Involvement of GATOR complex genes in familial focal epilepsies and focal cortical dysplasia von Weckhuysen, Sarah, Marsan, Elise, Lambrecq, Virginie, Marchal, Cécile, Morin‐Brureau, Mélanie, An‐Gourfinkel, Isabelle, Baulac, Michel, Fohlen, Martine, Kallay Zetchi, Christine, Seeck, Margitta, Grange, Pierre, Dermaut, Bart, Meurs, Alfred, Thomas, Pierre, Chassoux, Francine, Leguern, Eric, Picard, Fabienne, Baulac, Stéphanie

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Cannabidiol Treatment for Adult Patients with Drug‐Resistant Epilepsies: A Real‐World Study in a Tertiary Center von Calonge, Quentin, Besnard, Aurore, Bailly, Laurent, Damiano, Maria, Pichit, Phintip, Dupont, Sophie, Gourfinkel‐An, Isabelle, Navarro, Vincent

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STXBP1‐related encephalopathy presenting as infantile spasms and generalized tremor in three patients von Mignot, Cyril, Moutard, Marie‐Laure, Trouillard, Oriane, Gourfinkel‐An, Isabelle, Jacquette, Aurélia, Arveiler, Benoit, Morice‐Picard, Fanny, Lacombe, Didier, Chiron, Catherine, Ville, Dorothée, Charles, Perrine, LeGuern, Eric, Depienne, Christel, Héron, Delphine

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Mutations and deletions in PCDH19 account for various familial or isolated epilepsies in females von Depienne, Christel, Trouillard, Oriane, Bouteiller, Delphine, Gourfinkel-An, Isabelle, Poirier, Karine, Rivier, François, Berquin, Patrick, Nabbout, Rima, Chaigne, Denys, Steschenko, Dominique, Gautier, Agnès, Hoffman-Zacharska, Dorota, Lannuzel, Annie, Lackmy-Port-Lis, Marilyn, Maurey, Hélène, Dusser, Anne, Bru, Marie, Gilbert-Dussardier, Brigitte, Roubertie, Agathe, Kaminska, Anna, Whalen, Sandra, Mignot, Cyril, Baulac, Stéphanie, Lesca, Gaetan, Arzimanoglou, Alexis, LeGuern, Eric

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Sporadic infantile epileptic encephalopathy caused by mutations in PCDH19 resembles Dravet syndrome but mainly affects females von Depienne, Christel, Bouteiller, Delphine, Keren, Boris, Cheuret, Emmanuel, Poirier, Karine, Trouillard, Oriane, Benyahia, Baya, Quelin, Chloé, Carpentier, Wassila, Julia, Sophie, Afenjar, Alexandra, Gautier, Agnès, Rivier, François, Meyer, Sophie, Berquin, Patrick, Hélias, Marie, Py, Isabelle, Rivera, Serge, Bahi-Buisson, Nadia, Gourfinkel-An, Isabelle, Cazeneuve, Cécile, Ruberg, Merle, Brice, Alexis, Nabbout, Rima, Leguern, Eric

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First genetic evidence of GABAA receptor dysfunction in epilepsy: a mutation in the γ2-subunit gene von Baulac, Stéphanie, Huberfeld, Gilles, Gourfinkel-An, Isabelle, Mitropoulou, Georgia, Beranger, Alexandre, Prud'homme, Jean-François, Baulac, Michel, Brice, Alexis, Bruzzone, Roberto, LeGuern, Eric

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Does epilepsy in multiplex autism pedigrees define a different subgroup in terms of clinical characteristics and genetic risk? von Amiet, Claire, Gourfinkel-An, Isabelle, Laurent, Claudine, Bodeau, Nicolas, Génin, Bérengère, Leguern, Eric, Tordjman, Sylvie, Cohen, David

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Parental mosaicism can cause recurrent transmission of SCN1A mutations associated with severe myoclonic epilepsy of infancy von Depienne, Christel, Arzimanoglou, Alexis, Trouillard, Oriane, Fedirko, Estelle, Baulac, Stéphanie, Saint-Martin, Cécile, Ruberg, Merle, Dravet, Charlotte, Nabbout, Rima, Baulac, Michel, Gourfinkel-An, Isabelle, Leguern, Eric

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Two novel CLCN2 mutations accelerating chloride channel deactivation are associated with idiopathic generalized epilepsy von Saint-Martin, Cécile, Gauvain, Grégory, Teodorescu, Georgeta, Gourfinkel-An, Isabelle, Fedirko, Estelle, Weber, Yvonne G, Maljevic, Snezana, Ernst, Jan-Peter, Garcia-Olivares, Jennie, Fahlke, Christoph, Nabbout, Rima, LeGuern, Eric, Lerche, Holger, Christophe Poncer, Jean, Depienne, Christel

