Background: Phenylketonuria (PKU) is a chronic inborn error of amino acid metabolism that requires lifelong follow-up and intervention, which may represent strains on Quality of Life (QoL). This observational study evaluated QoL in a cohort of PKU patients, using updated and detailed instruments. Methods: 22 patients with mild PKU respondent to BH4 and 21 patients with classical PKU treated with diet were recruited in this study. Adult patients completed WHOQOL questionnaire-100 (WHOQOL-100) and pediatric patients the Pediatric QoL inventory (PedsQL™). Psychiatric and mood disorders were also evaluated using TAD or BDI and STAI-Y inventories. A multivariable linear regression model was fitted to investigate the predictors of QoL, including ...
The aim of this study was to examine Health-Related Quality of Life (HRQoL) of patients with Phenylk...
OBJECTIVES: To assess quality of life and psychologic adjustment in children and adolescents with ea...
Early dietary treatment of phenylketonuria (PKU), an inborn error of phenylalanine (Phe) metabolism,...
Background: Phenylketonuria (PKU) is a chronic inborn error of amino acid metabolism that requires l...
The strict and demanding dietary treatment and mild cognitive abnormalities seen in PKU treated from...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
Abstract Background Phenylketonuria (PKU) is a rare inborn error of metabolism affecting the catabol...
Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydroxylase enzym...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
BACKGROUND: The aim of our study was to develop and validate the first set of PKU-specific Health-re...
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...
OBJECTIVES: To assess quality of life and psychologic adjustment in children and adolescents with ea...
Early dietary treatment of phenylketonuria (PKU), an inborn error of phenylalanine (Phe) metabolism,...
Background: Phenylketonuria (PKU) is a chronic inborn error of amino acid metabolism that requires l...
The strict and demanding dietary treatment and mild cognitive abnormalities seen in PKU treated from...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
Abstract Background Phenylketonuria (PKU) is a rare inborn error of metabolism affecting the catabol...
Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydroxylase enzym...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
BACKGROUND: The aim of our study was to develop and validate the first set of PKU-specific Health-re...
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...
OBJECTIVES: To assess quality of life and psychologic adjustment in children and adolescents with ea...
Early dietary treatment of phenylketonuria (PKU), an inborn error of phenylalanine (Phe) metabolism,...