STXBP1 encephalopathy: A neurodevelopmental disorder including epilepsy von Stamberger, Hannah, Nikanorova, Marina, Willemsen, Marjolein H, Accorsi, Patrizia, Angriman, Marco, Baier, Hartmut, Benkel-Herrenbrueck, Ira, Benoit, Valérie, Budetta, Mauro, Caliebe, Almuth, Cantalupo, Gaetano, Capovilla, Giuseppe, Casara, Gianluca, Courage, Carolina, Deprez, Marie, Destrée, Anne, Dilena, Robertino, Erasmus, Corrie E, Fannemel, Madeleine, Fjær, Roar, Giordano, Lucio, Helbig, Katherine L, Heyne, Henrike O, Klepper, Joerg, Kluger, Gerhard J, Lederer, Damien, Lodi, Monica, Maier, Oliver, Merkenschlager, Andreas, Michelberger, Nina, Minetti, Carlo, Muhle, Hiltrud, Phalin, Judith, Ramsey, Keri, Romeo, Antonino, Schallner, Jens, Schanze, Ina, Shinawi, Marwan, Sleegers, Kristel, Sterbova, Katalin, Syrbe, Steffen, Traverso, Monica, Tzschach, Andreas, Uldall, Peter, Van Coster, Rudy, Verhelst, Helene, Viri, Maurizio, Winter, Susan, Wolff, Markus, Zenker, Martin, Zoccante, Leonardo, De Jonghe, Peter, Helbig, Ingo, Striano, Pasquale, Lemke, Johannes R, Møller, Rikke S, Weckhuysen, Sarah

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Sex‐based electroclinical differences and prognostic factors in epilepsy with eyelid myoclonia von Cerulli Irelli, Emanuele, Cocchi, Enrico, Ramantani, Georgia, Morano, Alessandra, Riva, Antonella, Caraballo, Roberto H., Giuliano, Loretta, Yilmaz, Tülay, Panagiotakaki, Eleni, Operto, Francesca F., Giraldez, Beatriz Gonzalez, Balestrini, Simona, Silvennoinen, Katri, Casciato, Sara, Comajuan, Marion, Fortunato, Francesco, Giallonardo, Anna T., Gamirova, Rimma, Coppola, Antonietta, Di Gennaro, Giancarlo, Labate, Angelo, Sofia, Vito, Kluger, Gerhard J., Gambardella, Antonio, Kasteleijn‐Nolst Trenite, Dorothee, Baykan, Betul, Sisodiya, Sanjay M., Arzimanoglou, Alexis, Striano, Pasquale, Di Bonaventura, Carlo, Fisco, Giacomo, Meletti, Stefano, Liukshina, Natalia, Tomenko, Tatiana, Gobbi, Giuseppe, Buti, Daniela, Casellato, Susanna, Striano, Salvatore, Messana, Tullio, Giordano, Lucio, Ferlazzo, Edoardo, Vignoli, Aglaia, Viri, Maurizio, Bagnasco, Irene, Bebek, Nerses, Altıokka‐Uzun, Gunes

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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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Co‐occurring malformations of cortical development and SCN1A gene mutations von Barba, Carmen, Parrini, Elena, Coras, Roland, Galuppi, Anna, Craiu, Dana, Kluger, Gerhard, Parmeggiani, Antonia, Pieper, Tom, Schmitt‐Mechelke, Thomas, Striano, Pasquale, Giordano, Flavio, Blumcke, Ingmar, Guerrini, Renzo

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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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Reader response: SYNGAP1 encephalopathy: A distinctive generalized developmental and epileptic encephalopathy von Wolf, Peter, von Stülpnagel, Celina, Hartlieb, Till, Møller, Rikke S., Kluger, Gerhard J.

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Electroclinical Features and Long-term Seizure Outcome in Patients With Eyelid Myoclonia With Absences von Cerulli Irelli, Emanuele, Cocchi, Enrico, Ramantani, Georgia, Caraballo, Roberto H., Giuliano, Loretta, Yilmaz, Tulay, Morano, Alessandra, Panagiotakaki, Eleni, Operto, Francesca F., Gonzalez Giraldez, Beatriz, Silvennoinen, Katri, Casciato, Sara, Comajuan, Marion, Balestrini, Simona, Fortunato, Francesco, Coppola, Antonietta, Di Gennaro, Giancarlo, Labate, Angelo, Sofia, Vito, Kluger, Gerhard J., Kasteleijn-Nolst Trenité, Dorothée G.A., Gambardella, Antonio, Baykan, Betul, Sisodiya, Sanjay M., Arzimanoglou, Alexis, Striano, Pasquale, Di Bonaventura, Carlo

