Large neutral amino acids (LNAA) have been used on a limited number of patients with phenylketonuria (PKU) with the purpose of decreasing the influx of phenylalanine (Phe) to the brain. In an open-label study using LNAA, a surprising decline of blood Phe concentration was found in patients with PKU in metabolic treatment centres in Russia, the Ukraine, and the United States. To validate the data obtained from this trial, a short-term double-blind placebo control study was done using LNAA in patients with PKU, with the participation of three additional metabolic centres Milan, Padua and Rio de Janeiro. The results of the short trial showed significant lowering of blood Phe concentration by an average of 39% from baseline. The data from the d...
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...
Phenylketonuria (PKU) is a rare metabolic disorder characterized by impaired conversion of phenylala...
Large neutral amino acids (LNAA) have been used on a limited number of patients with phenylketonuria...
Click on the DOI link to access the article (may not be free).Large neutral amino acids (LNAAs) have...
Notwithstanding the success of the traditional dietary phenylalanine restriction treatment in phenyl...
Purpose: Phenylketonuria (PKU) is an inherited metabolic disease caused by low levels of the enzyme ...
Phenylketonuria (PKU) is an autosomal recessive disease caused by deficient activity of phenylalanin...
Controversies exist on the role of tyrosine in the pathogenesis of phenylketonuria (PKU) and, conseq...
Controversies exist on the role of tyrosine in the pathogenesis of phenylketonuria (PKU) and, conseq...
Objective: To determine the effects of large neutral amino acid (LNAA) supplements on brain and plas...
Phenylketonuria is an inborn error of phenylalanine (Phe) metabolism diagnosed by newborn screening ...
The mainstay of phenylketonuria treatment is a low protein diet, supplemented with phenylalanine (Ph...
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...
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...
Phenylketonuria (PKU) is a rare metabolic disorder characterized by impaired conversion of phenylala...
Large neutral amino acids (LNAA) have been used on a limited number of patients with phenylketonuria...
Click on the DOI link to access the article (may not be free).Large neutral amino acids (LNAAs) have...
Notwithstanding the success of the traditional dietary phenylalanine restriction treatment in phenyl...
Purpose: Phenylketonuria (PKU) is an inherited metabolic disease caused by low levels of the enzyme ...
Phenylketonuria (PKU) is an autosomal recessive disease caused by deficient activity of phenylalanin...
Controversies exist on the role of tyrosine in the pathogenesis of phenylketonuria (PKU) and, conseq...
Controversies exist on the role of tyrosine in the pathogenesis of phenylketonuria (PKU) and, conseq...
Objective: To determine the effects of large neutral amino acid (LNAA) supplements on brain and plas...
Phenylketonuria is an inborn error of phenylalanine (Phe) metabolism diagnosed by newborn screening ...
The mainstay of phenylketonuria treatment is a low protein diet, supplemented with phenylalanine (Ph...
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...
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...
Phenylketonuria (PKU) is a rare metabolic disorder characterized by impaired conversion of phenylala...