Abstract Background Children with Phenylketonuria (PKU) need a special diet to avoid a variety of physical and psychological complications. The aim of this study was to compare and assess the effects of two interventions on and levels of phenylalanine and micronutrients in children with PKU. Methods Forty-six children with PKU (ages 1–12 years) and their caregivers were randomly assigned to one of two 10-week interventions: a caregiver educational intervention based on the Integrative Model of Behvioral Prediction (IMBP) and supplementary low-protein-modified foods. Outcomes consisted of Children's plasma phenylalanine and micronutrients (i.e., vitamin B12, vitamin D3, and zinc) and hemoglobin levels. To assess the sustainability of outcome...
Introduction: In phenylketonuria (PKU), evidence suggests that casein glycomacropeptide supplemented...
This study addressed two questions: is there an effect of dietary interventions that induce relative...
In recent years, an increasing number of national guidelines on the treatment of phenylketonuria (PK...
Fruits and vegetables containing phenylalanine ≤ 75 mg/100 g (except potatoes) have little impact on...
CONTEXT: Dietary phenylalanine (PA) restriction is the most effective form for reducing its excess i...
Phenylketonuria (PKU) is the most common autosomal recessive disease. Hyperphenylalaninemia is cause...
Hyperphenylalaninaemia (HPA) is an inherited disorder that results in raised plasma phenylalanine le...
A wider understanding of the impact of each of the dietary components on blood phenylalanine concent...
Patients with phenylketonuria (PKU) must follow a strict low-phenylalanine (Phe) diet in order to mi...
In phenylketonuria (PKU), an important component of the UK dietary management system is a 50 mg phen...
Patients with phenylketonuria (PKU) must follow a strict low-phenylalanine (Phe) diet in order to mi...
Patients with phenylketonuria (PKU) must follow a strict low-phenylalanine (Phe) diet in order to mi...
Hyperphenylalaninaemia (HPA) is an inherited disorder that results in raised plasma phenylalanine le...
ObjectiveTo compare a gram protein exchange system (1g=50-mg Phenylalanine) with a unit exchange sys...
There is currently no known method to cure PKU completely. With a disorder and a special type of met...
Introduction: In phenylketonuria (PKU), evidence suggests that casein glycomacropeptide supplemented...
This study addressed two questions: is there an effect of dietary interventions that induce relative...
In recent years, an increasing number of national guidelines on the treatment of phenylketonuria (PK...
Fruits and vegetables containing phenylalanine ≤ 75 mg/100 g (except potatoes) have little impact on...
CONTEXT: Dietary phenylalanine (PA) restriction is the most effective form for reducing its excess i...
Phenylketonuria (PKU) is the most common autosomal recessive disease. Hyperphenylalaninemia is cause...
Hyperphenylalaninaemia (HPA) is an inherited disorder that results in raised plasma phenylalanine le...
A wider understanding of the impact of each of the dietary components on blood phenylalanine concent...
Patients with phenylketonuria (PKU) must follow a strict low-phenylalanine (Phe) diet in order to mi...
In phenylketonuria (PKU), an important component of the UK dietary management system is a 50 mg phen...
Patients with phenylketonuria (PKU) must follow a strict low-phenylalanine (Phe) diet in order to mi...
Patients with phenylketonuria (PKU) must follow a strict low-phenylalanine (Phe) diet in order to mi...
Hyperphenylalaninaemia (HPA) is an inherited disorder that results in raised plasma phenylalanine le...
ObjectiveTo compare a gram protein exchange system (1g=50-mg Phenylalanine) with a unit exchange sys...
There is currently no known method to cure PKU completely. With a disorder and a special type of met...
Introduction: In phenylketonuria (PKU), evidence suggests that casein glycomacropeptide supplemented...
This study addressed two questions: is there an effect of dietary interventions that induce relative...
In recent years, an increasing number of national guidelines on the treatment of phenylketonuria (PK...