Outcome of pregnancy in the rat with mild hyperphenylalaninaemia and hypertyrosinaemia: Implications for the management of “human maternal PKU”
Author:
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/BF01819292
Reference15 articles.
1. Anderson, V.E. and Guroff, G. Enduring behavioural changes in rats with experimental phenylketonuria.Proc. Natl. Acad. Sci. USA 69 (1972) 863–867
2. Anderson, V. E. and Siegel, F. S. Behavioural and biochemical correlates of diet change in phenylketonuria.Pediatr. Res. 10 (1976) 10–17
3. Cloninger, M. R. and Baldwin, R. E. Aspartylphenylalanine methyl ester: A low calorie sweetner.Science 170 (1970) 81–82
4. Delvalle, J. A., Dienel, G. and Greengard, O. Comparison of α-methylphenylalanine andp-chlorophenylalanine as inducers of chronic hyperphenylalaninaemia in developing rats.Biochem. J. 170 (1978) 449–459
5. Delvalle, J. A. and Greengard, O. Phenylalanine hydroxlase and tyrosine aminotransferase in human fetal and adult liver.Pediatr. Res. 11 (1977) 2
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2. The complete European guidelines on phenylketonuria: diagnosis and treatment;Orphanet Journal of Rare Diseases;2017-10-12
3. Maternal and fetal tyrosinemia type I;Journal of Inherited Metabolic Disease;2010-12
4. Phenylketonuria: tyrosine supplementation in phenylalanine-restricted diets;The American Journal of Clinical Nutrition;2001-02-01
5. Large daily fluctuations in plasma tyrosine in treated patients with phenylketonuria;The American Journal of Clinical Nutrition;1996-12-01
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