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- ALLEN R. J., GIBSON R. M. Phenylketonuria with normal intelligence. Am J Dis Child. 1961 Jul;102:115–122. doi: 10.1001/archpedi.1961.02080010117019. [DOI] [PubMed] [Google Scholar]
- ARMSTRONG M. D., BINKLEY E. L., Jr Studies on phenylketonuria. V. Observations on a newborn infant with phenylketonuria. Proc Soc Exp Biol Med. 1956 Dec;93(3):418–420. doi: 10.3181/00379727-93-22775. [DOI] [PubMed] [Google Scholar]
- 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]
- CENTERWALL W. R., CENTERWALL S. A., ARMON V., MANN L. B. Phenylketonuria. II. Results of treatment of infants and young children. A report of 10 cases. J Pediatr. 1961 Jul;59:102–118. doi: 10.1016/s0022-3476(61)80217-5. [DOI] [PubMed] [Google Scholar]
- 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]
- COATES S. Results of treatment in phenylketonuria. Br Med J. 1961 Mar 18;1(5228):767–771. doi: 10.1136/bmj.1.5228.767. [DOI] [PMC free article] [PubMed] [Google Scholar]
- FUJIKI N., DREW A. L., MIYAKE M., NEMOTO H., SUJAKU C., SHIMADA T. A case of phenylketonuria in the Eta resulting from the mating of a homozygous father and a heterozygous mother. Am J Hum Genet. 1961 Mar;13:64–68. [PMC free article] [PubMed] [Google Scholar]
- HORNER F. A., STREAMER C. W. Phenylketonuria treated from earliest infancy; report of three cases. AMA J Dis Child. 1959 Mar;97(3):345–347. doi: 10.1001/archpedi.1959.02070010347014. [DOI] [PubMed] [Google Scholar]
- 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]
- HSIA D. Y., KNOX W. E., QUINN K. V., PAINE R. S. A one-year, controlled study of the effect of low-phenylalanine diet on phenylketonuria. Pediatrics. 1958 Feb;21(2):178–202. [PubMed] [Google Scholar]
- JERVIS G. A. Phenylpyruvic oligophrenia (phenylketonuria). Res Publ Assoc Res Nerv Ment Dis. 1954;33:259–282. [PubMed] [Google Scholar]
- KNOX W. E. An evaluation of the treatment of phenylketonuria with diets low in phenylalanine. Pediatrics. 1960 Jul;26:1–11. [PubMed] [Google Scholar]
- 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]
- PARTINGTON M. W. The early symptoms of phenylketonuria. Pediatrics. 1961 Mar;27:465–473. [PubMed] [Google Scholar]
- UDENFRIEND S., COOPER J. R. The chemical estimation of tyrosine and tyramine. J Biol Chem. 1952 May;196(1):227–233. [PubMed] [Google Scholar]
- WOOLF L. I., OUNSTED C., LEE D., HUMPHREY M., CHESHIRE N. M., STEED G. R. Atypical phenylketonuria in sisters with normal offspring. Lancet. 1961 Aug 26;2(7200):464–465. doi: 10.1016/s0140-6736(61)92434-5. [DOI] [PubMed] [Google Scholar]