Výsledky vyhledávání - Hirsch, Edouard

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

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Corticotropin-releasing Hormone—induced Seizures in Infant Rats Originate in the Amygdala Autor 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) Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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 Autor 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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