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10.3389/fped.2017.00053 http://scihub22266oqcxt.onion/10.3389/fped.2017.00053 C5362630!5362630!28386535     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       Front+Pediatr 2017 ; 5 (ä): ä Nephropedia Template TP {{tp|p=28386535|t=2017. Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease |pdf=|usr=}}{{28386535}} gab.com Text Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease JO: Front Pediatr http://www.kidney.de/pget.php?&tw=1&pmid=28386535 #FOAvip Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is associated with concerning long-term implications for kidney function and cardiovascular health. Early intervention is needed in order to mitigate these long-term complications. Herein, we review important findings from recent clinical trials in ADPKD and their relevance to affected children and young adults and consider future directions for intervention. Recent clinical trials support aggressive control of blood pressure with blockade of the renin-angiotensin-aldosterone system as well as potential benefit of pravastatin therapy in children and young adults with ADPKD. There are several other candidate therapies, some of which have shown benefit in adult ADPKD, which require further investigation in affected children. Twit Text FOAVip Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease ????Front Pediatr http://www.kidney.de/pget.php?&tw=1&pmid=28386535 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28386535 #FOAvip English Wikipedia <ref>{{Cite pmid|28386535}}</ref> Clinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Disease #MMPMID28386535 Cadnapaphornchai MA Front Pediatr 2017[]; 5 (ä): ä PMID28386535show ga Autosomal dominant polycystic kidney disease (ADPKD) is the most common hereditary kidney disease and is associated with concerning long-term implications for kidney function and cardiovascular health. Early intervention is needed in order to mitigate these long-term complications. Herein, we review important findings from recent clinical trials in ADPKD and their relevance to affected children and young adults and consider future directions for intervention. Recent clinical trials support aggressive control of blood pressure with blockade of the renin-angiotensin-aldosterone system as well as potential benefit of pravastatin therapy in children and young adults with ADPKD. There are several other candidate therapies, some of which have shown benefit in adult ADPKD, which require further investigation in affected children. äClinical Trials in Pediatric Autosomal Dominant Polycystic Kidney Dise(epmc).pdf DeepDyve Pubget Overpricing