Critical incidents, nocturnal supervision, and caregiver knowledge on SUDEP in patients with Dravet syndrome: A prospective multicenter study in Germany by Maltseva, Margarita, Rosenow, Felix, Schubert‐Bast, Susanne, Flege, Silke, Wolff, Markus, von Spiczak, Sarah, Trollmann, Regina, Syrbe, Steffen, Ruf, Susanne, Polster, Tilman, Neubauer, Bernd A., Mayer, Thomas, Jacobs, Julia, Kurlemann, Gerhard, Kluger, Gerhard, Klotz, Kerstin A., Kieslich, Matthias, Kay, Lara, Hornemann, Frauke, Bettendorf, Ulrich, Bertsche, Astrid, Bast, Thomas, Strzelczyk, Adam

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Aberrant Inclusion of a Poison Exon Causes Dravet Syndrome and Related SCN1A-Associated Genetic Epilepsies by 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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L-Serine Treatment is Associated with Improvements in Behavior, EEG, and Seizure Frequency in Individuals with GRIN-Related Disorders Due to Null Variants by Krey, Ilona, von Spiczak, Sarah, Johannesen, Kathrine M., Hikel, Christiane, Kurlemann, Gerhard, Muhle, Hiltrud, Beysen, Diane, Dietel, Tobias, Møller, Rikke S., Lemke, Johannes R., Syrbe, Steffen

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The spectrum of intermediate SCN8A‐related epilepsy by Johannesen, Katrine M., Gardella, Elena, Encinas, Alejandra C., Lehesjoki, Anna‐Elina, Linnankivi, Tarja, Petersen, Michael B., Lund, Ida Charlotte Bay, Blichfeldt, Susanne, Miranda, Maria J., Pal, Deb K., Lascelles, Karine, Procopis, Peter, Orsini, Alessandro, Bonuccelli, Alice, Giacomini, Thea, Helbig, Ingo, Fenger, Christina D., Sisodiya, Sanjay M., Hernandez‐Hernandez, Laura, Krithika, Sundararaman, Rumple, Melissa, Masnada, Silvia, Valente, Marialuisa, Cereda, Cristina, Giordano, Lucio, Accorsi, Patrizia, Bürki, Sarah E., Mancardi, Margherita, Korff, Christian, Guerrini, Renzo, Spiczak, Sarah, Hoffman‐Zacharska, Dorota, Mazurczak, Tomasz, Coppola, Antonietta, Buono, Salvatore, Vecchi, Marilena, Hammer, Michael F., Varesio, Costanza, Veggiotti, Pierangelo, Lal, Dennis, Brünger, Tobias, Zara, Federico, Striano, Pasquale, Rubboli, Guido, Møller, Rikke S.

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Genome-wide copy number variation in epilepsy: novel susceptibility loci in idiopathic generalized and focal epilepsies by Mefford, Heather C, Muhle, Hiltrud, Ostertag, Philipp, von Spiczak, Sarah, Buysse, Karen, Baker, Carl, Franke, Andre, Malafosse, Alain, Genton, Pierre, Thomas, Pierre, Gurnett, Christina A, Schreiber, Stefan, Bassuk, Alexander G, Guipponi, Michel, Stephani, Ulrich, Helbig, Ingo, Eichler, Evan E

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Corticosteroids versus clobazam for treatment of children with epileptic encephalopathy with spike-wave activation in sleep (RESCUE ESES): a multicentre randomised controlled trial by van Arnhem, Marleen M L, van den Munckhof, Bart, Arzimanoglou, Alexis, Perucca, Emilio, Metsähonkala, Liisa, Rubboli, Guido, Søndergaard Khinchi, Marianne, de Saint-Martin, Anne, Klotz, Kerstin A, Jacobs, Julia, Cross, J Helen, Garcia Morales, Irene, Otte, Wim M, van Teeseling, Heleen C, Leijten, Frans S S, Braun, Kees P J, Jansen, Floor E, Jansen, Anna, Lagae, Lieven, Bast, Thomas, von Spiczak, Sarah, Kluger, Gerhard, van Bogaert, Patrick, Gaily, Eija, Baer, Sarah, Auvin, Stéphane, Chin, Richard, Zuberi, Sameer, Dimova, Petia, Craiu, C Dana, Veggiotti, Pierangelo, Ramantani, Georgia