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Lennox-Gastaut syndrome: a consensus approach on diagnosis, assessment, management, and trial methodology von Arzimanoglou, Alexis, MD, French, Jacqueline, MD, Blume, Warren T, MD, Cross, J Helen, MD, Ernst, Jan-Peter, MD, Feucht, Martha, MD, Genton, Pierre, MD, Guerrini, Renzo, MD, Kluger, Gerhard, MD, Pellock, John M, MD, Perucca, Emilio, MD, Wheless, James W, MD

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Clinical spectrum of STX1B-related epileptic disorders von Wolking, Stefan, May, Patrick, Mei, Davide, Møller, Rikke S, Balestrini, Simona, Helbig, Katherine L, Altuzarra, Cecilia Desmettre, Chatron, Nicolas, Kaiwar, Charu, Stöhr, Katharina, Widdess-Walsh, Peter, Mendelsohn, Bryce A, Numis, Adam, Cilio, Maria R, Van Paesschen, Wim, Svendsen, Lene L, Oates, Stephanie, Hughes, Elaine, Goyal, Sushma, Brown, Kathleen, Sifuentes Saenz, Margarita, Dorn, Thomas, Muhle, Hiltrud, Pagnamenta, Alistair T, Vavoulis, Dimitris V, Knight, Samantha J.L, Taylor, Jenny C, Canevini, Maria Paola, Darra, Francesca, Gavrilova, Ralitza H, Powis, Zöe, Tang, Shan, Marquetand, Justus, Armstrong, Martin, McHale, Duncan, Klee, Eric W, Kluger, Gerhard J, Lowenstein, Daniel H, Weckhuysen, Sarah, Pal, Deb K, Helbig, Ingo, Guerrini, Renzo, Thomas, Rhys H, Rees, Mark I, Lesca, Gaetan, Sisodiya, Sanjay M, Weber, Yvonne G, Lal, Dennis, Marini, Carla, Lerche, Holger, Schubert, Julian

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Electro-Clinical Features and Functional Connectivity Analysis in SYN1-Related Epilepsy von Moya Quiros, Vincent, Adham, Ahmed, Convers, Philippe, Lesca, Gaetan, Mauguiere, François, Soulier, Hugo, Arzimanoglou, Alexis, Bayat, Allan, Braakman, Hilde, Camdessanche, Jean-Philippe, Casenave, Philippe, Chaton, Laurence, Chaix, Yves, Chochoi, Maxime, Depienne, Christel, Desportes, Vincent, De Ridder, Jessie, Dinkelacker, Vera, Gardella, Elena, Kluger, Gerhard J, Jung, Julien, Lemesle Martin, Martine, Mancardi, Maria Margherita, Mueller, Markus, Poulat, Anne-Lise, Platzer, Konrad, Roubertie, Agathe, Stokman, Marijn F, Vulto-van Silfhout, Anneke T, Wiegand, Gert, Mazzola, Laure

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Sleep quality, anxiety, symptoms of depression, and caregiver burden among those caring for patients with Dravet syndrome: a prospective multicenter study in Germany von Maltseva, Margarita, Schubert-Bast, Susanne, Zöllner, Johann Philipp, Bast, Thomas, Mayer, Thomas, von Spiczak, Sarah, Ruf, Susanne, Trollmann, Regina, Wolff, Markus, Hornemann, Frauke, Klotz, Kerstin A, Jacobs, Julia, Kurlemann, Gerhard, Neubauer, Bernd A, Polster, Tilman, Syrbe, Steffen, Bertsche, Astrid, Bettendorf, Ulrich, Kluger, Gerhard, Flege, Silke, Rosenow, Felix, Kay, Lara, Strzelczyk, Adam

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No evidence of neuronal/glial autoantibodies in febrile infection-related epilepsy syndrome (FIRES): a prospective clinic-serologic analysis von Soler Wenglein, Janina, Kluger, Gerhard, Leypoldt, Frank, Wandinger, Klaus-Peter, van Baalen, Andreas

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DEPDC5 mutations in genetic focal epilepsies of childhood von Lal, Dennis, Reinthaler, Eva M., Schubert, Julian, Muhle, Hiltrud, Riesch, Erik, Kluger, Gerhard, Jabbari, Kamel, Kawalia, Amit, Bäumel, Christine, Holthausen, Hans, Hahn, Andreas, Feucht, Martha, Neophytou, Birgit, Haberlandt, Edda, Becker, Felicitas, Altmüller, Janine, Thiele, Holger, Lemke, Johannes R., Lerche, Holger, Nürnberg, Peter, Sander, Thomas, Weber, Yvonne, Zimprich, Fritz, Neubauer, Bernd A.

