Live feed enrichments using microalgae for pikeperch ( Sander lucioperca ) larval culture von Yanes‐Roca, C., Štěrbová, K., Mráz, J., Veselý, L., Malinovskyi, O., Pěnka, T., Masojídek, J., Policar, T.

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Novel variants in the NARS2 gene as a cause of infantile-onset severe epilepsy leading to fatal refractory status epilepticus: case study and literature review von Štěrbová, K., Vlčková, M., Hansíková, H., Sebroňová, V., Sedláčková, L., Pavlíček, P., Laššuthová, Petra

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In response to: Fatal status epilepticus—the broad phenotypic heterogeneity of NARS2 variants. Author: Prof. Josef Finsterer: Regarding our manuscript: Novel variants in the NARS2... von Štěrbová, K., Vlčková, M., Hansíková, H., Sebroňová, V., Sedláčková, L., Pavlíček, P., Laššuthová, P.

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Brivaracetam use in children with epilepsy: A retrospective multicenter study von Špilárová, Z, Sládková, S, Bělohlávková, A, Česká, K, Hanáková, P, Horák, O, Jahodová, A, Knedlíková, L, Kolář, S, Ebel, M, Kudr, M, Ošlejšková, H, Ryzí, M, Španělová, K, Štěrbová, K, Koubová, A, Kršek, P, Danhofer, P

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Synchronization as adjustment of information rates: detection from bivariate time series von Palus, M, Komárek, V, Hrncír, Z, Sterbová, K

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The effectiveness of night-time video EEG monitoring in nocturnal enuresis is low von Štěrbová, K., Tesfayeová, A.

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In response to: Fatal status epilepticus—the broad phenotypic heterogeneity of NARS2 variants. Author: Prof. Josef Finsterer von Štěrbová, K, Vlčková, M, Hansíková, H, Sebroňová, V, Sedláčková, L, Pavlíček, P, Laššuthová, P

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Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients von Kovel, Carolien G.F., Brilstra, Eva H., Kempen, Marjan J.A., Slot, Ruben, Nijman, Isaac J., Afawi, Zaid, De Jonghe, Peter, Djémié, Tania, Guerrini, Renzo, Hardies, Katia, Helbig, Ingo, Hendrickx, Rik, Kanaan, Moine, Kramer, Uri, Lehesjoki, Anna‐Elina E., Lemke, Johannes R., Marini, Carla, Mei, Davide, Møller, Rikke S., Pendziwiat, Manuela, Stamberger, Hannah, Suls, Arvid, Weckhuysen, Sarah, Koeleman, Bobby P.C., R, Balling, N, Barisic, S, Baulac, HS, Caglayan, DC, Craiu, C, Depienne, P, Gormley, H, Hjalgrim, D, Hoffman‐Zacharska, J, Jähn, KM, Klein, V, Komarek, E, LeGuern, H, Lerche, P, May, H, Muhle, D, Pal, A, Palotie, F, Rosenow, K, Selmer, JM, Serratosa, SM, Sisodiya, U, Stephani, K, Sterbova, P, Striano, T, Talvik, M, van Haelst, N, Verbeek, S, von Spiczak, YG, Weber

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Postnatal hypobaric hypoxia in rats impairs water maze learning and the morphology of neurones and macroglia in cortex and hippocampus von SIMONOVA, Zuzana, STERBOVA, Katalin, BROZEK, Gustav, KOMAREK, Vladimir, SYKOVA, Eva

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Epileptiform activity in children with developmental dysphasia: quantification of discharges in overnight sleep video-EEG von Neuschlova, L, Sterbova, K, Zackova, J, Komarek, V

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A Development and Overview of the Use of Chemotherapy and the Role of Radiotherapy and Surgery in Patients with Newly Diagnosed Pancreatic Tumor and Cancer in the Current 5-year Ce... von Vokurka, S, Votavová, M, Kulhánková, J, Korunková, H, Fiala, O, Štěrbová, K, Svoboda, T, Vojtíšek, R, Matějka, V M, Fínek, J

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Synchronization and information flow in EEGs of epileptic patients von Palus, M., Komarek, V., Prochazka, T., Hrncir, Z., Sterbova, K.

