Epilepsy diagnostic and treatment needs identified with a collaborative database involving tertiary centers in France von Chipaux, Mathilde, Szurhaj, William, Vercueil, Laurent, Milh, Mathieu, Villeneuve, Nathalie, Cances, Claude, Auvin, Stéphane, Chassagnon, Serge, Napuri, Sylvia, Allaire, Catherine, Derambure, Philippe, Marchal, Cécile, Caubel, Isabelle, Ricard‐Mousnier, Brigitte, N'Guyen the Tich, Sylvie, Pinard, Jean‐Marc, Bahi‐Buisson, Nadia, Baracé, Claire, Kahane, Philippe, Gautier, Agnès, Hamelin, Sophie, Coste‐Zeitoun, Delphine, Rosenberg, Sarah‐Dominique, Clerson, Pierre, Nabbout, Rima, Kuchenbuch, Mathieu, Picot, Marie‐Christine, Kaminska, Anna

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Clinical and molecular delineation of Tetrasomy 9p syndrome: Report of 12 new cases and literature review von El Khattabi, Laïla, Jaillard, Sylvie, Andrieux, Joris, Pasquier, Laurent, Perrin, Laurence, Capri, Yline, Benmansour, Abdelmadjid, Toutain, Annick, Marcorelles, Pascale, Vincent-Delorme, Catherine, Journel, Hubert, Henry, Catherine, De Barace, Claire, Devisme, Louise, Dubourg, Christèle, Demurger, Florence, Lucas, Josette, Belaud-Rotureau, Marc-Antoine, Amiel, Jeanne, Malan, Valérie, De Blois, Marie-Christine, De Pontual, Loïc, Lebbar, Aziza, Le DÛ, Nathalie, Germain, Dominique P., Pinard, Jean-Marc, Pipiras, Eva, Tabet, Anne-Claude, Aboura, Azzedine, Verloes, Alain

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Magnetic resonance imaging and histological studies of corpus callosal and hippocampal abnormalities linked to doublecortin deficiency von Kappeler, Caroline, Dhenain, Marc, Phan Dinh Tuy, Françoise, Saillour, Yoann, Marty, Serge, Fallet-Bianco, Catherine, Souville, Isabelle, Souil, Evelyne, Pinard, Jean-Marc, Meyer, Gundela, Encha-Razavi, Ferechté, Volk, Andreas, Beldjord, Cherif, Chelly, Jamel, Francis, Fiona

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A prion protein epitope selective for the pathologically misfolded conformation von Paramithiotis, Eustache, Pinard, Marc, Lawton, Trebor, LaBoissiere, Sylvie, Leathers, Valerie L, Zou, Wen-Quan, Estey, Lisa A, Lamontagne, Julie, Lehto, Marty T, Kondejewski, Leslie H, Francoeur, Gregory P, Papadopoulos, Maria, Haghighat, Ashkan, Spatz, Stephen J, Head, Mark, Will, Robert, Ironside, James, O'Rourke, Katherine, Tonelli, Quentin, Ledebur, Harry C, Chakrabartty, Avi, Cashman, Neil R

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A Novel CNS Gene Required for Neuronal Migration and Involved in X-Linked Subcortical Laminar Heterotopia and Lissencephaly Syndrome von Portes, Vincent des, Pinard, Jean Marc, Billuart, Pierre, Vinet, Marie Claude, Koulakoff, Annette, Carrié, Alain, Gelot, Antoinette, Dupuis, Elisabeth, Motte, Jacques, Berwald-Netter, Yoheved, Catala, Martin, Kahn, Axel, Beldjord, Cherif, Chelly, Jamel

