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Recent Advances in the Pathogenesis and Drug Action in Periodic Paralyses and Related Channelopathies

The periodic paralysis (PP) are rare autosomal-dominant disorders associated to mutations in the skeletal muscle sodium, calcium, and potassium channel genes characterized by muscle fiber depolarization with un-excitability, episodes of weakness with variations in serum potassium concentrations. Rec...

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Detalhes bibliográficos
Main Authors: Tricarico, Domenico, Camerino, Diana Conte
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Research Foundation 2011
Assuntos:
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC3108473/
https://ncbi.nlm.nih.gov/pubmed/21687503
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fphar.2011.00008
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