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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]
- ARROW V. K., WESTALL R. G. Amino acid clearances in cystinuria. J Physiol. 1958 Jun 18;142(1):141–146. doi: 10.1113/jphysiol.1958.sp006004. [DOI] [PMC free article] [PubMed] [Google Scholar]
- BARON D. N., DENT C. E., HARRIS H., HART E. W., JEPSON J. B. Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria, and other bizarre biochemical features. Lancet. 1956 Sep 1;271(6940):421–428. doi: 10.1016/s0140-6736(56)91914-6. [DOI] [PubMed] [Google Scholar]
- BARRETT A. M., FAIRWEATHER D. V., MCCANCE R. A., MORRISON A. B. Genetic, clinical, biochemical, and pathological features of hypophosphatasia; based on the study of a family. Q J Med. 1956 Oct;25(100):523–537. [PubMed] [Google Scholar]
- BICKEL H., SMELLIE J. M. Cystine storage disease with amino-aciduria. Lancet. 1952 May 31;1(6718):1093–1095. doi: 10.1016/s0140-6736(52)90750-2. [DOI] [PubMed] [Google Scholar]
- Berenblum I., Chain E. An improved method for the colorimetric determination of phosphate. Biochem J. 1938 Feb;32(2):295–298. doi: 10.1042/bj0320295. [DOI] [PMC free article] [PubMed] [Google Scholar]
- CRUMPLER H. R., DENT C. E., HARRIS H., WESTALL R. G. beta-Aminoisobutyric acid (alpha-methyl-beta-alanine); a new amino-acid obtained from human urine. Nature. 1951 Feb 24;167(4243):307–308. doi: 10.1038/167307a0. [DOI] [PubMed] [Google Scholar]
- CUSWORTH D. C. The isolation and identification of phosphoethanolamine from the urine of a case of hypophosphatasia. Biochem J. 1958 Feb;68(2):262–264. doi: 10.1042/bj0680262. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DENT C. E. Chromatography in the study of amino-acid metabolism. Lect Sci Basis Med. 1952 1953;2:213–234. [PubMed] [Google Scholar]
- DENT C. E., HARRIS H. Hereditary forms of rickets and osteomalacia. J Bone Joint Surg Br. 1956 Feb;38-B(1):204–226. doi: 10.1302/0301-620X.38B1.204. [DOI] [PubMed] [Google Scholar]
- DENT C. E., SENIOR B. Studies on the treatment of cystinuria. Br J Urol. 1955 Dec;27(4):317–332. doi: 10.1111/j.1464-410x.1955.tb03486.x. [DOI] [PubMed] [Google Scholar]
- DENT C. E. The renal amino-acidurias. Exp Med Surg. 1954;12(2):229–232. doi: 10.1159/000382344. [DOI] [PubMed] [Google Scholar]
- DOOLAN P. D., HARPER H. A., HUTCHIN M. E., ALPEN E. L. The renal tubular response to amino acid loading. J Clin Invest. 1956 Aug;35(8):888–896. doi: 10.1172/JCI103341. [DOI] [PMC free article] [PubMed] [Google Scholar]
- DOOLAN P. D., HARPER H. A., HUTCHIN M. E., SHREEVE W. W. Renal clearance of eighteen individual amino acids in human subjects. J Clin Invest. 1955 Aug;34(8):1247–1255. doi: 10.1172/JCI103171. [DOI] [PMC free article] [PubMed] [Google Scholar]
- Dent C. E. The amino-aciduria in Fanconi syndrome. A study making extensive use of techniques based on paper partition chromatography. Biochem J. 1947;41(2):240–253. doi: 10.1042/bj0410240. [DOI] [PMC free article] [PubMed] [Google Scholar]
- EVERED D. F. The excretion of amino acids by the human; a quantitative study with ion-exchange chromatography. Biochem J. 1956 Mar;62(3):416–427. doi: 10.1042/bj0620416. [DOI] [PMC free article] [PubMed] [Google Scholar]
