Intermodality in European metropolises: The current state of the art, and the results of an expert survey covering Berlin, Copenhagen, Hamburg and Paris von Goletz, Mirko, Haustein, Sonja, Wolking, Christina, L’Hostis, Alain

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Activation of AMP-activated kinase modulates sensitivity of glioma cells against epidermal growth factor receptor inhibition von HARTEL, INES, RONELLENFITSCH, MICHAEL, WANKA, CHRISTINA, WOLKING, STEFAN, STEINBACH, JOACHIM P, RIEGER, JOHANNES

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The modified ultrasound pattern sum score mUPSS as additional diagnostic tool for genetically distinct hereditary neuropathies von Grimm, Alexander, Rasenack, Maria, Athanasopoulou, Ioanna M., Dammeier, Nele Maria, Lipski, Christina, Wolking, Stefan, Vittore, Debora, Décard, Bernhard F., Axer, Hubertus

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Ultrasound pattern sum score, homogeneity score and regional nerve enlargement index for differentiation of demyelinating inflammatory and hereditary neuropathies von Grimm, Alexander, Vittore, Debora, Schubert, Victoria, Lipski, Christina, Heiling, Bianka, Décard, Bernhard F., Axer, Hubertus

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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals von Howrigan, Daniel P., Abbott, Liam E., Tashman, Katherine, Singh, Tarjinder, Watts, Nick, Lal, Dennis, Hakonarson, Hakon, Weckhuysen, Sarah, Petrovski, Slavé, Cossette, Patrick, Cotsapas, Chris, De Jonghe, Peter, Guerrini, Renzo, Marson, Anthony G., Depondt, Chantal, Striano, Pasquale, Freyer, Catharine, Regan, Brigid M., Leu, Costin, Johns, Esther M.C., Macdonald, Alexandra, Bahlo, Melanie, Todaro, Marian, Stamberger, Hannah, Sadoway, Tara R., Kousiappa, Ioanna, Tanteles, George A., Štěrbová, Katalin, Kunz, Wolfram S., Zsurka, Gábor, Elger, Christian E., Rademacher, Michael, van Baalen, Andreas, von Spiczak, Sarah, Afawi, Zaid, Canavati, Christina, Kluger, Gerhard, Blatt, Ilan, Weber, Yvonne G., Wolking, Stefan, Rau, Sarah, Steinhoff, Bernhard J., Schulze-Bonhage, Andreas, Borggräfe, Ingo, Madeleyn, Rene, Kälviäinen, Reetta, Linnankivi, Tarja, Chung, Seo-Kyung, Balestrini, Simona, Braatz, Vera, Johnson, Michael R., Auce, Pauls, Sham, Pak C., Lui, Colin H.T., Doherty, Colin P., Shukralla, Arif, El-Naggar, Hany, Vari, Maria Stella, Salpietro, Vincenzo, Tinuper, Paolo, Gagliardi, Monica, Montomoli, Martino, Doccini, Viola, Inoue, Yushi, Yamakawa, Kazuhiro, Tumiene, Birute, Sadleir, Lynette G., Caglayan, S. Hande, Arslan, Mutluay, Yis, Uluc, Topaloglu, Pınar, Baykan, Betül, Salman, Barış, Haryanyan, Garen, Özkara, Çiğdem, Poduri, Annapurna, Shiedley, Beth R., Shain, Catherine, French, Jacqueline A., Kuzniecky, Ruben I., Hegde, Manu, Helbig, Katherine L., Piras, Federica, Reif, Andreas, McQuillin, Andrew, Johnstone, Mandy, Palotie, Aarno, Carvalho, Celia Barreto, Achtyes, Eric D., Azevedo, Maria Helena, Kotov, Roman, Lehrer, Douglas S., Marder, Stephen R., Medeiros, Helena, Morley, Christopher P., Rapaport, Mark H., Knowles, James A., McCarroll, Steven A., Lowenstein, Daniel H., Goldstein, David B.

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Identification of a macrocyclic compound targeting the lassa virus polymerase von Aida-Ficken, Virginia, Kelly, Jamie A., Chatterjee, Payel, Jenks, M. Harley, McMullan, Laura K., Albariño, César G., Montgomery, Joel M., Seley-Radtke, Katherine L., Spiropoulou, Christina F., Flint, Mike

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Combined electrophysiological and morphological phenotypes in patients with genetic generalized epilepsy and their healthy siblings von Stier, Christina, Loose, Markus, Kotikalapudi, Raviteja, Elshahabi, Adham, Li Hegner, Yiwen, Marquetand, Justus, Braun, Christoph, Lerche, Holger, Focke, Niels K.