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Spinocerebellar Ataxia Type 7 (SCA7): A Neurodegenerative Disorder With Neuronal Intranuclear Inclusions von Holmberg, Monica, Duyckaerts, Charles, Dürr, Alexandra, Cancel, Géraldine, Gourfinkel-An, Isabelle, Damier, Philippe, Faucheux, Baptiste, Trottier, Yvon, Hirsch, Etienne C., Agid, Yves, Brice, Alexis

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Malignant catatonia due to anti-NMDA-receptor encephalitis in a 17-year-old girl: case report von Consoli, Angèle, Ronen, Karine, An-Gourfinkel, Isabelle, Barbeau, Martine, Marra, Donata, Costedoat-Chalumeau, Nathalie, Montefiore, Delphine, Maksud, Philippe, Bonnot, Olivier, Didelot, Adrien, Amoura, Zahir, Vidailhet, Marie, Cohen, David

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Genes in infantile epileptic encephalopathies von Depienne, Christel, Gourfinkel‐An, Isabelle, Baulac, Stéphanie, LeGuern, Eric

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Familial form of typical childhood absence epilepsy in a consanguineous context von Abouda, Hanen, Hizem, Yosr, Gargouri, Amina, Depienne, Christel, Bouteiller, Delphine, Riant, Florence, Tournier‐Lasserve, Elisabeth, Gourfinkel‐An, Isabelle, LeGuern, Eric, Gouider, Riadh

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Differential distribution of the normal and mutated forms of huntingtin in the human brain von Gourfinkel-An, Isabelle, Cancel, Géraldine, Trottier, Yvon, Devys, Didier, Tora, Laszlo, Lutz, Yves, Imbert, Georges, Saudou, Frédéric, Stevanin, Giovanni, Agid, Yves, Brice, Alexis, Mandel, Jean-Louis, Hirsch, Etienne C.

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A French experience of type 3 Gaucher disease: Phenotypic diversity and neurological outcome of 10 patients von Kraoua, Ichraf, Sedel, Frédéric, Caillaud, Catherine, Froissart, Roseline, Stirnemann, Jérôme, Chaurand, Guy, Flodrops, Hugues, Tari, Saliha, Gourfinkel-An, Isabelle, Mathieu, Sophie, Belmatoug, Nadia, Billette de Villemeur, Thierry, Mignot, Cyril

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Absence of mutations in the LGI1 receptor ADAM22 gene in autosomal dominant lateral temporal epilepsy von Chabrol, Elodie, Gourfinkel-An, Isabelle, Scheffer, Ingrid E, Picard, Fabienne, Couarch, Philippe, Berkovic, Samuel F, McMahon, Jacinta M, Bajaj, Nandita, Mota-Vieira, Luisa, Mota, Rui, Trouillard, Oriane, Depienne, Christel, Baulac, Michel, LeGuern, Eric, Baulac, Stéphanie

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Heterogeneous Intracellular Localization and Expression of Ataxin-3 von Trottier, Yvon, Cancel, Géraldine, An-Gourfinkel, Isabelle, Lutz, Yves, Weber, Chantal, Brice, Alexis, Hirsch, Etienne, Mandel, Jean-Louis

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Mechanisms for variable expressivity of inherited SCN1A mutations causing Dravet syndrome von Depienne, Christel, Trouillard, Oriane, Gourfinkel-An, Isabelle, Saint-Martin, Cécile, Bouteiller, Delphine, Graber, Denis, Barthez-Carpentier, Marie-Anne, Gautier, Agnès, Villeneuve, Nathalie, Dravet, Charlotte, Livet, Marie-Odile, Rivier-Ringenbach, Clothilde, Adam, Claude, Dupont, Sophie, Baulac, Stéphanie, Héron, Delphine, Nabbout, Rima, LeGuern, Eric

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Correction: Sporadic Infantile Epileptic Encephalopathy Caused by Mutations in PCDH19 Resembles Dravet Syndrome but Mainly Affects Females von Depienne, Christel, Bouteiller, Delphine, Keren, Boris, Cheuret, Emmanuel, Poirier, Karine, Trouillard, Oriane, Benyahia, Baya, Quelin, Chloé, Carpentier, Wassila, Julia, Sophie, Afenjar, Alexandra, Gautier, Agnès, Rivier, François, Meyer, Sophie, Berquin, Patrick, Hélias, Marie, Py, Isabelle, Rivera, Serge, Bahi-Buisson, Nadia, Gourfinkel-An, Isabelle, Cazeneuve, Cécile, Ruberg, Merle, Brice, Alexis, Nabbout, Rima, LeGuern, Eric

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Epilepsy in Autism is Associated with Intellectual Disability and Gender: Evidence from a Meta-Analysis von Amiet, Claire, Gourfinkel-An, Isabelle, Bouzamondo, Anissa, Tordjman, Sylvie, Baulac, Michel, Lechat, Philippe, Mottron, Laurent, Cohen, David

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