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10.4103/2152-7806.169561 http://scihub22266oqcxt.onion/10.4103/2152-7806.169561 C4653353!4653353!26629397     free     free     free Deprecated: Implicit conversion from float 231.6 to int loses precision in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 534       Surg+Neurol+Int 2015 ; 6 (ä): ä Nephropedia Template TP {{tp|p=26629397|t=2015. A comprehensive review of amyotrophic lateral sclerosis |pdf=|usr=}}{{26629397}} gab.com Text A comprehensive review of amyotrophic lateral sclerosis JO: Surg Neurol Int http://www.kidney.de/pget.php?&tw=1&pmid=26629397 #FOAvip Amyotrophic lateral sclerosis (ALS) is a late-onset fatal neurodegenerative disease affecting motor neurons with an incidence of about 1/100,000. Most ALS cases are sporadic, but 5?10% of the cases are familial ALS. Both sporadic and familial ALS (FALS) are associated with degeneration of cortical and spinal motor neurons. The etiology of ALS remains unknown. However, mutations of superoxide dismutase 1 have been known as the most common cause of FALS. In this study, we provide a comprehensive review of ALS. We cover all aspects of the disease including epidemiology, comorbidities, environmental risk factor, molecular mechanism, genetic factors, symptoms, diagnostic, treatment, and even the available supplement and management of ALS. This will provide the reader with an advantage of receiving a broad range of information about the disease. Twit Text FOAVip A comprehensive review of amyotrophic lateral sclerosis ????Surg Neurol Int http://www.kidney.de/pget.php?&tw=1&pmid=26629397 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=26629397 #FOAvip English Wikipedia <ref>{{Cite pmid|26629397}}</ref> A comprehensive review of amyotrophic lateral sclerosis #MMPMID26629397 Zarei S; Carr K; Reiley L; Diaz K; Guerra O; Altamirano PF; Pagani W; Lodin D; Orozco G; Chinea A Surg Neurol Int 2015[]; 6 (ä): ä PMID26629397show ga Amyotrophic lateral sclerosis (ALS) is a late-onset fatal neurodegenerative disease affecting motor neurons with an incidence of about 1/100,000. Most ALS cases are sporadic, but 5?10% of the cases are familial ALS. Both sporadic and familial ALS (FALS) are associated with degeneration of cortical and spinal motor neurons. The etiology of ALS remains unknown. However, mutations of superoxide dismutase 1 have been known as the most common cause of FALS. In this study, we provide a comprehensive review of ALS. We cover all aspects of the disease including epidemiology, comorbidities, environmental risk factor, molecular mechanism, genetic factors, symptoms, diagnostic, treatment, and even the available supplement and management of ALS. This will provide the reader with an advantage of receiving a broad range of information about the disease. äA comprehensive review of amyotrophic lateral sclerosis (epmc).pdf DeepDyve Pubget Overpricing