Invited reviewMaternal phenylketonuria (PKU) — A review
References (65)
Studies on phenylpyruvic oligophrenia. The position of the metabolic error
J Biol Chem
(1947)- et al.
The enzymatic conversion of phenylalanine to tyrosine
J Biol Chem
(1952) - et al.
A third allele at the phenylalanine-hydroxylase locus in mild phenylketonuria (hyperphenylalaninemia)
Lancet
(1968) - et al.
Phenylketonuria: Mental development behavior and termination of low phenylalanine diet
J Pediatr
(1968) - et al.
Preliminary report on the effect of diet discontinuation in PKU
Pediatrics
(1982) - et al.
Development changes in amino acid concentrations in human amniotic fluid
Am J Obstet Gynecol
(1971) - et al.
Maternal phenylketonuria. Results of dietary therapy
Am J Obstet Gynecol
(1982) - et al.
Maternal hyperphenylalaninemia fetal effects
J Pediatr
(1984) Maternal nutrition in pregnancy and later achievement of offspring: a personal interpretation
Early Human Dev
(1985)- et al.
Amniotic fluid infections in an African city
J Pediatr
(1977)
Maternal phenylketonuria
Lancet
(1979)
Uber Ausscheidung von Phenbrenztraubensaute in den Harn als Stoffwechselanomalie in verbindug mit imbezillitat
Hoppe Seyler Z Physiol Chem
(1934)
Prenatal diagnosis and carrier detection of classical phenylketonuria by gene analysis
Pediatrics
(1984)
The influence of phenylalanine intake on the chemistry and behaviour of a phenylketonuric child
Acta Pediatr Scand
(1954)
Treatment of phenylketonuria with a diet low in phenylalanine
Br Med J
(1955)
A simple phenylalanine method for detecting phenylketonuria in large populations of newborn infants
Pediatrics
(1963)
Phenylalanine
Atypical phenylketonuria. An approach to diagnosis and management
Arch Dis Child
(1970)
Different phenotypes for phenylalanine hydroxylase deficiency
Ann Clin Biochem
(1977)
Hyperphenylaninemia without phenylketonuria
Am J Dis Child
(1967)
The early treatment of phenylketonuria
Am J Dis Child
(1967)
Phenylalaninaemia. Differential diagnosis
Arch Dis Child
(1974)
Phenylalaninemia and phenylketonuria
Atypical phenylketonuria accompanied by a severe progressive neurological illness unresponsive to dietary treatment
Arch Dis Child
(1974)
A new molecular defect in phenylketonuria
Lancet
(1974)
Phenylketonuria due to a deficiency of dihydropteridine reductase
N Engl J Med
(1975)
Tetrahydrobiopterin therapy for hyperphenylalaninemia caused by defective synthesis of tetrahydrobiopterin
Ann Neurol
(1983)
Correlates of intelligence test results in treated phenylketonuric children
Pediatrics
(1981)
Effect of age at loss of dietary control on intellectual performance and behavior in children with phenylketonuria
N Engl J Med
(1986)
Projections of mental retardation from PKU
Pediatr Res
(1979)
Projections of a rebound in frequency of mental retardation from phenylketonuria
Appl Res Ment Retard
(1982)
Discussion of Armstrong MD. Relation of biochemical abnormality to development of mental defect in phenylketonuria
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Copyright © 1987 Published by Elsevier Inc.