Review: Challenges in the histopathological classification of ganglioglioma and DNT: microscopic agreement studies and a preliminary genotype‐phenotype analysis von Blümcke, I., Coras, R., Wefers, A. K., Capper, D., Aronica, E., Becker, A., Honavar, M., Stone, T. J., Jacques, T. S., Miyata, H., Mühlebner, A., Pimentel, J., Söylemezoğlu, F., Thom, M.

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New insights into a spectrum of developmental malformations related to mTOR dysregulations: challenges and perspectives von Mühlebner, A., Bongaarts, A., Sarnat, H. B., Scholl, T., Aronica, E.

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Seizure outcome and use of antiepileptic drugs after epilepsy surgery according to histopathological diagnosis: a retrospective multicentre cohort study von Otte, Willem M, Braun, Kees P J, Aichholzer, Martin, Amorim, Isabel, Aparicio, Javier, Aronica, Eleonora, Beck, Jürgen, Becker, Albert, Bodi, Istvan, Chassoux, Francine, Chipaux, Mathilde, Cloppenborg, Thomas, Coras, Roland, Cross, J Helen, De Tisi, Jane, Duncan, John S, Elger, Christian, Ernst, Katharina, Feucht, Martha, Gadze, Zeljka Petelin, Jacques, Thomas S, Jakovcevic, Antonia, Jutila, Leena, Kalina, Adam, Koenig, Kristina, Kudernatsch, Manfred, Marusic, Petr, Özkara, Çiğdem, Pieper, Tom, Pimentel, Jose, Raicevic, Savo, Rheims, Sylvain, Ribeiro, Joana, Rosenow, Felix, Sales, Francisco, Schaller, Karl Lothar, Scholl, Theresa, Schramm, Johannes, Schulze-Bonhage, Andreas, Sciot, Raf, Seeck, Margitta, Sokic, Dragoslav, Specchio, Nicola, Delgado, Rafael Toledano, Van Paesschen, Wim, Leijten, Frans, Spliet, Wim GM, Mühlebner, Angelika, Fauser, Susanne, Polster, Tilman, Kalbhenn, Thilo, McEvoy, Andrew, Turak, Bares, Ferrand-Sorbets, Sarah, Scheiwe, Christian, Tisdall, Martin, Eltze, Christin, Akkol, Serdar, Deniz, Kaancan, Holthausen, Hans, Streichenberger, Nathalie, Guenot, Marc, Isnard, Jean, Valentijn, Antonio, Chang, Amanda, Mullatti, Nandini, Zamecnik, Josef, Zarubova, Jana, Tomasek, Martin, Immonen, Arto, Saarela, Anni, Rauramaa, Tuomas, Lobrinus, Johannes A, Momjian, Shahan, Lohr, Hannah, Kroell, Judith, Vermeulen, Lynn, Samueli, Sharon, Czech, Thomas, Spreafico, Roberto, Villani, Flavio, Rossini, Laura, Hermsen, Anke, Belohlavkova, Anezka, Benova, Barbora, Hoogland, Govert, Candela-Cantó, Santiago, Ostrowsky-Coste, Karine, Panagiotakaki, Eleni, Montavont, Alexandra, Kosal, Pascale Keo, Gokce-Samar, Zeynep, Milleret, Clara, Sulentic, Vlatko, Mrak, Goran, CarfíPavia, Giusy, Vojvodic, Nikola, Ristic, Aleksandar, Aledo-Serrano, Angel, Garcia-Morales, Irene

