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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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related]
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 [Abstract] [Full Text] [Related] Page: [Next] [New Search]