Despite extensive clinical and biochemical re-search, the relationship of the metabolic error in phenylketonuria to the clinical symptomatology is unknown (1, 2). The specific biochemical de
Phenylalanine (Phe) is the most reliable indicator for the diagnosis of phenylketonuria (PKU). The p...
Fluctuations in blood phenylalanine concentrations may be an important determinant of intellectual o...
peer reviewedPhenylketonuria is an inherited metabolic disease, of autosomal recessive transmission,...
Phenylalanine and its metabolites were determined in serum and urine of phenylketonuric subjects and...
Gas-liquid chromatographic methods have been developed for the analysis of: urinary phenylalanine me...
Monitoring phenylalanine (Phe) concentrations is critical for the management of phenylketonuria (PKU...
BACKGROUND: Reliable measurement of phenylalanine (Phe) is a prerequisite for adequate follow-up of ...
Introduction: Metabolic control of phenylketonuria (PKU) and compliance with the low-phenylalanine (...
Non treated phenylketonuria (PKU) has serious consequences such as growth retardation and intellectu...
The absence of a convenient, direct enzymatic assay for detecting phenylketonuria (PKU) heterozygote...
Phenylketonuria (PKU) is caused by deficient activity of phenylalanine hydroxylase (PAH), responsibl...
and phenylethylamine, were measured in the urine of PKU patients. In general correlation was found b...
Phenylketonuria is an inborn error of metabolism, involving, in most cases, a deficient activity of ...
International audienceFluctuations in blood phenylalanine concentrations may be an important determi...
grantor: University of TorontoTyrosine requirements and resting energy expenditure (REE) w...
Phenylalanine (Phe) is the most reliable indicator for the diagnosis of phenylketonuria (PKU). The p...
Fluctuations in blood phenylalanine concentrations may be an important determinant of intellectual o...
peer reviewedPhenylketonuria is an inherited metabolic disease, of autosomal recessive transmission,...
Phenylalanine and its metabolites were determined in serum and urine of phenylketonuric subjects and...
Gas-liquid chromatographic methods have been developed for the analysis of: urinary phenylalanine me...
Monitoring phenylalanine (Phe) concentrations is critical for the management of phenylketonuria (PKU...
BACKGROUND: Reliable measurement of phenylalanine (Phe) is a prerequisite for adequate follow-up of ...
Introduction: Metabolic control of phenylketonuria (PKU) and compliance with the low-phenylalanine (...
Non treated phenylketonuria (PKU) has serious consequences such as growth retardation and intellectu...
The absence of a convenient, direct enzymatic assay for detecting phenylketonuria (PKU) heterozygote...
Phenylketonuria (PKU) is caused by deficient activity of phenylalanine hydroxylase (PAH), responsibl...
and phenylethylamine, were measured in the urine of PKU patients. In general correlation was found b...
Phenylketonuria is an inborn error of metabolism, involving, in most cases, a deficient activity of ...
International audienceFluctuations in blood phenylalanine concentrations may be an important determi...
grantor: University of TorontoTyrosine requirements and resting energy expenditure (REE) w...
Phenylalanine (Phe) is the most reliable indicator for the diagnosis of phenylketonuria (PKU). The p...
Fluctuations in blood phenylalanine concentrations may be an important determinant of intellectual o...
peer reviewedPhenylketonuria is an inherited metabolic disease, of autosomal recessive transmission,...
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