The Clinical Team Looks At Phenylketonuria : Problems of the Disease From the Viewpoint of the Biochemist, Pediatrician, Medical Social Worker, Public Health Nurse, Psychologist And Nutritionist

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He-ftor, F. A., et al: Termination of Dietary Treatment of Phenyl- ketonuria. New England Journal of Medicine, 266:79, 1962.
33. Kretchmer, N., and Etzwiler, D. D.: Disorders Associated with Metabolism of Phenylalanine and Tyrosine. Pediatrics, 21:445, 1958.
34. PKU. A Diet Guide for Parents of Children with Phenylketonuria, Prepared by the Bureau of Public Health Nutrition of the California State Department of Health, 1961.
35. Shaw, K. F., Koch, R., Schild, S., Fishier, K., and Ragsdale, N.:
...The Team Approach to Phenylketonuria. Published by the Childrens Bureau of the Department of Health, Education, and Welfare, Washington, D. C, 1961.
36. Umbarger, B.: Phenylketonuria - Treating the Disease and Feeding the Child. American Journal of Diseases of Children, 100:908, 1960.
37. Berman, P. W., Graham, F. K., Eichman, P. L., Waisman, H. A.: Psychologic and Neurologic Status of Diet-Treated Phenyl- ketonuric Children and Their Siblings. Pediatrics, 28:924, 1961.
- 20 FAMILY ATTITUDES AND THE LOW PHENYLALANINE DIET By Sylvia Schild, M.S.W.


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