BACKGROUND Metabolic control and dietary management of patients with phenylketonuria (PKU) are based on single blood samples obtained at variable intervals. Sampling conditions are often not well-specified and intermittent variation of phenylalanine concentrations between two measurements remains unknown. We determined phenylalanine and tyrosine concentrations in blood over 24 hours. Additionally, the impact of food intake and physical exercise on phenylalanine and tyrosine concentrations was examined. Subcutaneous microdialysis was evaluated as a tool for monitoring phenylalanine and tyrosine concentrations in PKU patients. METHODS Phenylalanine and tyrosine concentrations of eight adult patients with PKU were determined at 60 minute in...
BACKGROUND: Treatment of hereditary tyrosinemia type 1 with nitisinone and phenylalanine and tyrosin...
Treatment of phenylketonuria (PKU) consists of restriction of natural protein and provision of a pro...
In phenylketonuria (PKU) patients, diurnal fluctuations of blood phenylalanine (Phe) are different f...
BACKGROUND Metabolic control and dietary management of patients with phenylketonuria (PKU) are base...
In patients with phenylketonuria (PKU), extra tyrosine supplementation is advocated in addition to t...
Background In patients with Phenylketonuria (PKU) target ranges of blood phenylalanine (Phe) concent...
Background/Aims: In patients with phenylketonuria (PKU), target ranges of blood phenylalanine (Phe) ...
Fluctuations in blood phenylalanine concentrations may be an important determinant of intellectual o...
International audienceFluctuations in blood phenylalanine concentrations may be an important determi...
Objective. To achieve smooth control of plasma phenylalanine concentrations in phenylketonuric patie...
Objective. To achieve smooth control of plasma phenylalanine concentrations in phenylketonuric patie...
BACKGROUND: In patients with phenylketonuria, stability of blood phenylalanine and tyrosine concentr...
grantor: University of TorontoTyrosine requirements and resting energy expenditure (REE) w...
Dietary adherence in phenylketonuria (PKU) –measured as plasma phenylalanine concentrations (Phe)- i...
Tyrosinemia type 1 (TT1) treatment with 2-(2-nitro-4-trifluormethyl-benzyl)-1,3-cyclohexanedione (NT...
BACKGROUND: Treatment of hereditary tyrosinemia type 1 with nitisinone and phenylalanine and tyrosin...
Treatment of phenylketonuria (PKU) consists of restriction of natural protein and provision of a pro...
In phenylketonuria (PKU) patients, diurnal fluctuations of blood phenylalanine (Phe) are different f...
BACKGROUND Metabolic control and dietary management of patients with phenylketonuria (PKU) are base...
In patients with phenylketonuria (PKU), extra tyrosine supplementation is advocated in addition to t...
Background In patients with Phenylketonuria (PKU) target ranges of blood phenylalanine (Phe) concent...
Background/Aims: In patients with phenylketonuria (PKU), target ranges of blood phenylalanine (Phe) ...
Fluctuations in blood phenylalanine concentrations may be an important determinant of intellectual o...
International audienceFluctuations in blood phenylalanine concentrations may be an important determi...
Objective. To achieve smooth control of plasma phenylalanine concentrations in phenylketonuric patie...
Objective. To achieve smooth control of plasma phenylalanine concentrations in phenylketonuric patie...
BACKGROUND: In patients with phenylketonuria, stability of blood phenylalanine and tyrosine concentr...
grantor: University of TorontoTyrosine requirements and resting energy expenditure (REE) w...
Dietary adherence in phenylketonuria (PKU) –measured as plasma phenylalanine concentrations (Phe)- i...
Tyrosinemia type 1 (TT1) treatment with 2-(2-nitro-4-trifluormethyl-benzyl)-1,3-cyclohexanedione (NT...
BACKGROUND: Treatment of hereditary tyrosinemia type 1 with nitisinone and phenylalanine and tyrosin...
Treatment of phenylketonuria (PKU) consists of restriction of natural protein and provision of a pro...
In phenylketonuria (PKU) patients, diurnal fluctuations of blood phenylalanine (Phe) are different f...