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. 1968 May 11;2(5601):367. doi: 10.1136/bmj.2.5601.367

Phenylketonuria.

H Hansen
PMCID: PMC1985593  PMID: 5648984

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Page 367

367

Selected References

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

  1. Brown E. S., Waisman H. A. Intelligence of the unidentified phenylketonuric child. Pediatrics. 1967 Aug;40(2):247–249. [PubMed] [Google Scholar]
  2. Castells S., LaCamera R. G., Wessel M. A., Brandt I. K. Transient hyperphenylalaninemia. J Pediatr. 1968 Apr;72(4):530–533. doi: 10.1016/s0022-3476(68)80345-2. [DOI] [PubMed] [Google Scholar]
  3. O'Flynn M. E., Hsia D. Some observations on the dietary treatment of phenylketonuria. J Pediatr. 1968 Feb;72(2):260–262. doi: 10.1016/s0022-3476(68)80320-8. [DOI] [PubMed] [Google Scholar]
  4. Solomons G., Keleske L., Opitz E. Evaluation of the effects of terminating the diet in phenylketonuria. J Pediatr. 1966 Oct;69(4):596–602. doi: 10.1016/s0022-3476(66)80046-x. [DOI] [PubMed] [Google Scholar]
  5. 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]

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