- FRASER D., YENDT E. R., CHRISTIE F. H. Metabolic abnormalities in hypophosphatasia. Lancet. 1955 Feb 5;268(6858):286–286. doi: 10.1016/s0140-6736(55)90112-4. [DOI] [PubMed] [Google Scholar]
- GOLDBERG A., RIMINGTON C. Fate of porphobilinogen in the rat: relation to acute porphyria in man. Lancet. 1954 Jul 24;267(6830):172–173. doi: 10.1016/s0140-6736(54)90143-9. [DOI] [PubMed] [Google Scholar]
- HARRISON H. E., HARRISON H. C. Aminoaciduria in relation to deficiency diseases and kidney function. J Am Med Assoc. 1957 Aug 3;164(14):1571–1577. doi: 10.1001/jama.1957.62980140006008. [DOI] [PubMed] [Google Scholar]
- JEPSON J. B. Paper chromatography of urinary indoles. Lancet. 1955 Nov 12;269(6898):1009–1011. doi: 10.1016/s0140-6736(55)93432-2. [DOI] [PubMed] [Google Scholar]
- JONXIS J. H., HUISMAN T. H. Amino-aciduria in rachitic children. Lancet. 1953 Aug 29;265(6783):428–431. doi: 10.1016/s0140-6736(53)90204-9. [DOI] [PubMed] [Google Scholar]
- King E. J., Armstrong A. R. A CONVENIENT METHOD FOR DETERMINING SERUM AND BILE PHOSPHATASE ACTIVITY. Can Med Assoc J. 1934 Oct;31(4):376–381. [PMC free article] [PubMed] [Google Scholar]
- LOWE C. U., TERREY M., MacLACHLAN E. A. Organic-aciduria, decreased renal ammonia production, hydrophthalmos, and mental retardation; a clinical entity. AMA Am J Dis Child. 1952 Feb;83(2):164–184. doi: 10.1001/archpedi.1952.02040060030004. [DOI] [PubMed] [Google Scholar]
- MOORE S., STEIN W. H. A modified ninhydrin reagent for the photometric determination of amino acids and related compounds. J Biol Chem. 1954 Dec;211(2):907–913. [PubMed] [Google Scholar]
- MOORE S., STEIN W. H. Procedures for the chromatographic determination of amino acids on four per cent cross-linked sulfonated polystyrene resins. J Biol Chem. 1954 Dec;211(2):893–906. [PubMed] [Google Scholar]
- McCANCE R. A., MORRISON A. B., DENT C. E. The excretion of phosphoethanolamine and hypophosphatasia. Lancet. 1955 Jan 15;268(6855):131–131. doi: 10.1016/s0140-6736(55)91704-9. [DOI] [PubMed] [Google Scholar]
- Neuberger A., Rimington C., Wilson J. M. Studies on alcaptonuria: 2. Investigations on a case of human alcaptonuria. Biochem J. 1947;41(3):438–449. [PMC free article] [PubMed] [Google Scholar]
- ROSE G. A., LUMB F. H., DENT C. E. Discussion on generalized aches and pains from metabolic bone disease. Proc R Soc Med. 1957 May;50(5):371–380. [PMC free article] [PubMed] [Google Scholar]
- SERENI F., McNAMARA H., SHIBUYA M., KRETCHMER N., BARNETT H. L. Concentration in plasma and rate of urinary excretion of amino acids in premature infants. Pediatrics. 1955 May;15(5):575–585. [PubMed] [Google Scholar]
- STEIN W. H. A chromatographic investigation of the amino acid constituents of normal urine. J Biol Chem. 1953 Mar;201(1):45–58. [PubMed] [Google Scholar]
- STEIN W. H., MOORE S. The free amino acids of human blood plasma. J Biol Chem. 1954 Dec;211(2):915–926. [PubMed] [Google Scholar]
- WESTALL R. G. The amino acids and other ampholytes of urine. 3. Unidentified substances excreted in normal human urine. Biochem J. 1955 Jun;60(2):247–255. doi: 10.1042/bj0600247. [DOI] [PMC free article] [PubMed] [Google Scholar]