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10.1055/s-0036-1586162 http://scihub22266oqcxt.onion/10.1055/s-0036-1586162 C5495599!5495599!28680488     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=28680488&cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215 Deprecated: Implicit conversion from float 225.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534 Deprecated: Implicit conversion from float 225.6 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\28680488.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Int+Arch+Otorhinolaryngol 2017 ; 21 (3): 213-23 Nephropedia Template TP {{tp|p=28680488|t=2017. Sudden Sensorioneural Hearing Loss and Autoimmune Systemic Diseases |pdf=|usr=}}{{28680488}} gab.com Text Sudden Sensorioneural Hearing Loss and Autoimmune Systemic Diseases JO: Int Arch Otorhinolaryngol http://www.kidney.de/pget.php?&tw=1&pmid=28680488 #FOAvip Introduction ?Several authors have demonstrated the relationship between sudden sensorineural hearing loss (SNHL) and systemic autoimmune diseases (SAD). Immune-mediated SNHL can rarely present as unilateral sudden SNHL and manifests itself in the contralateral ear only after years. It presents clinical relevance for being one of the few SNHL that may be reversible given that early and appropriate treatment is applied. Objective ?The objective of this study is to describe the clinical presentations and audiological findings from patients with idiopathic sudden SNHL and SAD associated with a probable diagnosis of immune-mediated SNHL. Furthermore, we strive to estimate the prevalence of SAD in patients with sudden SNHL. Methods ?This is an observational retrospective cohort. We have selected and studied patients with SAD. Revision of available literature on scientific repositories. Results ?We evaluated 339 patients with sudden SNHL. Among them, 13 (3.83%) patients suffered from SAD. Three patients had bilateral involvement, a total of 16 ears. We evaluate and describe various clinical, epidemiological, and audiological aspects of this sample. Conclusion ?In our sample of patients with sudden SNHL, the prevalence of SAD was found relevant. The majority had tinnitus and dizziness concomitant hearing loss, unilateral involvement and had experienced profound hearing loss at the time of the installation. In spite of instituted treatment, most cases showed no improvement in audiometric thresholds. Apparently, patients with sudden SNHL and SAD have a more severe initial impairment, higher percentage of bilateral, lower response to treatment, and worse prognosis than patients with sudden SNHL of unknown etiology. Twit Text FOAVip Sudden Sensorioneural Hearing Loss and Autoimmune Systemic Diseases ????Int Arch Otorhinolaryngol http://www.kidney.de/pget.php?&tw=1&pmid=28680488 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28680488 #FOAvip English Wikipedia <ref>{{Cite pmid|28680488}}</ref> Sudden Sensorioneural Hearing Loss and Autoimmune Systemic Diseases #MMPMID28680488 Rossini BAA; Penido Nde O; Munhoz MSL; Bogaz EA; Curi RS Int Arch Otorhinolaryngol 2017[Jul]; 21 (3): 213-23 PMID28680488show ga Introduction ?Several authors have demonstrated the relationship between sudden sensorineural hearing loss (SNHL) and systemic autoimmune diseases (SAD). Immune-mediated SNHL can rarely present as unilateral sudden SNHL and manifests itself in the contralateral ear only after years. It presents clinical relevance for being one of the few SNHL that may be reversible given that early and appropriate treatment is applied. Objective ?The objective of this study is to describe the clinical presentations and audiological findings from patients with idiopathic sudden SNHL and SAD associated with a probable diagnosis of immune-mediated SNHL. Furthermore, we strive to estimate the prevalence of SAD in patients with sudden SNHL. Methods ?This is an observational retrospective cohort. We have selected and studied patients with SAD. Revision of available literature on scientific repositories. Results ?We evaluated 339 patients with sudden SNHL. Among them, 13 (3.83%) patients suffered from SAD. Three patients had bilateral involvement, a total of 16 ears. We evaluate and describe various clinical, epidemiological, and audiological aspects of this sample. Conclusion ?In our sample of patients with sudden SNHL, the prevalence of SAD was found relevant. The majority had tinnitus and dizziness concomitant hearing loss, unilateral involvement and had experienced profound hearing loss at the time of the installation. In spite of instituted treatment, most cases showed no improvement in audiometric thresholds. Apparently, patients with sudden SNHL and SAD have a more severe initial impairment, higher percentage of bilateral, lower response to treatment, and worse prognosis than patients with sudden SNHL of unknown etiology. äSudden Sensorioneural Hearing Loss and Autoimmune Systemic Diseases (epmc).pdf DeepDyve Pubget Overpricing