The pharmacologic treatment of Dravet syndrome von Chiron, Catherine, Dulac, Olivier

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Acute encephalopathy with inflammation-mediated status epilepticus von Nabbout, Rima, Dr, Vezzani, Annamaria, PhD, Dulac, Olivier, Prof, Chiron, Catherine, MD

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Efficacy of ketogenic diet in severe refractory status epilepticus initiating fever induced refractory epileptic encephalopathy in school age children (FIRES) von Nabbout, Rima, Mazzuca, Michel, Hubert, Philippe, Peudennier, Sylviane, Allaire, Catherine, Flurin, Vincent, Aberastury, Marina, Silva, Walter, Dulac, Olivier

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De novo gain-of-function KCNT1 channel mutations cause malignant migrating partial seizures of infancy von Barcia, Giulia, Fleming, Matthew R, Deligniere, Aline, Gazula, Valeswara-Rao, Brown, Maile R, Langouet, Maeva, Chen, Haijun, Kronengold, Jack, Abhyankar, Avinash, Cilio, Roberta, Nitschke, Patrick, Kaminska, Anna, Boddaert, Nathalie, Casanova, Jean-Laurent, Desguerre, Isabelle, Munnich, Arnold, Dulac, Olivier, Kaczmarek, Leonard K, Colleaux, Laurence, Nabbout, Rima

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Ketogenic diet for super-refractory status epilepticus (SRSE) with NORSE and FIRES: Single tertiary center experience and literature data von Nabbout, Rima, Matricardi, Sara, De Liso, Paola, Dulac, Olivier, Oualha, Mehdi

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Epileptic Encephalopathy von Dulac, Olivier

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Neuronal chloride accumulation and excitatory GABA underlie aggravation of neonatal epileptiform activities by phenobarbital von NARDOU, Romain, YAMAMOTO, Sumii, CHAZAL, Geneviève, BHAR, Asma, FERRAND, Nadine, DULAC, Olivier, BEN-ARI, Yehezkel, KHALILOV, Ilgam

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From genotype to phenotype in Dravet disease von Gataullina, Svetlana, Dulac, Olivier

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New insights in phenomenology and treatment of epilepsy in CDKL5 encephalopathy von Melikishvili, Gia, Epitashvili, Nino, Tabatadze, Nazi, Chikvinidze, Gocha, Dulac, Olivier, Bienvenu, Thierry, Gataullina, Svetlana

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Herpes Simplex Virus Encephalitis in Human UNC-93B Deficiency von Casrouge, Armanda, Zhang, Shen-Ying, Eidenschenk, Céline, Jouanguy, Emmanuelle, Puel, Anne, Yang, Kun, Alcais, Alexandre, Picard, Capucine, Mahfoufi, Nora, Nicolas, Nathalie, Lorenzo, Lazaro, Plancoulaine, Sabine, Sénéchal, Brigitte, Geissmann, Frédéric, Tabeta, Koichi, Hoebe, Kasper, Du, Xin, Miller, Richard L, Héron, Bénédicte, Mignot, Cyril, Villemeur, Thierry Billette de, Lebon, Pierre, Dulac, Olivier, Rozenberg, Flore, Beutler, Bruce, Tardieu, Marc, Abel, Laurent, Casanova, Jean-Laurent

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Occasional seizures, epilepsy, and inborn errors of metabolism von Dulac, Olivier, Prof, Plecko, Barbara, Prof, Gataullina, Svetlana, MD, Wolf, Nicole I, MD

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Genotypic and phenotypic spectrum of pyridoxine-dependent epilepsy (ALDH7A1 deficiency) von Mills, Philippa B., Footitt, Emma J., Mills, Kevin A., Tuschl, Karin, Aylett, Sarah, Varadkar, Sophia, Hemingway, Cheryl, Marlow, Neil, Rennie, Janet, Baxter, Peter, Dulac, Olivier, Nabbout, Rima, Craigen, William J., Schmitt, Bernhard, Feillet, François, Christensen, Ernst, De Lonlay, Pascale, Pike, Mike G., Hughes, M. Imelda, Struys, Eduard A., Jakobs, Cornelis, Zuberi, Sameer M., Clayton, Peter T.

