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Journal Abstract Search
127 related items for PubMed ID: 8311084
1. Long-term prognosis in primary hyperoxaluria type II (L-glyceric aciduria). Chlebeck PT, Milliner DS, Smith LH. Am J Kidney Dis; 1994 Feb; 23(2):255-9. PubMed ID: 8311084 [Abstract] [Full Text] [Related]
3. Nephrocalcinosis in a patient with primary hyperoxaluria type 2. Kemper MJ, Müller-Wiefel DE. Pediatr Nephrol; 1996 Aug; 10(4):442-4. PubMed ID: 8865239 [Abstract] [Full Text] [Related]
4. 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]
5. 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 Aug; 10(8):1381-5. PubMed ID: 8538930 [Abstract] [Full Text] [Related]
8. 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]
9. d-Glyceric aciduria does not cause nonketotic hyperglycinemia: A historic co-occurrence. Swanson MA, Garcia SM, Spector E, Kronquist K, Creadon-Swindell G, Walter M, Christensen E, Van Hove JLK, Sass JO. Mol Genet Metab; 2017 Jun; 121(2):80-82. PubMed ID: 28462797 [Abstract] [Full Text] [Related]
10. A randomised Phase II/III study to evaluate the efficacy and safety of orally administered Oxalobacter formigenes to treat primary hyperoxaluria. Milliner D, Hoppe B, Groothoff J. Urolithiasis; 2018 Aug; 46(4):313-323. PubMed ID: 28718073 [Abstract] [Full Text] [Related]
13. Systematic assessment of urinary hydroxy-oxo-glutarate for diagnosis and follow-up of primary hyperoxaluria type III. Ventzke A, Feldkötter M, Wei A, Becker J, Beck BB, Hoppe B. Pediatr Nephrol; 2017 Dec; 32(12):2263-2271. PubMed ID: 28711958 [Abstract] [Full Text] [Related]
15. Severe child form of primary hyperoxaluria type 2 - a case report revealing consequence of GRHPR deficiency on metabolism. Konkoľová J, Chandoga J, Kováčik J, Repiský M, Kramarová V, Paučinová I, Böhmer D. BMC Med Genet; 2017 May 31; 18(1):59. PubMed ID: 28569194 [Abstract] [Full Text] [Related]
16. Primary hyperoxaluria (L-glyceric aciduria) in the cat: a newly recognised inherited disease. McKerrell RE, Blakemore WF, Heath MF, Plumb J, Bennett MJ, Pollitt RJ, Danpure CJ. Vet Rec; 1989 Jul 08; 125(2):31-4. PubMed ID: 2773220 [Abstract] [Full Text] [Related]
18. Primary hyperoxaluria type 2 in children. Johnson SA, Rumsby G, Cregeen D, Hulton SA. Pediatr Nephrol; 2002 Aug 08; 17(8):597-601. PubMed ID: 12185464 [Abstract] [Full Text] [Related]
19. Predictors of Incident ESRD among Patients with Primary Hyperoxaluria Presenting Prior to Kidney Failure. Zhao F, Bergstralh EJ, Mehta RA, Vaughan LE, Olson JB, Seide BM, Meek AM, Cogal AG, Lieske JC, Milliner DS, Investigators of Rare Kidney Stone Consortium. Clin J Am Soc Nephrol; 2016 Jan 07; 11(1):119-26. PubMed ID: 26656319 [Abstract] [Full Text] [Related]
20. Restrictive cardiomyopathy in a patient with primary hyperoxaluria type II. Schulze MR, Wachter R, Schmeisser A, Fischer R, Strasser RH. Clin Res Cardiol; 2006 Apr 07; 95(4):235-40. PubMed ID: 16598594 [Abstract] [Full Text] [Related] Page: [Next] [New Search]