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Selected References
These references are in PubMed. This may not be the complete list of references from this article.
- ALLAN J. D., CUSWORTH D. C., DENT C. E., WILSON V. K. A disease, probably hereditary characterised by severe mental deficiency and a constant gross abnormality of aminoacid metabolism. Lancet. 1958 Jan 25;1(7013):182–187. doi: 10.1016/s0140-6736(58)90666-4. [DOI] [PubMed] [Google Scholar]
- ARMSTRONG M. D., LOW N. L., BOSMA J. F. Studies on phenylketonuria. IX. Further observations on the effect of phenylalanine-restricted diet on patients with phenylketonuria. Am J Clin Nutr. 1957 Sep-Oct;5(5):543–554. doi: 10.1093/ajcn/5.5.543. [DOI] [PubMed] [Google Scholar]
- DANCIS J., LEVITZ M., MILLER S., WESTALL R. G. Maple syrup urine disease. Br Med J. 1959 Jan 10;1(5114):91–93. doi: 10.1136/bmj.1.5114.91. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DUSTIN J. P., MOORE S., BIGWOOD E. J. Chromatographic studies on the excretion of amino acids in early infancy. Metabolism. 1955 Jan;4(1):75–79. [PubMed] [Google Scholar]
- EADES C. H., Jr, POLLACK R. L., HARDY J. D. Thermal burns in man. IX. Urinary amino acid patterns. J Clin Invest. 1955 Dec;34(12):1756–1759. doi: 10.1172/JCI103230. [DOI] [PMC free article] [PubMed] [Google Scholar]
- FOWLER D. I., NORTON P. M., CHEUNG M. W., PRATT E. L. Observations on the urinary amino acid excretion in man; the influence of age and diet. Arch Biochem Biophys. 1957 Jun;68(2):452–466. doi: 10.1016/0003-9861(57)90376-4. [DOI] [PubMed] [Google Scholar]
- HURLEY K. E., WILLIAMS R. J. Urinary amino acids, creatinine and phosphate in muscular dystrophy. Arch Biochem Biophys. 1955 Feb;54(2):384–391. doi: 10.1016/0003-9861(55)90051-5. [DOI] [PubMed] [Google Scholar]
- JONXIS J. H., HUISMAN T. H. Amino aciduria and ascorbic acid deficiency. Pediatrics. 1954 Sep;14(3):238–244. [PubMed] [Google Scholar]
- LATHEM W., BAKER K., BRADLEY S. E. Urinary amino acid excretion in renal disease, with observations on the Fanconi syndrome. Am J Med. 1955 Feb;18(2):249–258. doi: 10.1016/0002-9343(55)90240-0. [DOI] [PubMed] [Google Scholar]
- Levine S. Z., Gordon H. H., Marples E. A DEFECT IN THE METABOLISM OF TYROSINE AND PHENYLALANINE IN PREMATURE INFANTS. II. SPONTANEOUS OCCURRENCE AND ERADICATION BY VITAMIN C. J Clin Invest. 1941 Mar;20(2):209–219. doi: 10.1172/JCI101213. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MACKENZIE D. Y., WOOLF L. I. Maple syrup urine disease; an inborn error of the metabolism of valine, leucine, and isoleucine associated with gross mental deficiency. Br Med J. 1959 Jan 10;1(5114):90–91. doi: 10.1136/bmj.1.5114.90. [DOI] [PMC free article] [PubMed] [Google Scholar]
- MENKES J. H., HURST P. L., CRAIG J. M. A new syndrome: progressive familial infantile cerebral dysfunction associated with an unusual urinary substance. Pediatrics. 1954 Nov;14(5):462–467. [PubMed] [Google Scholar]
- Medes G. A new error of tyrosine metabolism: tyrosinosis. The intermediary metabolism of tyrosine and phenylalanine. Biochem J. 1932;26(4):917–940. doi: 10.1042/bj0260917. [DOI] [PMC free article] [PubMed] [Google Scholar]
- NARDI G. L. Essential and nonessential amino acids in the urine of severely burned patients. J Clin Invest. 1954 Jun;33(6):847–854. doi: 10.1172/JCI102957. [DOI] [PMC free article] [PubMed] [Google Scholar]
- SHREEVE W. W., HUTCHIN M. E., HARPER H. A., MILLER C. D., DOOLAN P. D. Excretion of amino acids in nephrosis. Proc Soc Exp Biol Med. 1955 Apr;88(4):510–514. doi: 10.3181/00379727-88-21635. [DOI] [PubMed] [Google Scholar]
- WALLRAFF E. B., BRODIE E. C., BORDEN A. L. Urinary excretion of amino acids in pregnancy. J Clin Invest. 1950 Nov;29(11):1542–1544. doi: 10.1172/JCI102395. [DOI] [PMC free article] [PubMed] [Google Scholar]