Severity and disability related to epilepsy from the perspective of patients and physicians: A cross-cultural adaptation of the GASE and GAD scales von Duarte, Edson Pillotto, Corrêa, Catarina Dantas, Marques, Bruna Souza, Mendonça, Guilherme Simone, Braatz, Vera Lúcia, Harger, Rodrigo, Fagundes, Diego Antônio, Walz, Roger, Wiebe, Samuel, Lunardi, Mariana dos Santos, Lin, Katia

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Cutaneous adverse reactions associated with antiseizure medication: clinical characteristics and implications in epilepsy treatment von Tensini, Tallulah Spina, Von Glehn, Cristina Q. C., Bettinotti, Maria P., Iglehart, Brian, de Paola, Luciano, Lohr, Alfredo, Rodrigues, Marcelo, Tensini, Fernando Spina, Braatz, Vera L., Silvado, Carlos E. S.

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Ketogenic therapy in childhood and adolescence: recommendations of the Brazilian experts group von de Brito Sampaio, Letícia Pereira, Henriques-Souza, Adélia Maria de Miranda, Lin, Katia, Neri, Lenycia de Cassya Lopes, Inuzuka, Luciana Midori, Uchôa, Ludmila Inácio de Lima, Gregório, Marcela Marques de Oliveira, Guilhoto, Laura Maria, Montenegro, Maria Augusta, Lunardi, Mariana, Veiga, Marielza, de Lima, Patricia Azevedo, Braatz, Vera

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Guillain–Barré syndrome after coronavirus disease 2019 vaccine: A temporal association von Silva, Gustavo Figueiredo, Silva, Caroline Figueiredo, Oliveira, Raddib Eduardo Noleto da Nobrega, Romancini, Fabiana, Mendes, Rafael Marques, Locks, Amanda, Longo, Maria Francisca Moro, Moro, Carla Heloisa Cabral, Longo, Alexandre Luiz, Braatz, Vera Lucia

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Response to “Nerve conduction studies support the classification of SARSCoV‐2 associated Guillain‐Barre subtypes” von Silva, Gustavo Figueiredo, Silva, Caroline Figueiredo, Nobrega Oliveira, Raddib Eduardo Noleto, Romancini, Fabiana, Mendes, Rafael Marques, Locks, Amanda, Longo, Maria Francisca Moro, Moro, Carla Heloisa Cabral, Longo, Alexandre Luiz, Braatz, Vera Lucia

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Dopamine transporter imaging in clinically unclear cases of parkinsonism and the importance of scans without evidence of dopaminergic deficit (SWEDDs) von Utiumi, Marco A T, Felício, André C, Borges, Conrado R, Braatz, Vera L, Rezende, Sheyla A S, Munhoz, Renato P, Bressan, Rodrigo A, Ferraz, Henrique B, Teive, Hélio A G

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Brainstem reversible leukoencephalopathy syndrome von Braatz, Vera L, Lorenzoni, Paulo José, Kay, Cláudia S K, Chula, Domingos C, Scola, Rosana H, Werneck, Lineu C

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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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Polygenic burden in focal and generalized epilepsies von Leu, Costin, Stevelink, Remi, Smith, Alexander W, Goleva, Slavina B, Kanai, Masahiro, Ferguson, Lisa, Campbell, Ciaran, Kamatani, Yoichiro, Okada, Yukinori, Sisodiya, Sanjay M, Cavalleri, Gianpiero L, Koeleman, Bobby P C, Lerche, Holger, Jehi, Lara, Davis, Lea K, Najm, Imad M, Palotie, Aarno, Daly, Mark J, Busch, Robyn M, Lal, Dennis

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Neurological diagnoses in the emergency room: differences between younger and older patients von Lange, Marcos C, Braatz, Vera L, Tomiyoshi, Carolina, Nóvak, Felipe M, Fernandes, Artur F, Zamproni, Laura N, Piovesan, Elcio J, Nóvak, Edison M, Teive, Helio A G, Werneck, Lineu C

