Title: | What the internist should know about hereditary muscle channelopathies |
Journal : | Acta clinica Belgica, 73, 1 |
Authors: | Bissay V, Author ; Van Malderen SCH |
Material Type: | Article |
Publication Date: | 2018 |
Languages: | English |
Keywords : | Andersen syndrome ; chlorine channel disease ; familial hyperkalemic periodic paralysis ; familial hypokalemic periodic paralysis ; ion channel disease ; medical treatment ; muscle stiffness ; myotonia congenita ; myotonic dystrophy ; myotonic dystrophy type 1 ; myotonic dystrophy type 2 ; non dystrophic myotonic disease ; periodic paralysis ; skeletal muscle ; sodium channel disease |
Keywords: | Myotonia;channelopathy;dystrophy;paralysis;periodic; |
Pubmed / DOI : | DOI : 10.1080/17843286.2017.1396674 / Pubmed : 29088983 |
Link for e-copy: | http://www.ncbi.nlm.nih.gov/pubmed/29088983 |