Search Results - Hirsch, Edouard

Short-interval amygdala kindling in neonatal rats by Baram, Tallie Z., Hirsch, Edouard, Schultz, Linda

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Corticotropin-releasing Hormone—induced Seizures in Infant Rats Originate in the Amygdala by Baram, Tallie Z., Hirsch, Edouard, Snead, O. Carter, Schultz, Linda

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Genetic generalized epilepsy and generalized onset seizures with focal evolution (GOFE) by Lamy, Florian, Valenti-Hirsch, Maria-Paola, Gauer, Lucas, Gérard, Bénédicte, Obeid, Mohamed, de Saint-Martin, Anne, Dinkelacker, Vera, Baer, Sarah, Hirsch, Edouard

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Molecular networks implicated in speech-related disorders: FOXP2 regulates the SRPX2/uPAR complex by Roll, Patrice, Vernes, Sonja C., Bruneau, Nadine, Cillario, Jennifer, Ponsole-Lenfant, Magali, Massacrier, Annick, Rudolf, Gabrielle, Khalife, Manal, Hirsch, Edouard, Fisher, Simon E., Szepetowski, Pierre

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Classification of the epilepsies: New concepts for discussion and debate—Special report of the ILAE Classification Task Force of the Commission for Classification and Terminology by Scheffer, Ingrid E., French, Jacqueline, Hirsch, Edouard, Jain, Satish, Mathern, Gary W., Moshé, Solomon L, Perucca, Emilio, Tomson, Torbjorn, Wiebe, Samuel, Zhang, Yue‐Hua, Zuberi, Sameer M.

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Mutations of DEPDC5 cause autosomal dominant focal epilepsies by Ishida, Saeko, Picard, Fabienne, Rudolf, Gabrielle, Noé, Eric, Achaz, Guillaume, Thomas, Pierre, Genton, Pierre, Mundwiller, Emeline, Wolff, Markus, Marescaux, Christian, Miles, Richard, Baulac, Michel, Hirsch, Edouard, Leguern, Eric, Baulac, Stéphanie

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Mild malformations of cortical development in sleep‐related hypermotor epilepsy due to KCNT1 mutations by Rubboli, Guido, Plazzi, Giuseppe, Picard, Fabienne, Nobili, Lino, Hirsch, Edouard, Chelly, Jamel, Prayson, Richard A., Boutonnat, Jean, Bramerio, Manuela, Kahane, Philippe, Dibbens, Leanne M., Gardella, Elena, Baulac, Stéphanie, Møller, Rikke S.

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Illusory own body perceptions mapped in the cingulate cortex—An intracranial stimulation study by Popa, Irina, Barborica, Andrei, Scholly, Julia, Donos, Cristian, Bartolomei, Fabrice, Lagarde, Stanislas, Hirsch, Edouard, Valenti‐Hirsch, Maria‐Paola, Maliia, Mihai Dragos, Arbune, Anca Adriana, Daneasa, Andrei, Ciurea, Jean, Bajenaru, Ovidiu‐Alexandru, Mindruta, Ioana

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Use of suggestive seizure manipulation methods in the investigation of patients with possible psychogenic nonepileptic seizures—An international ILAE survey by Gras, Adrien, Wardrope, Alistair, Hirsch, Edouard, Asadi Pooya, Ali A, Duncan, Rod, Gigineishvili, David, Hingray, Coraline, Kanemoto, Kousuke, Ladino, Lady, LaFrance, William Curt, McGonigal, Aileen, Pretorius, Chrisma, Valenti Hirsch, Paola, Vidailhet, Pierre, Zhou, Dong, Reuber, Markus

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ILAE Classification of the Epilepsies Position Paper of the ILAE Commission for Classification and Terminology by Scheffer, Ingrid E, Berkovic, Samuel, Capovilla, Giuseppe, Connolly, Mary B, French, Jacqueline, Guilhoto, Laura, Hirsch, Edouard, Jain, Satish, Mathern, Gary W., Moshé, Solomon L, Nordli, Douglas R, Perucca, Emilio, Tomson, Torbjörn, Wiebe, Samuel, Zhang, Yue-Hua, Zuberi, Sameer M

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Efficacy of naloxone in reducing postictal central respiratory dysfunction in patients with epilepsy: study protocol for a double-blind, randomized, placebo-controlled trial by Rheims, Sylvain, Valton, Luc, Michel, Véronique, Maillard, Louis, Navarro, Vincent, Convers, Philippe, Bartolomei, Fabrice, Biraben, Arnaud, Crespel, Arielle, Derambure, Philippe, de Toffol, Bertrand, Hirsch, Edouard, Kahane, Philippe, Martin, Martine Lemesle, Tourniaire, Didier, Boulogne, Sébastien, Mercier, Catherine, Roy, Pascal, Ryvlin, Philippe

