Phenylketonuria due to a deficiency of dihydropteridine reductase.

Phenylalanine has no effect on dihydropteridine reductase activity in phenylketonuria fibroblasts.

Insertion of an extra codon for threonine is a cause of dihydropteridine reductase deficiency.

Clinical characteristics of epileptic seizures in a case of dihydropteridine reductase deficiency.

Adverse effects of trimethoprim-sulfamethoxazole in a child with dihydropteridine reductase deficiency.

Production of antibodies to sheep liver dihydropteridine reductase: characterization and use to study the enzyme defect in a variant form of phenylketonuria.

Hyperphenylalaninemia due to a deficiency of biopterin. A variant form of phenylketonuria.

Crystal structure of rat liver dihydropteridine reductase.

Dihydropteridine reductase from Escherichia coli exhibits dihydrofolate reductase activity.

Atypical (mild) forms of dihydropteridine reductase deficiency: neurochemical evaluation and mutation detection.

Dihydropteridine reductase may function in tetrahydrofolate metabolism.

Male pseudohermaphroditism due to testicular 17-ketosteroid reductase deficiency.

QDPR gene mutation and clinical follow-up in Chinese patients with dihydropteridine reductase deficiency.

Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic fluid cells.

A new enzyme, NADPH-dihydropteridine reductase in bovine liver.

Isolation and characterization of dihydropteridine reductase from Pseudomonas species.

Morphologic studies in a patient with homocystinuria due to 5, 10-methylenetetrahydrofolate reductase deficiency.

Dihydropteridine reductase from bovine liver. Purification, crystallization, and isolation of a binary complex with NADH.

Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment.

Tetrahydrobiopterin therapy of atypical phenylketonuria due to defective dihydrobiopterin biosynthesis.

Congenital methemoglobinemia due to methemoglobin reductase deficiency in two unrelated American black families.

A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiency.

Failures Due to Language Deficiency.

Atypical PKU with normal phenylalanine hydroxylase and dihydropteridine reductase activity in vitro.

West syndrome due to vitamin B12 deficiency.

Suggest Documents

Phenylalanine has no effect on dihydropteridine reductase activity in phenylketonuria fibroblasts.

Insertion of an extra codon for threonine is a cause of dihydropteridine reductase deficiency.

Clinical characteristics of epileptic seizures in a case of dihydropteridine reductase deficiency.

Adverse effects of trimethoprim-sulfamethoxazole in a child with dihydropteridine reductase deficiency.

Production of antibodies to sheep liver dihydropteridine reductase: characterization and use to study the enzyme defect in a variant form of phenylketonuria.

Hyperphenylalaninemia due to a deficiency of biopterin. A variant form of phenylketonuria.

Crystal structure of rat liver dihydropteridine reductase.

Dihydropteridine reductase from Escherichia coli exhibits dihydrofolate reductase activity.

Atypical (mild) forms of dihydropteridine reductase deficiency: neurochemical evaluation and mutation detection.

Dihydropteridine reductase may function in tetrahydrofolate metabolism.

Male pseudohermaphroditism due to testicular 17-ketosteroid reductase deficiency.

QDPR gene mutation and clinical follow-up in Chinese patients with dihydropteridine reductase deficiency.

Hyperphenylalaninemia due to dihydropteridine reductase deficiency. Assay of the enzyme in fibroblasts from affected infants, heterozygotes, and in normal amniotic fluid cells.

A new enzyme, NADPH-dihydropteridine reductase in bovine liver.

Isolation and characterization of dihydropteridine reductase from Pseudomonas species.

Morphologic studies in a patient with homocystinuria due to 5, 10-methylenetetrahydrofolate reductase deficiency.

Dihydropteridine reductase from bovine liver. Purification, crystallization, and isolation of a binary complex with NADH.

Familial hyperlysinaemia due to L-lysine alpha-ketoglutarate reductase deficiency: results of attempted treatment.

Tetrahydrobiopterin therapy of atypical phenylketonuria due to defective dihydrobiopterin biosynthesis.

Congenital methemoglobinemia due to methemoglobin reductase deficiency in two unrelated American black families.

A peroxisomal disorder of severe intellectual disability, epilepsy, and cataracts due to fatty acyl-CoA reductase 1 deficiency.

Failures Due to Language Deficiency.

Atypical PKU with normal phenylalanine hydroxylase and dihydropteridine reductase activity in vitro.

West syndrome due to vitamin B12 deficiency.

Phenylketonuria due to a deficiency of dihydropteridine reductase.

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