نتائج البحث - Stephani, Ulrich

A data-driven model of the generation of human EEG based on a spatially distributed stochastic wave equation حسب Galka, Andreas, Ozaki, Tohru, Muhle, Hiltrud, Stephani, Ulrich, Siniatchkin, Michael

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Representation and propagation of epileptic activity in absences and generalized photoparoxysmal responses حسب Moeller, Friederike, Muthuraman, Muthuraman, Stephani, Ulrich, Deuschl, Günther, Raethjen, Jan, Siniatchkin, Michael

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Seizure control in a patient with Dravet syndrome and cystic fibrosis() حسب Schmalbach, Barbara, Moeller, Bettina, von Spiczak, Sarah, Muhle, Hiltrud, Stephani, Ulrich, Lang, Nicolas

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Developmental changes of the contingent negative variation in migraine and healthy children حسب Siniatchkin, Michael, Jonas, Anne, Baki, Huelya, van Baalen, Andreas, Gerber, Wolf-Dieter, Stephani, Ulrich

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Absence seizures: Individual patterns revealed by EEG-fMRI حسب Moeller, Friederike, LeVan, Pierre, Muhle, Hiltrud, Stephani, Ulrich, Dubeau, Francois, Siniatchkin, Michael, Gotman, Jean

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Dynamic Imaging of Coherent Sources Reveals Different Network Connectivity Underlying the Generation and Perpetuation of Epileptic Seizures حسب Elshoff, Lydia, Muthuraman, Muthuraman, Anwar, Abdul Rauf, Deuschl, Günther, Stephani, Ulrich, Raethjen, Jan, Siniatchkin, Michael

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A Computational Study of Stimulus Driven Epileptic Seizure Abatement حسب Taylor, Peter Neal, Wang, Yujiang, Goodfellow, Marc, Dauwels, Justin, Moeller, Friederike, Stephani, Ulrich, Baier, Gerold

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Variability of the hemodynamic response as a function of age and frequency of epileptic discharge in children with epilepsy حسب Jacobs, Julia, Hawco, Colin, Kobayashi, Eliane, Boor, Rainer, LeVan, Pierre, Stephani, Ulrich, Siniatchkin, Michael, Gotman, Jean

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Altered information processing in children with focal epilepsies with and without intellectual disability حسب Japaridze, Natia, Schark, Mamke, von-Ondarza, Gisela, Boor, Rainer, Muhle, Hiltrud, Gerber, Wolf-Dieter, Stephani, Ulrich, Siniatchkin, Michael

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Absence seizures with intellectual disability as a phenotype of the 15q13.3 microdeletion syndrome حسب Muhle, Hiltrud, Mefford, Heather C, Obermeier, Tanja, von Spiczak, Sarah, Eichler, Evan E, Stephani, Ulrich, Sander, Thomas, Helbig, Ingo

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MIPAS-Family—evaluation of a new multi-modal behavioral training program for pediatric headaches: clinical effects and the impact on quality of life حسب Gerber, Wolf-Dieter, Petermann, Franz, Gerber-von Müller, Gabriele, Dollwet, Maren, Darabaneanu, Stephanie, Niederberger, Uwe, Schulte, Ilva Elena, Stephani, Ulrich, Andrasik, Frank

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Neuronal Networks during Burst Suppression as Revealed by Source Analysis حسب Japaridze, Natia, Muthuraman, Muthuraman, Reinicke, Christine, Moeller, Friederike, Anwar, Abdul Rauf, Mideksa, Kidist Gebremariam, Pressler, Ronit, Deuschl, Günther, Stephani, Ulrich, Siniatchkin, Michael

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Investigating the genetic basis of fever-associated syndromic epilepsies using copy number variation analysis حسب Hartmann, Corinna, von Spiczak, Sarah, Suls, Arvid, Weckhuysen, Sarah, Buyse, Gunnar, Vilain, Catheline, Van Bogaert, Patrick, De Jonghe, Peter, Cook, Joseph, Muhle, Hiltrud, Stephani, Ulrich, Helbig, Ingo, Mefford, Heather C.

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Fenfluramine for Treatment-Resistant Seizures in Patients With Dravet Syndrome Receiving Stiripentol-Inclusive Regimens: A Randomized Clinical Trial حسب Nabbout, Rima, Mistry, Arun, Zuberi, Sameer, Villeneuve, Nathalie, Gil-Nagel, Antonio, Sanchez-Carpintero, Rocio, Stephani, Ulrich, Laux, Linda, Wirrell, Elaine, Knupp, Kelly, Chiron, Catherine, Farfel, Gail, Galer, Bradley S., Morrison, Glenn, Lock, Michael, Agarwal, Anupam, Auvin, Stéphane

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Genome-Wide Copy Number Variation in Epilepsy: Novel Susceptibility Loci in Idiopathic Generalized and Focal Epilepsies حسب Mefford, Heather C., Muhle, Hiltrud, Ostertag, Philipp, von Spiczak, Sarah, Buysse, Karen, Baker, Carl, Franke, Andre, Malafosse, Alain, Genton, Pierre, Thomas, Pierre, Gurnett, Christina A., Schreiber, Stefan, Bassuk, Alexander G., Guipponi, Michel, Stephani, Ulrich, Helbig, Ingo, Eichler, Evan E.

