Skip to main content
PMC home page
Archives of Disease in Childhood logoLink to Archives of Disease in Childhood
. 1965 Oct;40(213):485–491. doi: 10.1136/adc.40.213.485

The metabolic error in primary hyperoxaluria.

T D Hockaday, J E Clayton, L H Smith Jr
PMCID: PMC2019460  PMID: 5829992

Full text

PDF
490

Selected References

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

  1. APONTE G. E., FETTER T. R. Familial idiopathic oxalate nephrocalcinosis. Am J Clin Pathol. 1954 Dec;24(12):1363–1373. doi: 10.1093/ajcp/24.12.1363. [DOI] [PubMed] [Google Scholar]
  2. ARCHER H. E., DORMER A. E., SCOWEN E. F., WATTS R. W. Primary hyperoxaluria. Lancet. 1957 Aug 17;273(6990):320–322. doi: 10.1016/s0140-6736(57)92210-9. [DOI] [PubMed] [Google Scholar]
  3. ATKINS G. L., DEAN B. M., GRIFFIN W. J., SCOWEN E. F., WATTS R. W. PRIMARY HYPEROXALURIA. THE RELATION BETWEEN ASCORBIC ACID AND THE INCREASED URINARY EXCRETION OF OXALATE. Lancet. 1963 Nov 23;2(7317):1096–1097. doi: 10.1016/s0140-6736(63)92863-0. [DOI] [PubMed] [Google Scholar]
  4. Baudhuin P., Beaufay H., Rahman-Li Y., Sellinger O. Z., Wattiaux R., Jacques P., De Duve C. Tissue fractionation studies. 17. Intracellular distribution of monoamine oxidase, aspartate aminotransferase, alanine aminotransferase, D-amino acid oxidase and catalase in rat-liver tissue. Biochem J. 1964 Jul;92(1):179–184. doi: 10.1042/bj0920179. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Beadle G. W., Tatum E. L. Genetic Control of Biochemical Reactions in Neurospora. Proc Natl Acad Sci U S A. 1941 Nov 15;27(11):499–506. doi: 10.1073/pnas.27.11.499. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. CRAWHALL J. C., SCOWEN E. F., DE MOWBRAY R. R., WATTS R. W. Conversion of glycine to oxalate in a normal subject. Lancet. 1959 Nov 14;2(7107):810–810. doi: 10.1016/s0140-6736(59)90752-4. [DOI] [PubMed] [Google Scholar]
  7. CRAWHALL J. C., SCOWEN E. F., WATTS R. W. Conversion of glycine to oxalate in primary hyperoxaluria. Lancet. 1959 Nov 14;2(7107):806–809. doi: 10.1016/s0140-6736(59)90751-2. [DOI] [PubMed] [Google Scholar]
  8. Crawhall J. C., Watts R. W. The metabolism of glyoxylate by human- and rat-liver mitochondria. Biochem J. 1962 Oct;85(1):163–171. doi: 10.1042/bj0850163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. DANIELS R. A., MICHELS R., AISEN P., GOLDSTEIN G. Familial hyperoxaluria. Report of a family, review of the literature. Am J Med. 1960 Nov;29:820–831. doi: 10.1016/0002-9343(60)90116-9. [DOI] [PubMed] [Google Scholar]
  10. DEMPSEY E. F., FORBES A. P., MELICK R. A., HENNEMAN P. H. Urinary oxalate excretion. Metabolism. 1960 Jan;9:52–58. [PubMed] [Google Scholar]
  11. ELDER T. D., WYNGAARDEN J. B. The biosynthesis and turnover of oxalate in normal and hyperoxaluric subjects. J Clin Invest. 1960 Aug;39:1337–1344. doi: 10.1172/JCI104151. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. FREDERICK E. W., RABKIN M. T., RICHIE R. H., Jr, SMITH L. H., Jr STUDIES ON PRIMARY HYPEROXALURIA. I. IN VIVO DEMONSTRATION OF A DEFECT IN GLYOXYLATE METABOLISM. N Engl J Med. 1963 Oct 17;269:821–829. doi: 10.1056/NEJM196310172691601. [DOI] [PubMed] [Google Scholar]
  13. GERSHOFF S. N., FARAGALLA F. F., NELSON D. A., ANDRUS S. B. Vitamin B6 deficiency and oxalate nephrocalcinosis in the cat. Am J Med. 1959 Jul;27(1):72–80. doi: 10.1016/0002-9343(59)90062-2. [DOI] [PubMed] [Google Scholar]
