No evidence that SCN9A variants are associated with epilepsy von Brunklaus, A.

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Prognostic, clinical and demographic features in SCN1A mutation-positive Dravet syndrome von BRUNKLAUS, A, ELLIS, R, REAVEY, E, FORBES, G. H, ZUBERI, S. M

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Genotype―phenotype associations in SCN1A-related epilepsies von ZUBERI, S. M, BRUNKLAUS, A, BIRCH, R, REAVEY, E, DUNCAN, J, FORBES, G. H

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Genetic diversity analysis of Moroccan lentil (Lens culinaris Medik.) landraces using Simple Sequence Repeat and Amplified Fragment Length Polymorphisms reveals functional adaptati... von Idrissi, Omar, Udupa, Sripada M., Houasli, Chafika, De Keyser, Ellen, Van Damme, Patrick, De Riek, Jan

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The value of cardiac MRI versus echocardiography in the pre-operative assessment of patients with Duchenne muscular dystrophy von Brunklaus, A, Parish, E, Muntoni, F, Scuplak, S, Tucker, S.K, Fenton, M, Hughes, M.L, Manzur, A.Y

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Safety and efficacy of ganaxolone in patients with CDKL5 deficiency disorder: results from the double-blind phase of a randomised, placebo-controlled, phase 3 trial von Knight, Elia M Pestana, Amin, Sam, Bahi-Buisson, Nadia, Benke, Tim A, Cross, J Helen, Demarest, Scott T, Olson, Heather E, Specchio, Nicola, Fleming, Thomas R, Aimetti, Alex A, Gasior, Maciej, Devinsky, Orrin, Belousova, Elena, Belyaev, Oleg, Ben-Zeev, Bruria, Brunklaus, Andreas, Ciliberto, Michael A., Darra, Francesca, Davis, Ronald, De Giorgis, Valentina, Doronina, Olga, Fahey, Michael, Guerrini, Renzo, Heydemann, Peter, Khaletskaya, Olga, Lisewski, Pawel, Marsh, Eric D., Moosa, Ahsan N., Perry, Scott, Philip, Sunny, Rajaraman, Rajsekar R., Renfroe, Ben, Saneto, Russell P., Scheffer, Ingrid E., Sogawa, Yoshimi, Suter, Bernhardt, Sweney, Matthew T., Tarquinio, Daniel, Veggiotti, Pierangelo, Wallace, Geoff, Weisenberg, Judy, Wilfong, Angus, Wirrell, Elaine C., Zafar, Muhammad, Zolnowska, Marta

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The Genetic Landscape of Epilepsy of Infancy with Migrating Focal Seizures von Burgess, Rosemary, Wang, Shuyu, McTague, Amy, Boysen, Katja E., Yang, Xiaoling, Zeng, Qi, Myers, Kenneth A., Rochtus, Anne, Trivisano, Marina, Gill, Deepak, Sadleir, Lynette G., Specchio, Nicola, Guerrini, Renzo, Marini, Carla, Zhang, Yue‐Hua, Mefford, Heather C., Kurian, Manju A., Poduri, Annapurna H., Scheffer, Ingrid E.

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High sensitivity and specificity of the light-adapted ERG for neuronal ceroid lipofuscinoses (NCLs) von Morris, W, Brunklaus, A, Horrocks, I.A, Macleod, S, O'Regan, M.E, Spowart, K, Yeo, T.H, Zuberi, S, Hamilton, R

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International consensus recommendations for management of new onset refractory status epilepticus (NORSE) including febrile infection‐related epilepsy syndrome (FIRES): Summary and... von Wickström, Ronny, Taraschenko, Olga, Dilena, Robertino, Payne, Eric T., Specchio, Nicola, Nabbout, Rima, Koh, Sookyong, Gaspard, Nicolas, Hirsch, Lawrence J., Auvin, Stephane, Baalen, Andreas, Beghi, Ettore, Benseler, Susanne M., Bergin, Peter, Bleck, Tom, Brunklaus, Andreas, Caraballo, Roberto H., Cervenka, Mackenzie, Costello, Daniel, Drislane, Frank, Farias‐Moeller, Raquel, Gallantine, William, Gilmore, Emily J., Gofton, Teneille, Jimenez, Maria Angeles Perez, Hocker, Sara, Kaliakatsos, Marios, Kellogg, Marissa, Lee, Jong Woo, Loddenkemper, Tobias, Meletti, Stefano, Mizugushi, Masashi, Muscal, Eyal, Riviello, James J., Rosenthal, Eric S., Rossetti, Andrea O., Ruegg, Stefan, Said, Rana, Sculier, Claudine, Schmitt, Sarah, Schuele, Stephan, Stredny, Coral, Trinka, Eugen, Wainwright, Mark, VanHaerents, Stephen, Wells, Elisabeth, Wirrell, Elaine, Zuberi, Sameer M.

