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10.4184/asj.2015.9.5.794 http://scihub22266oqcxt.onion/10.4184/asj.2015.9.5.794 C4591454!4591454!26435801     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=26435801&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       Asian+Spine+J 2015 ; 9 (5): 794-7 Nephropedia Template TP {{tp|p=26435801|t=2015. Severe Spinal Injury in Hirayama Disease |pdf=|usr=}}{{26435801}} gab.com Text Severe Spinal Injury in Hirayama Disease JO: Asian Spine J http://www.kidney.de/pget.php?&tw=1&pmid=26435801 #FOAvip Hirayama disease is a rare neurological disorder characterized by an insidious progressive subacute unilateral or bilateral weakness of the hands and forearm muscles leading to a painless amyotrophy. The disease primarily affects young men in the second to third decades of life. It has always been described as a second motor neuron disease, thus sparing the pyramidal and sensitive pathways. It usually has a slow progression course of 3 to 5 years followed by stabilization. Since its initial description by Keyzo Hirayama in 1959, most cases have been reported in Asia, particularly Japan and India, although the disease reportedly has worldwide distribution. Twit Text FOAVip Severe Spinal Injury in Hirayama Disease ????Asian Spine J http://www.kidney.de/pget.php?&tw=1&pmid=26435801 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26435801 #FOAvip English Wikipedia <ref>{{Cite pmid|26435801}}</ref> Severe Spinal Injury in Hirayama Disease #MMPMID26435801 Quarracino C; Aguirre F; Rugilo CA; Negri LD; Villa AM Asian Spine J 2015[Oct]; 9 (5): 794-7 PMID26435801show ga Hirayama disease is a rare neurological disorder characterized by an insidious progressive subacute unilateral or bilateral weakness of the hands and forearm muscles leading to a painless amyotrophy. The disease primarily affects young men in the second to third decades of life. It has always been described as a second motor neuron disease, thus sparing the pyramidal and sensitive pathways. It usually has a slow progression course of 3 to 5 years followed by stabilization. Since its initial description by Keyzo Hirayama in 1959, most cases have been reported in Asia, particularly Japan and India, although the disease reportedly has worldwide distribution. äSevere Spinal Injury in Hirayama Disease (epmc).pdf DeepDyve Pubget Overpricing