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Pathogenic variants in SMARCA1 cause an X-linked neurodevelopmental disorder modulated by NURF complex composition von Picketts, D, Mirzaa, G, Yan, K, Relator, R, Timpano, S, Yalcin, B, Collins, S, Ziegler, A, Pao, E, Oyama, N, Brischoux-Boucher, E, Piard, J, Monaghan, K, Sacoto, MG, Dobyns, W, Park, K, Fernández-Mayoralas, D, Fernández-Jaén, A, Jayakar, P, Brusco, A, Antona, V, Giorgio, E, Kvarnung, M, Isidor, B, Conrad, S, Cogné, B, Deb, W, Stuurman, KE, Sterbova, K, Smal, N, Weckhuysen, S, Oegema, R, Innes, M, Latsko, M, Ben-Omran, T, Yeh, R, Kruer, M, Bakhtiari, S, Papavasiliou, A, Moutton, S, Nambot, S, Chanprasert, S, Paolucci, S, Miller, K, Burton, B, Kim, K, O'Heir, E, Bruwer, Z, Donald, K, Kleefstra, T, Goldstein, A, Angle, B, Bontempo, K, Miny, P, Joset, P, Demurger, F, Hobson, E, Pang, L, Carpenter, L, Li, D, Bonneau, D, Sadikovic, B

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SLEEP EEG ANALYSIS IN CHILDHOOD AUTISM von Komárek, V, Kulisek, R, Hrdlicka, M, Hrncir, Z, Sterbova, K, Faladova, L

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Genome-wide identification and phenotypic characterization of seizure-associated copy number variations in 741,075 individuals von Montanucci, L, Lewis-Smith, D, Collins, RL, Niestroj, LM, Parthasarathy, S, Xian, J, Ganesan, S, Macnee, M, Brünger, T, Thomas, RH, Talkowski, M, Motelow, JE, Povysil, G, Dhindsa, RS, Stanley, KE, Allen, AS, Goldstein, DB, Feng, YCA, Howrigan, DP, Abbott, LE, Tashman, K, Cerrato, F, Cusick, C, Singh, T, Heyne, H, Byrnes, AE, Churchhouse, C, Watts, N, Solomonson, M, Lal, D, Gupta, N, Neale, BM, Berkovic, SF, Lerche, H, Lowenstein, DH, Cavalleri, GL, Cossette, P, Cotsapas, C, De Jonghe, P, Dixon-Salazar, T, Guerrini, R, Hakonarson, H, Heinzen, EL, Helbig, I, Kwan, P, Marson, AG, Petrovski, S, Kamalakaran, S, Sisodiya, SM, Stewart, R, Weckhuysen, S, Depondt, C, Dlugos, DJ, Scheffer, IE, Striano, P, Freyer, C, Krause, R, May, P, McKenna, K, Regan, BM, Bennett, CA, Leech, SL, Leu, C, O’Brien, TJ, Todaro, M, Stamberger, H, Depondti, C, Andrade, DM, Ali, QZ, Sadoway, TR, Krestel, H, Schaller, A, Papacostas, SS, Kousiappa, I, Tanteles, GA, Yiolanda, C, Šterbová, K, Vlcková, M, Sedlácková, L, Laššuthová, P, Klein, KM, Rosenow, F, Reif, PS, Knake, S, Neubauer, BA, Zimprich, F, Feucht, M, Reinthaler, E, Kunz, WS, Zsurka, G, Surges, R, Baumgartner, TH, Von Wrede, R, Pendziwiat, M, Muhle, H, Rademacher, A, Van Baalen, A, Von Spiczak, S

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A Recurrent Missense Variant in AP2M1 Impairs Clathrin-Mediated Endocytosis and Causes Developmental and Epileptic Encephalopathy von Helbig, I, Lopez-Hernandez, T, Shor, O, Galer, P, Ganesan, S, Pendziwiat, M, Rademacher, A, Ellis, CA, Hümpfer, N, Schwarz, N, Seiffert, S, Peeden, J, Shen, J, Štěrbová, K, Hammer, TB, Møller, RS, Shinde, DN, Tang, S, Smith, L, Poduri, A, Krause, R, Benninger, F, Helbig, KL, Haucke, V, Weber, YG, EuroEPINOMICS-RES Consortium, GRIN Consortium

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Application of rare variant transmission disequilibrium tests to epileptic encephalopathy trio sequence data von Allen, AS, Berkovic, SF, Bridgers, J, Cossette, P, Dlugos, D, Epstein, MP, Glauser, T, Goldstein, DB, Heinzen, EL, Jiang, Y, Johnson, MR, Kuzniecky, R, Lowenstein, DH, Marson, AG, Mefford, HC, O'Brien, TJ, Ottman, R, Petrou, S, Petrovski, S, Poduri, A, Ren, Z, Scheffer, IE, Sherr, E, Wang, Q, Balling, R, Barisic, N, Baulac, S, Caglayan, H, Craiu, D, De Jonghe, P, Depienne, C, Guerrini, R, Helbig, I, Hjalgrim, H, Hoffman-Zacharska, D, Jaehn, J, Klein, KM, Komarek, V, Krause, R, Leguern, E, Lehesjoki, A-E, Lemke, JR, Lerche, H, Linnankivi, T, Marini, C, May, P, Moller, RS, Muhle, H, Pal, D, Palotie, A, Rosenow, F, Selmer, K, Serratosa, JM, Sisodiya, S, Stephani, U, Sterbova, K, Striano, P, Suls, A, Talvik, T, von Spiczak, S, Weber, Y, Weckhuysen, S, Zara, F, Abou-Khalil, B, Alldredge, BK, Andermann, E, Andermann, F, Bluvstein, J, Cascino, GD, Consalvo, D, Crumrine, P, Devinsky, O, Fiol, ME, Fountain, NB, Friedman, D, Haas, K, Haut, SR, Hayward, J, Joshi, S, Kanner, A, Kirsch, HE, Kossoff, EH, Kuperman, R, McGuire, SM, Motika, PV, Novotny, EJ, Paolicchi, JM, Parent, J, Park, K, Shellhaas, RA, Sirven, J, Smith, MC, Sullivan, J, Thio, LL, Venkat, A, Vining, EPG, Von Allmen, GK, Weisenberg, JL, Widdess-Walsh, P, Winawer, MR