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GWAS meta-analysis of over 29,000 people with epilepsy identifies 26 risk loci and subtype-specific genetic architecture von Stevelink, Remi, Campbell, Ciarán, Chen, Siwei, Abou-Khalil, Bassel, Adesoji, Oluyomi M., Afawi, Zaid, Amadori, Elisabetta, Anderson, Alison, Anderson, Joseph, Andrade, Danielle M., Annesi, Grazia, Auce, Pauls, Avbersek, Andreja, Bahlo, Melanie, Baker, Mark D., Balagura, Ganna, Balestrini, Simona, Barba, Carmen, Barboza, Karen, Bartolomei, Fabrice, Bast, Thomas, Baum, Larry, Baumgartner, Tobias, Baykan, Betül, Bebek, Nerses, Becker, Albert J., Becker, Felicitas, Bennett, Caitlin A., Berghuis, Bianca, Berkovic, Samuel F., Beydoun, Ahmad, Bianchini, Claudia, Bisulli, Francesca, Blatt, Ilan, Bobbili, Dheeraj R., Borggraefe, Ingo, Bosselmann, Christian, Braatz, Vera, Bradfield, Jonathan P., Brockmann, Knut, Brody, Lawrence C., Buono, Russell J., Busch, Robyn M., Caglayan, Hande, Campbell, Ellen, Canafoglia, Laura, Canavati, Christina, Cascino, Gregory D., Castellotti, Barbara, Catarino, Claudia B., Cavalleri, Gianpiero L., Cerrato, Felecia, Chassoux, Francine, Cherny, Stacey S., Cheung, Ching-Lung, Chinthapalli, Krishna, Chou, I-Jun, Chung, Seo-Kyung, Churchhouse, Claire, Clark, Peggy O., Cole, Andrew J., Compston, Alastair, Coppola, Antonietta, Cosico, Mahgenn, Cossette, Patrick, Craig, John J., Cusick, Caroline, Daly, Mark J., Davis, Lea K., de Haan, Gerrit-Jan, Delanty, Norman, Depondt, Chantal, Derambure, Philippe, Devinsky, Orrin, Di Vito, Lidia, Dlugos, Dennis J., Doccini, Viola, Doherty, Colin P., El-Naggar, Hany, Elger, Christian E., Ellis, Colin A., Eriksson, Johan G., Faucon, Annika, Feng, Yen-Chen A., Ferguson, Lisa, Ferraro, Thomas N., Ferri, Lorenzo, Feucht, Martha, Fitzgerald, Mark, Fonferko-Shadrach, Beata, Fortunato, Francesco, Franceschetti, Silvana, Franke, Andre, French, Jacqueline A., Freri, Elena, Gagliardi, Monica, Gambardella, Antonio, Geller, Eric B., Giangregorio, Tania, Gjerstad, Leif

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Fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography imaging in the investigation of Lambert-Eaton myasthenic syndrome von Braatz, Vera L, Kay, Cláudia S K, Lorenzoni, Paulo J, Ludwig, Vinicius B, Junior, Milton M Machota, Ioshii, Sergio O, Scola, Rosana H, Werneck, Lineu C

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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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Postictal Psychosis in Epilepsy: A Clinicogenetic Study von Braatz, Vera, Martins Custodio, Helena, Leu, Costin, Agrò, Luigi, Wang, Baihan, Calafato, Stella, Rayner, Genevieve, Doyle, Michael G., Hengsbach, Christian, Bisulli, Francesca, Weber, Yvonne G., Gambardella, Antonio, Delanty, Norman, Cavalleri, Gianpiero, Foong, Jacqueline, Scheffer, Ingrid E., Berkovic, Samuel F., Bramon, Elvira, Balestrini, Simona, Sisodiya, Sanjay M.

