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10.4103/jpn.JPN_140_16 http://scihub22266oqcxt.onion/10.4103/jpn.JPN_140_16 C5437791!5437791!28553383     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       J+Pediatr+Neurosci 2017 ; 12 (1): 55-60 Nephropedia Template TP {{tp|p=28553383|t=2017. Hemophagocytic Lymphohistiocytosis: A Diagnostic Conundrum |pdf=|usr=}}{{28553383}} gab.com Text Hemophagocytic Lymphohistiocytosis: A Diagnostic Conundrum JO: J Pediatr Neurosci http://www.kidney.de/pget.php?&tw=1&pmid=28553383 #FOAvip Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of excessive immune activation causing widespread inflammation and tissue destruction leading to multi-organ dysfunction and failure. Making the diagnosis of HLH could be quite challenging due to the broad range of presenting symptoms and their lack of specificity. After ruling out considerations for differential diagnoses, recognizing the most common presenting signs and symptoms of HLH, including neurologic dysfunction, and having a high clinical suspicion for HLH in the setting of inflammatory/demyelinating diseases are important for prompt diagnosis and treatment. Twit Text FOAVip Hemophagocytic Lymphohistiocytosis: A Diagnostic Conundrum ????J Pediatr Neurosci http://www.kidney.de/pget.php?&tw=1&pmid=28553383 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=28553383 #FOAvip English Wikipedia <ref>{{Cite pmid|28553383}}</ref> Hemophagocytic Lymphohistiocytosis: A Diagnostic Conundrum #MMPMID28553383 Grzybowski B; Vishwanath VA J Pediatr Neurosci 2017[Jan]; 12 (1): 55-60 PMID28553383show ga Hemophagocytic lymphohistiocytosis (HLH) is a syndrome of excessive immune activation causing widespread inflammation and tissue destruction leading to multi-organ dysfunction and failure. Making the diagnosis of HLH could be quite challenging due to the broad range of presenting symptoms and their lack of specificity. After ruling out considerations for differential diagnoses, recognizing the most common presenting signs and symptoms of HLH, including neurologic dysfunction, and having a high clinical suspicion for HLH in the setting of inflammatory/demyelinating diseases are important for prompt diagnosis and treatment. äHemophagocytic Lymphohistiocytosis: A Diagnostic Conundrum (epmc).pdf DeepDyve Pubget Overpricing