The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations of phenylalanine in the blood and brain, and as a consequence neurotransmitter metabolism, white matter, and synapse functioning are affected. A specific nutrient combination (SNC) has been shown to improve synapse formation, morphology and function. This could become an interesting new nutritional approach for PKU. To assess whether treatment with SNC can affect synapses, we treated PKU mice with SNC or an isocaloric control diet and wild-type (WT) mice with an isocaloric control for 12 weeks, starting at postnatal day 31. Immunostaining for post-synaptic density protein 95 (PSD-95), a post-synaptic density marker, was carried out in the hipp...
48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary tr...
Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be pre...
In humans, lack of phenylalanine hydroxylase (Pah) activity results in phenylketonuria (PKU), which ...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
BACKGROUND: Phenylketonuria treatment consists mainly of a Phe-restricted diet, which leads to subop...
Background Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction c...
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...
Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be pre...
In humans, lack of phenylalanine hydroxylase (Pah) activity results in phenylketonuria (PKU), which ...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
BACKGROUND: Phenylketonuria treatment consists mainly of a Phe-restricted diet, which leads to subop...
Background Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction c...
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...
Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be pre...
In humans, lack of phenylalanine hydroxylase (Pah) activity results in phenylketonuria (PKU), which ...