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Journal Abstract Search

115 related items for PubMed ID: 4159786

  • 1.
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  • 2. The metabolic error in primary hyperoxaluria.
    Hockaday TD, Clayton JE, Smith LH.
    Arch Dis Child; 1965 Oct; 40(213):485-91. PubMed ID: 5829992
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  • 3. Dietary intake, absorption, metabolism, and excretion of oxalate.
    Williams AW, Wilson DM.
    Semin Nephrol; 1990 Jan; 10(1):2-8. PubMed ID: 2404326
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  • 4. Quantitative aspects of ascorbic acid metabolism in patients with primary hyperoxaluria.
    Atkins GL, Dean BM, Griffin WJ, Scowen EF, Watts RW.
    Clin Sci; 1965 Oct; 29(2):305-14. PubMed ID: 5840978
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  • 5. [Primary hyperoxaluria in children].
    Iur'eva EA, Kablukova EK, Korovina NA, Balandina EK, Cherniavskaia NA.
    Vopr Okhr Materin Det; 1977 Oct; 22(10):13-7. PubMed ID: 605528
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  • 7. The renal clearance of oxalate in normal subjects and patients with primary hyperoxaluria.
    Williams HE, Johnson GA, Smith LH.
    Clin Sci; 1971 Sep; 41(3):213-8. PubMed ID: 5571501
    [No Abstract] [Full Text] [Related]

  • 8. Renal homotransplantation in a patient with primary familial oxalosis.
    Deodhar SD, Tung KS, Zühlke V, Nakamoto S.
    Arch Pathol; 1969 Jan; 87(1):118-24. PubMed ID: 4881324
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  • 9. The identification of the enzymes that catalyse the oxidation of glyoxylate to oxalate in the 100000 g supernatant fraction of human hyperoxaluric and control liver and heart tissue.
    Gibbs DA, Watts RW.
    Clin Sci; 1973 Mar; 44(3):227-41. PubMed ID: 4348266
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  • 17. The conversion of [1-13C]glycine and [2-13C]glycine to [13C]oxalate in primary hyperoxaluria: evidence for the existence of more than one metabolic pathway from glycine to oxalate in man.
    Dean BM, Watts RW, Westwick WJ.
    Clin Sci; 1968 Oct; 35(2):325-35. PubMed ID: 5721235
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  • 18. Glyoxylate metabolism by blood cells from normal subjects and patients with primary hyperoxaluria.
    Fisher V, Watts RW.
    Biochem J; 1967 Sep; 104(3):42P. PubMed ID: 6049869
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