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10.1590/abd1806-4841.20164449 http://scihub22266oqcxt.onion/10.1590/abd1806-4841.20164449 C5087238!5087238 !27828653     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 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\27828653 .jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       An+Bras+Dermatol 2016 ; 91 (5 ): 683-685 Nephropedia Template TP {{tp|p=27828653 |t=2016. Syndrome in question: antisynthetase syndrome (anti-PL-7) |pdf=|usr=}}{{27828653 }} gab.com Text Syndrome in question: antisynthetase syndrome (anti-PL-7) JO: An Bras Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=27828653 #FOAvip Antisynthetase syndrome is a rare autoimmune disease characterized by interstitial lung disease and/or inflammatory myositis, with positive antisynthetase antibodies (anti-Jo-1, anti-PL-7, anti-PL-12, ZO, OJ, anti-KE or KS). Other symptoms described include: non-erosive arthritis, fever, Raynaud's phenomenon, and "mechanic's hands." The first therapeutic option is corticotherapy, followed by other immunosuppressants. The prognosis of the disease is quite limited when compared to other inflammatory myopathies with negative antisynthetase antibodies. Twit Text FOAVip Syndrome in question: antisynthetase syndrome (anti-PL-7) ????An Bras Dermatol http://www.kidney.de/pget.php?&tw=1&pmid=27828653 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27828653 #FOAvip English Wikipedia <ref>{{Cite pmid|27828653 }}</ref> Syndrome in question: antisynthetase syndrome (anti-PL-7) #MMPMID27828653 Esposito AC ; Gige TC ; Miot HA An Bras Dermatol 2016[Sep]; 91 (5 ): 683-685 PMID27828653 show ga Antisynthetase syndrome is a rare autoimmune disease characterized by interstitial lung disease and/or inflammatory myositis, with positive antisynthetase antibodies (anti-Jo-1, anti-PL-7, anti-PL-12, ZO, OJ, anti-KE or KS). Other symptoms described include: non-erosive arthritis, fever, Raynaud's phenomenon, and "mechanic's hands." The first therapeutic option is corticotherapy, followed by other immunosuppressants. The prognosis of the disease is quite limited when compared to other inflammatory myopathies with negative antisynthetase antibodies. |Adult [MESH] |Female [MESH] |Hand Dermatoses/complications [MESH] |Humans [MESH] |Lung Diseases, Interstitial/complications/diagnostic imaging [MESH] |Myositis/complications/*diagnosis [MESH] |Nail Diseases/complications [MESH]Syndrome in question: antisynthetase syndrome (anti-PL-7) (epmc).pdf DeepDyve Pubget Overpricing