The neuropediatric emergency in the neurologist’s office: Differential diagnosis and management by Borggräfe, I

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Ultra-Rare Genetic Variation in the Epilepsies: A Whole-Exome Sequencing Study of 17,606 Individuals by 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 by 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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Genetic predisposition in anti‐LGI1 and anti‐NMDA receptor encephalitis by Mueller, Stefanie H., Färber, Anna, Golombeck, Kristin S., Kümpfel, Tania, Kaufmann, Max, Ringelstein, Marius, Kellinghaus, Christoph, Ehrlich, Sven, Then Bergh, Florian, Faiss, Jürgen H., Franke, Andre, Lyss, Birgit, Wallenfelsova, Eva, Othman, Jalal, Bogarin, Yuri, Schwabe, Julia, Handreka, Robert, Rostasy, Kevin, Körber, Rüdiger, Heide, Wolfgang, Geis, Tobias, Dogan, Muejgan, Bien, Christian, Kramme, Corinna, Pulkowski, Ulrich, Hoepner, Robert, Schindler, Kaspar, Lippert, Julian, Ewering, Carina, Reimann, Gemot, Schimrigk, Sebastian, Urbanek, Christian, Schön, Frauke, Finke, Alexander, Henningsen, Henning, Küpper, Philipp, Kellinghaus, Christoph, Hofstadt, Ulrich, Trendelenburg, George, Heider, Steffen, Thaler, Franziska, Muth, Carolin, Borggräfe, Ingo, Blaschek, Astrid, Kümpfel, Tania, Bieniek, Rolf, Philipsen, Alexandra, Winter, Benjamin, Gass, Achim, Hagenah, Ulrich, Hausler, Martin Georg, Tauber, Simone, Elger, Christian, Spruth, Eike, Paul, Friedemann, Finke, Carsten, Prüss, Harald, Wöpking, Sigrid, Schneider, Auke, Seitz, Rüdiger, Ringelstein, Marius, Aktas, Orhan, Huttner, Hagen, Stich, Oliver, Baumgartner, Annette, Neubauer, Bemd, Döppner, Thorsten, Süße, M, Heesen, Christoph, Friese, Manuel, Sühs, Kurt‐Wolfram, Trebst, Corinna, Wildemann, Brigitte, Bösel, Julian, Roepke, Luise, Brämer, Dirk, Strubl, Julia, Günther, Albrecht, Bergh, Florian Then, Schilling, Ruth, Bittner, Daniel, Spreer, Annette, Methner, Axel, Pledl, Hans‐Wemer, Anlonso, Angelika, Szabo, Kristina, Philipp, Konstanze, Möning, Constanze, Weissert, Robert, Retzlaff, Nele, Fousse, Mathias, Ragoschke‐Schumm, Andreas, Stumer, Klarissa, Berg, Daniela, Schmütz, Isa, Bartsch, Thorsten, Falk, Kim Christin, Hummel, Katja, Tumani, Hayrettin, Lewerenz, Jan

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Arterial ischemic stroke in childhood and adolescence by Gerstl, L, Borggräfe, I, Heinen, F, Olivieri, M

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Arteriell ischämischer Schlaganfall im Kindes- und Jugendalter: Zeitkritischer Notfall in der Pädiatrie by Gerstl, L., Borggräfe, I., Heinen, F., Olivieri, M.

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Exome sequencing of 20,979 individuals with epilepsy reveals shared and distinct ultra-rare genetic risk across disorder subtypes by 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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Distinct gene-set burden patterns underlie common generalized and focal epilepsies by 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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Arteriell ischämischer Schlaganfall im Kindes- und Jugendalter: Zeitkritischer Notfall in der Pädiatrie by Gerstl, L., Borggräfe, I., Heinen, F., Olivieri, M.

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Therapie des akuten epileptischen Anfalls by Tacke, M., Kieslich, M., Borggräfe, I.

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Arterial ischemic stroke in childhood and adolescence by Gerstl, L, Borggräfe, I, Heinen, F, Olivieri, M

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Anforderungen an ein Epilepsiezentrum für Kinder und Jugendliche by Borggräfe, I., Heinen, F., Noachtar, S.

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Akut ischämischer Schlaganfall bei einem 9‑jährigen Jungen by Frenz, S., Bonfert, M., Reiter, K., Hübner, J., Borggräfe, I., Olivieri, M., Gerstl, L.

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Fieberkrämpfe: Diagnostik, Therapie und Beratung by Borggräfe, I., Heinen, F., Gerstl, L.

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Fieberkrämpfe: Diagnostik, Therapie und Beratung by Borggräfe, I., Heinen, F., Gerstl, L.

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Komorbiditäten bei Zerebralparesen: Epilepsien by Borggräfe, I., Heinen, F.

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Dystonien im Kindesalter by Ensslen, M., Mehrkens, J.-H., Bötzel, K., Schröder, A.S., Müller-Felber, W., Heinen, F., Borggräfe, I.

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Robotergestützte Laufbandtherapie für Kinder mit zentralen Gangstörungen by Borggräfe, I., Kumar, A., Schäfer, J.-S., Berweck, S., Meyer-Heim, A., Hufschmidt, A., Heinen, Florian

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Kongenitale myotone Dystrophie: Fallbericht und Literaturübersicht by Borggräfe, I., Enders, A., Müller-Felber, W., Heinen, F.

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Grafikgestützter Konsensus für die Behandlung von Bewegungsstörungen bei Kindern mit bilateralen spastischen Zerebralparesen (BS-CP): Therapiekurven – CP-Motorik by Heinen, F., Schröder, A.S., Döderlein, L., Voss, W., Hustedt, U., Mall, V., Borggräfe, I., Wiedenhöfer, B., Manolikakis, G., Huss, K., Sprinz, A., Wissel, J., Behrens, K.E., Benecke, R., Fietzek, U.M., Breuer, U., Warken, B., Böhle, B., Krägeloh-Mann, I., Berweck, S.

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