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Sub-genic intolerance, ClinVar, and the epilepsies: A whole-exome sequencing study of 29,165 individuals von Povysil, Gundula, Allen, Andrew S., Howrigan, Daniel P., Tashman, Katherine, Cerrato, Felecia, Cusick, Caroline, Heyne, Henrike, Churchhouse, Claire, Watts, Nick, Lal, Dennis, Gupta, Namrata, Cavalleri, Gianpiero L., Hakonarson, Hakon, Marson, Anthony G., Petrovski, Slavé, Sisodiya, Sanjay M., Depondt, Chantal, Scheffer, Ingrid E., Krause, Roland, Regan, Brigid M., Leu, Costin, Leech, Stephanie L., Todaro, Marian, Stamberger, Hannah, Kousiappa, Ioanna, Tanteles, George A., Christou, Yiolanda, Laššuthová, Petra, Knake, Susanne, Kunz, Wolfram S., Zsurka, Gábor, Surges, Rainer, Rademacher, Annika, von Spiczak, Sarah, Kanaan, Moien, Canavati, Christina, Lemke, Johannes R., Krey, Ilona, Weber, Yvonne G., Wolking, Stefan, Kegele, Josua, Borggräfe, Ingo, Mayer, Thomas, Brockmann, Knut, Madeleyn, Rene, Saarela, Anni, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Derambure, Philippe, Hirsch, Edouard, Chassoux, Francine, Chung, Seo-Kyung, Schneider, Natascha, Balestrini, Simona, Zagaglia, Sara, Johnson, Michael R., Auce, Pauls, Barišić, Nina, Canafoglia, Laura, Franceschetti, Silvana, Castellotti, Barbara, Granata, Tiziana, Ragona, Francesca, Iacomino, Michele, Riva, Antonella, Vari, Maria Stella, Salpietro, Vincenzo, Mancardi, Maria Margherita, Nobili, Lino, Bisulli, Francesca, Pippucci, Tommaso, Licchetta, Laura, Tinuper, Paolo, Gambardella, Antonio, Labate, Angelo, Annesi, Grazia, Manna, Lorella, Parrini, Elena, Bianchini, Claudia, Montomoli, Martino, Hirose, Shinichi, Yamakawa, Kazuhiro, Beydoun, Ahmad, Sadleir, Lynette G., Topaloglu, Pınar, Baykan, Betül, Özkara, YeşÇiğdem, Ho, Chen-Jui, Chou, I-Jun, Shain, Catherine, Goldman, Alicia, Busch, Robyn M., Jehi, Lara, Ferguson, Lisa, Clark, Peggy O., Privitera, Michael, Schachter, Steven, Cosico, Mahgenn, Lowenstein, Daniel H., Goldstein, David B.

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Quantitative determination of SLC2A1 variant functional effects in GLUT1 deficiency syndrome von Tayebi, Naeimeh, Leon‐Ricardo, Brian, McCall, Kevin, Mehinovic, Elvisa, Engelstad, Kristin, Huynh, Vincent, Turner, Tychele N., Weisenberg, Judy, Thio, Liu L., Hruz, Paul, Williams, Robin S. B., De Vivo, Darryl C., Petit, Vincent, Haller, Gabe, Gurnett, Christina A.

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A Clinical Drug‐Drug Interaction Study Assessing a Novel Drug Transporter Phenotyping Cocktail With Adefovir, Sitagliptin, Metformin, Pitavastatin, and Digoxin von Trueck, Christina, Hsin, Chih‐hsuan, Scherf‐Clavel, Oliver, Schaeffeler, Elke, Lenssen, Rebekka, Gazzaz, Malaz, Gersie, Marleen, Taubert, Max, Quasdorff, Maria, Schwab, Matthias, Kinzig, Martina, Sörgel, Fritz, Stoffel, Marc S., Fuhr, Uwe

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How are large-scale One Health initiatives targeting infectious diseases and antimicrobial resistance evaluated? A scoping review von Delesalle, Léa, Sadoine, Margaux L., Mediouni, Sarah, Denis-Robichaud, José, Zinszer, Kate, Zarowsky, Christina, Aenishaenslin, Cécile, Carabin, Hélène