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Histopathological Findings in Brain Tissue Obtained during Epilepsy Surgery von Blumcke, Ingmar, Spreafico, Roberto, Haaker, Gerrit, Coras, Roland, Kobow, Katja, Bien, Christian G, Pfäfflin, Margarete, Elger, Christian, Widman, Guido, Schramm, Johannes, Becker, Albert, Braun, Kees P, Leijten, Frans, Baayen, Johannes C, Aronica, Eleonora, Chassoux, Francine, Hamer, Hajo, Stefan, Hermann, Rössler, Karl, Thom, Maria, Walker, Matthew C, Sisodiya, Sanjay M, Duncan, John S, McEvoy, Andrew W, Pieper, Tom, Holthausen, Hans, Kudernatsch, Manfred, Meencke, H. Joachim, Kahane, Philippe, Schulze-Bonhage, Andreas, Zentner, Josef, Heiland, Dieter H, Urbach, Horst, Steinhoff, Bernhard J, Bast, Thomas, Tassi, Laura, Lo Russo, Giorgio, Özkara, Cigdem, Oz, Buge, Krsek, Pavel, Vogelgesang, Silke, Runge, Uwe, Lerche, Holger, Weber, Yvonne, Honavar, Mrinalini, Pimentel, José, Arzimanoglou, Alexis, Ulate-Campos, Adriana, Noachtar, Soheyl, Hartl, Elisabeth, Schijns, Olaf, Guerrini, Renzo, Barba, Carmen, Jacques, Thomas S, Cross, J. Helen, Feucht, Martha, Mühlebner, Angelika, Grunwald, Thomas, Trinka, Eugen, Winkler, Peter A, Gil-Nagel, Antonio, Toledano Delgado, Rafael, Mayer, Thomas, Lutz, Martin, Zountsas, Basilios, Garganis, Kyriakos, Rosenow, Felix, Hermsen, Anke, von Oertzen, Tim J, Diepgen, Thomas L, Avanzini, Giuliano

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Expression of microRNAs miR21, miR146a, and miR155 in tuberous sclerosis complex cortical tubers and their regulation in human astrocytes and SEGA-derived cell cultures von van Scheppingen, J., Iyer, A. M., Prabowo, A. S., Mühlebner, A., Anink, J. J., Scholl, T., Feucht, M., Jansen, F. E., Spliet, W. G., Krsek, P., Zamecnik, J., Buccoliero, A. M., Giordano, F., Genitori, L., Kotulska, K., Jozwiak, S., Jaworski, J., Liszewska, E., van Vliet, E. A., Aronica, E.

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OP52 – 2694: The ketogenic diet versus ACTH in the treatment of infantile spasms: A prospective randomised study von Dressler, A, Trimmel-Schwahofer, P, Reithofer, E, Gröppel, G, Mühlebner, A, Samueli, S, Abraham, K, Benninger, F, Feucht, M

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OP57 – 2589: Temporal lobe epilepsy in children: Beyond hippocampal sclerosis von Mühlebner, A, Breu, M, Stefanits, H, Scholl, T, Gröppel, G, Kasprian, G, Schmook, M.T, Dressler, A, Prayer, D, Czech, T, Hainfellner, J, Feucht, M

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Promoter-Specific Hypomethylation Correlates with IL-1β Overexpression in Tuberous Sclerosis Complex (TSC) von Fuso, A., Iyer, A. M., van Scheppingen, J., Maccarrone, M., Scholl, T., Hainfellner, J. A., Feucht, M., Jansen, F. E., Spliet, W. G., Krsek, P., Zamecnik, J., Mühlebner, A., Aronica, E.

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Dysregulation of the (immuno)proteasome pathway in malformations of cortical development von van Scheppingen, J, Broekaart, D W M, Scholl, T, Zuidberg, M R J, Anink, J J, Spliet, W G, van Rijen, P C, Czech, T, Hainfellner, J A, Feucht, M, Mühlebner, A, van Vliet, E A, Aronica, E

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ID 361 – Remission of ESES after functional hemispherotomy is associated with significant language development von Gröppel, G, Dorfer, C, Dressler, A, Mühlebner-Fahrngruber, A, Porsche, B, Hainfellner, J.A, Czech, T, Feucht, M

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Diffuse, IDH-wildtype gliomas in adults with minimal histological change and isolated TERT promoter mutation: not simply CNS WHO grade 4 von Priesterbach-Ackley, L. P., Cordier, F., de Witt Hamer, P., Snijders, T. J., Robe, P. A., Küsters, B., de Leng, W. W. J., den Dunnen, W. F. A., Brandsma, D., Jansen, C., Wesseling, P., Muhlebner, A.

