48 Homozygous wild-types (WT, +/+) and 96 PKU BTBRPah2 (-/-) male and female mice started dietary treatment on postnatal day 31 up to 10 months of age in the following six groups: WT control diet (WT C-HP), WT normal diet plus specific nutrient combination (WT SNC-HP), PKU normal diet (PKU C-HP), PKU normal diet plus specific nutrient combination (PKU SNC-HP), PKU low-Phe diet (PKU C-LP), and PKU low-Phe diet plus specific nutrient combination (PKU SNC-LP). Mice were tested three times (4,7, and 10 months) after treatment initiation during four behavioural tasks: open field (OF), novel object recognition task (NOR), spatial object recognition task (SOR), and balance beam task (BB). The results are stored in three zipped folders: Measurement...
Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be pre...
Phenylketonuria (PKU) is an inborn error of metabolism caused by a deficiency in functional phenylal...
"Phenylketonuria (PKU) is one of the most common inborn errors of metabolism and is due to a deficit...
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...
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...
Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenyla...
Background Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction c...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenyla...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be pre...
Phenylketonuria (PKU) is an inborn error of metabolism caused by a deficiency in functional phenylal...
"Phenylketonuria (PKU) is one of the most common inborn errors of metabolism and is due to a deficit...
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...
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...
Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenyla...
Background Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction c...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
Phenylketonuria (PKU) is one of the most common human inborn errors of metabolism, caused by phenyla...
The inherited metabolic disease phenylketonuria (PKU) is characterized by increased concentrations o...
Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be pre...
Phenylketonuria (PKU) is an inborn error of metabolism caused by a deficiency in functional phenylal...
"Phenylketonuria (PKU) is one of the most common inborn errors of metabolism and is due to a deficit...