Sapropterin treatment, with or without dietary treatment, improves blood phenylalanine control, increases phenylalanine tolerance, and may reduce the day-to-day dietary treatment burden in a subset of patients with phenylketonuria (PKU). Balancing the need for maintained control of blood phenylalanine with diet relaxation is complex when administering sapropterin. We present a series of seven patient cases with PKU that illustrate important aspects of using sapropterin with diet in the management of the disorder. (C) 2012 Elsevier Inc. All rights reserved.</p
Phenylketonuria (PKU) is an inherited metabolic disease characterized by phenylalanine (Phe) accumul...
Phenylketonuria (PKU) is an inherited disorder of phenylalanine (Phe) metabolism. Until recently, th...
Hyperphenylalaninemia is caused by deficient enzyme activity of phenylalanine hydroxylase. It was on...
Sapropterin treatment, with or without dietary treatment, improves blood phenylalanine control, incr...
Sapropterin treatment, with or without dietary treatment, improves blood phenylalanine control, incr...
Sapropterin treatment, with or without dietary treatment, improves blood phenylalanine control, incr...
In a Phase I study, 20% of subjects with phenylketonuria (96/485) responded with a = 30% reduction i...
Phenylketonuria (PKU) is caused by mutations in the phenylalanine hydroxylase (PAH) gene, leading to...
The usual treatment for phenylketonuria (PKU) is a phenylalanine-restricted diet. Following this die...
The usual treatment for phenylketonuria (PKU) is a phenylalanine-restricted diet. Following this die...
Phenylketonuria (PKU) is caused by mutations in the phenylalanine hydroxylase (PAH) gene, leading to...
Background and objective: Untreated phenylketonuria is characterized by neurocognitive and neuromoto...
The usual treatment for phenylketonuria (PKU) is a phenylalanine-restricted diet. Following this die...
The usual treatment for phenylketonuria (PKU) is a phenylalanine-restricted diet. Following this die...
Background and objective: Untreated phenylketonuria is characterized by neurocognitive and neuromoto...
Phenylketonuria (PKU) is an inherited metabolic disease characterized by phenylalanine (Phe) accumul...
Phenylketonuria (PKU) is an inherited disorder of phenylalanine (Phe) metabolism. Until recently, th...
Hyperphenylalaninemia is caused by deficient enzyme activity of phenylalanine hydroxylase. It was on...
Sapropterin treatment, with or without dietary treatment, improves blood phenylalanine control, incr...
Sapropterin treatment, with or without dietary treatment, improves blood phenylalanine control, incr...
Sapropterin treatment, with or without dietary treatment, improves blood phenylalanine control, incr...
In a Phase I study, 20% of subjects with phenylketonuria (96/485) responded with a = 30% reduction i...
Phenylketonuria (PKU) is caused by mutations in the phenylalanine hydroxylase (PAH) gene, leading to...
The usual treatment for phenylketonuria (PKU) is a phenylalanine-restricted diet. Following this die...
The usual treatment for phenylketonuria (PKU) is a phenylalanine-restricted diet. Following this die...
Phenylketonuria (PKU) is caused by mutations in the phenylalanine hydroxylase (PAH) gene, leading to...
Background and objective: Untreated phenylketonuria is characterized by neurocognitive and neuromoto...
The usual treatment for phenylketonuria (PKU) is a phenylalanine-restricted diet. Following this die...
The usual treatment for phenylketonuria (PKU) is a phenylalanine-restricted diet. Following this die...
Background and objective: Untreated phenylketonuria is characterized by neurocognitive and neuromoto...
Phenylketonuria (PKU) is an inherited metabolic disease characterized by phenylalanine (Phe) accumul...
Phenylketonuria (PKU) is an inherited disorder of phenylalanine (Phe) metabolism. Until recently, th...
Hyperphenylalaninemia is caused by deficient enzyme activity of phenylalanine hydroxylase. It was on...