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10.5001/omj.2018.20 http://scihub22266oqcxt.onion/10.5001/omj.2018.20 C5889841!5889841!29657677     free     free     free Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\29657677.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Oman+Med+J 2018 ; 33 (2): 97-103 Nephropedia Template TP {{tp|p=29657677|t=2018. Immunoglobulin G4-Related Disease: An Update |pdf=|usr=}}{{29657677}} gab.com Text Immunoglobulin G4-Related Disease: An Update JO: Oman Med J http://www.kidney.de/pget.php?&tw=1&pmid=29657677 #FOAvip Immunoglobulin G4-related disease (IgG4-RD) is an increasingly recognized immune-mediated condition comprised of a collection of disorders that share specific pathological, serological, and clinical features. IgG4-RD is a fibroinflammatory condition with a tendency to form tumors with inflammatory infiltrate with IgG4 rich plasma cells and elevation of serum IgG4, which may affect virtually every organ and tissue. IgG4-related ophthalmic disease may present as dacryoadenitis, myositis, or involvement of other orbital tissue. Hypophysitis or pachymeningitis may manifest as cranial neuropathies. The diagnosis of IgG4-RD is based on a typical clinical scenario, supportive laboratory test, expected radiological characteristics, and distinct histopathological and immunohistochemical features. Corticosteroids and immunosuppressives form the mainline treatment. Twit Text FOAVip Immunoglobulin G4-Related Disease: An Update ????Oman Med J http://www.kidney.de/pget.php?&tw=1&pmid=29657677 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=29657677 #FOAvip English Wikipedia <ref>{{Cite pmid|29657677}}</ref> Immunoglobulin G4-Related Disease: An Update #MMPMID29657677 Al-Mujaini A; Al-Khabori M; Shenoy K; Wali U Oman Med J 2018[Mar]; 33 (2): 97-103 PMID29657677show ga Immunoglobulin G4-related disease (IgG4-RD) is an increasingly recognized immune-mediated condition comprised of a collection of disorders that share specific pathological, serological, and clinical features. IgG4-RD is a fibroinflammatory condition with a tendency to form tumors with inflammatory infiltrate with IgG4 rich plasma cells and elevation of serum IgG4, which may affect virtually every organ and tissue. IgG4-related ophthalmic disease may present as dacryoadenitis, myositis, or involvement of other orbital tissue. Hypophysitis or pachymeningitis may manifest as cranial neuropathies. The diagnosis of IgG4-RD is based on a typical clinical scenario, supportive laboratory test, expected radiological characteristics, and distinct histopathological and immunohistochemical features. Corticosteroids and immunosuppressives form the mainline treatment. äImmunoglobulin G4-Related Disease: An Update (epmc).pdf DeepDyve Pubget Overpricing