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Targeted sequencing of 351 candidate genes for epileptic encephalopathy in a large cohort of patients von de Kovel, CGF, Brilstra, EH, Van Kempen, MJA, Van‘t Slot, R, Nijman, IJ, Afawi, Z, De Jonghe, P, Djémié, T, Guerrini, R, Hardies, K, Helbig, I, Hendrickx, R, Kanaan, M, Kramer, U, Lehesjoki, AEE, Lemke, JR, Marini, C, Mei, D, Møller, RS, Pendziwiat, M, Stamberger, H, Suls, A, Weckhuysen, S, Balling, R, Barisic, N, Baulac, S, Caglayan, HS, Craiu, DC, Depienne, C, Gormley, P, Hjalgrim, H, Hoffman-Zacharska, D, Jähn, J, Klein, KM, Komarek, V, LeGuern, E, Lerche, H, May, P, Muhle, H, Pal, D, Palotie, A, Rosenow, F, Selmer, K, Serratosa, JM, Sisodiya, SM, Stephani, U, Sterbova, K, Striano, P, Talvik, T, van Haelst, M, Verbeek, N, von Spiczak, S, Weber, YG, Koeleman, BPC

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Variation in depressive symptom trajectories in a large sample of couples von Csajbók, Zsófia, Štěrbová, Zuzana, Jonason, Peter K., Cermakova, Pavla, Dóka, Ádám, Havlíček, Jan

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De Novo Mutations in Synaptic Transmission Genes Including DNM1 Cause Epileptic Encephalopathies von Appenzeller, Silke, Balling, Rudi, Barisic, Nina, Baulac, Stéphanie, Caglayan, Hande, De Jonghe, Peter, Depienne, Christel, Dimova, Petia, Djémié, Tania, Gormley, Padhraig, Guerrini, Renzo, Helbig, Ingo, Hjalgrim, Helle, Jähn, Johanna, Klein, Karl Martin, Koeleman, Bobby, Komarek, Vladimir, Krause, Roland, Kuhlenbäumer, Gregor, Lemke, Johannes R., Lerche, Holger, Linnankivi, Tarja, Marini, Carla, May, Patrick, Møller, Rikke S., Muhle, Hiltrud, Palotie, Aarno, Pendziwiat, Manuela, Roelens, Filip, Rosenow, Felix, Selmer, Kaja, Serratosa, Jose M., Sisodiya, Sanjay, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Suls, Arvid, Talvik, Tiina, von Spiczak, Sarah, Weckhuysen, Sarah, Abou-Khalil, Bassel, Alldredge, Brian K., Andermann, Eva, Andermann, Frederick, Amron, Dina, Bautista, Jocelyn F., Berkovic, Samuel F., Bluvstein, Judith, Boro, Alex, Consalvo, Damian, Crumrine, Patricia, Devinsky, Orrin, Dlugos, Dennis, Epstein, Michael P., Fiol, Miguel, French, Jacqueline, Friedman, Daniel, Geller, Eric B., Glauser, Tracy, Glynn, Simon, Haas, Kevin, Haut, Sheryl R., Hayward, Jean, Helmers, Sandra L., Joshi, Sucheta, Kanner, Andres, Knowlton, Robert C., Kossoff, Eric H., Kuperman, Rachel, Kuzniecky, Ruben, Lowenstein, Daniel H., Motika, Paul V., Novotny, Edward J., Ottman, Ruth, Paolicchi, Juliann M., Parent, Jack, Park, Kristen, Scheffer, Ingrid E., Shellhaas, Renée A., Sherr, Elliott, Singh, Rani, Smith, Michael C., Sullivan, Joe, Venkat, Anu, Vining, Eileen P.G., Von Allmen, Gretchen K., Weisenberg, Judith L., Winawer, Melodie R., Cossette, Patrick, Delanty, Norman, Eichler, Evan E., Goldstein, David B., Han, Yujun, Heinzen, Erin L., Marson, Anthony G., Nieh, Sahar Esmaeeli, O’Brien, Terence J., Petrou, Stephen, Petrovski, Slavé, Ruzzo, Elizabeth K.

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