BACKGROUND: The 24- and 48-hour tetrahydrobiopterin (BH4) loading test (BLT) performed at a minimum baseline phenylalanine concentration of 400 mumol/l is commonly used to test phenylketonuria patients for BH4 responsiveness. This study aimed to analyze differences between the 24- and 48-hour BLT and the necessity of the 400 mumol/l minimum baseline phenylalanine concentration. METHODS: Data on 186 phenylketonuria patients were collected. Patients were supplemented with phenylalanine if phenylalanine was /= 30% reduction in phenylalanine concentration at >/= 1 time point. RESULTS: Eighty-six (46.2%) patients were responsive. Among responders 84% showed a >/= 30% response at T = 48. Fifty-three percent had their maximal decrease at T = 48. F...
Background: How to efficiently diagnose tetrahydrobiopterin (BH4) responsiveness in patients with ph...
The oral loading test with tetrahydrobiopterin (BH4) is used to discriminate between variants of hyp...
Phenylketonuria (PKU), is an autosomal recessive inborn error of metabolism, in most of cases (about...
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 ...
Item does not contain fulltextBACKGROUND: The 24- and 48-hour tetrahydrobiopterin (BH4) loading test...
Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may be...
Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may be...
Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may be...
BACKGROUND: Phenylketonuria (PKU) is an inborn error of phenylalanine (Phe) metabolism. Besides diet...
Background: How to efficiently diagnose tetrahydrobiopterin (BH4) responsiveness in patients with ph...
Pharmacological levels of the phenylalanine hydroxylase enzyme cofactor, tetrahydrobiopterin (BH4), ...
Background: It is unknown whether the neonatal tetrahydrobiopterin (BH4) loading test is adequate to...
INTRODUCTION: Pharmacological levels of the phenylalanine hydroxylase enzyme cofactor, tetrahydrobio...
BACKGROUND: It is unknown whether the neonatal tetrahydrobiopterin (BH4) loading test is adequate to...
Background: How to efficiently diagnose tetrahydrobiopterin (BH4) responsiveness in patients with ph...
The oral loading test with tetrahydrobiopterin (BH4) is used to discriminate between variants of hyp...
Phenylketonuria (PKU), is an autosomal recessive inborn error of metabolism, in most of cases (about...
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 ...
Item does not contain fulltextBACKGROUND: The 24- and 48-hour tetrahydrobiopterin (BH4) loading test...
Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may be...
Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may be...
Patients with tetrahydrobiopterin (BH4)-responsive phenylalanine hydroxylase (PAH) deficiency may be...
BACKGROUND: Phenylketonuria (PKU) is an inborn error of phenylalanine (Phe) metabolism. Besides diet...
Background: How to efficiently diagnose tetrahydrobiopterin (BH4) responsiveness in patients with ph...
Pharmacological levels of the phenylalanine hydroxylase enzyme cofactor, tetrahydrobiopterin (BH4), ...
Background: It is unknown whether the neonatal tetrahydrobiopterin (BH4) loading test is adequate to...
INTRODUCTION: Pharmacological levels of the phenylalanine hydroxylase enzyme cofactor, tetrahydrobio...
BACKGROUND: It is unknown whether the neonatal tetrahydrobiopterin (BH4) loading test is adequate to...
Background: How to efficiently diagnose tetrahydrobiopterin (BH4) responsiveness in patients with ph...
The oral loading test with tetrahydrobiopterin (BH4) is used to discriminate between variants of hyp...
Phenylketonuria (PKU), is an autosomal recessive inborn error of metabolism, in most of cases (about...