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PRRT2 links infantile convulsions and paroxysmal dyskinesia with migraine by Cloarec, Robin, Bruneau, Nadine, Rudolf, Gabrielle, Massacrier, Annick, Salmi, Manal, Bataillard, Marc, Boulay, Clotilde, Caraballo, Roberto, Fejerman, Natalio, Genton, Pierre, Hirsch, Edouard, Hunter, Alasdair, Lesca, Gaetan, Motte, Jacques, Roubertie, Agathe, Sanlaville, Damien, Wong, Sau-Wei, Fu, Ying-Hui, Rochette, Jacques, Ptáček, Louis J., Szepetowski, Pierre

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GRIN2A-related disorders: genotype and functional consequence predict phenotype by Strehlow, Vincent, Heyne, Henrike O, Vlaskamp, Danique R M, Marwick, Katie F M, Rudolf, Gabrielle, de Bellescize, Julitta, Biskup, Saskia, Brilstra, Eva H, Brouwer, Oebele F, Callenbach, Petra M C, Hentschel, Julia, Hirsch, Edouard, Kind, Peter C, Mignot, Cyril, Platzer, Konrad, Rump, Patrick, Skehel, Paul A, Wyllie, David J A, Hardingham, Giles E, van Ravenswaaij-Arts, Conny M A, Lesca, Gaetan, Lemke, Johannes R

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Biallelic PDE2A variants: a new cause of syndromic paroxysmal dyskinesia by Doummar, Diane, Dentel, Christel, Lyautey, Romane, Metreau, Julia, Keren, Boris, Drouot, Nathalie, Malherbe, Ludivine, Bouilleret, Viviane, Courraud, Jérémie, Valenti-Hirsch, Maria Paola, Minotti, Lorella, Dozieres-Puyravel, Blandine, Bär, Séverine, Scholly, Julia, Schaefer, Elise, Nava, Caroline, Wirth, Thomas, Nasser, Hala, de Salins, Marie, de Saint Martin, Anne, Warde, Marie Thérèse Abi, Kahane, Philippe, Hirsch, Edouard, Anheim, Mathieu, Friant, Sylvie, Chelly, Jamel, Mignot, Cyril, Rudolf, Gabrielle

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Probabilistic functional tractography of the human cortex revisited by Trebaul, Lena, Deman, Pierre, Tuyisenge, Viateur, Jedynak, Maciej, Hugues, Etienne, Rudrauf, David, Bhattacharjee, Manik, Tadel, François, Chanteloup-Foret, Blandine, Saubat, Carole, Reyes Mejia, Gina Catalina, Adam, Claude, Nica, Anca, Pail, Martin, Dubeau, François, Rheims, Sylvain, Trébuchon, Agnès, Wang, Haixiang, Liu, Sinclair, Blauwblomme, Thomas, Garcés, Mercedes, De Palma, Luca, Valentin, Antonio, Metsähonkala, Eeva-Liisa, Petrescu, Ana Maria, Landré, Elizabeth, Szurhaj, William, Hirsch, Edouard, Valton, Luc, Rocamora, Rodrigo, Schulze-Bonhage, Andreas, Mindruta, Ioana, Francione, Stefano, Maillard, Louis, Taussig, Delphine, Kahane, Philippe, David, Olivier

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Mutations in the novel protein PRRT2 cause paroxysmal kinesigenic dyskinesia with infantile convulsions by Lee, Hsien-Yang, Huang, Yong, Bruneau, Nadine, Roll, Patrice, Roberson, Elisha D.O., Hermann, Mark, Quinn, Emily, Maas, James, Edwards, Robert, Ashizawa, Tetsuo, Baykan, Betul, Bhatia, Kailash, Bressman, Susan, Bruno, Michiko K., Brunt, Ewout R., Caraballo, Roberto, Echenne, Bernard, Fejerman, Natalio, Frucht, Steve, Gurnett, Christina A., Hirsch, Edouard, Houlden, Henry, Jankovic, Joseph, Lee, Wei-Ling, Lynch, David R., Mohamed, Shehla, Müller, Ulrich, Nespeca, Mark P., Renner, David, Rochette, Jacques, Rudolf, Gabrielle, Saiki, Shinji, Soong, Bing-Wen, Swoboda, Kathryn J., Tucker, Sam, Wood, Nicholas, Hanna, Michael, Bowcock, Anne, Szepetowski, Pierre, Fu, Ying-Hui, Ptáček, Louis J.

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Loss of function of the retinoid-related nuclear receptor (RORB) gene and epilepsy by Rudolf, Gabrielle, Lesca, Gaetan, Mehrjouy, Mana M, Labalme, Audrey, Salmi, Manal, Bache, Iben, Bruneau, Nadine, Pendziwiat, Manuela, Fluss, Joel, de Bellescize, Julitta, Scholly, Julia, Møller, Rikke S, Craiu, Dana, Tommerup, Niels, Valenti-Hirsch, Maria Paola, Schluth-Bolard, Caroline, Sloan-Béna, Frédérique, Helbig, Katherine L, Weckhuysen, Sarah, Edery, Patrick, Coulbaut, Safia, Abbas, Mohamed, Scheffer, Ingrid E, Tang, Sha, Myers, Candace T, Stamberger, Hannah, Carvill, Gemma L, Shinde, Deepali N, Mefford, Heather C, Neagu, Elena, Huether, Robert, Lu, Hsiao-Mei, Dica, Alice, Cohen, Julie S, Iliescu, Catrinel, Pomeran, Cristina, Rubenstein, James, Helbig, Ingo, Sanlaville, Damien, Hirsch, Edouard, Szepetowski, Pierre

