Seizures, Febrile

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Saksa, D., Sun, L. S., Rodean, J., Berry, J., Hall, M., Leahy, I., Ferrari, L., & Huang, Y. Y. (2022). Variability in Resource Utilization in the Evaluation and Management of Simple Febrile Seizures Inpatients in US Children’s Hospitals. Journal of Neurosurgical Anesthesiology, 35(1), 153–159. https://doi.org/10.1097/ana.0000000000000887
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Platzer, K., Sticht, H., Bupp, C., Ganapathi, M., Pereira, E. M., Le Guyader, G., Bilan, F., Henderson, L. B., Lemke, J. R., Taschenberger, H., Brose, N., Abou Jamra, R., & Wojcik, S. M. (2022). De Novo Missense Variants in SLC32A1 Cause a Developmental and Epileptic Encephalopathy Due to Impaired GABAergic Neurotransmission. Annals of Neurology, 92(6), 958–973. Portico. https://doi.org/10.1002/ana.26485
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Cornejo-Sanchez, D. M., Acharya, A., Bharadwaj, T., Marin-Gomez, L., Pereira-Gomez, P., Nouel-Saied, L. M., Nickerson, D. A., Bamshad, M. J., Mefford, H. C., Schrauwen, I., Carrizosa-Moog, J., Cornejo-Ochoa, W., Pineda-Trujillo, N., & Leal, S. M. (2022). SCN1A Variants as the Underlying Cause of Genetic Epilepsy with Febrile Seizures Plus in Two Multi-Generational Colombian Families. Genes, 13(5), 754. https://doi.org/10.3390/genes13050754
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Cerulli Irelli, E., Cocchi, E., Ramantani, G., Caraballo, R. H., Giuliano, L., Yilmaz, T., Morano, A., Panagiotakaki, E., Operto, F. F., Gonzalez Giraldez, B., Silvennoinen, K., Casciato, S., Comajuan, M., Balestrini, S., Fortunato, F., Coppola, A., Di Gennaro, G., Labate, A., … Sofia, V. (2022). Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences. Neurology, 98(18). https://doi.org/10.1212/wnl.0000000000200165
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