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Journal Abstract Search

107 related items for PubMed ID: 9510895

  • 1. Availability of assays for definitive diagnosis of primary hyperoxaluria types 1 and 2.
    Rumsby G, Samuell C.
    Clin Chem; 1998 Mar; 44(3):694. PubMed ID: 9510895
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  • 3. L-glyceric aciduria. A new genetic variant of primary hyperoxaluria.
    Williams HE, Smith LH.
    N Engl J Med; 1968 Feb 01; 278(5):233-8. PubMed ID: 5635456
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  • 8. A new case of hyperoxaluria type II.
    Vilarinho L, Araujo R, Vilarinho A, Pereira E, Abdo K, Bardet J, Parvy P, Rabier D.
    J Inherit Metab Dis; 1993 Feb 01; 16(5):896-7. PubMed ID: 8295409
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  • 11. Detection of primary hyperoxaluria type 2 (L-glyceric aciduria) in patients with maintained renal function or end-stage renal failure.
    Marangella M, Petrarulo M, Cosseddu D, Vitale C, Cadario A, Barbos MP, Gurioli L, Linari F.
    Nephrol Dial Transplant; 1995 Feb 01; 10(8):1381-5. PubMed ID: 8538930
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  • 12. Hyperoxaluria in L-glyceric aciduria: possible pathogenic mechanism.
    Williams HE, Smith LH.
    Science; 1971 Jan 29; 171(3969):390-1. PubMed ID: 4321474
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  • 14. Simultaneous analysis of urinary metabolites for preliminary identification of primary hyperoxaluria.
    Clifford-Mobley O, Hewitt L, Rumsby G.
    Ann Clin Biochem; 2016 Jul 29; 53(Pt 4):485-94. PubMed ID: 26342005
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  • 17. The synthesis of oxylate from hydroxypyruvate by isolated perfused rat liver. The mechanism of hyperoxaluria in L-glyceric aciduria.
    Liao LL, Richardson KE.
    Biochim Biophys Acta; 1978 Jan 03; 538(1):76-86. PubMed ID: 620064
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  • 18. 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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  • 19. Disorders of oxalate metabolism.
    Williams HE, Smith LH.
    Am J Med; 1968 Nov 15; 45(5):715-35. PubMed ID: 4879833
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