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http://scihub22266oqcxt.onion/ C4852070!4852070!27141276     free     free     free Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27141276&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 Warning: imagejpeg(C:\Inetpub\vhosts\kidney.de\httpdocs\phplern\27141276.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117       Iran+J+Neurol 2016 ; 15 (1): 46-53 Nephropedia Template TP {{tp|p=27141276|t=2016. Myotonic disorders: A review article |pdf=|usr=}}{{27141276}} gab.com Text Myotonic disorders: A review article JO: Iran J Neurol http://www.kidney.de/pget.php?&tw=1&pmid=27141276 #FOAvip The myotonic disorders are a heterogeneous group of genetically determined diseases that are unified by the presence of myotonia, which is defined as failure of muscle relaxation after activation. The presentation of these disorders can range from asymptomatic electrical myotonia, as seen in some forms of myotonia congenita (MC), to severe disability with muscle weakness, cardiac conduction defects, and other systemic features as in myotonic dystrophy type I (DM1). In this review, we describe the clinical features and pathophysiology of the different myotonic disorders, their laboratory and electrophysiologic findings and briefly review the currently available treatments. Twit Text FOAVip Myotonic disorders: A review article ????Iran J Neurol http://www.kidney.de/pget.php?&tw=1&pmid=27141276 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=27141276 #FOAvip English Wikipedia <ref>{{Cite pmid|27141276}}</ref> Myotonic disorders: A review article #MMPMID27141276 Hahn C; Salajegheh MK Iran J Neurol 2016[Jan]; 15 (1): 46-53 PMID27141276show ga The myotonic disorders are a heterogeneous group of genetically determined diseases that are unified by the presence of myotonia, which is defined as failure of muscle relaxation after activation. The presentation of these disorders can range from asymptomatic electrical myotonia, as seen in some forms of myotonia congenita (MC), to severe disability with muscle weakness, cardiac conduction defects, and other systemic features as in myotonic dystrophy type I (DM1). In this review, we describe the clinical features and pathophysiology of the different myotonic disorders, their laboratory and electrophysiologic findings and briefly review the currently available treatments. äMyotonic disorders: A review article (epmc).pdf DeepDyve Pubget Overpricing