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http://scihub22266oqcxt.onion/ 17657107!ä!17657107 Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=17657107&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215       Saudi+J+Kidney+Dis+Transpl 2003 ; 14 (3): 351-7 Nephropedia Template TP {{tp|p=17657107|t=2003. Cystinosis and cystinuria: differences in outcome |pdf=|usr=}}{{17657107}} gab.com Text Cystinosis and cystinuria: differences in outcome JO: Saudi J Kidney Dis Transpl http://www.kidney.de/pget.php?&tw=1&pmid=17657107 #FOAvip Cystinosis and cystinuria, both recessive genetic disorders, are fundamentally different in their pathophysiologic mechanisms. Cystinosis is a disease of cystine storage in which the kidney is the initial, but not the sole target organ. Cystinuria is a disease of renal tubular cystine transport in which excessive loss of this insoluble amino acid causes precipitation at physiologic urine pH and concentration. The former disorder uniformly results in the need for renal allograft despite recent advances in medical therapy. Cystinuria has a variable severity of expression and may be amenable to long-term medical treatment in some patients. Others may have frequent stone recurrence and infection and progress to chronic renal failure in the long term. It is the purpose of this review to provide the reader with an understanding of the respective diseases and the reasons for the differences in their prognoses and long-term outcomes. Twit Text FOAVip Cystinosis and cystinuria: differences in outcome ????Saudi J Kidney Dis Transpl http://www.kidney.de/pget.php?&tw=1&pmid=17657107 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=17657107 #FOAvip English Wikipedia <ref>{{Cite pmid|17657107}}</ref> Cystinosis and cystinuria: differences in outcome #MMPMID17657107 Roth KS; Chan JC Saudi J Kidney Dis Transpl 2003[Jul]; 14 (3): 351-7 PMID17657107show ga Cystinosis and cystinuria, both recessive genetic disorders, are fundamentally different in their pathophysiologic mechanisms. Cystinosis is a disease of cystine storage in which the kidney is the initial, but not the sole target organ. Cystinuria is a disease of renal tubular cystine transport in which excessive loss of this insoluble amino acid causes precipitation at physiologic urine pH and concentration. The former disorder uniformly results in the need for renal allograft despite recent advances in medical therapy. Cystinuria has a variable severity of expression and may be amenable to long-term medical treatment in some patients. Others may have frequent stone recurrence and infection and progress to chronic renal failure in the long term. It is the purpose of this review to provide the reader with an understanding of the respective diseases and the reasons for the differences in their prognoses and long-term outcomes. äCystinosis and cystinuria: differences in outcome (epmc).pdf DeepDyve Pubget Overpricing