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The time window for successful right-hemispheric language reorganization in children von Lidzba, Karen, PhD, Küpper, Hanna, MD, Kluger, Gerhard, MD, Staudt, Martin, MD

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Direct and indirect costs and cost-driving factors of Tuberous sclerosis complex in children, adolescents, and caregivers: a multicenter cohort study von Grau, Janina, Zöllner, Johann Philipp, Schubert-Bast, Susanne, Kurlemann, Gerhard, Hertzberg, Christoph, Wiemer-Kruel, Adelheid, Bast, Thomas, Bertsche, Astrid, Bettendorf, Ulrich, Fiedler, Barbara, Hahn, Andreas, Hartmann, Hans, Hornemann, Frauke, Immisch, Ilka, Jacobs, Julia, Kieslich, Matthias, Klein, Karl Martin, Klotz, Kerstin A, Kluger, Gerhard, Knuf, Markus, Mayer, Thomas, Marquard, Klaus, Meyer, Sascha, Muhle, Hiltrud, Müller-Schlüter, Karen, Noda, Anna H, Ruf, Susanne, Sauter, Matthias, Schlump, Jan-Ulrich, Syrbe, Steffen, Thiels, Charlotte, Trollmann, Regina, Wilken, Bernd, Willems, Laurent M, Rosenow, Felix, Strzelczyk, Adam

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Glutamate-mediated upregulation of the multidrug resistance protein 2 in porcine and human brain capillaries von Luna-Munguia, Hiram, Salvamoser, Josephine D, Pascher, Bettina, Pieper, Tom, Getzinger, Thekla, Kudernatsch, Manfred, Kluger, Gerhard, Potschka, Heidrun

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Network for Therapy in Rare Epilepsies (NETRE): Lessons From the Past 15 Years von von Stülpnagel, Celina, van Baalen, Andreas, Borggraefe, Ingo, Eschermann, Kirsten, Hartlieb, Till, Kiwull, Lorenz, Pringsheim, Milka, Wolff, Markus, Kudernatsch, Manfred, Wiegand, Gert, Striano, Pasquale, Kluger, Gerhard

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Exploring the relationships between composite scores of disease severity, seizure-freedom and quality of life in Dravet syndrome von Strzelczyk, Adam, Kurlemann, Gerhard, Bast, Thomas, Bettendorf, Ulrich, Kluger, Gerhard, Mayer, Thomas, Neubauer, Bernd A, Polster, Tilman, von Spiczak, Sarah, Trollmann, Regina, Wolff, Markus, Toward, Toby, Gruenert, Jens, Gibson, Eddie, Pritchard, Clive, Carroll, Joe, Rosenow, Felix, Schubert-Bast, Susanne

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KCNQ2 R144 variants cause neurodevelopmental disability with language impairment and autistic features without neonatal seizures through a gain-of-function mechanism von Miceli, Francesco, Millevert, Charissa, Soldovieri, Maria Virginia, Mosca, Ilaria, Ambrosino, Paolo, Carotenuto, Lidia, Schrader, Dewi, Lee, Hyun Kyung, Riviello, James, Hong, William, Risen, Sarah, Emrick, Lisa, Amin, Hitha, Ville, Dorothée, Edery, Patrick, de Bellescize, Julitta, Michaud, Vincent, Van-Gils, Julien, Goizet, Cyril, Willemsen, Marjolein H., Kleefstra, Tjitske, Møller, Rikke S, Bayat, Allan, Devinsky, Orrin, Sands, Tristan, Korenke, G. Christoph, Kluger, Gerhard, Mefford, Heather C., Brilstra, Eva, Lesca, Gaetan, Milh, Mathieu, Cooper, Edward C., Taglialatela, Maurizio, Weckhuysen, Sarah

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Epilepsy is a possible feature in Williams-Beuren syndrome patients harboring typical deletions of the 7q11.23 critical region von Nicita, Francesco, Garone, Giacomo, Spalice, Alberto, Savasta, Salvatore, Striano, Pasquale, Pantaleoni, Chiara, Spartà, Maria Valentina, Kluger, Gerhard, Capovilla, Giuseppe, Pruna, Dario, Freri, Elena, D'Arrigo, Stefano, Verrotti, Alberto

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