These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.
4. An 8-year-old boy with renal failure, nephrolithiasis and bone pain. Yalçinkaya F; Tümer N; Onder S; Kuzu I Eur J Pediatr; 1998 Mar; 157(3):255-6. PubMed ID: 9537497 [No Abstract] [Full Text] [Related]
5. Primary hyperoxaluria presenting with early renal allograft dysfunction. Rathnamalala NK; Lanerolle RD; Hoppe B; Beck B Nephrology (Carlton); 2012 May; 17(4):431. PubMed ID: 22509767 [No Abstract] [Full Text] [Related]
8. Atypical features of primary hyperoxaluria in end-stage renal disease. Absy MM Am J Nephrol; 1991; 11(4):301-4. PubMed ID: 1799188 [TBL] [Abstract][Full Text] [Related]
10. Primary hyperoxaluria type 1. Cochat P Kidney Int; 1999 Jun; 55(6):2533-47. PubMed ID: 10354306 [No Abstract] [Full Text] [Related]
11. Is there a genotype-phenotype correlation in primary hyperoxaluria type 1? Beck BB; Hoppe B Kidney Int; 2006 Sep; 70(6):984-6. PubMed ID: 16957746 [TBL] [Abstract][Full Text] [Related]
12. [Oxalate: a poorly soluble organic waste with consequences]. Lu Y; Bonny O Praxis (Bern 1994); 2015 Mar; 104(7):353-9. PubMed ID: 25804778 [TBL] [Abstract][Full Text] [Related]
13. Infantile primary hyperoxaluria type 1 with end stage renal failure. Khoo JJ; Pee S; Kamaludin DP Pathology; 2006 Aug; 38(4):371-4. PubMed ID: 16916735 [No Abstract] [Full Text] [Related]
15. Primary Hyperoxaluria: The Patient and Caregiver Perspective. Lawrence JE; Wattenberg DJ Clin J Am Soc Nephrol; 2020 Jul; 15(7):909-911. PubMed ID: 32165441 [No Abstract] [Full Text] [Related]
16. Primary hyperoxaluria: effect of treatment with vitamin B6 and shock waves. Amato M; Donzelli S; Lombardi M; Salvadori M; Carini M; Selli C; Caudarella R Contrib Nephrol; 1987; 58():190-2. PubMed ID: 3691125 [No Abstract] [Full Text] [Related]
17. Primary Hyperoxaluria: A Need for New Perspectives in an Era of New Therapies. Somers MJG Am J Kidney Dis; 2023 Feb; 81(2):131-133. PubMed ID: 36184293 [No Abstract] [Full Text] [Related]
18. Novel AGXT gene mutation in a Sri Lankan family with primary Hyperoxaluria type 1. Sirisena ND; Tantrigoda NH; Kariyawasam KJ; Jayasekara RW; Dissanayake VH Nephrology (Carlton); 2016 Jan; 21(1):75-6. PubMed ID: 26693850 [No Abstract] [Full Text] [Related]