Concurrent Quinidine and Phenobarbital in the Treatment of a Patient with 2 KCNT1 Mutations

Epilepsy of infancy with migrating focal seizures is a devastating pediatric neurologic disorder that often results in treatment-resistant seizure activity and developmental delay. The condition has been associated with mutations in the KCNT1 gene that cause a gain of function in neuronal sodium-act...

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Detalles Bibliográficos
Autores principales: Passey, Camerin C., Erramouspe, John, Castellanos, Peter, O'Donnell, Elizabeth C., Denton, David M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2019
Materias:
Review Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6677567/
https://www.ncbi.nlm.nih.gov/pubmed/31388363
http://dx.doi.org/10.1016/j.curtheres.2019.02.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6677567/
https://www.ncbi.nlm.nih.gov/pubmed/31388363
http://dx.doi.org/10.1016/j.curtheres.2019.02.002

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