylketonuric children. Fluorimetry, paper and column chromatogra...
A positive ferric chloride reaction was found at routine examination of the urine of a 14 year old m...
The occurrence of γ-glutamylphenylalanine in the urine of patients with phenylketonuria could be dem...
Phenylalanine (Phe) is the most reliable indicator for the diagnosis of phenylketonuria (PKU). The p...
The absence of a convenient, direct enzymatic assay for detecting phenylketonuria (PKU) heterozygote...
Despite extensive clinical and biochemical re-search, the relationship of the metabolic error in phe...
Phenylketonuria (PKU) is caused by deficient activity of phenylalanine hydroxylase (PAH), responsibl...