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Structural genomic variation in childhood epilepsies with complex phenotypes حسب Helbig, Ingo, Swinkels, Marielle E M, Aten, Emmelien, Caliebe, Almuth, van 't Slot, Ruben, Boor, Rainer, von Spiczak, Sarah, Muhle, Hiltrud, Jähn, Johanna A, van Binsbergen, Ellen, van Nieuwenhuizen, Onno, Jansen, Floor E, Braun, Kees P J, de Haan, Gerrit-Jan, Tommerup, Niels, Stephani, Ulrich, Hjalgrim, Helle, Poot, Martin, Lindhout, Dick, Brilstra, Eva H, Møller, Rikke S, Koeleman, Bobby PC

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Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood حسب Vögtle, F.-Nora, Brändl, Björn, Larson, Austin, Pendziwiat, Manuela, Friederich, Marisa W., White, Susan M., Basinger, Alice, Kücükköse, Cansu, Muhle, Hiltrud, Jähn, Johanna A., Keminer, Oliver, Helbig, Katherine L., Delto, Carolyn F., Myketin, Lisa, Mossmann, Dirk, Burger, Nils, Miyake, Noriko, Burnett, Audrey, van Baalen, Andreas, Lovell, Mark A., Matsumoto, Naomichi, Walsh, Maie, Yu, Hung-Chun, Shinde, Deepali N., Stephani, Ulrich, Van Hove, Johan L.K., Müller, Franz-Josef, Helbig, Ingo

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Linking pre-existing biorepositories for medical research: the PopGen 2.0 Network حسب Lieb, Wolfgang, Jacobs, Gunnar, Wolf, Andreas, Richter, Gesine, Gaede, Karoline I., Schwarz, Jeanette, Arnold, Norbert, Böhm, Ruwen, Buyx, Alena, Cascorbi, Ingolf, Franke, Andre, Glinicke, Christine, Held-Feindt, Janka, Junker, Ralf, Kalthoff, Holger, Kramer, Hans-Heiner, Leypoldt, Frank, Maass, Nicolai, Maetzler, Walter, May, Sandra, Mehdorn, H. Maximilian, Röcken, Christoph, Schafmayer, Clemens, Schrappe, Martin, Schreiber, Stefan, Sebens, Susanne, Stephani, Ulrich, Synowitz, Michael, Weimer, Jörg, Zabel, Peter, Nöthlings, Ute, Röder, Christian, Krawczak, Michael

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Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly حسب Hardies, Katia, May, Patrick, Djémié, Tania, Tarta-Arsene, Oana, Deconinck, Tine, Craiu, Dana, Helbig, Ingo, Suls, Arvid, Balling, Rudy, Weckhuysen, Sarah, De Jonghe, Peter, Hirst, Jennifer, Afawi, Zaid, Barisic, Nina, Baulac, Stéphanie, Caglayan, Hande, Depienne, Christel, De Kovel, Carolien G.F., Dimova, Petia, Guerrero-López, Rosa, Guerrini, Renzo, Hjalgrim, Helle, Hoffman-Zacharska, Dorota, Jahn, Johanna, Klein, Karl Martin, Koeleman, Bobby P.C., Leguern, Eric, Lehesjoki, Anna-Elina, Lemke, Johannes, Lerche, Holger, Marini, Carla, Muhle, Hiltrud, Rosenow, Felix, Serratosa, Jose M., Møller, Rikke S., Stephani, Ulrich, Striano, Pasquale, Talvik, Tiina, Von Spiczak, Sarah, Weber, Yvonne, Zara, Federico

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Burden Analysis of Rare Microdeletions Suggests a Strong Impact of Neurodevelopmental Genes in Genetic Generalised Epilepsies حسب Lal, Dennis, Ruppert, Ann-Kathrin, Trucks, Holger, Schulz, Herbert, de Kovel, Carolien G., Kasteleijn-Nolst Trenité, Dorothée, Sonsma, Anja C. M., Koeleman, Bobby P., Lindhout, Dick, Weber, Yvonne G., Lerche, Holger, Kapser, Claudia, Schankin, Christoph J., Kunz, Wolfram S., Surges, Rainer, Elger, Christian E., Gaus, Verena, Schmitz, Bettina, Helbig, Ingo, Muhle, Hiltrud, Stephani, Ulrich, Klein, Karl M., Rosenow, Felix, Neubauer, Bernd A., Reinthaler, Eva M., Zimprich, Fritz, Feucht, Martha, Møller, Rikke S., Hjalgrim, Helle, De Jonghe, Peter, Suls, Arvid, Lieb, Wolfgang, Franke, Andre, Strauch, Konstantin, Gieger, Christian, Schurmann, Claudia, Schminke, Ulf, Nürnberg, Peter, Sander, Thomas

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