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10.1136/bcr-2016-215981 http://scihub22266oqcxt.onion/10.1136/bcr-2016-215981 C4986154!4986154!27469383     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       BMJ+Case+Rep 2016 ; 2016 (ä): ä Nephropedia Template TP {{tp|p=27469383|t=2016. Expanding the range of immunopathology in neuromyelitis optica spectrum disorder |pdf=|usr=}}{{27469383}} gab.com Text Expanding the range of immunopathology in neuromyelitis optica spectrum disorder JO: BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=27469383 #FOAvip Neuromyelitis optica (NMO) spectrum disorder typically associates with a pathognomonic antibody response directed against aquaporin 4 and a unique immunopathological signature characterised by loss of aquaporin 4 expression. We describe a tumefactive presentation of NMO in which a biopsy specimen demonstrated active demyelination and reactive astrocytes with preserved surface aquaporin 4 immunoreactivity and dystrophic processes. While the astrocytic pathology is more typical of classical multiple sclerosis, a positive NMO-IgG (1:80) and subsequent clinical presentation with an area postrema syndrome is consistent with a diagnosis of NMO spectrum disorder. This report expands the immunopathological features that have been reported in NMO spectrum disorder. Twit Text FOAVip Expanding the range of immunopathology in neuromyelitis optica spectrum disorder ????BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=27469383 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27469383 #FOAvip English Wikipedia <ref>{{Cite pmid|27469383}}</ref> Expanding the range of immunopathology in neuromyelitis optica spectrum disorder #MMPMID27469383 Massey J; Buckland ME; Barnett Y; Sutton I BMJ Case Rep 2016[]; 2016 (ä): ä PMID27469383show ga Neuromyelitis optica (NMO) spectrum disorder typically associates with a pathognomonic antibody response directed against aquaporin 4 and a unique immunopathological signature characterised by loss of aquaporin 4 expression. We describe a tumefactive presentation of NMO in which a biopsy specimen demonstrated active demyelination and reactive astrocytes with preserved surface aquaporin 4 immunoreactivity and dystrophic processes. While the astrocytic pathology is more typical of classical multiple sclerosis, a positive NMO-IgG (1:80) and subsequent clinical presentation with an area postrema syndrome is consistent with a diagnosis of NMO spectrum disorder. This report expands the immunopathological features that have been reported in NMO spectrum disorder. äExpanding the range of immunopathology in neuromyelitis optica spectru(epmc).pdf DeepDyve Pubget Overpricing