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10.3892/etm.2018.5841 http://scihub22266oqcxt.onion/10.3892/etm.2018.5841 C5840950!5840950!29545831     free     free     free Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 219.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Exp+Ther+Med 2018 ; 15 (4): 3169-72 Nephropedia Template TP {{tp|p=29545831|t=2018. Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report |pdf=|usr=}}{{29545831}} gab.com Text Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report JO: Exp Ther Med http://www.kidney.de/pget.php?&tw=1&pmid=29545831 #FOAvip Primary hyperoxaluria type 2 is a rare autosomal recessive disorder caused by glyoxylate reductase/hydroxypyruvate reductase deficiency and characterized by recurrent episodes of nephrolithiasis and nephrocalcinosis. Herein, we describe a case of primary hyperoxaluria type 2 in a 33-year-old man who failed to respond to conventional therapies; thus renal transplantation was performed. This case demonstrated that, although primary hyperoxaluria type 2 is rare, hyperoxaluria should be suspected and blood oxalate and stone component be examined in patients with recurrent episodes of nephrolithiasis, particularly in those who are unresponsive to conventional therapies. Combined liver-kidney transplant may be required as kidney transplant alone is not likely to be successful. Twit Text FOAVip Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report ????Exp Ther Med http://www.kidney.de/pget.php?&tw=1&pmid=29545831 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29545831 #FOAvip English Wikipedia <ref>{{Cite pmid|29545831}}</ref> Recurrent primary hyperoxaluria type 2 leads to early post-transplant renal function loss: A case report #MMPMID29545831 Liu S; Gao B; Wang G; Wang W; Lian X; Wu S; Yu J; Fu Y; Zhou H Exp Ther Med 2018[Apr]; 15 (4): 3169-72 PMID29545831show ga Primary hyperoxaluria type 2 is a rare autosomal recessive disorder caused by glyoxylate reductase/hydroxypyruvate reductase deficiency and characterized by recurrent episodes of nephrolithiasis and nephrocalcinosis. Herein, we describe a case of primary hyperoxaluria type 2 in a 33-year-old man who failed to respond to conventional therapies; thus renal transplantation was performed. This case demonstrated that, although primary hyperoxaluria type 2 is rare, hyperoxaluria should be suspected and blood oxalate and stone component be examined in patients with recurrent episodes of nephrolithiasis, particularly in those who are unresponsive to conventional therapies. Combined liver-kidney transplant may be required as kidney transplant alone is not likely to be successful. äRecurrent primary hyperoxaluria type 2 leads to early post-transplant (epmc).pdf DeepDyve Pubget Overpricing