Treffer 1 - 20 von 36 für Suche 'Kwan, Chris C H', Suchdauer: 1,10s Treffer weiter einschränken
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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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    Electrodiagnostic subtyping in Guillain–Barré syndrome patients in the International Guillain–Barré Outcome Study von Arends, Samuel, Drenthen, Judith, Hadden, Robert D. M., Kuwabara, Satoshi, Reisin, Ricardo C., Shahrizaila, Nortina, Ajroud‐Driss, Senda, Antonini, Giovanni, Attarian, Shahram, Balducci, Claudia, Brannagan, Thomas H., Chavada, Govind, Dillmann, Klaus‐Ulrich, Dimachkie, Mazen M., Galassi, Giuliana, Gutiérrez‐Gutiérrez, Gerardo, Islam, Badrul, Islam, Zhahirul, Katzberg, Hans, Miller, James A. L., Pardo, Julio, Rajabally, Yusuf A., Vytopil, Michal, Cornblath, David R., Badrising, Umesh A., Bateman, Kathleen, Bella, Isabelita, Bhavaraju‐Sanka, Ratna, Casasnovas, Carlos, Conti, Eugenia, Dalakas, Marinos, Damme, Philip, Davidson, Amy, Doets, Alex, Echaniz‐Laguna, Andoni, Eftimov, Filip, Faber, Karin G., Fazio, Raffaella, Fehmi, Janev, Garssen, Marcel P.J., Gijsbers, Cees J., Gilchrist, James M., Gilhuis, Job, Goldstein, Jonathan M., Gorson, Kenneth C., Gutmann, Ludwig, Holt, James K.L., Hsieh, Sung‐Tsang, Htut, Min, Hughes, Richard A.C., Kaida, Kenichi, Karafiath, Summer, Khoshnoodi, Mohammad Ali, Kiers, Lynette, Kleiweg, Ruud P., Kolb, Noah A., Kooi, Anneke J., Kramers, Hans, Kwan, Justin Y., Ladha, Shafeeq S., Lassen, Lisbeth Landschoff, Lawson, Victoria H., Cejas, Luciana Leon, Leonhard, Sonja E., Manji, Hadi, Marfia, Girolama A., Martín‐Aguilar, Lorena, Martinez‐Hernandez, Eugenia, Mataluni, Giorgia, Mattiazzi, Marcelo, Meekins, Gregg, Mohammad, Quazi Deen, Tassa, Germán Moris, Nobile‐Orazio, Eduardo, Pelouto, Farah, Pulley, Michael T., Gutiérrez, Luis Querol, Reddel, Stephen W., Rinaldi, Simon, Ripellino, Paolo, Roberts, Rhys C., Rojas‐Marcos, Iñigo, Roodbol, Joyce, Samijn, Johnny P.A., Santoro, Lucio, Tous, Maria José Sedano, Silvestri, Nicholas Joseph, Sundrup, Soeren H., Sommer, Claudia, Stein, Beth, Stino, Amro Maher, Varrato, Jay D., Vermeij, Frederique H., Verschuuren, Jan, Visser, Leo H., Walgaard, Christa, Wang, Yuzhong, Willison, Hugh J., Wirtz, Paul W., Zivkovic, Sascha A.

    Veröffentlicht in European journal of neurology

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