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10.1093/qjmed/hcu012 http://scihub22266oqcxt.onion/10.1093/qjmed/hcu012 C4071293!4071293!24453283     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=24453283&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 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       QJM 2014 ; 107 (7): 515-9 Nephropedia Template TP {{tp|p=24453283|t=2014. Vascular remodelling in the pathogenesis of idiopathic pulmonary fibrosis |pdf=|usr=}}{{24453283}} gab.com Text Vascular remodelling in the pathogenesis of idiopathic pulmonary fibrosis JO: QJM http://www.kidney.de/pget.php?&tw=1&pmid=24453283 #FOAvip Idiopathic pulmonary fibrosis (IPF) is a progressive and irreversible fibrosing interstitial pneumonia of unknown aetiology that usually leads to respiratory failure and death within 5 years of diagnosis. Alveolar epithelial cell injury, disruption of alveolar capillary membrane integrity and abnormal vascular repair and remodelling have all been proposed as possible pathogenic mechanisms. This review summarizes our current knowledge of the abnormalities in vascular remodelling observed in IPF and highlights several of the cytokines thought to play a pathogenic role, which may ultimately prove to be future therapeutic targets. Twit Text FOAVip Vascular remodelling in the pathogenesis of idiopathic pulmonary fibrosis ????QJM http://www.kidney.de/pget.php?&tw=1&pmid=24453283 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24453283 #FOAvip English Wikipedia <ref>{{Cite pmid|24453283}}</ref> Vascular remodelling in the pathogenesis of idiopathic pulmonary fibrosis #MMPMID24453283 Barratt S; Millar A QJM 2014[Jul]; 107 (7): 515-9 PMID24453283show ga Idiopathic pulmonary fibrosis (IPF) is a progressive and irreversible fibrosing interstitial pneumonia of unknown aetiology that usually leads to respiratory failure and death within 5 years of diagnosis. Alveolar epithelial cell injury, disruption of alveolar capillary membrane integrity and abnormal vascular repair and remodelling have all been proposed as possible pathogenic mechanisms. This review summarizes our current knowledge of the abnormalities in vascular remodelling observed in IPF and highlights several of the cytokines thought to play a pathogenic role, which may ultimately prove to be future therapeutic targets. äVascular remodelling in the pathogenesis of idiopathic pulmonary fibro(epmc).pdf DeepDyve Pubget Overpricing