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10.12688/f1000research.9045.1 http://scihub22266oqcxt.onion/10.12688/f1000research.9045.1 C4991528!4991528!27594986     free     free     free Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       F1000Res 2016 ; 5 (ä): ä Nephropedia Template TP {{tp|p=27594986|t=2016. Autosomal dominant polycystic kidney disease: recent advances in clinical management |pdf=|usr=}}{{27594986}} gab.com Text Autosomal dominant polycystic kidney disease: recent advances in clinical management JO: F1000Res http://www.kidney.de/pget.php?&tw=1&pmid=27594986 #FOAvip The first clinical descriptions of autosomal dominant polycystic kidney disease (ADPKD) go back at least 500 years to the late 16 th century. Advances in understanding disease presentation and pathophysiology have mirrored the progress of clinical medicine in anatomy, pathology, physiology, cell biology, and genetics. The identification of PKD1 and PKD2, the major genes mutated in ADPKD, has stimulated major advances, which in turn have led to the first approved drug for this disorder and a fresh reassessment of patient management in the 21 st century. In this commentary, we consider how clinical management is likely to change in the coming decade. Twit Text FOAVip Autosomal dominant polycystic kidney disease: recent advances in clinical management ????F1000Res http://www.kidney.de/pget.php?&tw=1&pmid=27594986 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27594986 #FOAvip English Wikipedia <ref>{{Cite pmid|27594986}}</ref> Autosomal dominant polycystic kidney disease: recent advances in clinical management #MMPMID27594986 Mao Z; Chong J; Ong ACM F1000Res 2016[]; 5 (ä): ä PMID27594986show ga The first clinical descriptions of autosomal dominant polycystic kidney disease (ADPKD) go back at least 500 years to the late 16 th century. Advances in understanding disease presentation and pathophysiology have mirrored the progress of clinical medicine in anatomy, pathology, physiology, cell biology, and genetics. The identification of PKD1 and PKD2, the major genes mutated in ADPKD, has stimulated major advances, which in turn have led to the first approved drug for this disorder and a fresh reassessment of patient management in the 21 st century. In this commentary, we consider how clinical management is likely to change in the coming decade. äAutosomal dominant polycystic kidney disease: recent advances in clini(epmc).pdf DeepDyve Pubget Overpricing