Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText. Kick-your-searchterm to multiple Engines kick-your-query now !>

A dictionary by aggregated review articles of nephrology, medicine and the life sciences Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

10.1161/CIRCRESAHA.115.301146 http://scihub22266oqcxt.onion/10.1161/CIRCRESAHA.115.301146 C4096686!4096686!24951762     free     free     free Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Circ+Res 2014 ; 115 (1): 115-30 Nephropedia Template TP {{tp|p=24951762|t=2014. Pulmonary Arterial Hypertension: The Clinical Syndrome |pdf=|usr=}}{{24951762}} gab.com Text Pulmonary Arterial Hypertension: The Clinical Syndrome JO: Circ Res http://www.kidney.de/pget.php?&tw=1&pmid=24951762 #FOAvip Pulmonary arterial hypertension (PAH) is a progressive disorder in which endothelial dysfunction and vascular remodeling obstruct small pulmonary arteries, resulting in increased pulmonary vascular resistance and pulmonary pressures. This leads to reduced cardiac output, right heart failure, and ultimately death. In this review, we attempt to answer some important questions commonly asked by patients diagnosed with PAH pertaining to the disease, and aim to provide an explanation in terms of classification, diagnosis, pathophysiology, genetic etiologies, demographics, and prognostic factors. Furthermore, important molecular pathways that are central to the pathogenesis of PAH are reviewed, including nitric oxide, prostacyclin, endothelin-1, reactive oxygen species, and endothelial and smooth muscle proliferation. Twit Text FOAVip Pulmonary Arterial Hypertension: The Clinical Syndrome ????Circ Res http://www.kidney.de/pget.php?&tw=1&pmid=24951762 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24951762 #FOAvip English Wikipedia <ref>{{Cite pmid|24951762}}</ref> Pulmonary Arterial Hypertension: The Clinical Syndrome #MMPMID24951762 Lai YC; Potoka KC; Champion HC; Mora AL; Gladwin MT Circ Res 2014[Jun]; 115 (1): 115-30 PMID24951762show ga Pulmonary arterial hypertension (PAH) is a progressive disorder in which endothelial dysfunction and vascular remodeling obstruct small pulmonary arteries, resulting in increased pulmonary vascular resistance and pulmonary pressures. This leads to reduced cardiac output, right heart failure, and ultimately death. In this review, we attempt to answer some important questions commonly asked by patients diagnosed with PAH pertaining to the disease, and aim to provide an explanation in terms of classification, diagnosis, pathophysiology, genetic etiologies, demographics, and prognostic factors. Furthermore, important molecular pathways that are central to the pathogenesis of PAH are reviewed, including nitric oxide, prostacyclin, endothelin-1, reactive oxygen species, and endothelial and smooth muscle proliferation. äPulmonary Arterial Hypertension: The Clinical Syndrome (epmc).pdf DeepDyve Pubget Overpricing