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10.1093/ndtplus/sfq036 http://scihub22266oqcxt.onion/10.1093/ndtplus/sfq036 C5477959!5477959!28657066     free     free     free 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       NDT+Plus 2010 ; 3 (3): 303-5 Nephropedia Template TP {{tp|p=28657066|t=2010. Fabry disease in donor kidneys with 3- and 12-year follow-up after transplantation |pdf=|usr=}}{{28657066}} gab.com Text Fabry disease in donor kidneys with 3- and 12-year follow-up after transplantation JO: NDT Plus http://www.kidney.de/pget.php?&tw=1&pmid=28657066 #FOAvip Enzyme replacement therapy (ERT) has been introduced for Fabry disease and has been reported to clear some renal cell types of accumulated glycolipids and to reduce the accumulation in other cell types. We describe two patients without Fabry disease who were transplanted with kidney allografts from a male donor with Fabry disease. Biopsies were taken at transplantation and after 3 years in the first case and after 12 years in the second case. Even though these Fabry kidney allografts for many years had been exposed to normal levels of circulating ?-galactosidase A (?-gal-A), the amount of accumulated lysosomal deposits in the podocytes remained unchanged. Additionally, small deposits were also found in tubular cells and glomerular endothelial cells as long as 12 years after transplantation. Twit Text FOAVip Fabry disease in donor kidneys with 3- and 12-year follow-up after transplantation ????NDT Plus http://www.kidney.de/pget.php?&tw=1&pmid=28657066 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28657066 #FOAvip English Wikipedia <ref>{{Cite pmid|28657066}}</ref> Fabry disease in donor kidneys with 3- and 12-year follow-up after transplantation #MMPMID28657066 Aasebø W; Strøm EH; Hovig T; Undset LH; Heiberg A; Jenssen T NDT Plus 2010[Jun]; 3 (3): 303-5 PMID28657066show ga Enzyme replacement therapy (ERT) has been introduced for Fabry disease and has been reported to clear some renal cell types of accumulated glycolipids and to reduce the accumulation in other cell types. We describe two patients without Fabry disease who were transplanted with kidney allografts from a male donor with Fabry disease. Biopsies were taken at transplantation and after 3 years in the first case and after 12 years in the second case. Even though these Fabry kidney allografts for many years had been exposed to normal levels of circulating ?-galactosidase A (?-gal-A), the amount of accumulated lysosomal deposits in the podocytes remained unchanged. Additionally, small deposits were also found in tubular cells and glomerular endothelial cells as long as 12 years after transplantation. äFabry disease in donor kidneys with 3- and 12-year follow-up after tra(epmc).pdf DeepDyve Pubget Overpricing