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. 1968 Apr;43(228):137–140. doi: 10.1136/adc.43.228.137

Mass screening of the newborn for metabolic disease.

L I Woolf
PMCID: PMC2019823  PMID: 5645685

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Selected References

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

  1. BERRY H. K. Use of micromethod for phenylalanine in management of phenylketonuric patients. Clin Chem. 1962 Apr;8:172–173. [PubMed] [Google Scholar]
  2. BEUTLER E., BALUDA M., DONNELL G. N. A NEW METHOD FOR THE DETECTION OF GALACTOXEMIA AND ITS CARRIER STATE. J Lab Clin Med. 1964 Oct;64:694–705. [PubMed] [Google Scholar]
  3. Berry H. K., Umbarger B., Sutherland B. S. Procedures for monitoring the low-phenylalanine diet in treatment of phenylketonuria. J Pediatr. 1965 Oct;67(4):609–616. doi: 10.1016/s0022-3476(65)80432-2. [DOI] [PubMed] [Google Scholar]
  4. Bessman S. P. Legislation and advances in medical knowledge--acceleration or inhibition? J Pediatr. 1966 Aug;69(2):334–338. doi: 10.1016/s0022-3476(66)80350-5. [DOI] [PubMed] [Google Scholar]
  5. CARTER C. O., WOOLF L. I. The birthplaces of parents and grandparents of a series of patients with phenylketonuria in in south-east England. Ann Hum Genet. 1961 May;25:57–64. doi: 10.1111/j.1469-1809.1961.tb01497.x. [DOI] [PubMed] [Google Scholar]
  6. Cahalane S. F. Phenylketonuria. Mass screening of newborns in Ireland. Arch Dis Child. 1968 Apr;43(228):141–144. doi: 10.1136/adc.43.228.141. [DOI] [PMC free article] [PubMed] [Google Scholar]
  7. Carson N. A., Carré I. J., Neill D. W. Results of routine screening for phenylketonuria in early infancy, Northern Ireland (1960-67). Arch Dis Child. 1968 Apr;43(228):145–146. doi: 10.1136/adc.43.228.145. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. EFRON M. L., YOUNG D., MOSER H. W., MACCREADY R. A. A SIMPLE CHROMATOGRAPHIC SCREENING TEST FOR THE DETECTION OF DISORDERS OF AMINO ACID METABOLISM. A TECHNIC USING WHOLE BLOOD OR URINE COLLECTED ON FILTER PAPER. N Engl J Med. 1964 Jun 25;270:1378–1383. doi: 10.1056/NEJM196406252702602. [DOI] [PubMed] [Google Scholar]
  9. 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]
  10. GUTHRIE R., SUSI A. A SIMPLE PHENYLALANINE METHOD FOR DETECTING PHENYLKETONURIA IN LARGE POPULATIONS OF NEWBORN INFANTS. Pediatrics. 1963 Sep;32:338–343. [PubMed] [Google Scholar]
  11. HILL J. B., SUMMER G. K., PENDER M. W., ROSZEL N. O. AN AUTOMATED PROCEDURE FOR BLOOD PHENYLALANINE. Clin Chem. 1965 May;11:541–546. [PubMed] [Google Scholar]
  12. Hsia D. Y. Phenylketonuria 1967. Dev Med Child Neurol. 1967 Oct;9(5):531–540. doi: 10.1111/j.1469-8749.1967.tb02321.x. [DOI] [PubMed] [Google Scholar]
  13. Justice P., O'Flynn M. E., Hsia D. Y. Phenylalanine-hydroxylase activity in hyperphenylalaninaemia. Lancet. 1967 Apr 29;1(7496):928–929. doi: 10.1016/s0140-6736(67)91490-0. [DOI] [PubMed] [Google Scholar]
  14. Mellon J. P., Stiven A. G. A rapid method for the detection of plasma phenylalanine. J Med Lab Technol. 1966 Jul;23(3):204–206. [PubMed] [Google Scholar]
  15. SCRIVER C. R., DAVIES E., CULLEN A. M. APPLICATION OF A SIMPLE MICROMETHOD TO THE SCREENING OF PLASMA FOR A VARIETY OF AMINOACIDOPATHIES. Lancet. 1964 Aug 1;2(7353):230–232. doi: 10.1016/s0140-6736(64)90183-7. [DOI] [PubMed] [Google Scholar]
  16. Scriver C. R. Diagnosis and treatment: interpreting the positive screening test in the newborn infant. Pediatrics. 1967 May;39(5):764–768. [PubMed] [Google Scholar]
  17. Searle B., Mijuskovic M. B., Widelock D., Davidow B. A manual fluorometric paper disc method for detecting phenylketonuria. Clin Chem. 1967 Aug;13(8):621–625. [PubMed] [Google Scholar]
  18. Stephenson J. B., McBean M. S. Diagnosis of phenylketonuria (phenylalanine hydroxylase deficiency, temporary and permanent). Br Med J. 1967 Sep 2;3(5565):579–581. doi: 10.1136/bmj.3.5565.579. [DOI] [PMC free article] [PubMed] [Google Scholar]

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