Lack of fetal effect on blood phenylalanine concentration in maternal phenylketonuria
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference14 articles.
1. Maternal phenylketonuria and hyperphenylalaninemia: An international survey of the outcome of untreated and treated pregnancies;Lenke;N Engl J Med,1980
2. Maternal phenylketonuria: Results of dietary therapy;Lenke;Am J Obstet Gynecol,1982
3. Diet, genetics and mental retardation: Interaction between phenylketonuric heterozygous, mother and fetus to produce nonspecific diminution of IQ. Evidence in support of the justification hypothesis;Bessman;Proc Natl Acad Sci USA,1978
4. Hepatic metabolism of phenylalanine during development;Kenney;J Clin Invest,1959
5. Phenylalanine hydroxylase in human liver during development;Räihä;Pediatr Res,1973
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1. Dietary management in pregnant Phenylketonuria (PKU) patients: comparison with protein and phenylalanine requirements in healthy pregnancies;2023-03-16
2. The Impact of the Quality of Nutrition and Lifestyle in the Reproductive Years of Women with PKU on the Long-Term Health of Their Children;Nutrients;2022-02-28
3. The complete European guidelines on phenylketonuria: diagnosis and treatment;Orphanet Journal of Rare Diseases;2017-10-12
4. Phenylketonuria: tyrosine supplementation in phenylalanine-restricted diets;The American Journal of Clinical Nutrition;2001-02-01
5. Neurological Implications of the Genetic Mouse Models for Human Phenylketonuria and Hyperphenylalaninemia;Mouse Models in the Study of Genetic Neurological Disorders;1999
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