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10.2450/2015.0096-15 http://scihub22266oqcxt.onion/10.2450/2015.0096-15 C4781787!4781787 !26710352     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26710352 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\26710352 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Blood+Transfus 2016 ; 14 (2 ): 175-84 Nephropedia Template TP {{tp|p=26710352 |t=2016. The evolution of anticoagulant therapy |pdf=|usr=}}{{26710352 }} gab.com Text The evolution of anticoagulant therapy JO: Blood Transfus http://www.kidney.de/pget.php?&tw=1&pmid=26710352 #FOAvip Arterial and venous thromboembolism are leading causes of morbidity and mortality around the world. For almost 70 years, heparins (unfractionated heparin and low molecular weight heparins) and vitamin K antagonists have been the leading therapeutic medical options for the treatment and prevention of thromboembolic disorders. Nevertheless, the many limitations of these traditional anticoagulants have fuelled the search for novel agents over the past 15 years, and a new class of oral anticoagulants that specifically target activated factor X and thrombin has been developed and is now commercially available. In this narrative review, the evolution of anticoagulant therapy is summarised, with a focus on newer oral anticoagulants. Twit Text FOAVip The evolution of anticoagulant therapy ????Blood Transfus http://www.kidney.de/pget.php?&tw=1&pmid=26710352 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26710352 #FOAvip English Wikipedia <ref>{{Cite pmid|26710352 }}</ref> The evolution of anticoagulant therapy #MMPMID26710352 Franchini M ; Liumbruno GM ; Bonfanti C ; Lippi G Blood Transfus 2016[Mar]; 14 (2 ): 175-84 PMID26710352 show ga Arterial and venous thromboembolism are leading causes of morbidity and mortality around the world. For almost 70 years, heparins (unfractionated heparin and low molecular weight heparins) and vitamin K antagonists have been the leading therapeutic medical options for the treatment and prevention of thromboembolic disorders. Nevertheless, the many limitations of these traditional anticoagulants have fuelled the search for novel agents over the past 15 years, and a new class of oral anticoagulants that specifically target activated factor X and thrombin has been developed and is now commercially available. In this narrative review, the evolution of anticoagulant therapy is summarised, with a focus on newer oral anticoagulants. |Administration, Oral [MESH] |Factor Xa Inhibitors/history/*therapeutic use [MESH] |Heparin/history/*therapeutic use [MESH] |History, 20th Century [MESH] |History, 21st Century [MESH] |Humans [MESH] |Venous Thromboembolism/*drug therapy/history [MESH]The evolution of anticoagulant therapy (epmc).pdf DeepDyve Pubget Overpricing