Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy von Simkin, Dina, Marshall, Kelly A, Vanoye, Carlos G, Desai, Reshma R, Bustos, Bernabe I, Piyevsky, Brandon N, Ortega, Juan A, Forrest, Marc, Robertson, Gabriella L, Penzes, Peter, Laux, Linda C, Lubbe, Steven J, Millichap, John J, George, Alfred L, Kiskinis, Evangelos

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Open-label use of highly purified CBD (Epidiolex®) in patients with CDKL5 deficiency disorder and Aicardi, Dup15q, and Doose syndromes von Devinsky, Orrin, Verducci, Chloe, Thiele, Elizabeth A., Laux, Linda C., Patel, Anup D., Filloux, Francis, Szaflarski, Jerzy P., Wilfong, Angus, Clark, Gary D., Park, Yong D., Seltzer, Laurie E., Bebin, E. Martina, Flamini, Robert, Wechsler, Robert T., Friedman, Daniel

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Long‐term safety and treatment effects of cannabidiol in children and adults with treatment‐resistant epilepsies: Expanded access program results von Szaflarski, Jerzy P., Bebin, Elizabeth Martina, Comi, Anne M., Patel, Anup D., Joshi, Charuta, Checketts, Daniel, Beal, Jules C., Laux, Linda C., De Boer, Lisa M., Wong, Matthew H., Lopez, Merrick, Devinsky, Orrin, Lyons, Paul D., Zentil, Pilar Pichon, Wechsler, Robert, Chez, Michael, Flamini, Robert, Marsh, Eric D., Miller, Ian, Park, Yong, Segal, Eric, Seltzer, Laurie, Thiele, Elizabeth A., Weinstock, Arie

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Seizure Outcomes in Children Following Electrocorticography-Guided Single-Stage Surgical Resection von Bansal, Seema, Kim, Andrew J., Berg, Anne T., Koh, Sookyong, Laux, Linda C., Nangia, Srishti, Millichap, John J., Shaw, Alexandra, Fisher, Breanne, Dezort, Catherine, DiPatri, Arthur J., Alden, Tord D., Nordli, Douglas R.

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Long-term safety and efficacy of cannabidiol in children and adults with treatment resistant Lennox-Gastaut syndrome or Dravet syndrome: Expanded access program results von Laux, Linda C., Bebin, E. Martina, Checketts, Daniel, Chez, Michael, Flamini, Robert, Marsh, Eric D., Miller, Ian, Nichol, Kathryn, Park, Yong, Segal, Eric, Seltzer, Laurie, Szaflarski, Jerzy P., Thiele, Elizabeth A., Weinstock, Arie

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Severe peri-ictal respiratory dysfunction is common in Dravet syndrome von Kim, YuJaung, Bravo, Eduardo, Thirnbeck, Caitlin K, Smith-Mellecker, Lori A, Kim, Se Hee, Gehlbach, Brian K, Laux, Linda C, Zhou, Xiuqiong, Nordli, Jr, Douglas R, Richerson, George B

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Phenotypes of Dravet Syndrome von Garcia-Sosa, Rebecca, Laux, Linda C

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The ketogenic diet in children 3 years of age or younger: a 10-year single-center experience von Kim, Se Hee, Shaw, Alexandra, Blackford, Robyn, Lowman, Wesley, Laux, Linda C., Millichap, John J., Nordli, Douglas R.

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Alleged cases of vaccine encephalopathy rediagnosed years later as Dravet syndrome von Reyes, Ila S, Hsieh, David T, Laux, Linda C, Wilfong, Angus A

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Child Neurology: Dravet syndrome: when to suspect the diagnosis von Millichap, John J, Koh, Sookyong, Laux, Linda C, Nordli, Jr, Douglas R

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When do seizures usually improve with the ketogenic diet? von Kossoff, Eric H., Laux, Linda C., Blackford, Robyn, Morrison, Peter F., Pyzik, Paula L., Hamdy, Rana M., Turner, Zahava, Nordli, Douglas R.

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Ictal asystole and anti-N-methyl-D-aspartate receptor antibody encephalitis von Millichap, John J, Goldstein, Joshua L, Laux, Linda C, Nordli, Jr, Douglas R, Stack, Cynthia V, Wainwright, Mark S

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Pediatric Psychogenic Nonepileptic Seizures in the Emergency Department: Recognition and Interventions von Plioplys, Sigita, MD, Laux, Linda C., MD

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Functional Consequences of Epilepsy-Associated KCNQ2 Variants Determinend by Automated Electrophysiology von Vanoye, Carlos G., Desai, Reshma R., Gallagher, Shannon L., Sinkim, Dina, Laux, Linda C., Millichap, John J., Kiskinis, Evangelos, George, Alfred L.

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Return of individual results in epilepsy genomic research: A view from the field von Ottman, Ruth, Freyer, Catharine, Mefford, Heather C., Poduri, Annapurna, Lowenstein, Daniel H., Appelbaum, Paul S., Burke, Wylie, Dixon‐Salazar, Tracy, Dlugos, Dennis, Fisher, Robert S., Helbig, Katherine L., Herraiz, Laurie, Holm, Ingrid, Huntley, Melanie, Koenig, Barbara, Laux, Linda C., Porter, Brenda, Sewards, Shannon, Sheidley, Beth R.

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Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy von Simkin, Dina, Marshall, Kelly A, Vanoye, Carlos G, Desai, Reshma R, Bustos, Bernabe I, Piyevsky, Brandon N, Ortega Cano, Juan Alberto, Forrest, Marc, Robertson, Gabriella L, Penzes, Peter, Laux, Linda C, Lubbe, Steven J, Millichap, John J, George Jr, Alfred L, Kiskinis, Evangelos

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Seizure Outcomes in Children Following ECoG-Guided Single-Stage Surgical Resection von Bansal, Seema, Kim, Andrew J, Berg, Anne T, Koh, Sookyong, Laux, Linda C, Nangia, Srishti, Millichap, John J, Shaw, Alexandra, Fisher, Breanne, Dezort, Catherine, DiPatri, Arthur J, Alden, Tord D, Nordli, Douglas R

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Dyshomeostatic modulation of Ca 2+ -activated K + channels in a human neuronal model of KCNQ2 encephalopathy von Simkin, Dina, Marshall, Kelly A, Vanoye, Carlos G, Desai, Reshma R, Bustos, Bernabe I, Piyevsky, Brandon N, Ortega, Juan A, Forrest, Marc, Robertson, Gabriella L, Penzes, Peter, Laux, Linda C, Lubbe, Steven J, Millichap, John J, George, Jr, Alfred L, Kiskinis, Evangelos

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Optimizing the Diagnosis and Management of Dravet Syndrome: Recommendations from A North American Consensus Panel von Wirrell, Elaine C., MD, Laux, Linda, MD, Donner, Elizabeth, MD, Jette, Nathalie, MD, Knupp, Kelly, MD, Meskis, Mary Anne, Miller, Ian, MD, Sullivan, Joseph, MD, Welborn, Michelle, Pharm D, Berg, Anne T., PhD

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Trial of Cannabidiol for Drug-Resistant Seizures in the Dravet Syndrome von Devinsky, Orrin, Cross, J. Helen, Laux, Linda, Marsh, Eric, Miller, Ian, Nabbout, Rima, Scheffer, Ingrid E, Thiele, Elizabeth A, Wright, Stephen

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