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- ARMSTRONG M. D., ROBINSON K. S. On the excretion of indole derivatives in phenylketonuria. Arch Biochem Biophys. 1954 Sep;52(1):287–288. doi: 10.1016/0003-9861(54)90115-0. [DOI] [PubMed] [Google Scholar]
- ARMSTRONG M. D., TYLER F. H. Studies on phenylketonuria. I. Restricted phenylalanine intake in phenylketonuria. J Clin Invest. 1955 Apr;34(4):565–580. doi: 10.1172/JCI103105. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BERRY J. P., WOOLF L. I. Estimation of phenylpyruvic acid. Nature. 1952 Feb 2;169(4292):202–203. doi: 10.1038/169202a0. [DOI] [PubMed] [Google Scholar]
- BICKEL H., GERRARD J., HICKMANS E. M. Influence of phenylalanine intake on phenylketonuria. Lancet. 1953 Oct 17;265(6790):812–813. doi: 10.1016/s0140-6736(53)90473-5. [DOI] [PubMed] [Google Scholar]
- BLAINEY J. D., GULLIFORD R. Phenylalanine-restricted diets in the treatment of phenylketonuria. Arch Dis Child. 1956 Dec;31(160):452–466. doi: 10.1136/adc.31.160.452. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BLASCHKO H., DATTA S. P., HARRIS H. Pyridoxin deficiency in the rat; liver L-cysteic acid decarboxylase activity and urinary amino-acids. Br J Nutr. 1953;7(4):364–371. doi: 10.1079/bjn19530046. [DOI] [PubMed] [Google Scholar]
- BRAUDE H. Phenylketonuria; a case report in a European child treated with a diet low in phenylalanine. S Afr Med J. 1956 Jan 28;30(4):83–85. [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]
- COLLINS R. A., HARPER A. E., SCHREIBER M., ELVEHJEM C. A. The folic acid and vitamin B12 content of the milk of various species. J Nutr. 1951 Feb;43(2):313–321. doi: 10.1093/jn/43.2.313. [DOI] [PubMed] [Google Scholar]
- COWIE V. Phenylpyruvic oligophrenia. J Ment Sci. 1951 Jul;97(408):505–531. doi: 10.1192/bjp.97.408.505. [DOI] [PubMed] [Google Scholar]
- DANCIS J., BALIS M. E. A possible mechanism for disturbance in tyrosine metabolism in phenylpyruvic oligophrenia. Pediatrics. 1955 Jan;15(1):63–66. [PubMed] [Google Scholar]
- HORNER F. A., STREAMER C. W. Effect of a phenylalanine-restricted diet on patients with phenylketonuria; clinical observations in three cases. J Am Med Assoc. 1956 Aug 25;161(17):1628–1630. doi: 10.1001/jama.1956.62970170004005b. [DOI] [PubMed] [Google Scholar]
- MUNRO H. N., THOMSON W. S. Influence of glucose on amino acid metabolism. Metabolism. 1953 Jul;2(4):354–361. [PubMed] [Google Scholar]
- PARE C. M., SANDLER M., STACEY R. S. 5-Hydroxytryptamine deficiency in phenylketonuria. Lancet. 1957 Mar 16;272(6968):551–553. doi: 10.1016/s0140-6736(57)90920-0. [DOI] [PubMed] [Google Scholar]
- PENROSE L. S. Measurement of pleiotropic effects in phenylketonuria. Ann Eugen. 1951 Sep;16(2):134–141. doi: 10.1111/j.1469-1809.1951.tb02467.x. [DOI] [PubMed] [Google Scholar]
- WOLF H. Zur Behandlung des sogenannten Phenylbrenztraubensäure-Schwachsinns (Oligophrenia phenylpyruvica). Medizinische. 1956 Jun 16;(24):883–886. [PubMed] [Google Scholar]
- WOOLF L. I., VULLIAMY D. G. Phenylketonuria with a study of the effect upon it of glutamic acid. Arch Dis Child. 1951 Dec;26(130):487–494. doi: 10.1136/adc.26.130.487. [DOI] [PMC free article] [PubMed] [Google Scholar]