The role of opioids in restless legs syndrome: an [11C]diprenorphine PET study von von Spiczak, Sarah, Whone, Alan L., Hammers, Alexander, Asselin, Marie-Claude, Turkheimer, Federico, Tings, Tobias, Happe, Svenja, Paulus, Walter, Trenkwalder, Claudia, Brooks, David J.

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Klinische Charakteristika und Lebensqualität beim Dravet-Syndrom: Ergebnisse der deutschen Kohorte des „Dravet syndrome caregiver survey“ (DISCUSS) von Strzelczyk, A, Lagae, L, Kurlemann, G, Flege, S, Bast, T, Polster, T, Pringsheim, M, von Spiczak, S, Hipp, P, Schubert-Bast, S

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G.P.17.01 Intravenous inotropic treatment of end stage heart failure in neuromuscular disorders von van Baalen, A, Fischer, G, von Spiczak, S, Wiegand, G, Stephani, U

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Genetic heterogeneity in infantile spasms von Muir, Alison M., Myers, Candace T., Nguyen, Nancy T., Saykally, Julia, Craiu, Dana, De Jonghe, Peter, Helbig, Ingo, Hoffman-Zacharska, Dorota, Guerrini, Renzo, Lehesjoki, Anna-Elina, Marini, Carla, Møller, Rikke S., Serratosa, Jose, Štěrbová, Katalin, Striano, Pasquale, von Spiczak, Sarah, Weckhuysen, Sarah, Mefford, Heather C.

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Clinical characteristics and quality of life with Dravet syndrome: results of the German cohort of the Dravet syndrome caregiver survey (DISCUSS) von Strzelczyk, A, Lagae, L, Kurlemann, G, Flege, S, Bast, T, Polster, T, Pringsheim, M, von Spiczak, S, Hipp, P, Schubert-Bast, S

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Familial and sporadic 15q13.3 microdeletions in idiopathic generalized epilepsy: precedent for disorders with complex inheritance von Dibbens, Leanne M., Mullen, Saul, Helbig, Ingo, Mefford, Heather C., Bayly, Marta A., Bellows, Susannah, Leu, Costin, Trucks, Holger, Obermeier, Tanja, Wittig, Michael, Franke, Andre, Caglayan, Hande, Yapici, Zuhal, Sander, Thomas, Eichler, Evan E., Scheffer, Ingrid E., Mulley, John C., Berkovic, Samuel F.

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Genetische Ursachen epileptischer Enzephalopathien von von Spiczak, S, Caliebe, A, Muhle, H, Helbig, I, Stephani, U

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PND78 - SOCIO-ECONOMIC IMPACT OF DRAVET SYNDROME IN GERMANY: A REAL-WORLD STUDY von Irwin, J, Strzelczyk, A, Kalski, M, Bast, T, Wiemer-Kruel, A., Bettendorf, U, Kieslich, M, Kluger, G, Kurlemann, G, Mayer, T, Neubauer, B.A., Polster, T, Herting, A, von Spiczak, S., Trollmann, R, Wolff, M, Klein, KM, Rosenow, F, Schubert-Bast, S., Carroll, J, MacDonald, D, Gibson, E