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Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes von Chen, Siwei, Abou-Khalil, Bassel W., Afawi, Zaid, Ali, Quratulain Zulfiqar, Amadori, Elisabetta, Anderson, Alison, Anderson, Joe, Andrade, Danielle M., Annesi, Grazia, Arslan, Mutluay, Auce, Pauls, Bahlo, Melanie, Baker, Mark D., Balagura, Ganna, Balestrini, Simona, Banks, Eric, Barba, Carmen, Barboza, Karen, Bartolomei, Fabrice, Bass, Nick, Baum, Larry W., Baumgartner, Tobias H., Baykan, Betül, Bebek, Nerses, Becker, Felicitas, Bennett, Caitlin A., Beydoun, Ahmad, Bianchini, Claudia, Bisulli, Francesca, Blackwood, Douglas, Blatt, Ilan, Borggräfe, Ingo, Bosselmann, Christian, Braatz, Vera, Brand, Harrison, Brockmann, Knut, Buono, Russell J., Busch, Robyn M., Caglayan, S. Hande, Canafoglia, Laura, Canavati, Christina, Castellotti, Barbara, Cavalleri, Gianpiero L., Cerrato, Felecia, Chassoux, Francine, Cherian, Christina, Cherny, Stacey S., Cheung, Ching-Lung, Chou, I-Jun, Chung, Seo-Kyung, Churchhouse, Claire, Ciullo, Valentina, Clark, Peggy O., Cole, Andrew J., Cosico, Mahgenn, Cossette, Patrick, Cotsapas, Chris, Cusick, Caroline, Daly, Mark J., Davis, Lea K., Jonghe, Peter De, Delanty, Norman, Dennig, Dieter, Depondt, Chantal, Derambure, Philippe, Devinsky, Orrin, Vito, Lidia Di, Dickerson, Faith, Dlugos, Dennis J., Doccini, Viola, Doherty, Colin P., El-Naggar, Hany, Ellis, Colin A., Epstein, Leon, Evans, Meghan, Faucon, Annika, Feng, Yen-Chen Anne, Ferguson, Lisa, Ferraro, Thomas N., Silva, Izabela Ferreira Da, Ferri, Lorenzo, Feucht, Martha, Fields, Madeline C., Fitzgerald, Mark, Fonferko-Shadrach, Beata, Fortunato, Francesco, Franceschetti, Silvana, French, Jacqueline A., Freri, Elena, Fu, Jack M., Gabriel, Stacey, Gagliardi, Monica, Gambardella, Antonio, Gauthier, Laura, Giangregorio, Tania, Gili, Tommaso, Glauser, Tracy A., Goldberg, Ethan, Goldman, Alica, Goldstein, David B.

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Fluoro-2-deoxy-D-glucose positron emission tomography/computed tomography imaging in the investigation of LambertEaton myasthenic syndrome von Braatz, Vera L., Kay, Claudia S. K., Lorenzoni, Paulo J., Ludwig, Vinicius B., Junior, Milton M. Machota, Ioshii, Sergio O., Scola, Rosana H., Werneck, Lineu C.

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Pediatric acute-onset neuropsychiatric syndrome (PANS) misdiagnosed as autism spectrum disorder von Goncalves, Marcus Vinicius M., Harger, Rodrigo, Braatz, Vera, Parolin, Laura F., Eboni, Audred C. Biondo, Fontana, Maria Aparecida N., Anacleto, Andrea, Fragoso, Yara Dadalti

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Guidelines for the assessment and acceptance of potential brain-dead organ donors von Westphal, Glauco Adrieno, Garcia, Valter Duro, Souza, Rafael Lisboa de, Franke, Cristiano Augusto, Vieira, Kalinca Daberkow, Birckholz, Viviane Renata Zaclikevis, Machado, Miriam Cristine, Almeida, Eliana Régia Barbosa de, Machado, Fernando Osni, Sardinha, Luiz Antônio da Costa, Wanzuita, Raquel, Silvado, Carlos Eduardo Soares, Costa, Gerson, Braatz, Vera, Caldeira Filho, Milton, Furtado, Rodrigo, Tannous, Luana Alves, Albuquerque, André Gustavo Neves de, Abdala, Edson, Gonçalves, Anderson Ricardo Roman, Pacheco-Moreira, Lúcio Filgueiras, Dias, Fernando Suparregui, Fernandes, Rogério, Giovanni, Frederico Di, Carvalho, Frederico Bruzzi de, Fiorelli, Alfredo, Teixeira, Cassiano, Feijó, Cristiano, Camargo, Spencer Marcantonio, Oliveira, Neymar Elias de, David, André Ibrahim, Prinz, Rafael Augusto Dantas, Herranz, Laura Brasil, Andrade, Joel de

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Meropenem-induced myoclonus: A case report von Spina Silva, Tallulah, Dal-Prá Ducci, Renata, Zorzetto, Francis Paciornik, Braatz, Vera Lucia, de Paola, Luciano, Kowacs, Pedro André

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Parakinesia brachialis oscitans during thrombolytic therapy von Zorzetto, Francis Paciornik, Braatz, Vera Lucia, Walusinski, Olivier, Teive, Helio Afonso Guizoni

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