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The role of CNVs in the etiology of rare autosomal recessive disorders: the example of TRAPPC9-associated intellectual disability von Mortreux, Jérémie, Busa, Tiffany, Germain, Dominique P, Nadeau, Gwenaël, Puechberty, Jacques, Coubes, Christine, Gatinois, Vincent, Cacciagli, Pierre, Duffourd, Yannis, Pinard, Jean-Marc, Tevissen, Hélène, Villard, Laurent, Sanlaville, Damien, Philip, Nicole, Missirian, Chantal

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The location of DCX mutations predicts malformation severity in X-linked lissencephaly von Leger, Pierre-Louis, Souville, Isabelle, Boddaert, Nathalie, Elie, Caroline, Pinard, Jean Marc, Plouin, Perrine, Moutard, Marie Laure, des Portes, Vincent, Van Esch, Hilde, Joriot, Sylvie, Renard, Jean Louis, Chelly, Jamel, Francis, Fiona, Beldjord, Cherif, Bahi-Buisson, Nadia

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Brain MRI abnormalities in muscular dystrophy due to FKRP mutations von Quijano-Roy, Susana, Martí-Carrera, Itxaso, Makri, Samira, Mayer, Michèle, Maugenre, Svetlana, Richard, Pascale, Berard, Carole, Viollet, Louis, Leheup, Bruno, Guicheney, Pascale, Pinard, Jean-Marc, Estournet, Brigitte, Y. Carlier, Robert

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Pregabalin adjunctive therapy for focal onset seizures in children 1 month to <4 years of age: A double‐blind, placebo‐controlled, video‐electroencephalographic trial von Mann, Donald, Antinew, Jeremias, Knapp, Lloyd, Almas, Mary, Liu, Jing, Scavone, Joseph, Yang, Ruoyong, Modequillo, Margaret, Makedonska, Iryna, Ortiz, Marilyn, Kyrychenko, Alla, Nordli, Douglas, Farkas, Viktor, Farkas, Mark Kristof, Shalkevich, Leanid, Jansen, Anna, Ivanov, Ivan, Nedkova, Vania, Fang, Fang, Wang, Yi, Pinard, Jean‐Marc, Brandl, Ulrich, Zafeiriou, Dimitrios, Altmann, Anna, Berenyi, Marianne, Bessenyei, Monika, Fogaras, Andras, Szabo, Geza, Fattal‐Valevski, Aviva, Kim, Ki Joong, Beydoun, Ahmad, Hmaimess, Ghassan, Yahaya, Nor Azni, Barlaan‐Lukban, Marissa, Bolanos, Martha, De la Calzada, Jo Janette, Estrella Ibe, Maria, Valencia, Maria Antonia Aurora, Craiu, Dana, Diaconu, Georgeta, Antonova, Tatiana, Belousova, Elena, Karakulova, Yulia, Khaletskaya, Olga, Lvova, Olga, Strachunskaya, Maria, Kravljanac, Ruzica, Nikolic, Dimitrije, Lopez Pison, Francisco, Chang, Ying‐Chao, Chou, I‐Ching, Lee, Wang‐Tso, Nabangchang, Charcrin, Sanmaneechai, Oranee, Dundar, Nihal Olgac, Gencpinar, Pinar, Chomolyak, Yurii, Delva, Dmytro, Martyniuk, Volodymyr, Davis, Ronald, Ferreira, Jose, Tomasovic, Jerry

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Autism multiplex family with 16p11.2p12.2 microduplication syndrome in monozygotic twins and distal 16p11.2 deletion in their brother von TABET, Anne-Claude, PILORGE, Marion, DELORME, Richard, AMSELLEM, Frédérique, PINARD, Jean-Marc, LEBOYER, Marion, VERLOES, Alain, BENZACKEN, Brigitte, BETANCUR, Catalina

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DNA Methyltransferase Is a Downstream Effector of Cellular Transformation Triggered by Simian Virus 40 Large T Antigen von Slack, A, Cervoni, N, Pinard, M, Szyf, M

