|1.||Ichida, Kimiyoshi: 6 articles (10/2015 - 10/2008)|
|2.||Stiburkova, Blanka: 5 articles (10/2015 - 04/2011)|
|3.||Ganon, Liat: 4 articles (03/2012 - 05/2009)|
|4.||Dinour, Dganit: 4 articles (03/2012 - 05/2009)|
|5.||Sebesta, Ivan: 3 articles (10/2013 - 04/2011)|
|6.||Holtzman, Eliezer J: 3 articles (03/2012 - 01/2010)|
|7.||Sela, Ben-Ami: 3 articles (03/2012 - 01/2010)|
|8.||Nozu, Kandai: 3 articles (02/2012 - 04/2009)|
|9.||Hosoyamada, Makoto: 3 articles (12/2011 - 12/2003)|
|10.||Nakamura, Makiko: 2 articles (10/2015 - 10/2013)|
|1.||Acute Kidney Injury (Acute Renal Failure)
01/01/2014 - "Recurrent exercise-induced acute kidney injury by idiopathic renal hypouricemia with a novel mutation in the SLC2A9 gene and literature review."
01/01/2014 - "Recurrent exercise-induced acute renal failure in a young Pakistani man with severe renal hypouricemia and SLC2A9 compound heterozygosity."
11/01/2013 - "Posterior reversible encephalopathy syndrome with exercise-induced acute kidney injury in renal hypouricemia type 1."
01/01/2013 - "Novel URAT1 mutations caused acute renal failure after exercise in two Chinese families with renal hypouricemia."
02/01/2012 - "Although renal hypouricemia is mostly asymptomatic, it is known to present a high risk of exercise-induced acute renal failure, especially in young males. "
03/01/1997 - "We treated two cases of renal hypouricemia with nephrolithiasis. "
03/01/1997 - "Two cases of renal hypouricemia with nephrolithiasis."
03/01/2012 - "Hereditary renal hypouricemia type 1 (RHUC1) is caused by mutations in the renal tubular UA transporter URAT1 and can be complicated by nephrolithiasis and exercise-induced acute renal failure (EIARF). "
07/01/2011 - "Hereditary renal hypouricemia may be complicated by nephrolithiasis or exercise-induced acute renal failure. "
12/01/2011 - "Primary renal hypouricemia is a genetic disorder characterized by defective renal uric acid (UA) reabsorption with complications such as nephrolithiasis and exercise-induced acute renal failure. "
|3.||Inborn Genetic Diseases (Disease, Hereditary)
01/01/2013 - "Renal hypouricemia (RHUC), as an infrequent hereditary disease, is associated with severe complications such as exercise-induced acute renal failure (EIARF). "
06/01/2011 - "Renal hypouricemia (RHU) is a hereditary disease that predisposes affected people to exercise-induced acute renal failure (EIARF). "
06/01/2015 - "Renal hypouricemia (RHU) is an autosomal recessive hereditary disease characterized by impaired renal urate reabsorption and subsequent profound hypouricemia. "
06/01/2006 - "Idiopathic renal hypouricemia is a hereditary disease characterized by abnormally increased renal excretion of urate. "
07/01/2005 - "Idiopathic renal hypouricemia is a hereditary disease characterized by abnormally high renal uric acid clearance. "
02/01/2012 - "However, there is little information regarding the clinical features of urolithiasis as a complication in childhood renal hypouricemia. "
01/01/2015 - "However, individuals with renal hypouricemia have a high risk of urolithiasis and exercise-induced acute kidney injury, both of which are risk factors for reduced kidney function. "
01/01/1980 - "[Hereditary renal hypouricemia with hyperuricosuira, variably associated with hypercalciuria and urolithiasis: a new syndrome]."
01/01/1980 - "Hereditary renal hypouricemia with hyperuricosuria and variably absorptive hypercalciuria and urolithiasis--a new syndrome."
01/01/1993 - "These results suggest that renal hypouricemia due to enhanced tubular secretion of urate can result in urolithiasis and the alkalization of urine may be an effective treatment for uric acid stones."
01/01/2014 - "This is the first study of the impact of non-synonymous allelic variants on the function of GLUT9 except for patients suffering from renal hypouricemia type 2. The cohort consisted of 250 individuals (150 controls, 54 nonspecific hyperuricemics and 46 primary gout and/or hyperuricemia subjects). "
04/01/2013 - "It has been shown that mutations of the SLC22 genes encoding these transporters cause specific diseases like primary systemic carnitine deficiency and idiopathic renal hypouricemia and are correlated with diseases such as Crohn's disease and gout. "
01/01/1994 - "Acquired and hereditary diseases accompanied by hyperuricosuria and stone disease include: gout, in strong correlation with the amount of uric acid excreted, myelo- and lymphoproliferative disorders, multiple myeloma, secondary polycythemia, pernicious anemia and hemolytic disorders, hemoglobinopathies and thalassemia, the complete or partial deficiency of HGPRT, superactivity of PRPP synthetase, and hereditary renal hypouricemia. "
|1.||Uric Acid (Urate)
|5.||Citric Acid (Citrate)
|7.||Ribose-Phosphate Pyrophosphokinase (Phosphoribosyl Pyrophosphate Synthetase)
|10.||Hypoxanthine Phosphoribosyltransferase (Hypoxanthine Guanine Phosphoribosyltransferase)
|1.||Lithotripsy (Extracorporeal Shockwave Lithotripsy)