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Ultra-rare genetic variation in the epilepsies: A whole-exome sequencing study of 17,606 individuals von Feng, Y-CA, Howrigan, DP, Tashman, K, Cerrato, F, Churchhouse, C, Dhindsa, RS, Stanley, KE, Weckhuysen, S, Sisodiya, SM, Cotsapas, C, De Jonghe, P, Kwan, P, Marson, AG, Stewart, R, Dlugos, DJ, Scheffer, IE, Striano, P, Freyer, C, Bellows, ST, Leu, C, Macdonald, A, Burgess, R, Weckhuysen, D, Bahlo, M, Papacostas, SS, Laššuthová, P, Reif, PS, Kunz, WS, Zsurka, G, Elger, CE, Bauer, J, Rademacher, M, Pendziwiat, M, Rademacher, A, Kluger, G, Häusler, M, Becker, F, Rau, S, Steinhoff, BJ, Schubert-Bast, S, Borggräfe, I, Madeleyn, R, Saarela, A, Linnankivi, T, Rees, MI, Chung, S-K, Powell, R, Schneider, N, Braatz, V, Auce, P, Sham, PC, Delanty, N, McCormack, M, Canafoglia, L, Castellotti, B, Iacomino, M, Mancardi, MM, Tinuper, P, Licchetta, L, Stipa, C, Manna, L, Gagliardi, M, Parrini, E, Vetro, A, Bianchini, C, Doccini, V, Yamakawa, K, King, C, Arslan, M, Yapıcı, Z, Yis, U, Topaloglu, P, Uğur-İşeri, S, Baykan, B, Salman, B, Kesim, Y, Özkara, Ç, Shiedley, BR, Buono, RJ, Ferraro, TN, Privitera, M, Kuzniecky, RI, Hegde, M, Ellis, CA, Ciullo, V, Reif, A, McQuillin, A, McIntosh, A, Blackwood, D, Carvalho, CB, Malaspina, D, Morley, CP, Perkins, DO, Knowles, JA, McCarroll, SA, Gupta, N, Lander, ES, Goldstein, DB, Lerche, H, Neale, BM

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Klinische Charakteristika und Lebensqualität beim Dravet-Syndrom: Ergebnisse der deutschen Kohorte des „Dravet syndrome caregiver survey“ (DISCUSS) von Strzelczyk, A., Lagae, L., Kurlemann, G., Flege, S., Bast, T., Polster, T., Pringsheim, M., von Spiczak, S., Hipp, P., Schubert-Bast, S.

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P14.10 Levetiracetam and Lamotrigin May Increase Seizure Activity in Idiopathic or Cryptogenic Paediatric Epilepsies von Boor, R., Doege, C., Dreiwes, C., von Spiczak, S., Stephani, U.

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Mehr als Anfälle und Antiepileptika von von Spiczak, S, Stephani, U

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Mutations in GRIN2A and GRIN2B encoding regulatory subunits of NMDA receptors cause variable neurodevelopmental phenotypes von Endele, S, Rosenberger, G, Geider, K, Popp, B, Tamer, C, Stefanova, I, Milh, M, Kortüm, F, Fritsch, A, Pientka, F K, Hellenbroich, Y, Kalscheuer, V M, Kohlhase, J, Moog, U, Rappold, G, Rauch, A, Ropers, H H, von Spiczak, S, Tönnies, H, Villeneuve, N, Villard, L, Zabel, B, Zenker, M, Laube, B, Reis, A, Wieczorek, D, Van Maldergem, L, Kutsche, K

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De novo variants in neurodevelopmental disorders with epilepsy von Heyne, Henrike O., Singh, Tarjinder, Stamberger, Hannah, Abou Jamra, Rami, Caglayan, Hande, Craiu, Dana, De Jonghe, Peter, Guerrini, Renzo, Helbig, Katherine L., Koeleman, Bobby P. C., Kosmicki, Jack A., Linnankivi, Tarja, May, Patrick, Muhle, Hiltrud, Møller, Rikke S., Neubauer, Bernd A., Palotie, Aarno, Pendziwiat, Manuela, Striano, Pasquale, Tang, Sha, Wu, Sitao, Poduri, Annapurna, Weber, Yvonne G., Weckhuysen, Sarah, Sisodiya, Sanjay M., Daly, Mark J., Helbig, Ingo, Lal, Dennis, Lemke, Johannes R.

