Abstract Background Phenylketonuria (PKU) is a rare inborn error of metabolism affecting the catabolism of phenylalanine (Phe). To date, findings regarding health-related quality of life (HRQoL) in adults with early-treated classical PKU are discrepant. Moreover, little is known about metabolic, demographic, and cognitive factors associated with HRQoL. Hence, we aimed to investigate HRQoL and its association with demographic, metabolic, and cognitive characteristics in a large European sample of adults with early-treated classical PKU. Results This cross-sectional study included 124 adults with early-treated classical PKU from Hungary, Italy, Spain, Switzerland, and Turkey. All participants prospectively completed the PKU quality of life qu...
BACKGROUND: The aim of our study was to develop and validate the first set of PKU-specific Health-re...
Dietary treatment is the cornerstone of therapy for phenylketonuria (PKU), but adherence to low- phe...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
BACKGROUND Phenylketonuria (PKU) is a rare inborn error of metabolism affecting the catabolism of...
The strict and demanding dietary treatment and mild cognitive abnormalities seen in PKU treated from...
10Background: Phenylketonuria (PKU) is a chronic inborn error of amino acid metabolism that requires...
The aim of this study was to examine Health-Related Quality of Life (HRQoL) of patients with Phenylk...
The aim of this study was to examine Health-Related Quality of Life (HRQoL) of patients with Phenylk...
The aim of this study was to examine Health-Related Quality of Life (HRQoL) of patients with Phenylk...
Phenylketonuria (PKU; OMIM 261600) is an autosomal recessive disorder of phenylalanine metabolism ca...
BACKGROUND: The aim of our study was to develop and validate the first set of PKU-specific Health-re...
Dietary treatment is the cornerstone of therapy for phenylketonuria (PKU), but adherence to low- phe...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
BACKGROUND Phenylketonuria (PKU) is a rare inborn error of metabolism affecting the catabolism of...
The strict and demanding dietary treatment and mild cognitive abnormalities seen in PKU treated from...
10Background: Phenylketonuria (PKU) is a chronic inborn error of amino acid metabolism that requires...
The aim of this study was to examine Health-Related Quality of Life (HRQoL) of patients with Phenylk...
The aim of this study was to examine Health-Related Quality of Life (HRQoL) of patients with Phenylk...
The aim of this study was to examine Health-Related Quality of Life (HRQoL) of patients with Phenylk...
Phenylketonuria (PKU; OMIM 261600) is an autosomal recessive disorder of phenylalanine metabolism ca...
BACKGROUND: The aim of our study was to develop and validate the first set of PKU-specific Health-re...
Dietary treatment is the cornerstone of therapy for phenylketonuria (PKU), but adherence to low- phe...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...