OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an approved drug for the treatment of patients with BH4-responsive phenylketonuria (PKU). The purpose of this study was to assess genotypes and data on the long-term effects of BH4/sapropterin on metabolic control and patient-related outcomes in 6 large European countries.METHODS: A questionnaire was developed to assess phenotype, genotype, blood phenylalanine (Phe) levels, Phe tolerance, quality of life, mood changes, and adherence to diet in PKU patients from 16 medical centers.RESULTS: One hundred forty-seven patients, of whom 41.9% had mild hyperphenylalaninemia, 50.7% mild PKU, and 7.4% classic PKU, were followed up overCONCLUSIONS: Our data ...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
In a Phase I study, 20% of subjects with phenylketonuria (96/485) responded with a = 30% reduction i...
Phenylketonuria (PKU) is caused by mutations in the phenylalanine hydroxylase (PAH) gene, leading to...
OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an ap...
OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an ap...
OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an ap...
OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an a...
OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an ap...
Background: Sapropterin/BH4 is an approved drug for treatment of responsive PKU patients. The purpos...
Background: Phenylketonuria (PKU) is an autosomal recessive disorder caused by the deficiency of phe...
Background: Phenylketonuria (PKU) is an autosomal recessive disorder caused by the deficiency of phe...
Phenylketonuria (PKU) is an inherited metabolic disease characterized by phenylalanine (Phe) accumul...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
PubMedID: 28593914Background: Phenylketonuria (PKU) often requires a lifelong phenylalanine (Phe)-re...
Phenylketonuria (PKU) is caused by mutations in the phenylalanine hydroxylase (PAH) gene, leading to...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
In a Phase I study, 20% of subjects with phenylketonuria (96/485) responded with a = 30% reduction i...
Phenylketonuria (PKU) is caused by mutations in the phenylalanine hydroxylase (PAH) gene, leading to...
OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an ap...
OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an ap...
OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an ap...
OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an a...
OBJECTIVE: Sapropterin dihydrochloride, the synthetic form of 6R-tetrahydrobiopterin (BH4), is an ap...
Background: Sapropterin/BH4 is an approved drug for treatment of responsive PKU patients. The purpos...
Background: Phenylketonuria (PKU) is an autosomal recessive disorder caused by the deficiency of phe...
Background: Phenylketonuria (PKU) is an autosomal recessive disorder caused by the deficiency of phe...
Phenylketonuria (PKU) is an inherited metabolic disease characterized by phenylalanine (Phe) accumul...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
PubMedID: 28593914Background: Phenylketonuria (PKU) often requires a lifelong phenylalanine (Phe)-re...
Phenylketonuria (PKU) is caused by mutations in the phenylalanine hydroxylase (PAH) gene, leading to...
Background: Phenylketonuria (PKU) is a rare inborn error of metabolism caused by phenylalanine hydro...
In a Phase I study, 20% of subjects with phenylketonuria (96/485) responded with a = 30% reduction i...
Phenylketonuria (PKU) is caused by mutations in the phenylalanine hydroxylase (PAH) gene, leading to...