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Auditory stimuli mimicking ambient sounds drive temporal "delta-brushes" in premature infants von Chipaux, Mathilde, Colonnese, Matthew T, Mauguen, Audrey, Fellous, Laure, Mokhtari, Mostafa, Lezcano, Oscar, Milh, Mathieu, Dulac, Olivier, Chiron, Catherine, Khazipov, Rustem, Kaminska, Anna

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Mutations in QARS, Encoding Glutaminyl-tRNA Synthetase, Cause Progressive Microcephaly, Cerebral-Cerebellar Atrophy, and Intractable Seizures von Zhang, Xiaochang, Ling, Jiqiang, Barcia, Giulia, Jing, Lili, Wu, Jiang, Barry, Brenda J., Mochida, Ganeshwaran H., Hill, R. Sean, Weimer, Jill M., Stein, Quinn, Poduri, Annapurna, Partlow, Jennifer N., Ville, Dorothée, Dulac, Olivier, Yu, Tim W., Lam, Anh-Thu N., Servattalab, Sarah, Rodriguez, Jacqueline, Boddaert, Nathalie, Munnich, Arnold, Colleaux, Laurence, Zon, Leonard I., Söll, Dieter, Walsh, Christopher A., Nabbout, Rima

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Human slack potassium channel mutations increase positive cooperativity between individual channels von Kim, Grace E, Kronengold, Jack, Barcia, Giulia, Quraishi, Imran H, Martin, Hilary C, Blair, Edward, Taylor, Jenny C, Dulac, Olivier, Colleaux, Laurence, Nabbout, Rima, Kaczmarek, Leonard K

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Lamotrigine and Seizure Aggravation in Severe Myoclonic Epilepsy von Guerrini, Renzo, Dravet, Charlotte, Genton, Pierre, Belmonte, Anna, Kaminska, Anna, Dulac†, Olivier

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SCN1A duplications and deletions detected in Dravet syndrome: Implications for molecular diagnosis von Marini, Carla, Scheffer, Ingrid E., Nabbout, Rima, Mei, Davide, Cox, Kathy, Dibbens, Leanne M., McMahon, Jacinta M., Iona, Xenia, Carpintero, Rochio Sanchez, Elia, Maurizio, Cilio, Maria Roberta, Specchio, Nicola, Giordano, Lucio, Striano, Pasquale, Gennaro, Elena, Cross, J. Helen, Kivity, Sara, Neufeld, Miriam Y., Afawi, Zaid, Andermann, Eva, Keene, Daniel, Dulac, Olivier, Zara, Federico, Berkovic, Samuel F., Guerrini, Renzo, Mulley, John C.

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Taurine deficiency is a cause of vigabatrin-induced retinal phototoxicity von Jammoul, Firas, Wang, Qingping, Nabbout, Rima, Coriat, Caroline, Duboc, Agnès, Simonutti, Manuel, Dubus, Elisabeth, Craft, Cheryl M., Ye, Wen, Collins, Stephen D., Dulac, Olivier, Chiron, Catherine, Sahel, José A., Picaud, Serge

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Delineation of the motor disorder of Lesch–Nyhan disease von Jinnah, H. A., Visser, Jasper E., Harris, James C., Verdu, Alfonso, Larovere, Laura, Ceballos-Picot, Irene, Gonzalez-Alegre, Pedro, Neychev, Vladimir, Torres, Rosa J., Dulac, Olivier, Desguerre, Isabelle, Schretlen, David J., Robey, Kenneth L., Barabas, Gabor, Bloem, Bastiaan R., Nyhan, William, De Kremer, Raquel, Eddey, Gary E., Puig, Juan G., Reich, Stephen G.

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Severe myoclonic epilepsy in infancy: A systematic review and a meta‐analysis of individual patient data von Kassaï, Behrouz, Chiron, Catherine, Augier, Ségolène, Cucherat, Michel, Rey, Elisabeth, Gueyffier, François, Guerrini, Renzo, Vincent, Julien, Dulac, Olivier, Pons, Gérard

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