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Inhibition of Tumorigenesis by a Cytosine-DNA, Methyltransferase, Antisense Oligodeoxynucleotide von Ramchandani, Shyam, MacLeod, A. Robert, Pinard, Marc, Von Hofe, Eric, Szyf, Moshe

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Subependymal giant-cell astrocytomas in pediatric tuberous sclerosis disease : When should we operate? von DE RIBAUPIERRE, Sandrine, DORFMÜLLER, Georg, BULTEAU, Christine, FOHIEN, Martine, PINARD, Jean-Marc, CHIRON, Catherine, DELALANDE, Olivier, CHAPMAN, Paul H, POLLACK, Ian F, SUTTON, Leslie N

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Protein depletion from blood plasma using a volatile buffer von Sitnikov, Dmitri, Chan, Donovan, Thibaudeau, Eric, Pinard, Marc, Hunter, Joanna M.

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Creatine and guanidinoacetate reference values in a French population von Joncquel-Chevalier Curt, Marie, Cheillan, David, Briand, Gilbert, Salomons, Gajja S., Mention-Mulliez, Karine, Dobbelaere, Dries, Cuisset, Jean-Marie, Lion-François, Laurence, Des Portes, Vincent, Chabli, Allel, Valayannopoulos, Vassili, Benoist, Jean-François, Pinard, Jean-Marc, Simard, Gilles, Douay, Olivier, Deiva, Kumaran, Tardieu, Marc, Afenjar, Alexandra, Héron, Delphine, Rivier, François, Chabrol, Brigitte, Prieur, Fabienne, Cartault, François, Pitelet, Gaëlle, Goldenberg, Alice, Bekri, Soumeya, Gerard, Marion, Delorme, Richard, Porchet, Nicole, Vianey-Saban, Christine, Vamecq, Joseph

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Doublecortin Is the Major Gene Causing X-Linked Subcortical Laminar Heterotopia (SCLH) von des Portes, Vincent, Francis, Fiona, Pinard, Jean-Marc, Desguerre, Isabelle, Moutard, Marie-Laure, Snoeck, Irina, Meiners, Linda C., Capron, François, Cusmai, Raffaella, Ricci, Stefano, Motte, Jacques, Echenne, Bernard, Ponsot, Gérard, Dulac, Olivier, Chelly, Jamel, Beldjord, Cherif

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Screening for primary creatine deficiencies in French patients with unexplained neurological symptoms von Cheillan, David, Joncquel-Chevalier Curt, Marie, Briand, Gilbert, Salomons, Gajja S, Mention-Mulliez, Karine, Dobbelaere, Dries, Cuisset, Jean-Marie, Lion-François, Laurence, Portes, Vincent Des, Chabli, Allel, Valayannopoulos, Vassili, Benoist, Jean-François, Pinard, Jean-Marc, Simard, Gilles, Douay, Olivier, Deiva, Kumaran, Afenjar, Alexandra, Héron, Delphine, Rivier, François, Chabrol, Brigitte, Prieur, Fabienne, Cartault, François, Pitelet, Gaëlle, Goldenberg, Alice, Bekri, Soumeya, Gerard, Marion, Delorme, Richard, Tardieu, Marc, Porchet, Nicole, Vianey-Saban, Christine, Vamecq, Joseph

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Sleep-disordered breathing in children with congenital muscular dystrophies von Pinard, Jean-Marc, Azabou, Eric, Essid, Nouha, Quijano-Roy, Susana, Haddad, Samir, Cheliout-Héraut, Fawzia

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Sleep architecture impairment in epileptic children and putative role of anti epileptic drugs von Racaru, Valentina M., Cheliout-Heraut, Fawzia, Azabou, Eric, Essid, Nouha, Brami, Marc, Benga, Ileana, Pinard, Jean-Marc

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Sleep disorders in succinic semialdehyde dehydrogenase deficiency: A family report von Racaru, Valentina M, Pinard, Jean-Marc, Cheliout-Heraut, Fawzia

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