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10.1093/ckj/sfs143 http://scihub22266oqcxt.onion/10.1093/ckj/sfs143 C4400565!4400565!26069801     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Clin+Kidney+J 2012 ; 5 (6): 559-61 Nephropedia Template TP {{tp|p=26069801|t=2012. AA Amyloidosis in a patient with glycogen storage disorder and progressive chronic kidney disease |pdf=|usr=}}{{26069801}} gab.com Text AA Amyloidosis in a patient with glycogen storage disorder and progressive chronic kidney disease JO: Clin Kidney J http://www.kidney.de/pget.php?&tw=1&pmid=26069801 #FOAvip Type 1 glycogen storage diseases (GSD) are inherited metabolic diseases caused by defects in the activity of the glucose-6-phosphate transporter. We present the case of a 40-year-old male with glycogen storage disease type 1b (GSD1b) who was referred to our nephrology service for evaluation of his chronic kidney disease and found to have AA amyloid deposition on renal biopsy. Amyloid is a described complication of GSD1b. As the treatment of GSD has improved, patients are surviving longer and are now presenting more frequently to adult services. It is important that clinicians are aware of the possible renal complications of GSD1b. Twit Text FOAVip AA Amyloidosis in a patient with glycogen storage disorder and progressive chronic kidney disease ????Clin Kidney J http://www.kidney.de/pget.php?&tw=1&pmid=26069801 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26069801 #FOAvip English Wikipedia <ref>{{Cite pmid|26069801}}</ref> AA Amyloidosis in a patient with glycogen storage disorder and progressive chronic kidney disease #MMPMID26069801 Dick J; Kumar N; Horsfield C; Jayawardene S Clin Kidney J 2012[Dec]; 5 (6): 559-61 PMID26069801show ga Type 1 glycogen storage diseases (GSD) are inherited metabolic diseases caused by defects in the activity of the glucose-6-phosphate transporter. We present the case of a 40-year-old male with glycogen storage disease type 1b (GSD1b) who was referred to our nephrology service for evaluation of his chronic kidney disease and found to have AA amyloid deposition on renal biopsy. Amyloid is a described complication of GSD1b. As the treatment of GSD has improved, patients are surviving longer and are now presenting more frequently to adult services. It is important that clinicians are aware of the possible renal complications of GSD1b. äAA Amyloidosis in a patient with glycogen storage disorder and progres(epmc).pdf DeepDyve Pubget Overpricing