检索结果 - Widdess-Walsh, Peter
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Association of SLC32A1 Missense Variants With Genetic Epilepsy With Febrile Seizures Plus 由 Heron, Sarah E., Regan, Brigid M., Harris, Rebekah V., Gardner, Alison E., Coleman, Matthew J., Bennett, Mark F., Grinton, Bronwyn E., Helbig, Katherine L., Sperling, Michael R., Haut, Sheryl, Geller, Eric B., Widdess-Walsh, Peter, Pelekanos, James T., Bahlo, Melanie, Petrovski, Slavé, Heinzen, Erin L., Hildebrand, Michael S., Corbett, Mark A., Scheffer, Ingrid E., Gécz, Jozef, Berkovic, Samuel F.
出版 2021Text -
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Clinical spectrum of STX1B-related epileptic disorders 由 Wolking, Stefan, May, Patrick, Mei, Davide, Møller, Rikke S., Balestrini, Simona, Helbig, Katherine L., Altuzarra, Cecilia Desmettre, Chatron, Nicolas, Kaiwar, Charu, Stöhr, Katharina, Widdess-Walsh, Peter, Mendelsohn, Bryce A., Numis, Adam, Cilio, Maria R., Van Paesschen, Wim, Svendsen, Lene L., Oates, Stephanie, Hughes, Elaine, Goyal, Sushma, Brown, Kathleen, Sifuentes Saenz, Margarita, Dorn, Thomas, Muhle, Hiltrud, Pagnamenta, Alistair T., Vavoulis, Dimitris V., Knight, Samantha J.L., Taylor, Jenny C., Canevini, Maria Paola, Darra, Francesca, Gavrilova, Ralitza H., Powis, Zöe, Tang, Shan, Marquetand, Justus, Armstrong, Martin, McHale, Duncan, Klee, Eric W., Kluger, Gerhard J., Lowenstein, Daniel H., Weckhuysen, Sarah, Pal, Deb K., Helbig, Ingo, Guerrini, Renzo, Thomas, Rhys H., Rees, Mark I., Lesca, Gaetan, Sisodiya, Sanjay M., Weber, Yvonne G., Lal, Dennis, Marini, Carla, Lerche, Holger, Schubert, Julian
出版 2019Text