  14. GOLDSTONE A., ADAMS E. Metabolism of gamma-hydroxyglutamic acid. I. Conversion to alpha-hydroxy-gamma-ketoglutarate by purified glutamic-aspartic transaminase to rat liver. J Biol Chem. 1962 Nov;237:3476–3485. [PubMed] [Google Scholar]
  15. Gibson Q. H. The reduction of methaemoglobin in red blood cells and studies on the cause of idiopathic methaemoglobinaemia. Biochem J. 1948;42(1):13–23. doi: 10.1042/bj0420013. [DOI] [PMC free article] [PubMed] [Google Scholar]
  16. HALL E. G., SCOWEN E. F., WATTS R. W. Clinical manifestations of primary hyperoxaluria. Arch Dis Child. 1960 Feb;35:108–112. doi: 10.1136/adc.35.179.108. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. HOCKADAY T. D., CLAYTON J. E., FREDERICK E. W., SMITH L. H., Jr PRIMARY HYPEROXALURIA. Medicine (Baltimore) 1964 May;43:315–345. doi: 10.1097/00005792-196405000-00010. [DOI] [PubMed] [Google Scholar]
  18. HOCKADAY T. D., FREDERICK E. W., CLAYTON J. E., SMITH L. H., Jr STUDIES ON PRIMARY HYPEROXALURIA. II. URINARY OXALATE, GLYCOLATE, AND GLYOXYLATE MEASUREMENT BY ISOTOPE DILUTION METHODS. J Lab Clin Med. 1965 Apr;65:677–687. [PubMed] [Google Scholar]
  19. INGRAM V. M. Gene mutations in human haemoglobin: the chemical difference between normal and sickle cell haemoglobin. Nature. 1957 Aug 17;180(4581):326–328. doi: 10.1038/180326a0. [DOI] [PubMed] [Google Scholar]
  20. LAGRUE G., LAUDAT M. H., MEYER P., SAPIR M., MILLIEZ P. Oxalose familiale avec acidose hyperchlorémique secondaire. Sem Hop. 1959 Jun 18;35(28/6):2023–32/SP. [PubMed] [Google Scholar]
  21. MCLAURIN A. W., BEISEL W. R., MCCORMICK G. J., SCALETTAR R., HERMAN R. H. Primary hyperoxaluria. Ann Intern Med. 1961 Jul;55:70–80. doi: 10.7326/0003-4819-55-1-70. [DOI] [PubMed] [Google Scholar]
  22. MEISTER A. Enzymatic transamination reactions involving arginine and ornithine. J Biol Chem. 1954 Feb;206(2):587–596. [PubMed] [Google Scholar]
  23. MEISTER A., SOBER H. A., TICE S. V., FRASER P. E. Transamination and associated deamidation of asparagine and glutamine. J Biol Chem. 1952 May;197(1):319–330. [PubMed] [Google Scholar]
  24. NAKADA H. I. GLUTAMIC-GLYCINE TRANSAMINASE FROM RAT LIVER. J Biol Chem. 1964 Feb;239:468–471. [PubMed] [Google Scholar]
  25. NAKADA H. I., WEINHOUSE S. Studies of glycine oxidation in rat tissues. Arch Biochem Biophys. 1953 Feb;42(2):257–270. doi: 10.1016/0003-9861(53)90356-7. [DOI] [PubMed] [Google Scholar]
  26. SCOWEN E. F., WATTS R. W., HALL E. G. Further observations on the genetic basis of primary hyperoxaluria. Ann Hum Genet. 1959 Dec;23:367–381. doi: 10.1111/j.1469-1809.1959.tb01480.x. [DOI] [PubMed] [Google Scholar]
  27. SCRIVER C. R., HUTCHISON J. H. The vitamin B6 deficiency syndrome in human infancy: biochemical and clinical observations. Pediatrics. 1963 Feb;31:240–250. [PubMed] [Google Scholar]
  28. SHEPARD T. H., 2nd, KREBS E. G., LEE L. S., JOHNSON M. L. Primary hyperoxaluria. III. Nutritional and metabolic studies in a patient. Pediatrics. 1960 Jun;25:1008–1017. [PubMed] [Google Scholar]
  29. WEINHOUSE S., FRIEDMANN B. Metabolism of labeled 2-carbon acids in the intact rat. J Biol Chem. 1951 Aug;191(2):707–717. [PubMed] [Google Scholar]
  30. WEISSBACH A., SPRINSON D. B. The metabolism of 2-carbon compounds related to glycine. I. Glyoxylic acid. J Biol Chem. 1953 Aug;203(2):1023–1030. [PubMed] [Google Scholar]

Articles from Archives of Disease in Childhood are provided here courtesy of BMJ Publishing Group

RESOURCES