Rufinamide for generalized seizures associated with Lennox-Gastaut syndrome von GLAUSER, T, KLUGER, G, SACHDEO, R, KRAUSS, G, PERDOMO, C, ARROYO, S

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The core FOXG1 syndrome phenotype consists of postnatal microcephaly, severe mental retardation, absent language, dyskinesia, and corpus callosum hypogenesis von Kortüm, Fanny, Das, Soma, Flindt, Max, Morris-Rosendahl, Deborah J, Stefanova, Irina, Goldstein, Amy, Horn, Denise, Klopocki, Eva, Kluger, Gerhard, Martin, Peter, Rauch, Anita, Roumer, Agathe, Saitta, Sulagna, Walsh, Laurence E, Wieczorek, Dagmar, Uyanik, Gökhan, Kutsche, Kerstin, Dobyns, William B

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Limbic encephalitis in children and adolescents von Haberlandt, E, Bast, T, Ebner, A, Holthausen, H, Kluger, G, Kravljanac, R, Kröll-Seger, J, Kurlemann, G, Makowski, C, Rostasy, K, Tuschen-Hofstätter, E, Weber, G, Vincent, A, Bien, CG

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Clinical and genetic spectrum of SCN2A-associated episodic ataxia von Schwarz, N., Bast, T., Gaily, E., Golla, G., Gorman, K.M., Griffiths, L.R., Hahn, A., Hukin, J., King, M., Korff, C., Miranda, M.J., Møller, R.S., Neubauer, B., Smith, R.A., Smol, T., Striano, P., Stroud, B., Vaccarezza, M., Kluger, G., Lerche, H., Fazeli, W.

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Corrigendum to “Autoantibody status, neuroradiological and clinical findings in children with acute cerebellitis” [Eur. J. Paediatr. Neurol. 47 (2023) 118–130] von Quack, L., Glatter, S., Wegener-Panzer, A., Cleaveland, R., Bertolini, A., Endmayr, V., Seidl, R., Breu, M., Wendel, E., Schimmel, M., Baumann, M., Rauchenzauner, M., Pritsch, M., Boy, N., Muralter, T., Kluger, G., Makoswski, C., Kraus, V., Leiz, S., Loehr-Nilles, C., Kreth, J.H., Braig, S., Schilling, S., Kern, J., Blank, C., Baumann, B. Tro, Vieth, S., Wallot, M., Reindl, M., Ringl, H., Wandinger, K.P., Leypoldt, F., Höftberger, R., Rostàsy, K.

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Co-existence of self-limited focal epilepsies of childhood (SelFEC) and epileptiform discharges in the context of SelFEC in children with structural focal epilepsies and in childre... von Holthausen, H, Brockhaus, A, von Stülpnagel, C, Pieper, T, Zsoter, A, Kluger, G, Berweck, S, Hartlieb, T

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Autoantibody status, neuroradiological and clinical findings in children with acute cerebellitis von Quack, L, Glatter, S, Wegener-Panzer, A, Cleaveland, R, Bertolini, A, Endmayr, V, Seidl, R, Breu, M, Wendel, E, Schimmel, M, Baumann, M, Rauchenzauner, M, Pritsch, M, Boy, N, Muralter, T, Kluger, G, Makoswski, C, Kraus, V, Leiz, S, Loehr-Nilles, C, Kreth, J H, Braig, S, Schilling, S, Kern, J, Blank, C, Tro Baumann, B, Vieth, S, Wallot, M, Reindl, M, Ringl, H, Wandinger, K P, Leypoldt, F, Höftberger, R, Rostásy, K

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Retrospective evaluation of low long-term efficacy of antiepileptic drugs and ketogenic diet in 39 patients with CDKL5 -related epilepsy von Müller, A, Helbig, I, Jansen, C, Bast, T, Guerrini, R, Jähn, J, Muhle, H, Auvin, S, Korenke, G.C, Philip, S, Keimer, R, Striano, P, Wolf, N.I, Püst, B, Thiels, Ch, Fogarasi, A, Waltz, S, Kurlemann, G, Kovacevic-Preradovic, T, Ceulemans, B, Schmitt, B, Philippi, H, Tarquinio, D, Buerki, S, von Stülpnagel, C, Kluger, G

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Epilepsy in patients with GRIN2A alterations: genetics, neurodevelopment, epileptic phenotype and response to anticonvulsive drugs von Stülpnagel, C.v., M.D, Ensslen, M, Møller, R.S, Pal, D.K, Masnada, S, Veggiotti, P, Piazza, E, Dreesmann, M, Hartlieb, T, Herberhold, T, Hughes, E, Koch, M, Kutzer, C, Hoertnagel, K, Nitanda, J, Pohl, M, Rostásy, K, Haack, T.B, Stöhr, K, Kluger, G, Borggraefe, I

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Absence Seizures as a Feature of Juvenile Myoclonic Epilepsy in Rhodesian Ridgeback Dogs von Wielaender, F., James, F.M.K., Cortez, M.A., Kluger, G., Neßler, J.N., Tipold, A., Lohi, H., Fischer, A.

