Full text
PDF



Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- BERRY H. K. Use of micromethod for phenylalanine in management of phenylketonuric patients. Clin Chem. 1962 Apr;8:172–173. [PubMed] [Google Scholar]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
- 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]