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De Novo Loss-of-Function Mutations in CHD2 Cause a Fever-Sensitive Myoclonic Epileptic Encephalopathy Sharing Features with Dravet Syndrome by Suls, Arvid, Jaehn, Johanna A., Kecskés, Angela, Weber, Yvonne, Weckhuysen, Sarah, Craiu, Dana C., Siekierska, Aleksandra, Djémié, Tania, Afrikanova, Tatiana, Gormley, Padhraig, von Spiczak, Sarah, Kluger, Gerhard, Iliescu, Catrinel M., Talvik, Tiina, Talvik, Inga, Meral, Cihan, Caglayan, Hande S., Giraldez, Beatriz G., Serratosa, José, Lemke, Johannes R., Hoffman-Zacharska, Dorota, Szczepanik, Elzbieta, Barisic, Nina, Komarek, Vladimir, Hjalgrim, Helle, Møller, Rikke S., Linnankivi, Tarja, Dimova, Petia, Striano, Pasquale, Zara, Federico, Marini, Carla, Guerrini, Renzo, Depienne, Christel, Baulac, Stéphanie, Kuhlenbäumer, Gregor, Crawford, Alexander D., Lehesjoki, Anna-Elina, de Witte, Peter A.M., Palotie, Aarno, Lerche, Holger, Esguerra, Camila V., De Jonghe, Peter, Helbig, Ingo, Hendrickx, Rik, Holmgren, Philip, Stephani, Ulrich, Muhle, Hiltrud, Pendiziwiat, Manuela, Appenzeller, Silke, Selmer, Kaja, Brilstra, Eva, Koeleman, Bobby, Rosenow, Felix, Leguern, Eric, Sterbova, Katalin, Magdalena, Budisteanu, Rodica, Gherghiceanu, Arsene, Oana Tarta, Diana, Barca, Guerrero-Lopez, Rosa, Ortega, Laura, Todorova, Albena P., Kirov, Andrey V., Robbiano, Angela, Arslan, Mutluay, Yiş, Uluç, Ivanović, Vanja

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Semantic Similarity Analysis Reveals Robust Gene-Disease Relationships in Developmental and Epileptic Encephalopathies by Galer, Peter D., Ganesan, Shiva, Lewis-Smith, David, McKeown, Sarah E., Pendziwiat, Manuela, Helbig, Katherine L., Ellis, Colin A., Rademacher, Annika, Smith, Lacey, Poduri, Annapurna, Seiffert, Simone, von Spiczak, Sarah, Muhle, Hiltrud, van Baalen, Andreas, Thomas, Rhys H., Krause, Roland, Weber, Yvonne, Helbig, Ingo

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Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy by Chatron, Nicolas, Becker, Felicitas, Morsy, Heba, Schmidts, Miriam, Hardies, Katia, Tuysuz, Beyhan, Roselli, Sandra, Najafi, Maryam, Alkaya, Dilek Uludag, Ashrafzadeh, Farah, Nabil, Amira, Omar, Tarek, Maroofian, Reza, Karimiani, Ehsan Ghayoor, Hussien, Haytham, Kok, Fernando, Ramos, Luiza, Gunes, Nilay, Bilguvar, Kaya, Labalme, Audrey, Alix, Eudeline, Sanlaville, Damien, de Bellescize, Julitta, Poulat, Anne-Lise, Moslemi, Ali-Reza, Lerche, Holger, May, Patrick, Lesca, Gaetan, Weckhuysen, Sarah, Tajsharghi, Homa

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Biallelic VARS variants cause developmental encephalopathy with microcephaly that is recapitulated in vars knockout zebrafish by Siekierska, Aleksandra, Stamberger, Hannah, Deconinck, Tine, Oprescu, Stephanie N, Partoens, Michèle, Zhang, Yifan, Sourbron, Jo, Adriaenssens, Elias, Mullen, Patrick, Wiencek, Patrick, Hardies, Katia, Lee, Jeong-Soo, Giong, Hoi-Khoanh, Distelmaier, Felix, Elpeleg, Orly, Helbig, Katherine L, Hersh, Joseph, Isikay, Sedat, Jordan, Elizabeth, Karaca, Ender, Kecskes, Angela, Lupski, James R, Kovacs-Nagy, Reka, May, Patrick, Narayanan, Vinodh, Pendziwiat, Manuela, Ramsey, Keri, Rangasamy, Sampathkumar, Shinde, Deepali N, Spiegel, Ronen, Timmerman, Vincent, von Spiczak, Sarah, Helbig, Ingo, Weckhuysen, Sarah, Francklyn, Christopher, Antonellis, Anthony, de Witte, Peter, De Jonghe, Peter

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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 by 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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The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome by Larsen, Jan, Johannesen, Katrine Marie, Ek, Jakob, Tang, Shan, Marini, Carla, Blichfeldt, Susanne, Kibæk, Maria, Spiczak, Sarah, Weckhuysen, Sarah, Frangu, Mimoza, Neubauer, Bernd Axel, Uldall, Peter, Striano, Pasquale, Zara, Federico, Kleiss, Rebecca, Simpson, Michael, Muhle, Hiltrud, Nikanorova, Marina, Jepsen, Birgit, Tommerup, Niels, Stephani, Ulrich, Guerrini, Renzo, Duno, Morten, Hjalgrim, Helle, Pal, Deb, Helbig, Ingo, Møller, Rikke Steensbjerre, Craiu, DC, Caglayan, HS, Talvik, T, Weber, YG, Barisic, N