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Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies von Carvill, Gemma L., Engel, Krysta L., Ramamurthy, Aishwarya, Cochran, J. Nicholas, Roovers, Jolien, Stamberger, Hannah, Lim, Nicholas, Schneider, Amy L., Hollingsworth, Georgie, Holder, Dylan H., Regan, Brigid M., Lawlor, James, Lagae, Lieven, Ceulemans, Berten, Bebin, E. Martina, Nguyen, John, Striano, Pasquale, Zara, Federico, Helbig, Ingo, Møller, Rikke S., von Spiczak, Sarah, Muhle, Hiltrud, Caglayan, Hande, Sterbova, Katalin, Craiu, Dana, Hoffman, Dorota, Lehesjoki, Anna-Elina, Selmer, Kaja, Depienne, Christel, Lemke, Johannes, Marini, Carla, Guerrini, Renzo, Neubauer, Bernd, Talvik, Tiina, Leguern, Eric, de Jonghe, Peter, Weckhuysen, Sarah, Barsh, Gregory S., Weckhuysen, Sarah, Meisler, Miriam, Berkovic, Samuel F., De Jonghe, Peter, Scheffer, Ingrid E., Myers, Richard M., Cooper, Gregory M., Mefford, Heather C.

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Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy von Mignot, Cyril, von Stülpnagel, Celina, Nava, Caroline, Ville, Dorothée, Sanlaville, Damien, Lesca, Gaetan, Rastetter, Agnès, Gachet, Benoit, Marie, Yannick, Korenke, G Christoph, Borggraefe, Ingo, Hoffmann-Zacharska, Dorota, Szczepanik, Elżbieta, Rudzka-Dybała, Mariola, Yiş, Uluç, Çağlayan, Hande, Isapof, Arnaud, Marey, Isabelle, Panagiotakaki, Eleni, Korff, Christian, Rossier, Eva, Riess, Angelika, Beck-Woedl, Stefanie, Rauch, Anita, Zweier, Christiane, Hoyer, Juliane, Reis, André, Mironov, Mikhail, Bobylova, Maria, Mukhin, Konstantin, Hernandez-Hernandez, Laura, Maher, Bridget, Sisodiya, Sanjay, Kuhn, Marius, Glaeser, Dieter, Weckhuysen, Sarah, Myers, Candace T, Mefford, Heather C, Hörtnagel, Konstanze, Biskup, Saskia, Lemke, Johannes R, Héron, Delphine, Kluger, Gerhard, Depienne, Christel, Craiu, Dana, De Jonghe, Peter, Helbig, Ingo, Guerrini, Renzo, Lehesjoki, Anna-Elina, Marini, Carla, Muhle, Hiltrud, Møller, Rikke S, Neubauer, Bernd, Pal, Deb, Selmer, Kaja, Stephani, Ulrich, Sterbova, Katalin, Striano, Pasquale, Talvik, Tiina, von Spiczak, Sarah

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Clinical characteristics and quality of life with Dravet syndrome: results of the German cohort of the Dravet syndrome caregiver survey (DISCUSS) von Strzelczyk, A, Lagae, L, Kurlemann, G, Flege, S, Bast, T, Polster, T, Pringsheim, M, von Spiczak, S, Hipp, P, Schubert-Bast, S

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DYT11– Myoclonic Dystonia as a rare form of childhood dystonia von Spiczak, S von, Petersen, B, Muhle, H, Klein, C, Stephani, U

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Mutations in the GABA transporter SLC6A1 cause epilepsy with myoclonic atonic seizures von Carvill, Gemma L., McMahon, Jacinta M., Schneider, Amy, Zemel, Matthew, Myers, Candace T., Saykally, Julia, Nguyen, John, Robbiano, Angela, Zara, Federico, Specchio, Nicola, Mecarelli, Oriano, Smith, Robert L., Leventer, Richard J., Møller, Rikke S., Nikanorova, Marina, Dimova, Petia, Jordanova, Albena, Petrou, Steven, Helbig, Ingo, Striano, Pasquale, Weckhuysen, Sarah, Berkovic, Samuel F., Scheffer, Ingrid E., Mefford, Heather C.

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Myoklonisch-astatische Epilepsie von Doege, C, Kleiss, R, Stephani, U, von Spiczak, S

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