For almost all patients with PKU, a low phenylalanine diet is the basis of the treatment despite a widely varying natural protein tolerance. A vitamin and mineral supplement is essential and it is commonly added to a phenylalanine-free (phe-free) source of L-amino acids. In PKU, many phe-free L-amino acid supplements have age-specific vitamin and mineral profiles to meet individual requirements. The main micronutrient sources are chemically derived and their delivery dosage is usually advised in three or more doses throughout the day. Within the EU, the composition of VM (vitamin and mineral) phe-free L-amino acid supplements is governed by the Foods for Special Medical Purposes (FSMP) directive (European Commission Directive number 1999/21...
Phenylketonuria (PKU) is caused by the deficiency of the phenylalanine hydroxylase enzyme, which con...
Introduction: In phenylketonuria (PKU), a natural protein-restricted dietary treatment prevents seve...
Despite the appearance of new treatment, dietary approach remains the mainstay of PKU therapy. The n...
For almost all patients with PKU, a low phenylalanine diet is the basis of the treatment despite a w...
Patients with phenylketonuria (PKU) encompass an 'at risk' group for micronutrient imbalances. Optim...
Background & aims: Strict low-phenylalanine diet is associated with an increased risk of developing ...
The same basic principles are used to deliver dietary treatment in PKU that was developed sixty year...
Accumulating evidence suggests that hyperphenylalaninemia in phenylketonuria (PKU) can cause neurops...
Nutritional management is essential for Phenylketonuria (PKU) treatment, consisting in a semi-synthe...
Among aminoacidopathies, phenylketonuria (PKU) is the most prevalent one. Early diagnosis in the neo...
Background: Dietary phenylalanine restriction is the cornerstone of phenylketonuria (PKU) management...
Hyperphenylalaninemia (HPA) is an inborn error of phenylalanine metabolism, due to the deficiency of...
Abstract Phenylketonuria (PKU) is caused by a deficient activity of enzyme phenylalanine (Phe) hydro...
Phenylketonuria (PKU) is caused by the deficiency of the phenylalanine hydroxylase enzyme, which con...
Introduction: In phenylketonuria (PKU), a natural protein-restricted dietary treatment prevents seve...
Despite the appearance of new treatment, dietary approach remains the mainstay of PKU therapy. The n...
For almost all patients with PKU, a low phenylalanine diet is the basis of the treatment despite a w...
Patients with phenylketonuria (PKU) encompass an 'at risk' group for micronutrient imbalances. Optim...
Background & aims: Strict low-phenylalanine diet is associated with an increased risk of developing ...
The same basic principles are used to deliver dietary treatment in PKU that was developed sixty year...
Accumulating evidence suggests that hyperphenylalaninemia in phenylketonuria (PKU) can cause neurops...
Nutritional management is essential for Phenylketonuria (PKU) treatment, consisting in a semi-synthe...
Among aminoacidopathies, phenylketonuria (PKU) is the most prevalent one. Early diagnosis in the neo...
Background: Dietary phenylalanine restriction is the cornerstone of phenylketonuria (PKU) management...
Hyperphenylalaninemia (HPA) is an inborn error of phenylalanine metabolism, due to the deficiency of...
Abstract Phenylketonuria (PKU) is caused by a deficient activity of enzyme phenylalanine (Phe) hydro...
Phenylketonuria (PKU) is caused by the deficiency of the phenylalanine hydroxylase enzyme, which con...
Introduction: In phenylketonuria (PKU), a natural protein-restricted dietary treatment prevents seve...
Despite the appearance of new treatment, dietary approach remains the mainstay of PKU therapy. The n...