Mutational analysis of idiopathic renal hypouricemia in Korea
- 24 May 2005
- journal article
- case report
- Published by Springer Science and Business Media LLC in Pediatric Nephrology
- Vol. 20 (7), 886-890
- https://doi.org/10.1007/s00467-005-1863-3
Abstract
No abstract availableKeywords
This publication has 26 references indexed in Scilit:
- The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemiaPediatric Nephrology, 2004
- Is There a Pathogenetic Role for Uric Acid in Hypertension and Cardiovascular and Renal Disease?Hypertension, 2003
- Exercise-induced acute renal failure with renal hypouricemia: a case report and a review of the literatureClinical Nephrology, 2002
- Molecular identification of a renal urate–anion exchanger that regulates blood urate levelsNature, 2002
- Hematuria in Patients with Renal Hypouricemia.Internal Medicine, 1998
- Renal hypouricemia: Prevention of exercise-induced acute renal failure and a review of the literatureAmerican Journal of Kidney Diseases, 1995
- Renal Hypouricemia Due to Enhanced Tubular Secretion of Urate Associated with Urolithiasis; Successful Treatment of Urolithiasis by Alkalization of Urine K+, Na+-CitrateNephron, 1993
- Antioxidation mechanisms of uric acidJournal of the American Chemical Society, 1989
- Uric acid provides an antioxidant defense in humans against oxidant- and radical-caused aging and cancer: a hypothesis.Proceedings of the National Academy of Sciences, 1981
- Prediction of Creatinine Clearance from Serum CreatinineNephron, 1976