Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.1093/ckj/sft100 http://scihub22266oqcxt.onion/10.1093/ckj/sft100 C4438413!4438413!26064518     free     free     free Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Clin+Kidney+J 2013 ; 6 (5): 523-5 Nephropedia Template TP {{tp|p=26064518|t=2013. Hypouricaemia and hyperuricosuria in familial renal glucosuria |pdf=|usr=}}{{26064518}} gab.com Text Hypouricaemia and hyperuricosuria in familial renal glucosuria JO: Clin Kidney J http://www.kidney.de/pget.php?&tw=1&pmid=26064518 #FOAvip Familial renal glucosuria is a rare co-dominantly inherited benign phenotype characterized by the presence of glucose in the urine. It is caused by mutations in the SLC5A2 gene that encodes SGLT2, the Na+-glucose cotransporter responsible for the reabsorption of the bulk of glucose in the proximal tubule. We report a case of FRG displaying both severe glucosuria and renal hypouricaemia. We hypothesize that glucosuria can disrupt urate reabsorption in the proximal tubule, directly causing hyperuricosuria. Twit Text FOAVip Hypouricaemia and hyperuricosuria in familial renal glucosuria ????Clin Kidney J http://www.kidney.de/pget.php?&tw=1&pmid=26064518 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26064518 #FOAvip English Wikipedia <ref>{{Cite pmid|26064518}}</ref> Hypouricaemia and hyperuricosuria in familial renal glucosuria #MMPMID26064518 Aires I; Santos AR; Pratas J; Nolasco F; Calado J Clin Kidney J 2013[Oct]; 6 (5): 523-5 PMID26064518show ga Familial renal glucosuria is a rare co-dominantly inherited benign phenotype characterized by the presence of glucose in the urine. It is caused by mutations in the SLC5A2 gene that encodes SGLT2, the Na+-glucose cotransporter responsible for the reabsorption of the bulk of glucose in the proximal tubule. We report a case of FRG displaying both severe glucosuria and renal hypouricaemia. We hypothesize that glucosuria can disrupt urate reabsorption in the proximal tubule, directly causing hyperuricosuria. äHypouricaemia and hyperuricosuria in familial renal glucosuria (epmc).pdf DeepDyve Pubget Overpricing