Comorbidities of Rare Epilepsies: Results from the Rare Epilepsy Network by Ho, Nhan Thi, Kroner, Barbara, Grinspan, Zachary, Fureman, Brandy, Farrell, Kathleen, Zhang, Jingzhou, Buelow, Janice, Hesdorffer, Dale C., McDonald, Brianne, Weldon, Monica, Bradish, Juliann, Vogel-Farley, Vanessa, Nues, Paige, Dixon-Salazar, Tracy, Bliss, Geraldine, DeWoody, Yssa, Nakagawa, Jo Anne, Kroner, Barbara, Harris, Michael, Arm, Glen, Jackson, Heather, Miller, Ilene, Vozenilek, Gina, Wong, Nora, Davidow, Audrey, Wagner, Kira, Hecker, JayEtta, Egan, Lynn, Grabenstatter, Heidi, Meskis, Mary Anne, Bartenhagen, Mike, Sims, Scotty, Walters, Julie, Schoyer, Lisa, Nye, Kim

Get full text

Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy by Abreo, Timothy J, Thompson, Emma C, Madabushi, Anuraag, Park, Kristen L, Soh, Heun, Varghese, Nissi, Vanoye, Carlos G, Springer, Kristen, Johnson, Jim, Sims, Scotty, Ji, Zhigang, Chavez, Ana G, Jankovic, Miranda J, Habte, Bereket, Zuberi, Aamir R, Lutz, Cathleen M, Wang, Zhao, Krishnan, Vaishnav, Dudler, Lisa, Einsele-Scholz, Stephanie, Noebels, Jeffrey L, George, Alfred L, Maheshwari, Atul, Tzingounis, Anastasios, Cooper, Edward C

Get full text

Factors Associated with Caregiver Sleep Quality Related to Children with Rare Epilepsy Syndromes by Hesdorffer, Dale C., Kroner, Barbara L., Shen, Jing, Farrell, Kathleen, Roberds, Steve, Fureman, Brandy, McDonald, Brianne, Egan, Lynn, Jones, Monika, Weldon, Monica, Harris, Michael, Rice, Kim, Campbell, Vinez, Brandish, Juliann, Kercheval, Cindy, Villas, Nichole, Meskis, Mary Ann, Vogel-Farley, Vanessa, Miller, Ilene, Bartenhagen, Mike, Grabenstatter, Heidi, Utley, Karen, Nues, Paige, Cherry, Angela, Vozenilek, Gina, Sims, Scotty, Salazar, Tracy Dixon, SanInocencio, Christina, Forman, Stephanie, Wong, Nora, Bischoff, Kim, Walters, Julie, O’Boyle, Megan, Bliss, Geraldine, Davidow, Audrey, Schoyer, Lisa, DeWoody, Yssa, Wagner, Kira, Arcieri, Michael, Freed, Amber, Nye, Kim, Nakagawa, Jo Anne, Hecker, JayEtta

Get full text

Nonseizure consequences of Dravet syndrome, KCNQ2-DEE, KCNB1-DEE, Lennox–Gastaut syndrome, ESES: A functional framework by Berg, Anne T., Gaebler-Spira, Deborah, Wilkening, Greta, Zelko, Frank, Knupp, Kelly, Dixon-Salazar, Tracy, Villas, Nicole, Meskis, Mary Anne, Harwell, Vinez, Thompson, Tina, Sims, Scotty, Nesbitt, Gerry

Get full text

Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy by Abreo, Timothy J, Thompson, Emma C, Madabushi, Anuraag, Park, Kristen L, Soh, Heun, Varghese, Nissi, Vanoye, Carlos G, Springer, Kristen, Johnson, Jim, Sims, Scotty, Ji, Zhigang, Chavez, Ana G, Jankovic, Miranda J, Habte, Bereket, Zuberi, Aamir R, Lutz, Cathleen M, Wang, Zhao, Krishnan, Vaishnav, Dudler, Lisa, Einsele-Scholz, Stephanie, Noebels, Jeffrey L, George, Alfred L, Maheshwari, Atul, Tzingounis, Anastasios, Cooper, Edward C

Get full text