| scholarly article | Q13442814 |
| P356 | DOI | 10.1007/S00467-005-1863-3 |
| P698 | PubMed publication ID | 15912381 |
| P50 | author | Suhnggwon Kim | Q85792610 |
| P2093 | author name string | Takashi Igarashi | |
| Takashi Sekine | |||
| Hae Il Cheong | |||
| Yong Choi | |||
| Joo Hoon Lee | |||
| Il Soo Ha | |||
| Ju Hyung Kang | |||
| Fusako Komoda | |||
| P2860 | cites work | Molecular identification of a renal urate anion exchanger that regulates blood urate levels | Q24297979 |
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| Exercise-induced acute renal failure with renal hypouricemia: a case report and a review of the literature | Q34980460 | ||
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| Two male siblings with hereditary renal hypouricemia and exercise-induced ARF. | Q44679650 | ||
| The W258X mutation in SLC22A12 is the predominant cause of Japanese renal hypouricemia | Q44822748 | ||
| Regulation of renal urate excretion: a critical review. | Q52229377 | ||
| Acute renal failure with severe loin pain and patchy renal ischemia after anaerobic exercise in patients with or without renal hypouricemia. | Q53675111 | ||
| Causes of hypouricemia. | Q53725673 | ||
| Inborn hypouricemia due to isolated renal tubular defect | Q66921361 | ||
| Clinical significance of hypouricemia in hospitalized patients | Q67977242 | ||
| Hypouricemia due to familial isolated renal tubular uricosuria. Evaluation with the combined pyrazinamide-probenecid test | Q69792227 | ||
| Cause of persistent hypouricemia in outpatients | Q69944488 | ||
| Renal hypouricemia due to enhanced tubular secretion of urate associated with urolithiasis: successful treatment of urolithiasis by alkalization of urine K+, Na(+)-citrate | Q72759584 | ||
| Two cases of renal hypouricemia with nephrolithiasis | Q73325044 | ||
| Hematuria in patients with renal hypouricemia | Q74337292 | ||
| P433 | issue | 7 | |
| P921 | main subject | mutational analysis | Q1955810 |
| P304 | page(s) | 886-890 | |
| P577 | publication date | 2005-05-24 | |
| P1433 | published in | Pediatric Nephrology | Q15749796 |
| P1476 | title | Mutational analysis of idiopathic renal hypouricemia in Korea | |
| P478 | volume | 20 |
| Q38723885 | A Case Report of Familial Renal Hypouricemia Confirmed by Genotyping of SLC22A12, and a Literature Review |
| Q38405484 | A case of exercise-induced acute renal failure with G774A mutation in SCL22A12 causing renal hypouricemia |
| Q46984649 | Absence of SLC22A12 gene mutations in Greek Caucasian patients with primary renal hypouricaemia |
| Q36480292 | Analysis of mutations in the urate transporter 1 (URAT1) gene of Japanese patients with hypouricemia in northern Japan and review of the literature |
| Q28741258 | Clinical and functional characterization of URAT1 variants |
| Q36471761 | Clinical characteristics of acute renal failure with severe loin pain and patchy renal vasoconstriction |
| Q90575612 | Contribution of SLC22A12 on hypouricemia and its clinical significance for screening purposes |
| Q94475941 | Donor-derived hypouricemia in irrelevant recipients caused by kidney transplantation |
| Q38073215 | Genetics of hyperuricemia and gout: implications for the present and future |
| Q33562215 | Homozygous SLC2A9 mutations cause severe renal hypouricemia |
| Q37811961 | In Vitro and In Vivo Evidence of the Importance of Organic Anion Transporters (OATs) in Drug Therapy |
| Q45813994 | MicroRNA expression patterns of the kidney in hyperuricemia mice treated with Xiezhuo Chubi Decoction |
| Q36653405 | Molecular insights into the structure-function relationship of organic anion transporters OATs |
| Q57174959 | Multiple Membrane Transporters and Some Immune Regulatory Genes are Major Genetic Factors to Gout |
| Q46135588 | Non-urate transporter 1-related renal hypouricemia and acute renal failure in an Israeli-Arab family |
| Q36716533 | Organic anion transporters of the SLC22 family: biopharmaceutical, physiological, and pathological roles |
| Q81721908 | Physiology, structure, and regulation of the cloned organic anion transporters |
| Q44037103 | Posterior reversible encephalopathy syndrome with exercise-induced acute kidney injury in renal hypouricemia type 1. |
| Q37242604 | Prevalence and possible causes of hypouricemia at a tertiary care hospital. |
| Q58791430 | Renal hypouricemia caused by novel compound heterozygous mutations in the SLC22A12 gene: a case report with literature review |
| Q80218398 | Renal hypouricemia in school-aged children: screening of serum uric acid level before physical training |
| Q33834827 | Serum uric acid distribution according to SLC22A12 W258X genotype in a cross-sectional study of a general Japanese population |
| Q36316477 | Shared Ligands Between Organic Anion Transporters (OAT1 and OAT6) and Odorant Receptors |
| Q36829598 | Uric acid changes in urine and plasma: an effective tool in screening for purine inborn errors of metabolism and other pathological conditions. |
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