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Aperiodic Activity Indexes Neural Hyperexcitability in Generalized Epilepsy von Kopf, Markus, Martini, Jan, Stier, Christina, Ethofer, Silke, Braun, Christoph, Li Hegner, Yiwen, Focke, Niels K, Marquetand, Justus, Helfrich, Randolph F

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Distinct gene-set burden patterns underlie common generalized and focal epilepsies von Koko, Mahmoud, Krause, Roland, Sander, Thomas, Bobbili, Dheeraj Reddy, Lerche, Holger, Feng, Yen-Chen Anne, Abbott, Liam E, Tashman, Katherine, Singh, Tarjinder, Byrnes, Andrea, Churchhouse, Claire, Solomonson, Matthew, Dhindsa, Ryan S, Cavalleri, Gianpiero L, Weckhuysen, Sarah, Kamalakaran, Sitharthan, Sisodiya, Sanjay M, Cossette, Patrick, Cotsapas, Chris, Dlugos, Dennis J, Regan, Brigid M, Bellows, Susannah T, Leu, Costin, Weckhuysen, Dorien, Stamberger, Hannah, Andrade, Danielle M, Sadoway, Tara R, Mo, Kelly, Papacostas, Savvas S, Laššuthová, Petra, Knake, Susanne, Kunz, Wolfram S, Bauer, Jürgen, Muhle, Hiltrud, vanBaalen, Andreas, vonSpiczak, Sarah, Korczyn, Amos D, Häusler, Martin, Lemke, Johannes R, Weber, Yvonne G, Wolking, Stefan, Becker, Felicitas, Schubert-Bast, Susanne, Borggräfe, Ingo, Mayer, Thomas, Brockmann, Knut, Madeleyn, Rene, Linnankivi, Tarja, Lehesjoki, Anna-Elina, Rees, Mark I, Chung, Seo-Kyung, Powell, Robert, Sills, Graeme J, Baum, Larry W, Cherny, Stacey S, Delanty, Norman, El-Naggar, Hany, Zara, Federico, Madia, Francesca, Tinuper, Paolo, Stipa, Carlotta, Labate, Angelo, Gagliardi, Monica, Vetro, Annalisa, Montomoli, Martino, Doccini, Viola, Suzuki, Toshimitsu, Arslan, Mutluay, Kara, Bulent, Bebek, Nerses, Uğur-İşeri, Sibel, Baykan, Betül, Haryanyan, Garen, Özkara, Çiğdem, Shiedley, Beth R, Ferraro, Thomas N, Privitera, Michael, Schachter, Steven, Devinsky, Orrin, Hegde, Manu, Khankhanian, Pouya, Helbig, Katherine L, Spalletta, Gianfranco, McQuillin, Andrew, Blackwood, Douglas, Palotie, Aarno, Bromet, Evelyn J, Achtyes, Eric D, Azevedo, Maria Helena, Medeiros, Helena, Macciardi, Fabio, Rapaport, Mark H, Knowles, James A, Cohort, Genomic Psychiatry, Fanous, Ayman H, Gupta, Namrata, Daly, Mark J, Lowenstein, Daniel H, Goldstein, David B, Neale, Benjamin M

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Glut1 Deficiency Syndrome (Glut1DS): State of the art in 2020 and recommendations of the international Glut1DS study group von Klepper, Joerg, Akman, Cigdem, Armeno, Marisa, Auvin, Stéphane, Cervenka, Mackenzie, Cross, Helen J., De Giorgis, Valentina, Della Marina, Adela, Engelstad, Kristin, Heussinger, Nicole, Kossoff, Eric H., Leen, Wilhelmina G., Leiendecker, Baerbel, Monani, Umrao R., Oguni, Hirokazu, Neal, Elizabeth, Pascual, Juan M., Pearson, Toni S., Pons, Roser, Scheffer, Ingrid E., Veggiotti, Pierangelo, Willemsen, Michél, Zuberi, Sameer M., De Vivo, Darryl C.

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Thank you to our reviewers for 2023 von Sperling, Michael R.

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Résumés en français 2/2023

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THIRD ANNUAL TEXAS CHAPTERS CONFERENCE KEYNOTE ADDRESS von Cornyn, Senator John

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Acknowledgments

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Active members: Willinger-Zytnick

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Mothers and Daughters: Literary and Psychological Perspectives von Hirsch, Marianne, Rogoff, Mai-Lan

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