Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction could be prevented by dietary treatment. However, despite this effect, neuropsychological outcome in PKU still remains suboptimal and the phenylalanine-restricted diet is very demanding. To improve neuropsychological outcome and relieve the dietary restrictions for PKU patients, supplementation of large neutral amino acids (LNAA) is suggested as alternative treatment strategy that might correct all brain biochemical disturbances caused by high blood phenylalanine, and thereby improve neurocognitive functioning.As a proof-of-principle, this study aimed to investigate all hypothesized biochemical treatment objectives of LNAA supplementation (normalizing br...
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 is an inborn error of phenylalanine (Phe) metabolism diagnosed by newborn screening ...
Background Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction c...
BackgroundPhenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction co...
Background: Phenylketonuria treatment consists mainly of a Pherestricted diet, which leads to subopt...
Many phenylketonuria (PKU) patients cannot adhere to the severe dietary restrictions as advised by t...
Phenylketonuria treatment mainly consists of a phenylalanine-restricted diet but still results in su...
Notwithstanding the success of the traditional dietary phenylalanine restriction treatment in phenyl...
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...
BACKGROUND: Large neutral amino acid (LNAA) treatment has been suggested as alternative to the burde...
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 is an inborn error of phenylalanine (Phe) metabolism diagnosed by newborn screening ...
Background Phenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction c...
BackgroundPhenylketonuria (PKU) was the first disorder in which severe neurocognitive dysfunction co...
Background: Phenylketonuria treatment consists mainly of a Pherestricted diet, which leads to subopt...
Many phenylketonuria (PKU) patients cannot adhere to the severe dietary restrictions as advised by t...
Phenylketonuria treatment mainly consists of a phenylalanine-restricted diet but still results in su...
Notwithstanding the success of the traditional dietary phenylalanine restriction treatment in phenyl...
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...
BACKGROUND: Large neutral amino acid (LNAA) treatment has been suggested as alternative to the burde...
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 is an inborn error of phenylalanine (Phe) metabolism diagnosed by newborn screening ...