Many phenylketonuria (PKU) patients cannot adhere to the severe dietary restrictions as advised by the European PKU guidelines, which can be accompanied by aggravated neuropsychological impairments that, at least in part, have been attributed to brain monoaminergic neurotransmitter deficiencies. Supplementation of large neutral amino acids (LNAA) to an unrestricted diet has previously been shown to effectively improve brain monoamines in PKU mice of various ages. To determine the additive value of LNAA supplementation to a liberalized phenylalanine-restricted diet, brain and plasma monoamine and amino acid concentrations in 10 to 16-month-old adult C57Bl/6 PKU mice on a less severe phenylalanine-restricted diet with LNAA supplementation wer...
Phenylketonuria is an inborn error of phenylalanine (Phe) metabolism diagnosed by newborn screening ...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
Phenylketonuria treatment mainly consists of a phenylalanine-restricted diet but still results in su...
Many phenylketonuria (PKU) patients cannot adhere to the severe dietary restrictions as advised by t...
Many phenylketonuria (PKU) patients cannot adhere to the severe dietary restrictions as advised by t...
Background Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction c...
Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be pre...
Phenylketonuria treatment mainly consists of a phenylalanine-restricted diet but still results in su...
BACKGROUND: Phenylketonuria treatment consists mainly of a Phe-restricted diet, which leads to subop...
BackgroundPhenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction co...
Notwithstanding the success of the traditional dietary phenylalanine restriction treatment in phenyl...
BACKGROUND: Large neutral amino acid (LNAA) treatment has been suggested as alternative to the burde...
Phenylketonuria is an inborn error of phenylalanine (Phe) metabolism diagnosed by newborn screening ...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
Phenylketonuria treatment mainly consists of a phenylalanine-restricted diet but still results in su...
Many phenylketonuria (PKU) patients cannot adhere to the severe dietary restrictions as advised by t...
Many phenylketonuria (PKU) patients cannot adhere to the severe dietary restrictions as advised by t...
Background Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction c...
Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be pre...
Phenylketonuria treatment mainly consists of a phenylalanine-restricted diet but still results in su...
BACKGROUND: Phenylketonuria treatment consists mainly of a Phe-restricted diet, which leads to subop...
BackgroundPhenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction co...
Notwithstanding the success of the traditional dietary phenylalanine restriction treatment in phenyl...
BACKGROUND: Large neutral amino acid (LNAA) treatment has been suggested as alternative to the burde...
Phenylketonuria is an inborn error of phenylalanine (Phe) metabolism diagnosed by newborn screening ...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...
IntroductionIn phenylketonuria (PKU), a gene mutation in the phenylalanine metabolic pathway causes ...