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Low long-term efficacy and tolerability of add-on rufinamide in patients with Dravet syndrome von Mueller, A, Boor, R, Coppola, G, Striano, P, Dahlin, M, von Stuelpnagel, C, Lotte, J, Staudt, M, Kluger, G

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MRI-imaging and clinical findings of eleven children with tick-borne encephalitis and review of the literature von von Stülpnagel, C, Winkler, P, Koch, J, Zeches-Kansy, C, Schöttler-Glas, A, Wolf, G, Niller, H.H, Staudt, M, Kluger, G, Rostasy, K

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Changes in elementary finger–hand functions over time in preschool children with spastic cerebral palsy von Blank, R., Kluger, G.

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Levetiracetam as add-on therapy in different subgroups of “benign” idiopathic focal epilepsies in childhood von von Stülpnagel, C, Kluger, G, Leiz, S, Holthausen, H

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OP17 – 2537: Epilepsy, clinical presentation and MRI features in patients with COL4A1 mutations von Selch, C, Winkler, P, Pringsheim, M, Hasse, A, Baumeister, F, Staudt, M, Kluger, G

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First long-term experience with the orphan drug rufinamide in children with myoclonic-astatic epilepsy (Doose syndrome) von von Stülpnagel, C, Coppola, G, Striano, P, Müller, A, Staudt, M, Kluger, G

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Genetic epilepsies in childhood Exact molecular diagnosis as basis of an individual treatment? von von Stuelpnagel, C., Kluger, G.

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PP07.15 – 2633: Familial generalized epilepsy with absences with SCN9A mutation: Therapy with carbamazepine von Heil, S, Pringsheim, M, Betzler, C, Hoffmann, J, Grau, T, Hörtnagel, K, Staudt, M, Kluger, G

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Genetic and phenotypic heterogeneity suggest therapeutic implications in SCN2A-related disorders von Wolff, Markus, Johannesen, Katrine M, Hedrich, Ulrike B S, Masnada, Silvia, Rubboli, Guido, Gardella, Elena, Lesca, Gaetan, Ville, Dorothée, Milh, Mathieu, Villard, Laurent, Afenjar, Alexandra, Chantot-Bastaraud, Sandra, Mignot, Cyril, Lardennois, Caroline, Nava, Caroline, Schwarz, Niklas, Gérard, Marion, Perrin, Laurence, Doummar, Diane, Auvin, Stéphane, Miranda, Maria J, Hempel, Maja, Brilstra, Eva, Knoers, Nine, Verbeek, Nienke, van Kempen, Marjan, Braun, Kees P, Mancini, Grazia, Biskup, Saskia, Hörtnagel, Konstanze, Döcker, Miriam, Bast, Thomas, Loddenkemper, Tobias, Wong-Kisiel, Lily, Baumeister, Friedrich M, Fazeli, Walid, Striano, Pasquale, Dilena, Robertino, Fontana, Elena, Zara, Federico, Kurlemann, Gerhard, Klepper, Joerg, Thoene, Jess G, Arndt, Daniel H, Deconinck, Nicolas, Schmitt-Mechelke, Thomas, Maier, Oliver, Muhle, Hiltrud, Wical, Beverly, Finetti, Claudio, Brückner, Reinhard, Pietz, Joachim, Golla, Günther, Jillella, Dinesh, Linnet, Karen M, Charles, Perrine, Moog, Ute, Õiglane-Shlik, Eve, Mantovani, John F, Park, Kristen, Deprez, Marie, Lederer, Damien, Mary, Sandrine, Scalais, Emmanuel, Selim, Laila, Van Coster, Rudy, Lagae, Lieven, Nikanorova, Marina, Hjalgrim, Helle, Korenke, G Christoph, Trivisano, Marina, Specchio, Nicola, Ceulemans, Berten, Dorn, Thomas, Helbig, Katherine L, Hardies, Katia, Stamberger, Hannah, de Jonghe, Peter, Weckhuysen, Sarah, Lemke, Johannes R, Krägeloh-Mann, Ingeborg, Helbig, Ingo, Kluger, Gerhard, Lerche, Holger, Møller, Rikke S

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Peculiarities of Hemiplegic Migraine in Children von Moiseeva, S. L., Betzler, C., Herberholdt, T., Kluger, G., Staudt, M.

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