Title: | Myotonic disorders: A review article |
Journal : | Iranian journal of neurology, 15, 1 |
Authors: | Hahn C, Author ; Salajegheh MK |
Material Type: | Article |
Publication Date: | 2016 |
Size: | p 46 |
Languages: | English |
Keywords : | Becker myotonia congenita ; CLCN1 gene ; clinical presentation ; diagnosis ; diseases classifications ; diseases descriptions ; Eulenburg paramyotonia congenita ; familial hyperkalemic periodic paralysis ; medical treatment ; muscle stiffness ; myotonia fluctuans ; myotonic dystrophy type 1 ; myotonic dystrophy type 2 ; physiopathology ; prevalence ; review article ; SCN4A gene ; Thomsen myotonia congenita |
Keywords: | Hyperkalemic Periodic Paralysis;Myotonia;Myotonia Congenita;Myotonic Dystrophy;Paralysis Periodica Paramyotonia; |
Pubmed / DOI : | Pubmed : 27141276 |
Link for e-copy: | http://www.ncbi.nlm.nih.gov/pubmed/27141276 |