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10.21037/cdt.2017.12.07 http://scihub22266oqcxt.onion/10.21037/cdt.2017.12.07 C6039799!6039799!30057878     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 Deprecated: Implicit conversion from float 209.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Cardiovasc+Diagn+Ther 2018 ; 8 (3): 316-24 Nephropedia Template TP {{tp|p=30057878|t=2018. Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations: clinical aspects |pdf=|usr=}}{{30057878}} gab.com Text Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations: clinical aspects JO: Cardiovasc Diagn Ther http://www.kidney.de/pget.php?&tw=1&pmid=30057878 #FOAvip Hereditary hemorrhagic telangiectasia (HHT) is a genetic disorder of blood vessel formation resulting in mucocutaneous telangiectasias and visceral arteriovenous malformations. Nearly half of patients with HHT will have pulmonary arteriovenous malformations (PAVM) that place them at risk for potentially fatal complications that can occur when blood bypasses the pulmonary capillary circulation or as a result of PAVM rupture. Other manifestations of HHT outside the lung may increase the rate and severity of PAVM complications, creating unique clinical challenges. Management hinges on timely screening and diagnosis, followed by treatment of amenable PAVMs with transcatheter embolization in conjunction with medical management and prophylactic measures to treat and prevent complications. The purpose of this review is to highlight the clinical manifestations of PAVMs specific to patients with HHT and to detail screening and treatment strategies that can reduce the risk of developing life-threatening complications. Twit Text FOAVip Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations: clinical aspects ????Cardiovasc Diagn Ther http://www.kidney.de/pget.php?&tw=1&pmid=30057878 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=30057878 #FOAvip English Wikipedia <ref>{{Cite pmid|30057878}}</ref> Hereditary hemorrhagic telangiectasia and pulmonary arteriovenous malformations: clinical aspects #MMPMID30057878 Meier NM; Foster ML; Battaile JT Cardiovasc Diagn Ther 2018[Jun]; 8 (3): 316-24 PMID30057878show ga Hereditary hemorrhagic telangiectasia (HHT) is a genetic disorder of blood vessel formation resulting in mucocutaneous telangiectasias and visceral arteriovenous malformations. Nearly half of patients with HHT will have pulmonary arteriovenous malformations (PAVM) that place them at risk for potentially fatal complications that can occur when blood bypasses the pulmonary capillary circulation or as a result of PAVM rupture. Other manifestations of HHT outside the lung may increase the rate and severity of PAVM complications, creating unique clinical challenges. Management hinges on timely screening and diagnosis, followed by treatment of amenable PAVMs with transcatheter embolization in conjunction with medical management and prophylactic measures to treat and prevent complications. The purpose of this review is to highlight the clinical manifestations of PAVMs specific to patients with HHT and to detail screening and treatment strategies that can reduce the risk of developing life-threatening complications. äHereditary hemorrhagic telangiectasia and pulmonary arteriovenous malf(epmc).pdf DeepDyve Pubget Overpricing