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10.1155/2017/6501738 http://scihub22266oqcxt.onion/10.1155/2017/6501738 C5585673!5585673!28912820     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 Deprecated: Implicit conversion from float 211.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\28912820.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Case+Rep+Med 2017 ; 2017 (ä): ä Nephropedia Template TP {{tp|p=28912820|t=2017. Granulomatosis with Polyangiitis with Myocarditis and Ventricular Tachycardia |pdf=|usr=}}{{28912820}} gab.com Text Granulomatosis with Polyangiitis with Myocarditis and Ventricular Tachycardia JO: Case Rep Med http://www.kidney.de/pget.php?&tw=1&pmid=28912820 #FOAvip Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis, is a pulmonary-renal syndrome affecting small and medium sized blood vessels. The disease has a prevalence in studies ranging from 3 to 15.7 cases per 100,000, with a noted increasing incidence and prevalence in more recent studies. Pulmonary manifestations include hemorrhage, lung cavitary lesions, and pulmonary fibrosis. Within the kidney, GPA is known to cause rapidly progressive pauci-immune crescentic glomerulonephritis. Rare and severe cardiovascular manifestations include pericarditis, arrhythmias, myocarditis, and aortic valve disease. Our patient is a 43-year-old female with typical pulmonary and renal lesions from GPA and also acute myocarditis, multiple episodes of ventricular tachycardia, and a severe reactive thrombocytosis. Twit Text FOAVip Granulomatosis with Polyangiitis with Myocarditis and Ventricular Tachycardia ????Case Rep Med http://www.kidney.de/pget.php?&tw=1&pmid=28912820 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28912820 #FOAvip English Wikipedia <ref>{{Cite pmid|28912820}}</ref> Granulomatosis with Polyangiitis with Myocarditis and Ventricular Tachycardia #MMPMID28912820 Hanna RM; Lopez E; Wilson J Case Rep Med 2017[]; 2017 (ä): ä PMID28912820show ga Granulomatosis with polyangiitis (GPA), previously known as Wegener's granulomatosis, is a pulmonary-renal syndrome affecting small and medium sized blood vessels. The disease has a prevalence in studies ranging from 3 to 15.7 cases per 100,000, with a noted increasing incidence and prevalence in more recent studies. Pulmonary manifestations include hemorrhage, lung cavitary lesions, and pulmonary fibrosis. Within the kidney, GPA is known to cause rapidly progressive pauci-immune crescentic glomerulonephritis. Rare and severe cardiovascular manifestations include pericarditis, arrhythmias, myocarditis, and aortic valve disease. Our patient is a 43-year-old female with typical pulmonary and renal lesions from GPA and also acute myocarditis, multiple episodes of ventricular tachycardia, and a severe reactive thrombocytosis. äGranulomatosis with Polyangiitis with Myocarditis and Ventricular Tach(epmc).pdf DeepDyve Pubget Overpricing