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OP53 – 2462: The role of mTOR inhibitors in TSC associated epilepsy von Samueli, S, Abraham, K, Dressler, A, Gröppel, G, Mühlebner-Fahrngruber, A, Feucht, M

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MicroRNA-34a activation in tuberous sclerosis complex during early brain development may lead to impaired corticogenesis von Korotkov, A, Sim, N S, Luinenburg, M J, Anink, J J, van Scheppingen, J, Zimmer, T S, Bongaarts, A, Broekaart, D W M, Mijnsbergen, C, Jansen, F E, Van Hecke, W, Spliet, W G M, van Rijen, P C, Feucht, M, Hainfellner, J A, Krsek, P, Zamecnik, J, Crino, P B, Kotulska, K, Lagae, L, Jansen, A C, Kwiatkowski, D J, Jozwiak, S, Curatolo, P, Mühlebner, A, Lee, J H, Mills, J D, van Vliet, E A, Aronica, E

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PP01.13 – 2471: Sturge-Weber syndrome is associated with complex malformations of cortical development – A case report von Scholl, T, Samueli, S, Mühlebner-Fahrngruber, A, Dressler, A, Abraham, K, Gröppel, G, Hainfellner, J, Czech, T, Prayer, D, Laccone, F, Feucht, M

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Promoter-Specific Hypomethylation Correlates with IL-1[beta] Overexpression in Tuberous Sclerosis Complex (TSC) von Fuso, A, Iyer, A M, van Scheppingen, J, Maccarrone, M, Scholl, T, Hainfellner, J A, Feucht, M, Jansen, F E, Spliet, W G, Krsek, P, Zamecnik, J, Mühlebner, A, Aronica, E

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Promoter-Specific Hypomethylation Correlates with IL-1β Overexpression in Tuberous Sclerosis Complex (TSC) von Fuso, A, Iyer, A M, van Scheppingen, J, Maccarrone, M, Scholl, T, Hainfellner, J A, Feucht, M, Jansen, F E, Spliet, W G, Krsek, P, Zamecnik, J, Mühlebner, A, Aronica, E

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Dysregulation of the (immuno)proteasome pathway in malformations of cortical development von van Scheppingen, J, Broekaart, D W M, Scholl, T, Zuidberg, M R J, Anink, J J, Spliet, W G, van Rijen, P C, Czech, T, Hainfellner, J A, Feucht, M, Mühlebner, A, van Vliet, E.A, Aronica, E

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Toward a better definition of focal cortical dysplasia: An iterative histopathological and genetic agreement trial von Blümcke, I, Coras, R, Busch, RM, Morita-Sherman, M, Lal, D, Prayson, R, Cendes, F, Lopes-Cendes, I, Rogerio, F, Almeida, VS, Rocha, CS, Sim, NS, Lee, JH, Kim, SH, Baulac, S, Baldassari, S, Adle-Biassette, H, Walsh, CA, Bizzotto, S, Doan, RN, Morillo, KS, Aronica, E, Mühlebner, A, Becker, A, Cienfuegos, J, Garbelli, R, Giannini, C, Honavar, M, Jacques, TS, Thom, M, Mahadevan, A, Miyata, H, Niehusmann, P, Sarnat, HB, Söylemezoglu, F, Najm, I

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MicroRNA-34a activation in tuberous sclerosis complex during early brain development may lead to impaired corticogenesis von Korotkov, A, Sim, NS, Luinenburg, MJ, Anink, JJ, van Scheppingen, J, Zimmer, TS, Bongaarts, A, Broekaart, DWM, Mijnsbergen, C, Jansen, FE, Van Hecke, W, Spliet, WGM, van Rijen, PC, Feucht, M, Hainfellner, JA, Kršek, P, Zamecnik, J, Crino, PB, Kotulska, K, Lagae, L, Jansen, AC, Kwiatkowski, DJ, Jozwiak, S, Curatolo, P, Mühlebner, A, Lee, JH, Mills, JD, van Vliet, EA, Aronica, E

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Review: Challenges in the histopathological classification of ganglioglioma and DNT: microscopic agreement studies and a preliminary genotype‐phenotype analysis von Blümcke, I, Coras, R, Wefers, AK, Capper, D, Aronica, E, Becker, A, Honavar, M, Stone, TJ, Jacques, TS, Miyata, H, Mühlebner, A, Pimentel, J, Söylemezoğlu, F, Thom, M

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