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10.1007/s13730-014-0145-y http://scihub22266oqcxt.onion/10.1007/s13730-014-0145-y C5413714!5413714 !28509277     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28509277 &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 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\28509277 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       CEN+Case+Rep 2015 ; 4 (1 ): 85-89 Nephropedia Template TP {{tp|p=28509277 |t=2015. Two brothers with collagenofibrotic glomerulopathy |pdf=|usr=}}{{28509277 }} gab.com Text Two brothers with collagenofibrotic glomerulopathy JO: CEN Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=28509277 #FOAvip Collagenofibrotic glomerulopathy is a rare glomerular disease characterized by extensive accumulation of atypical type III collagen fibers within the mesangial matrix and subendothelial space. Laboratory evaluation of this disease shows a marked increase in serum procollagen III peptide (P III P) levels. Here, we report the case of two brothers with collagenofibrotic glomerulopathy confirmed by histology. Patient 1 presented with proteinuria and hypertension and patient 2 presented with nephrotic-range proteinuria. Immunohistochemistry revealed strong staining for antibodies to type III collagen in the widened subendothelial spaces in both patients. Electron microscopy revealed numerous collagenous fibers in the mesangium and subendothelial space. P III P levels were elevated in both patients. Most reported cases of collagenofibrotic glomerulopathy, including the adult-onset type, have been sporadic. Within the limits of our literature search, this is only the third report of adult siblings with collagenofibrotic glomerulopathy confirmed by histology. This report indicates that it may be beneficial to measure serum P III P levels in the siblings of patients diagnosed with adult-onset collagenofibrotic glomerulopathy. Twit Text FOAVip Two brothers with collagenofibrotic glomerulopathy ????CEN Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=28509277 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28509277 #FOAvip English Wikipedia <ref>{{Cite pmid|28509277 }}</ref> Two brothers with collagenofibrotic glomerulopathy #MMPMID28509277 Aoki T ; Hayashi K ; Morinaga T ; Tomida H ; Hishida M ; Yamamoto S ; Kajiwara N ; Tamai H CEN Case Rep 2015[May]; 4 (1 ): 85-89 PMID28509277 show ga Collagenofibrotic glomerulopathy is a rare glomerular disease characterized by extensive accumulation of atypical type III collagen fibers within the mesangial matrix and subendothelial space. Laboratory evaluation of this disease shows a marked increase in serum procollagen III peptide (P III P) levels. Here, we report the case of two brothers with collagenofibrotic glomerulopathy confirmed by histology. Patient 1 presented with proteinuria and hypertension and patient 2 presented with nephrotic-range proteinuria. Immunohistochemistry revealed strong staining for antibodies to type III collagen in the widened subendothelial spaces in both patients. Electron microscopy revealed numerous collagenous fibers in the mesangium and subendothelial space. P III P levels were elevated in both patients. Most reported cases of collagenofibrotic glomerulopathy, including the adult-onset type, have been sporadic. Within the limits of our literature search, this is only the third report of adult siblings with collagenofibrotic glomerulopathy confirmed by histology. This report indicates that it may be beneficial to measure serum P III P levels in the siblings of patients diagnosed with adult-onset collagenofibrotic glomerulopathy. äTwo brothers with collagenofibrotic glomerulopathy (epmc).pdf DeepDyve Pubget Overpricing