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Studies of blood and breast milk amino acid concentrations in mothers with abnormal phenylalanine metabolism

  • J. Hyánek
  • J. Kobilková
  • H. Viletová
  • V. Kunová
  • J. Smítková
  • M. Kubík
Short Communication

Keywords

Public Health Internal Medicine Metabolic Disease Acid Concentration Phenylalanine 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Güttler, F. and Hansen, G. Heterozygote detection in phenylketonuria.Clin. Genet. 11 (1977) 137–146PubMedGoogle Scholar
  2. Hyánek, J., Trnka, V., Viletová, H. and Kunová, V. Results of screening and dietetic treatment of PKU and HPA during pregnancy. In Bickel, H. (ed.)Maternal Phenylketonuria, Int. Workshop., Frankfurt/Main 1980Google Scholar
  3. Komrower, G. M., Sardharwalla, I. B. and Coutts, J. M. I. Management of maternal phenylketonuria: an emerging problem.Br. Med. J. 1 (1979) 1383–1387PubMedGoogle Scholar
  4. Pueschel, S. M. and Hum. C. Nutritional management of the female with phenylketonuria during pregnancy.Am. J. Clin. Nutr. 30 (1977) 1153–1161PubMedGoogle Scholar

Copyright information

© SSIEM and MTP Press Limited 1983

Authors and Affiliations

  • J. Hyánek
    • 1
  • J. Kobilková
    • 1
  • H. Viletová
    • 1
  • V. Kunová
    • 1
  • J. Smítková
    • 1
  • M. Kubík
    • 1
  1. 1.Diagnostic Centre of Inherited Metabolic Disorders and Obstetrics and Gynaecology Clinic, Medical FacultyCharles UniversityPragueCSSR

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