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. 1961 May 6;84(18):985–991.

Observations on Phenylketonuria in Ontario

M W Partington
PMCID: PMC1939561  PMID: 13733038

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Selected References

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

  1. ARMSTRONG M. D., LOW N. L. Phenylketonuria VIII. Relation between age, serum phenylalanine level, and phenylpyruvic acid excretion. Proc Soc Exp Biol Med. 1957 Jan;94(1):142–146. doi: 10.3181/00379727-94-22880. [DOI] [PubMed] [Google Scholar]
  2. BERRY H. K., SUTHERLAND B., GUEST G. M., WARKANY J. Simple method for detection of phenylketonuria. J Am Med Assoc. 1958 Aug 30;167(18):2189–2190. doi: 10.1001/jama.1958.72990350004005a. [DOI] [PubMed] [Google Scholar]
  3. CENTERWALL W. R., CHINNOCK R. F., PUSAVAT A. Phenylketonuria: screening programs and testing methods. Am J Public Health Nations Health. 1960 Nov;50:1667–1677. doi: 10.2105/ajph.50.11.1667. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. COATES S., NORMAN A. P., WOOLF L. I. Phenylketonuria with normal intelligence and Gowers' muscular dystrophy. Arch Dis Child. 1957 Aug;32(164):313–317. doi: 10.1136/adc.32.164.313. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. DODGE P. R., MANCALL E., CRAWFORD J. D., KNAPP J., PAINE R. S. Hypoglycemia complicating treatment of phenylketonuria with a phenylalanine-deficient diet; report of two cases. N Engl J Med. 1959 May 28;260(22):1104–1111. doi: 10.1056/NEJM195905282602202. [DOI] [PubMed] [Google Scholar]
  6. GIBBS N. K., WOOLF L. I. Tests for phenylketonuria: results of a one-year programme for its detection in infancy and among mental defectives. Br Med J. 1959 Sep 26;2(5151):532–535. doi: 10.1136/bmj.2.5151.532. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. GIBSON R. Phenylketonuria; a survey of cases at the Manitoba School. Can Med Assoc J. 1956 Jun 1;74(11):897–900. [PMC free article] [PubMed] [Google Scholar]
  8. HASSEL C. W., Jr, BRUNSTING L. A. Phenylpyruvic oligophrenia; an evaluation of the light-sensitive and pigmentary characteristics of seventeen patients. AMA Arch Derm. 1959 Apr;79(4):458–465. doi: 10.1001/archderm.1959.01560160076010. [DOI] [PubMed] [Google Scholar]
  9. HSIA D. Y. Y. Phenylketonuria: the phenylalanine-tyrosine ratio in the detection of the heterozygous carrier. J Ment Defic Res. 1958 Jun;2(1):8–16. doi: 10.1111/j.1365-2788.1958.tb00380.x. [DOI] [PubMed] [Google Scholar]
  10. JERVIS G. A. Phenylpyruvic oligophrenia (phenylketonuria). Res Publ Assoc Res Nerv Ment Dis. 1954;33:259–282. [PubMed] [Google Scholar]
  11. KNOX W. E., HSIA D. Y. Pathogenetic problems in phenylketonuria. Am J Med. 1957 May;22(5):687–702. doi: 10.1016/0002-9343(57)90120-1. [DOI] [PubMed] [Google Scholar]
  12. PARTINGTON M. W. The early symptoms of phenylketonuria. Pediatrics. 1961 Mar;27:465–473. [PubMed] [Google Scholar]
  13. STADLER H. E., MEYER H., LELAND H. Phenylpyruvic oligophrenia in a mulatto; probable manifestation of the pleiotropic effect. J Nerv Ment Dis. 1956 Aug;124(2):205–207. doi: 10.1097/00005053-195608000-00011. [DOI] [PubMed] [Google Scholar]
  14. UDENFRIEND S., COOPER J. R. Assay of L-phenylalanine as phenylethylamine after enzymatic decarboxylation; application to isotopic studies. J Biol Chem. 1953 Aug;203(2):953–960. [PubMed] [Google Scholar]
  15. WRIGHT S. W., TARJAN G. Phenylketonuria. AMA J Dis Child. 1957 Apr;93(4):405–419. doi: 10.1001/archpedi.1957.02060040407009. [DOI] [PubMed] [Google Scholar]

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