Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may benefit from BH4 therapy instead or in addition to the low-phenylalanine diet. Different loading test protocols are currently used to detect these patients. As a consequence, data on the rate of BH4-responsiveness within patients with mild phenylketonuria (PKU) and/or more severe phenotypes show high variation and a more sensitive and standardised BH4 loading test protocol needs to be defined. We modified the current standard BH4 loading test (20 mg/kg) to a second administration of 20 mg/kg after 24 h and extended blood sampling to 48 h in 24 patients with PAH deficiency. Using this extended loading test (2 x 20 mg BH4/kg), the rate of BH4-res...
Neonatal loading studies with tetrahydrobiopterin (BH4) are used to detect hyperphenylalaninemia due...
Background: How to efficiently diagnose tetrahydrobiopterin (BH4) responsiveness in patients with ph...
Phenylketonuria (PKU), is an autosomal recessive inborn error of metabolism, in most of cases (about...
Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may be...
Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may be...
BACKGROUND: The 24- and 48-hour tetrahydrobiopterin (BH4) loading test (BLT) performed at a minimum ...
BACKGROUND: The 24- and 48-hour tetrahydrobiopterin (BH4) loading test (BLT) performed at a minimum ...
BACKGROUND: The 24- and 48-hour tetrahydrobiopterin (BH4) loading test (BLT) performed at a minimum ...
Pharmacological levels of the phenylalanine hydroxylase enzyme cofactor, tetrahydrobiopterin (BH4), ...
Background: How to efficiently diagnose tetrahydrobiopterin (BH4) responsiveness in patients with ph...
BACKGROUND: Phenylketonuria (PKU) is an inborn error of phenylalanine (Phe) metabolism. Besides diet...
The oral loading test with tetrahydrobiopterin (BH4) is used to discriminate between variants of hyp...
INTRODUCTION: Pharmacological levels of the phenylalanine hydroxylase enzyme cofactor, tetrahydrobio...
Neonatal loading studies with tetrahydrobiopterin (BH4) are used to detect hyperphenylalaninemia due...
Neonatal loading studies with tetrahydrobiopterin (BH4) are used to detect hyperphenylalaninemia due...
Background: How to efficiently diagnose tetrahydrobiopterin (BH4) responsiveness in patients with ph...
Phenylketonuria (PKU), is an autosomal recessive inborn error of metabolism, in most of cases (about...
Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may be...
Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may be...
BACKGROUND: The 24- and 48-hour tetrahydrobiopterin (BH4) loading test (BLT) performed at a minimum ...
BACKGROUND: The 24- and 48-hour tetrahydrobiopterin (BH4) loading test (BLT) performed at a minimum ...
BACKGROUND: The 24- and 48-hour tetrahydrobiopterin (BH4) loading test (BLT) performed at a minimum ...
Pharmacological levels of the phenylalanine hydroxylase enzyme cofactor, tetrahydrobiopterin (BH4), ...
Background: How to efficiently diagnose tetrahydrobiopterin (BH4) responsiveness in patients with ph...
BACKGROUND: Phenylketonuria (PKU) is an inborn error of phenylalanine (Phe) metabolism. Besides diet...
The oral loading test with tetrahydrobiopterin (BH4) is used to discriminate between variants of hyp...
INTRODUCTION: Pharmacological levels of the phenylalanine hydroxylase enzyme cofactor, tetrahydrobio...
Neonatal loading studies with tetrahydrobiopterin (BH4) are used to detect hyperphenylalaninemia due...
Neonatal loading studies with tetrahydrobiopterin (BH4) are used to detect hyperphenylalaninemia due...
Background: How to efficiently diagnose tetrahydrobiopterin (BH4) responsiveness in patients with ph...
Phenylketonuria (PKU), is an autosomal recessive inborn error of metabolism, in most of cases (about...