A computational study of stimulus driven epileptic seizure abatement von Taylor, Peter Neal, Wang, Yujiang, Goodfellow, Marc, Dauwels, Justin, Moeller, Friederike, Stephani, Ulrich, Baier, Gerold

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Comparison of different methods to suppress muscle artifacts in EEG signals von Santillán-Guzmán, Alina, Heute, Ulrich, Stephani, Ulrich, Galka, Andreas

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Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies von 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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Mutations in PMPCB Encoding the Catalytic Subunit of the Mitochondrial Presequence Protease Cause Neurodegeneration in Early Childhood von 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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A multicenter, matched case‐control analysis comparing burden‐of‐illness in Dravet syndrome to refractory epilepsy and seizure remission in patients and caregivers in Germany von Strzelczyk, Adam, Schubert‐Bast, Susanne, Bast, Thomas, Bettendorf, Ulrich, Fiedler, Barbara, Hamer, Hajo M., Herting, Arne, Kalski, Malin, Kay, Lara, Kieslich, Matthias, Klein, Karl Martin, Kluger, Gerhard, Kurlemann, Gerhard, Mayer, Thomas, Neubauer, Bernd A., Polster, Tilman, von Spiczak, Sarah, Stephani, Ulrich, Trollmann, Regina, Wiemer‐Kruel, Adelheid, Wolff, Markus, Irwin, John, Carroll, Joe, Pritchard, Clive, Rosenow, Felix

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Febrile infection–related epilepsy syndrome (FIRES): A nonencephalitic encephalopathy in childhood von Van Baalen, Andreas, Häusler, Martin, Boor, Rainer, Rohr, Axel, Sperner, Jürgen, Kurlemann, Gerhard, Panzer, Axel, Stephani, Ulrich, Kluger, Gerhard

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Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish von Siekierska, Aleksandra, Stamberger, Hannah, Deconinck, Tine, Oprescu, Stephanie N., Partoens, Michèle, Zhang, Yifan, Sourbron, Jo, Adriaenssens, Elias, Mullen, Patrick, Wiencek, Patrick, Hardies, Katia, Lee, Jeong-Soo, Giong, Hoi-Khoanh, Distelmaier, Felix, Elpeleg, Orly, Helbig, Katherine L., Hersh, Joseph, Isikay, Sedat, Jordan, Elizabeth, Karaca, Ender, Kecskes, Angela, Lupski, James R., Kovacs-Nagy, Reka, May, Patrick, Narayanan, Vinodh, Pendziwiat, Manuela, Ramsey, Keri, Rangasamy, Sampathkumar, Shinde, Deepali N., Spiegel, Ronen, Timmerman, Vincent, von Spiczak, Sarah, Helbig, Ingo, Weckhuysen, Sarah, Francklyn, Christopher, Antonellis, Anthony, de Witte, Peter, De Jonghe, Peter

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Changes in activity of striato–thalamo–cortical network precede generalized spike wave discharges von Moeller, Friederike, Siebner, Hartwig R., Wolff, Stephan, Muhle, Hiltrud, Boor, Rainer, Granert, Oliver, Jansen, Olav, Stephani, Ulrich, Siniatchkin, Michael

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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome von Larsen, Jan, Johannesen, Katrine Marie, Ek, Jakob, Tang, Shan, Marini, Carla, Blichfeldt, Susanne, Kibæk, Maria, Spiczak, Sarah, Weckhuysen, Sarah, Frangu, Mimoza, Neubauer, Bernd Axel, Uldall, Peter, Striano, Pasquale, Zara, Federico, Kleiss, Rebecca, Simpson, Michael, Muhle, Hiltrud, Nikanorova, Marina, Jepsen, Birgit, Tommerup, Niels, Stephani, Ulrich, Guerrini, Renzo, Duno, Morten, Hjalgrim, Helle, Pal, Deb, Helbig, Ingo, Møller, Rikke Steensbjerre, Craiu, DC, Caglayan, HS, Talvik, T, Weber, YG, Barisic, N

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Dynamic imaging of coherent sources reveals different network connectivity underlying the generation and perpetuation of epileptic seizures von Elshoff, Lydia, Muthuraman, Muthuraman, Anwar, Abdul Rauf, Deuschl, Günther, Stephani, Ulrich, Raethjen, Jan, Siniatchkin, Michael

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Neuronal Networks during Burst Suppression as Revealed by Source Analysis von 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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Recessive loss-of-function mutations in AP4S1 cause mild fever-sensitive seizures, developmental delay and spastic paraplegia through loss of AP-4 complex assembly von 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

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Seizure and cognitive outcomes of epilepsy surgery in infancy and early childhood von Ramantani, Georgia, Kadish, Navah Ester, Strobl, Karl, Brandt, Armin, Stathi, Angeliki, Mayer, Hans, Schubert-Bast, Susanne, Wiegand, Gert, Korinthenberg, Rudolf, Stephani, Ulrich, van Velthoven, Vera, Zentner, Josef, Schulze-Bonhage, Andreas, Bast, Thomas

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PRRT2 Mutations are the major cause of benign familial infantile seizures von Schubert, Julian, Paravidino, Roberta, Becker, Felicitas, Berger, Andrea, Bebek, Nerses, Bianchi, Amedeo, Brockmann, Knut, Capovilla, Giuseppe, Dalla Bernardina, Bernardo, Fukuyama, Yukio, Hoffmann, Georg F., Jurkat-Rott, Karin, Anttonen, Anna-Kaisa, Kurlemann, Gerhard, Lehesjoki, Anna-Elina, Lehmann-Horn, Frank, Mastrangelo, Massimo, Mause, Ulrike, Müller, Stephan, Neubauer, Bernd, Püst, Burkhard, Rating, Dietz, Robbiano, Angela, Ruf, Susanne, Schroeder, Christopher, Seidel, Andreas, Specchio, Nicola, Stephani, Ulrich, Striano, Pasquale, Teichler, Jens, Turkdogan, Dilsad, Vigevano, Federico, Viri, Maurizio, Bauer, Peter, Zara, Federico, Lerche, Holger, Weber, Yvonne G.

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EEG-MEG Integration Enhances the Characterization of Functional and Effective Connectivity in the Resting State Network von Muthuraman, Muthuraman, Moliadze, Vera, Mideksa, Kidist Gebremariam, Anwar, Abdul Rauf, Stephani, Ulrich, Deuschl, Günther, Freitag, Christine M, Siniatchkin, Michael

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EEG‐fMRI in atypical benign partial epilepsy von Moeller, Friederike, Moehring, Jan, Ick, Imke, Steinmann, Elisabeth, Wolff, Stephan, Jansen, Olav, Boor, Rainer, Stephani, Ulrich, Siniatchkin, Michael

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Folker Hanefeld, 1937-2022 von Stephani, Ulrich, Rating, Dietz

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A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndrome von Tro‐Baumann, Blanca, von Spiczak, Sarah, Lotte, Jan, Bast, Thomas, Haberlandt, Edda, Sassen, Robert, Freund, Alfred, Leiz, Steffen, Stephani, Ulrich, Boor, Rainer, Holthausen, Hans, Helbig, Ingo, Kluger, Gerhard

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Abnormal response of motor cortex to photic stimulation in idiopathic generalized epilepsy von Groppa, Sergiu, Siebner, Hartwig R., Kurth, Christoph, Stephani, Ulrich, Siniatchkin, Michael

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Simultaneous EEG and fMRI recordings (EEG‐fMRI) in children with epilepsy von Moeller, Friederike, Stephani, Ulrich, Siniatchkin, Michael

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