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10.4081/audiores.2017.162 http://scihub22266oqcxt.onion/10.4081/audiores.2017.162 C5391519!5391519!28458810     free     free     free Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 213.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Audiol+Res 2017 ; 7 (1): ä Nephropedia Template TP {{tp|p=28458810|t=2017. Autoimmune Ear Disease: Clinical and Diagnostic Relevance in Cogan?s Sydrome |pdf=|usr=}}{{28458810}} gab.com Text Autoimmune Ear Disease: Clinical and Diagnostic Relevance in Cogan s Sydrome JO: Audiol Res http://www.kidney.de/pget.php?&tw=1&pmid=28458810 #FOAvip The autoimmune inner ear disease is a clinical syndrome with uncertain pathogenesis that is often associated to rapidly progressive hearing loss that, especially at the early stages of disease, may be at monoaural localization, although more often it is at binaural localization. It usually occurs as a sudden deafness, or a rapidly progressive sensorineural hearing loss. In this study a particular form of autoimmune inner ear disease is described, Cogan?s syndrome. Cogan?s syndrome is a chronic inflammatory disorder that most commonly affects young adults. Clinical hallmarks are interstitial keratitis, vestibular and auditory dysfunction. Associations between Cogan?s syndrome and systemic vasculitis, as well as aortitis, also exist. We report a case of a young woman who presented audiological and systemic characteristics attributable to Cogan?s syndrome. In the description of the case we illustrate how the appearance and evolution of the disease presented. Twit Text FOAVip Autoimmune Ear Disease: Clinical and Diagnostic Relevance in Cogan s Sydrome ????Audiol Res http://www.kidney.de/pget.php?&tw=1&pmid=28458810 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28458810 #FOAvip English Wikipedia <ref>{{Cite pmid|28458810}}</ref> Autoimmune Ear Disease: Clinical and Diagnostic Relevance in Cogan?s Sydrome #MMPMID28458810 Maiolino L; Cocuzza S; Conti A; Licciardello L; Serra A; Gallina S Audiol Res 2017[Feb]; 7 (1): ä PMID28458810show ga The autoimmune inner ear disease is a clinical syndrome with uncertain pathogenesis that is often associated to rapidly progressive hearing loss that, especially at the early stages of disease, may be at monoaural localization, although more often it is at binaural localization. It usually occurs as a sudden deafness, or a rapidly progressive sensorineural hearing loss. In this study a particular form of autoimmune inner ear disease is described, Cogan?s syndrome. Cogan?s syndrome is a chronic inflammatory disorder that most commonly affects young adults. Clinical hallmarks are interstitial keratitis, vestibular and auditory dysfunction. Associations between Cogan?s syndrome and systemic vasculitis, as well as aortitis, also exist. We report a case of a young woman who presented audiological and systemic characteristics attributable to Cogan?s syndrome. In the description of the case we illustrate how the appearance and evolution of the disease presented. äAutoimmune Ear Disease: Clinical and Diagnostic Relevance in Cogan?s S(epmc).pdf DeepDyve Pubget Overpricing