Skip to main content
The Journal of Clinical Investigation logoLink to The Journal of Clinical Investigation
. 1955 Apr;34(4):565–580. doi: 10.1172/JCI103105

STUDIES ON PHENYLKETONURIA. I. RESTRICTED PHENYLALANINE INTAKE IN PHENYLKETONURIA 1

Marvin D Armstrong 1,2, Frank H Tyler 1,2
PMCID: PMC438662  PMID: 14367510

Full text

PDF
565

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. ARMSTRONG M. D., LEWIS J. D. The toxicity of o- and p-fluorophenyl-DL-alanines for the rat. J Biol Chem. 1951 Jan;188(1):91–95. [PubMed] [Google Scholar]
  2. ARMSTRONG M. D., ROBINSON K. S. On the excretion of indole derivatives in phenylketonuria. Arch Biochem Biophys. 1954 Sep;52(1):287–288. doi: 10.1016/0003-9861(54)90115-0. [DOI] [PubMed] [Google Scholar]
  3. BICKEL H., GERRARD J., HICKMANS E. M. The influence of phenylalanine intake on the chemistry and behaviour of a phenyl-ketonuric child. Acta Paediatr. 1954 Jan;43(1):64–77. doi: 10.1111/j.1651-2227.1954.tb04000.x. [DOI] [PubMed] [Google Scholar]
  4. BOREK E., BRECHER A., JERVIS G. A., WAELSCH H. Oligophrenia phenylpyruvica. II. Constancy of the metabolic error. Proc Soc Exp Biol Med. 1950 Oct;75(1):86–89. doi: 10.3181/00379727-75-18109. [DOI] [PubMed] [Google Scholar]
  5. BOSCOTT R. J., BICKEL H. Detection of some new abnormal metabolites in the urine of phenylketonuria. Scand J Clin Lab Invest. 1953;5(4):380–382. doi: 10.3109/00365515309094216. [DOI] [PubMed] [Google Scholar]
  6. HARPER H. A., HUTCHIN M. E., KIMMEL J. R. Concentrations of ninteen amino acids in plasma and urine of fasting normal males. Proc Soc Exp Biol Med. 1952 Aug-Sep;80(4):768–771. doi: 10.3181/00379727-80-19757. [DOI] [PubMed] [Google Scholar]
  7. JERVIS G. A. Excretion of phenylalanine and derivatives in phenylpyruvic oligophrenia. Proc Soc Exp Biol Med. 1950 Oct;75(1):83–86. doi: 10.3181/00379727-75-18108. [DOI] [PubMed] [Google Scholar]
  8. JERVIS G. A. Phenylpyruvic oligophrenia deficiency of phenylalanine-oxidizing system. Proc Soc Exp Biol Med. 1953 Mar;82(3):514–515. [PubMed] [Google Scholar]
  9. JERVIS G. A. Studies on phenylpyruvic oligophrenia; phenylpyruvic acid content on blood. Proc Soc Exp Biol Med. 1952 Dec;81(3):715–720. doi: 10.3181/00379727-81-19998. [DOI] [PubMed] [Google Scholar]
  10. Penrose L., Quastel J. H. Metabolic studies in phenylketonuria. Biochem J. 1937 Feb;31(2):266–274. doi: 10.1042/bj0310266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. RIMINGTON C. Diet and inborn errors of metabolism. Br J Nutr. 1950;4(2-3):242–252. doi: 10.1079/bjn19500040. [DOI] [PubMed] [Google Scholar]
  12. WOOLF L. I., VULLIAMY D. G. Phenylketonuria with a study of the effect upon it of glutamic acid. Arch Dis Child. 1951 Dec;26(130):487–494. doi: 10.1136/adc.26.130.487. [DOI] [PMC free article] [PubMed] [Google Scholar]

Articles from Journal of Clinical Investigation are provided here courtesy of American Society for Clinical Investigation

RESOURCES