Views of caregivers, clinicians, and epilepsy advocacy group representatives on survey instruments used to assess behavior, communication, and quality of life in individuals with Lennox-Gastaut syndrome

Epilepsy Research · Published 2026-07-31 · DOI 10.1016/j.eplepsyres.2026.107889

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Authors (11)

Nicole Villalba, Rya Muller, Marc Rosenman, Sandi Lam, Tracy Dixon-Salazar, Kathy Leavens, Megan Votoupal, Carolyn C. Foster, Mary Wojnaroski, Maura Carroll, Anup D. Patel

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Year

2026

Citation

Villalba, N., Muller, R., Rosenman, M., et al. (2026). Views of caregivers, clinicians, and epilepsy advocacy group representatives on survey instruments used to assess behavior, communication, and quality of life in individuals with Lennox-Gastaut syndrome. Epilepsy Research. https://doi.org/10.1016/j.eplepsyres.2026.107889

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