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Monogenic Epilepsies: Disease Mechanisms, Clinical Phenotypes, and Targeted Therapies

A monogenic etiology can be identified in up to 40% of people with severe epilepsy. To address earlier and more appropriate treatment strategies, clinicians are required to know the implications that specific genetic causes might have on pathophysiology, natural history, comorbidities, and treatment...

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Detalles Bibliográficos
Autores principales: Guerrini, Renzo, Balestrini, Simona, Wirrell, Elaine C., Walker, Matthew C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10336826/
https://www.ncbi.nlm.nih.gov/pubmed/34493617
http://dx.doi.org/10.1212/WNL.0000000000012744