Arama Sonuçları - Stephani, Ulrich

A data-driven model of the generation of human EEG based on a spatially distributed stochastic wave equation Yazar: 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 Yazar: 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() Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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 Yazar: 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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