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Journal Abstract Search

138 related items for PubMed ID: 3141704

  • 1. Diversity in residual alanine glyoxylate aminotransferase activity in hyperoxaluria type I: correlation with pyridoxine responsiveness.
    Wanders RJ, van Roermund CW, Jurriaans S, Schutgens RB, Tager JM, van den Bosch H, Wolff ED, Przyrembel H, Berger R, Schaaphok FG.
    J Inherit Metab Dis; 1988; 11 Suppl 2():208-11. PubMed ID: 3141704
    [No Abstract] [Full Text] [Related]

  • 2. Enzymatic heterogeneity in primary hyperoxaluria type 1 (hepatic peroxisomal alanine: glyoxylate aminotransferase deficiency).
    Danpure CJ, Jennings PR.
    J Inherit Metab Dis; 1988; 11 Suppl 2():205-7. PubMed ID: 3141703
    [No Abstract] [Full Text] [Related]

  • 3. Peroxisomal alanine:glyoxylate aminotransferase deficiency in primary hyperoxaluria type I.
    Danpure CJ, Jennings PR.
    FEBS Lett; 1986 May 26; 201(1):20-4. PubMed ID: 3709805
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  • 4. Alanine glyoxylate aminotransferase and the urinary excretion of oxalate and glycollate in hyperoxaluria type I and the Zellweger syndrome.
    Wanders RJ, van Roermund CW, Westra R, Schutgens RB, van der Ende MA, Tager JM, Monnens LA, Baadenhuysen H, Govaerts L, Przyrembel H.
    Clin Chim Acta; 1987 Jun 15; 165(2-3):311-9. PubMed ID: 3652453
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  • 5. Primary hyperoxaluria: therapeutic strategies for the 90's.
    Scheinman JI.
    Kidney Int; 1991 Sep 15; 40(3):389-99. PubMed ID: 1787639
    [No Abstract] [Full Text] [Related]

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  • 14. Successful treatment of primary hyperoxaluria type I by combined hepatic and renal transplantation.
    Watts RW, Calne RY, Rolles K, Danpure CJ, Morgan SH, Mansell MA, Williams R, Purkiss P.
    Lancet; 1987 Aug 29; 2(8557):474-5. PubMed ID: 2887776
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  • 15. The effect of pyridoxine on oxalate dynamics in three cases of primary hyperoxaluria (with glycollic aciduria).
    Watts RW, Veall N, Purkiss P, Mansell MA, Haywood EF.
    Clin Sci (Lond); 1985 Jul 29; 69(1):87-90. PubMed ID: 4064559
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  • 17. Pyridoxine-responsive nephrocalcinosis and glycolic aciduria in two siblings without hyperoxaluria and with normal alanine: glyoxalate aminotransferase activity.
    Kist-van Holthe JE, Onkenhout W, van der Heijden AJ.
    J Inherit Metab Dis; 2000 Feb 29; 23(1):91-2. PubMed ID: 10682315
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