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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 by 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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The role of opioids in restless legs syndrome: an [11C]diprenorphine PET study by 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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Exploring the relationships between composite scores of disease severity, seizure-freedom and quality of life in Dravet syndrome by 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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Zonisamide‐responsive myoclonus in SEMA6B‐associated progressive myoclonic epilepsy by Herzog, Rebecca, Hellenbroich, Yorck, Brüggemann, Norbert, Lohmann, Katja, Grimmel, Mona, Haack, Tobias B., Spiczak, Sarah, Münchau, Alexander

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Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers by Weckhuysen, Sarah, Holmgren, Philip, Hendrickx, Rik, Jansen, Anna C., Hasaerts, Daniele, Dielman, Charlotte, Bellescize, Julitta, Boutry‐Kryza, Nadia, Lesca, Gaetan, Spiczak, Sarah Von, Helbig, Ingo, Gill, Deepak, Yendle, Simone, Møller, Rikke S., Klitten, Laura, Korff, Christian, Godfraind, Catherine, Rijckevorsel, Kenou, Jonghe, Peter, Hjalgrim, Helle, Scheffer, Ingrid E., Suls, Arvid

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A retrospective study of the relation between vaccination and occurrence of seizures in Dravet syndrome by Tro‐Baumann, Blanca, von Spiczak, Sarah, Lotte, Jan, Bast, Thomas, Haberlandt, Edda, Sassen, Robert, Freund, Alfred, Leiz, Steffen, Stephani, Ulrich, Boor, Rainer, Holthausen, Hans, Helbig, Ingo, Kluger, Gerhard

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Mutations in the GABA transporter SLC6A1 cause epilepsy with myoclonic atonic seizures by 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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Genome-wide mega-analysis identifies 16 loci and highlights diverse biological mechanisms in the common epilepsies by Abou-Khalil, Bassel, Auce, Pauls, Bahlo, Melanie, Balding, David J., Bast, Thomas, Becker, Albert J., Berkovic, Samuel F., Boysen, Katja E., Bradfield, Jonathan P., Brody, Lawrence C., Campbell, Ellen, Cascino, Gregory D., Catarino, Claudia B., Cherny, Stacey S., Compston, Alastair, Coppola, Antonietta, Cossette, Patrick, Craig, John J., de Haan, Gerrit-Jan, de Kovel, Carolien G. F., Delanty, Norman, Depondt, Chantal, Devinsky, Orrin, Doherty, Colin P., Elger, Christian E., Eriksson, Johan G., Ferraro, Thomas N., Francis, Ben, Freytag, Saskia, Gaus, Verena, Geller, Eric B., Glauser, Tracy, Goldstein, David B., Gui, Hongsheng, Haas, Kevin F., Hakonarson, Hakon, Hallmann, Kerstin, Helbig, Ingo, Hengsbach, Christian, Hjalgrim, Helle, Iacomino, Michele, Jamnadas-Khoda, Jennifer, Johnson, Michael R., Kasperavičiūte, Dalia, Kasteleijn-Nolst Trenite, Dorothee, Knowlton, Robert C., Kuzniecky, Ruben, Lau, Yu-Lung, Lehesjoki, Anna-Elina, Lerche, Holger, Lieb, Wolfgang, Lindhout, Dick, Lo, Warren D., Lopes-Cendes, Iscia, Lowenstein, Daniel H., Marson, Anthony G., McCormack, Mark, Mills, James L., Mirza, Nasir, Møller, Rikke S., Newton, Mark, Ng, Ping-Wing, Oliver, Karen L., Palotie, Aarno, Peter, Sarah, Petrovski, Slavé, Privitera, Michael, Radtke, Rodney, Reif, Philipp S., Reinthaler, Eva M., Rosenow, Felix, Sander, Josemir W., Sander, Thomas, Scattergood, Theresa, Schankin, Christoph J., Scheffer, Ingrid E., Schmitz, Bettina, Schoch, Susanne, Sills, Graeme J., Sisodiya, Sanjay M., Slattery, Lisa, Smith, David F., Smith, Michael C., Smith, Philip E., Sperling, Michael R., Steinhoff, Bernhard J., Stephani, Ulrich, Striano, Pasquale, Stroink, Hans, Surges, Rainer, Thio, Liu Lin, Todaro, Marian, Vari, Maria S., Visscher, Frank, von Spiczak, Sarah, Walley, Nicole M., Weisenberg, Judith, Yang, Wanling, Zara, Federico, Zimprich, Fritz

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