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Clinical outcomes in a large cohort of boys and adolescents with Duchenne muscular dystrophy von Alshaikh, N, Brunklaus, A, Robb, S, Quinlivan, R, Munot, P, Sarkozy, A, Muntoni, F, Manzur, A

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Vitamin D in corticosteroid treated Duchenne muscular dystrophy: What dose achieves serum 25OH vitamin D sufficiency? von Alshaikh, N, Brunklaus, A, Davis, T, Robb, S, Quinlivan, R, Munot, P, Sarkozy, A, Muntoni, F, Manzur, A

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Genetic and immune findings in complex febrile seizures and the epidemiology of Dravet syndrome: A nationwide cohort study von Symonds, J.D, Lang, B, Vincent, A, Brunklaus, A, Dorris, L, Ellis, R, Jollands, A, Joss, S, Kirkpatrick, M, McLellan, A, MacLeod, S, O'Regan, M, Pilz, D.T, Reavey, E, Stewart, K, Williams, N, Zuberi, S.M

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ILAE Genetics Literacy series: Progressive myoclonus epilepsies von Cameron, Jillian M, Ellis, Colin A, Berkovic, Samuel F

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ILAE Genetic Literacy Series: Self‐limited familial epilepsy syndromes with onset in neonatal age and infancy von Millevert, Charissa, Weckhuysen, Sarah, Perucca, Piero, Cross, J. Helen, Lerche, Holger, Esterhuizen, Alina I., Lopes‐Cendes, Iscia, Tsai, Meng‐Han, Berkovic, Samuel F., Lowenstein, Daniel H., Tan, Nigel C. K., Helbig, Ingo, Mefford, Heather C., Brunklaus, Andreas, Lesca, Gaetan

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ILAE Genetic Literacy Series: Postmortem Genetic Testing in Sudden Unexpected Death in Epilepsy von Bagnall, Richard D., Perucca, Piero, Cross, J. Helen, Lerche, Holger, Esterhuizen, Alina I., Lopes‐Cendes, Iscia, Tsai, Meng‐Han, Berkovic, Samuel F., Lowenstein, Daniel H., Tan, Nigel C. K., Helbig, Ingo, Mefford, Heather C., Brunklaus, Andreas, Lesca, Gaetan

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ILAE genetic literacy series: Focal cortical dysplasia von Macdonald-Laurs, Emma, Leventer, Richard J

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Unraveling unmet needs in ketogenic dietary services: An ERN EpiCARE survey von De Giorgis, Valentina, Pasca, Ludovica, Aznar‐Lain, Gemma, Bibic, Irena, Bibic, Vedrana, Darra, Francesca, Dianin, Alice, Dressler, Anastasia, Jonsson, Henna, Komulainen‐Ebrahim, Jonna, Kverneland, Magnhild, Molteberg, Ellen, Ragona, Francesca, Saint‐Martin, Anne, Varesio, Costanza, Cross, J. Helen, Baumgartner, Tobias, Bjellvi, Johan, Brunklaus, Andreas, Buttle, Janette, Pereira, Cristina Duarte, Fonseca Samões, Ana Raquel, Freri, Elena, Guglielmetti, Monica, Hallböök, Tove, Karandiene, Jurgita, Kotulska, Katarzyna, Lo Barco, Tommaso, Malenica, Masa, Messana, Tullio, Neubauer, David, Eleni, Panagiotakaki, Papadopoulou, Maria, Quintas, Sofia, Volpi, Lilia, TrimmelSchwahofer, Petra, Ruiz, Sonika Garcia‐Ribera

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Proposal to optimize evaluation and treatment of Febrile infection‐related epilepsy syndrome (FIRES): A Report from FIRES workshop von Koh, Sookyong, Wirrell, Elaine, Vezzani, Annamaria, Nabbout, Rima, Muscal, Eyal, Kaliakatsos, Marios, Wickström, Ronny, Riviello, James J., Brunklaus, Andreas, Payne, Eric, Valentin, Antonio, Wells, Elizabeth, Carpenter, Jessica L., Lee, Kihyeong, Lai, Yi‐Chen, Eschbach, Krista, Press, Craig A., Gorman, Mark, Stredny, Coral M., Roche, William, Mangum, Tara

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P191 Can physician reported response to antiepileptic medication help predict a SCN1A gene mutation? von Brunklaus, A, Birch, R, Duncan, J, Stenhouse, S, Zuberi, S.M

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Advancements in Lithium-Based Batteries: Unraveling and Mitigating Performance-Limiting Phenomena in Negative Electrodes von Huang, Yu-Kai

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