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10.1186/s12882-016-0246-2 http://scihub22266oqcxt.onion/10.1186/s12882-016-0246-2 C4802583!4802583!27000031     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27000031&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 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 235.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       BMC+Nephrol 2016 ; 17 (ä): ä Nephropedia Template TP {{tp|p=27000031|t=2016. Glomerulopathy in patients with distal duplication of chromosome 6p |pdf=|usr=}}{{27000031}} gab.com Text Glomerulopathy in patients with distal duplication of chromosome 6p JO: BMC Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=27000031 #FOAvip Background: Duplication of the distal part of chromosome 6p is a rare genetic syndrome. Renal involvement has been reported in the majority of patients, including a wide range of congenital abnormalities of kidney and urinary tract and, occasionally, a proteinuric glomerulopathy. Case presentation: Here, we report a 13-year-old girl with 6p25.3p22.1 duplication who presented with proteinuria in infancy, was later diagnosed as focal segmental glomerulosclerosis, progressed to end-stage renal disease and was successfully transplanted. Conclusion: A systematic literature review suggests that 15?20 % of individuals with distal 6p duplication develop progressive proteinuric glomerulopathy. Monitoring of kidney function should be recommended in all cases. Electronic supplementary material: The online version of this article (doi:10.1186/s12882-016-0246-2) contains supplementary material, which is available to authorized users. Twit Text FOAVip Glomerulopathy in patients with distal duplication of chromosome 6p ????BMC Nephrol http://www.kidney.de/pget.php?&tw=1&pmid=27000031 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27000031 #FOAvip English Wikipedia <ref>{{Cite pmid|27000031}}</ref> Glomerulopathy in patients with distal duplication of chromosome 6p #MMPMID27000031 Jankauskien? A; Koczkowska M; Bjerre A; Bernaciak J; Schaefer F; Lipska-Zi?tkiewicz BS BMC Nephrol 2016[]; 17 (ä): ä PMID27000031show ga Background: Duplication of the distal part of chromosome 6p is a rare genetic syndrome. Renal involvement has been reported in the majority of patients, including a wide range of congenital abnormalities of kidney and urinary tract and, occasionally, a proteinuric glomerulopathy. Case presentation: Here, we report a 13-year-old girl with 6p25.3p22.1 duplication who presented with proteinuria in infancy, was later diagnosed as focal segmental glomerulosclerosis, progressed to end-stage renal disease and was successfully transplanted. Conclusion: A systematic literature review suggests that 15?20 % of individuals with distal 6p duplication develop progressive proteinuric glomerulopathy. Monitoring of kidney function should be recommended in all cases. Electronic supplementary material: The online version of this article (doi:10.1186/s12882-016-0246-2) contains supplementary material, which is available to authorized users. äGlomerulopathy in patients with distal duplication of chromosome 6p (epmc).pdf DeepDyve Pubget Overpricing