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PUBMED FOR HANDHELDS

Journal Abstract Search


151 related items for PubMed ID: 8592629

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  • 8. Extraction of glyceric and glycolic acids from urine with tetrahydrofuran: utility in detection of primary hyperoxaluria.
    Dietzen DJ, Wilhite TR, Kenagy DN, Milliner DS, Smith CH, Landt M.
    Clin Chem; 1997 Aug; 43(8 Pt 1):1315-20. PubMed ID: 9267307
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  • 9. Immunocytochemical localization of human hepatic alanine: glyoxylate aminotransferase in control subjects and patients with primary hyperoxaluria type 1.
    Cooper PJ, Danpure CJ, Wise PJ, Guttridge KM.
    J Histochem Cytochem; 1988 Oct; 36(10):1285-94. PubMed ID: 3418107
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  • 11. D-glyceric aciduria is caused by genetic deficiency of D-glycerate kinase (GLYCTK).
    Sass JO, Fischer K, Wang R, Christensen E, Scholl-Bürgi S, Chang R, Kapelari K, Walter M.
    Hum Mutat; 2010 Dec; 31(12):1280-5. PubMed ID: 20949620
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  • 15. Simultaneous analysis of urinary metabolites for preliminary identification of primary hyperoxaluria.
    Clifford-Mobley O, Hewitt L, Rumsby G.
    Ann Clin Biochem; 2016 Jul; 53(Pt 4):485-94. PubMed ID: 26342005
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  • 16. D-glyceric aciduria.
    Dimer NW, Schuck PF, Streck EL, Ferreira GC.
    An Acad Bras Cienc; 2015 Aug; 87(2 Suppl):1409-14. PubMed ID: 26247153
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  • 18. High-performance liquid chromatographic assay for L-glyceric acid in body fluids. Application in primary hyperoxaluria type 2.
    Petrarulo M, Marangella M, Cosseddu D, Linari F.
    Clin Chim Acta; 1992 Oct 30; 211(3):143-53. PubMed ID: 1458609
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  • 20. Kinetic analysis and tissue distribution of human D-glycerate dehydrogenase/glyoxylate reductase and its relevance to the diagnosis of primary hyperoxaluria type 2.
    Giafi CF, Rumsby G.
    Ann Clin Biochem; 1998 Jan 30; 35 ( Pt 1)():104-9. PubMed ID: 9463747
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