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10.2147/IJNRD.S126844 http://scihub22266oqcxt.onion/10.2147/IJNRD.S126844 C5436760!5436760!28546764     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28546764&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 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Int+J+Nephrol+Renovasc+Dis 2017 ; 10 (ä): 97-107 Nephropedia Template TP {{tp|p=28546764|t=2017. Optimal management of primary focal segmental glomerulosclerosis in adults |pdf=|usr=}}{{28546764}} gab.com Text Optimal management of primary focal segmental glomerulosclerosis in adults JO: Int J Nephrol Renovasc Dis http://www.kidney.de/pget.php?&tw=1&pmid=28546764 #FOAvip Focal segmental glomerulosclerosis (FSGS) is a frequent glomerular kidney disease that is revealed by proteinuria or even nephrotic syndrome. A diagnosis can be established from a kidney biopsy that shows focal and segmental glomerulosclerosis. This histopathological lesion may be caused by a primary podocyte injury (idiopathic FSGS) but is also associated with other pathologies (secondary FSGS). The first-line treatment for idiopathic FSGS with nephrotic syndrome is a prolonged course of corticosteroids. However, steroid resistance or steroid dependence is frequent, and despite intensified immunosuppressive treatment, FSGS can lead to end-stage renal failure. In addition, in some cases, FSGS can recur on a graft after kidney transplantation: an unidentified circulating factor may be implicated. Understanding of its physiopathology is unclear, and it remains an important challenge for the scientific community to identify a specific diagnostic biomarker and to develop specific therapeutics. This study reviews the treatment of primary FSGS and the recurrence of FSGS after kidney transplantation in adults. Twit Text FOAVip Optimal management of primary focal segmental glomerulosclerosis in adults ????Int J Nephrol Renovasc Dis http://www.kidney.de/pget.php?&tw=1&pmid=28546764 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28546764 #FOAvip English Wikipedia <ref>{{Cite pmid|28546764}}</ref> Optimal management of primary focal segmental glomerulosclerosis in adults #MMPMID28546764 Beaudreuil S; Lorenzo HK; Elias M; Nnang Obada E; Charpentier B; Durrbach A Int J Nephrol Renovasc Dis 2017[]; 10 (ä): 97-107 PMID28546764show ga Focal segmental glomerulosclerosis (FSGS) is a frequent glomerular kidney disease that is revealed by proteinuria or even nephrotic syndrome. A diagnosis can be established from a kidney biopsy that shows focal and segmental glomerulosclerosis. This histopathological lesion may be caused by a primary podocyte injury (idiopathic FSGS) but is also associated with other pathologies (secondary FSGS). The first-line treatment for idiopathic FSGS with nephrotic syndrome is a prolonged course of corticosteroids. However, steroid resistance or steroid dependence is frequent, and despite intensified immunosuppressive treatment, FSGS can lead to end-stage renal failure. In addition, in some cases, FSGS can recur on a graft after kidney transplantation: an unidentified circulating factor may be implicated. Understanding of its physiopathology is unclear, and it remains an important challenge for the scientific community to identify a specific diagnostic biomarker and to develop specific therapeutics. This study reviews the treatment of primary FSGS and the recurrence of FSGS after kidney transplantation in adults. äOptimal management of primary focal segmental glomerulosclerosis in ad(epmc).pdf DeepDyve Pubget Overpricing