Characterization of hyperkalemic periodic paralysis: a survey of genetically diagnosed individuals

This exploratory study aims to create an evidence-based comprehensive characterization of hyperkalemic periodic paralysis (hyperPP). HyperPP is a rare genetic disorder that causes episodes of flaccid paralysis. Disease descriptions in the literature are based upon isolated clinical encounters and ca...

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Detalles Bibliográficos
Autores principales: Charles, G., Zheng, C., Lehmann-Horn, F., Jurkat-Rott, K., Levitt, J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2013
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3824221/
https://www.ncbi.nlm.nih.gov/pubmed/23884711
http://dx.doi.org/10.1007/s00415-013-7025-9

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3824221/
https://www.ncbi.nlm.nih.gov/pubmed/23884711
http://dx.doi.org/10.1007/s00415-013-7025-9

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