Hypokalemic periodic paralysis: a 3-year follow-up study

BACKGROUND AND OBJECTIVES: Primary hypokalemic periodic paralysis (HypoPP) is an inherited channelopathy most commonly caused by mutations in CACNA1S. HypoPP can present with different phenotypes: periodic paralysis (PP), permanent muscle weakness (PW), and mixed weakness (MW) with both periodic and...

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Detalles Bibliográficos
Autores principales: Holm-Yildiz, Sonja, Krag, Thomas, Witting, Nanna, Pedersen, Britt Stævnsbo, Dysgaard, Tina, Sloth, Louise, Pedersen, Jonas, Kjær, Rebecca, Kannuberg, Linda, Dahlqvist, Julia, de Stricker Borch, Josefine, Solheim, Tuva, Fornander, Freja, Eisum, Anne-Sofie, Vissing, John
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2023
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632268/
https://www.ncbi.nlm.nih.gov/pubmed/37656291
http://dx.doi.org/10.1007/s00415-023-11964-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10632268/
https://www.ncbi.nlm.nih.gov/pubmed/37656291
http://dx.doi.org/10.1007/s00415-023-11964-z

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