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10.1002/rcr2.104 http://scihub22266oqcxt.onion/10.1002/rcr2.104 C4469147!4469147!26090118     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 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       Respirol+Case+Rep 2015 ; 3 (2): 78-81 Nephropedia Template TP {{tp|p=26090118|t=2015. Autoimmune disease leading to pulmonary AL amyloidosis and pulmonary hypertension |pdf=|usr=}}{{26090118}} gab.com Text Autoimmune disease leading to pulmonary AL amyloidosis and pulmonary hypertension JO: Respirol Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=26090118 #FOAvip A 33-year-old woman with past history of Sjögren's syndrome and systemic lupus erythematosus presented with dyspnea and syncope secondary to pulmonary hypertension. After progressive symptoms over 4 years, she received bilateral lung transplantation. Histopathology of the explanted lungs showed isolated pulmonary amyloid light-chain amyloidosis and pulmonary cysts. No evidence of systemic amyloidosis was found at the time of transplantation. Seven years post lung transplantation, she remains well with no evidence of systemic amyloidosis recurrence. Twit Text FOAVip Autoimmune disease leading to pulmonary AL amyloidosis and pulmonary hypertension ????Respirol Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=26090118 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26090118 #FOAvip English Wikipedia <ref>{{Cite pmid|26090118}}</ref> Autoimmune disease leading to pulmonary AL amyloidosis and pulmonary hypertension #MMPMID26090118 Ellender CM; McLean C; Williams TJ; Snell GI; Whitford HM Respirol Case Rep 2015[Jun]; 3 (2): 78-81 PMID26090118show ga A 33-year-old woman with past history of Sjögren's syndrome and systemic lupus erythematosus presented with dyspnea and syncope secondary to pulmonary hypertension. After progressive symptoms over 4 years, she received bilateral lung transplantation. Histopathology of the explanted lungs showed isolated pulmonary amyloid light-chain amyloidosis and pulmonary cysts. No evidence of systemic amyloidosis was found at the time of transplantation. Seven years post lung transplantation, she remains well with no evidence of systemic amyloidosis recurrence. äAutoimmune disease leading to pulmonary AL amyloidosis and pulmonary h(epmc).pdf DeepDyve Pubget Overpricing