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A brain atlas of axonal and synaptic delays based on modelling of cortico-cortical evoked potentials by Lemaréchal, Jean-Didier, Jedynak, Maciej, Trebaul, Lena, Boyer, Anthony, Tadel, François, Bhattacharjee, Manik, Deman, Pierre, Tuyisenge, Viateur, Ayoubian, Leila, Hugues, Etienne, Chanteloup-Forêt, Blandine, Saubat, Carole, Zouglech, Raouf, Reyes Mejia, Gina Catalina, Tourbier, Sébastien, Hagmann, Patric, Adam, Claude, Barba, Carmen, Bartolomei, Fabrice, Blauwblomme, Thomas, Curot, Jonathan, Dubeau, François, Francione, Stefano, Garcés, Mercedes, Hirsch, Edouard, Landré, Elizabeth, Liu, Sinclair, Maillard, Louis, Metsähonkala, Eeva-Liisa, Mindruta, Ioana, Nica, Anca, Pail, Martin, Petrescu, Ana Maria, Rheims, Sylvain, Rocamora, Rodrigo, Schulze-Bonhage, Andreas, Szurhaj, William, Taussig, Delphine, Valentin, Antonio, Wang, Haixiang, Kahane, Philippe, George, Nathalie, David, Olivier

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Unstable TTTTA/TTTCA expansions in MARCH6 are associated with Familial Adult Myoclonic Epilepsy type 3 by Florian, Rahel T., Kraft, Florian, Leitão, Elsa, Kaya, Sabine, Klebe, Stephan, Magnin, Eloi, van Rootselaar, Anne-Fleur, Buratti, Julien, Kühnel, Theresa, Schröder, Christopher, Giesselmann, Sebastian, Tschernoster, Nikolai, Altmueller, Janine, Lamiral, Anaide, Keren, Boris, Nava, Caroline, Bouteiller, Delphine, Forlani, Sylvie, Jornea, Ludmila, Kubica, Regina, Ye, Tao, Plassard, Damien, Jost, Bernard, Meyer, Vincent, Deleuze, Jean-François, Delpu, Yannick, Avarello, Mario D. M., Vijfhuizen, Lisanne S., Rudolf, Gabrielle, Hirsch, Edouard, Kroes, Thessa, Reif, Philipp S., Rosenow, Felix, Ganos, Christos, Vidailhet, Marie, Thivard, Lionel, Mathieu, Alexandre, Bourgeron, Thomas, Kurth, Ingo, Rafehi, Haloom, Steenpass, Laura, Horsthemke, Bernhard, LeGuern, Eric, Klein, Karl Martin, Labauge, Pierre, Bennett, Mark F., Bahlo, Melanie, Gecz, Jozef, Corbett, Mark A., Tijssen, Marina A. J., van den Maagdenberg, Arn M. J. M., Depienne, Christel

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Genetic and phenotypic dissection of 1q43q44 microdeletion syndrome and neurodevelopmental phenotypes associated with mutations in ZBTB18 and HNRNPU by Depienne, Christel, Nava, Caroline, Keren, Boris, Heide, Solveig, Rastetter, Agnès, Passemard, Sandrine, Chantot-Bastaraud, Sandra, Moutard, Marie-Laure, Agrawal, Pankaj B., VanNoy, Grace, Stoler, Joan M., Amor, David J., Billette de Villemeur, Thierry, Doummar, Diane, Alby, Caroline, Cormier-Daire, Valérie, Garel, Catherine, Marzin, Pauline, Scheidecker, Sophie, de Saint-Martin, Anne, Hirsch, Edouard, Korff, Christian, Bottani, Armand, Faivre, Laurence, Verloes, Alain, Orzechowski, Christine, Burglen, Lydie, Leheup, Bruno, Roume, Joelle, Andrieux, Joris, Sheth, Frenny, Datar, Chaitanya, Parker, Michael J., Pasquier, Laurent, Odent, Sylvie, Naudion, Sophie, Delrue, Marie-Ange, Le Caignec, Cédric, Vincent, Marie, Isidor, Bertrand, Renaldo, Florence, Stewart, Fiona, Toutain, Annick, Koehler, Udo, Häckl, Birgit, von Stülpnagel, Celina, Kluger, Gerhard, Møller, Rikke S., Pal, Deb, Jonson, Tord, Soller, Maria, Verbeek, Nienke E., van Haelst, Mieke M., de Kovel, Carolien, Koeleman, Bobby, Monroe, Glen, van Haaften, Gijs, Attié-Bitach, Tania, Boutaud, Lucile, Héron, Delphine, Mignot, Cyril

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