IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes accumulation of phenylalanine (Phe) in blood and brain. Although early introduction of a Phe-restricted diet can prevent severe symptoms from developing, patients who are diagnosed and treated early still experience deficits in cognitive functioning indicating shortcomings of current treatment. In the search for new and/or additional treatment strategies, a specific nutrient combination (SNC) was postulated to improve brain function in PKU. In this study, a long-term dietary intervention with a low-Phe diet, a specific combination of nutrients designed to improve brain function, or both concepts together was investigated in male and female BT...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
"Phenylketonuria (PKU) is one of the most common inborn errors of metabolism and is due to a deficit...
Phenylketonuria treatment mainly consists of a phenylalanine-restricted diet but still results in su...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
Background Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction c...
BACKGROUND: Phenylketonuria treatment consists mainly of a Phe-restricted diet, which leads to subop...
Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be pre...
Many phenylketonuria (PKU) patients cannot adhere to the severe dietary restrictions as advised by t...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
"Phenylketonuria (PKU) is one of the most common inborn errors of metabolism and is due to a deficit...
Phenylketonuria treatment mainly consists of a phenylalanine-restricted diet but still results in su...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
Background Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction c...
BACKGROUND: Phenylketonuria treatment consists mainly of a Phe-restricted diet, which leads to subop...
Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be pre...
Many phenylketonuria (PKU) patients cannot adhere to the severe dietary restrictions as advised by t...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
"Phenylketonuria (PKU) is one of the most common inborn errors of metabolism and is due to a deficit...
Phenylketonuria treatment mainly consists of a phenylalanine-restricted diet but still results in su...