학술논문
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'학술논문'
에서 검색결과 288건 | 목록
1~20
Academic Journal
Yang, Fang; Begemann, Anais; Reichhart, Nadine; Haeckel, Akvile; Steindl, Katharina; Schellenberger, Eyk; Sturm, Ronja Fini; Barth, Magalie; Bassani, Sissy; Boonsawat, Paranchai; Courtin, Thomas; Delobel, Bruno; Gunning, Boudewijn; Hardies, Katia; Jennesson, Melanie; Legoff, Louis; Linnankivi, Tarja; Prouteau, Clement; Smal, Noor; Spodenkiewicz, Marta; Toelle, Sandra P.; Van Gassen, Koen; Van Paesschen, Wim; Verbeek, Nienke; Ziegler, Alban; Zweier, Markus; Horn, Anselm H.C.; Sticht, Heinrich; Lerche, Holger; Weckhuysen, Sarah; Strauss, Olaf; Rauch, Anita
Am J Hum Genet
The American journal of human genetics
The American journal of human genetics
Academic Journal
Sullivan, Joseph; Gunning, Boudewijn; Zafar, Muhammad; Guerrini, Renzo; Gecz, Jozef; Kolc, Kristy L.; Zhao, Yufan; Gasior, Maciej; Aimetti, Alex A.; Samanta, Debopam
Epilepsy Research. 203
Academic Journal
Sullivan, Joseph ; Gunning, Boudewijn ; Zafar, Muhammad ; Guerrini, Renzo ; Gecz, Jozef ; Kolc, Kristy L. ; Zhao, Yufan ; Gasior, Maciej ; Aimetti, Alex A. ; Samanta, Debopam
In Epilepsy Research March 2023 191
Academic Journal
Bonardi, Claudia; Heyne, Henrike; Fiannacca, Martina; Fitzgerald, Mark; Gardella, Elena; Gunning, Boudewijn; Olofsson, Kern; Lesca, Gaétan; Verbeek, Nienke; Stamberger, Hannah; Striano, Pasquale; Zara, Federico; Mancardi, Maria; Nava, Caroline; Syrbe, Steffen; Buono, Salvatore; Baulac, Stephanie; Coppola, Antonietta; Weckhuysen, Sarah; Schoonjans, An-Sofie; Ceulemans, Berten; Sarret, Catherine; Baumgartner, Tobias; Muhle, Hiltrud; Portes, Vincent Des; Toulouse, Joseph; Nougues, Marie-Christine; Rossi, Massimiliano; Demarquay, Geneviève; Ville, Dorothée; Hirsch, Edouard; Maurey, Hélène; Willems, Marjolaine; de Bellescize, Julitta; Altuzarra, Cecilia Desmettre; Villeneuve, Nathalie; Bartolomei, Fabrice; Picard, Fabienne; Hornemann, Frauke; Koolen, David; Kroes, Hester; Reale, Chiara; Fenger, Christina; Tan, Wen-Hann; Dibbens, Leanne; Bearden, David; Møller, Rikke; Rubboli, Guido
Brain, 144, pp. 3635-3650
Brain, Vol. 144, No 12 (2021) pp. 3635-3650
Brain
Bonardi, C M, Heyne, H O, Fiannacca, M, Fitzgerald, M P, Gardella, E,Gunning , B, Olofsson, K, Lesca, G, Verbeek, N, Stamberger, H, Striano, P, Zara, F, Mancardi, M M, Nava, C, Syrbe, S, Buono, S, Baulac, S, Coppola, A, Weckhuysen, S, Schoonjans, A-S, Ceulemans, B, Sarret, C, Baumgartner, T, Muhle, H, des Portes, V, Toulouse, J, Nougues, M-C, Rossi, M, Demarquay, G, Ville, D, Hirsch, E, Maurey, H, Willems, M, de Bellescize, J, Altuzarra, C D, Villeneuve, N, Bartolomei, F, Picard, F, Hornemann, F, Koolen, D A, Kroes, H Y, Reale, C, Fenger, C D, Tan, W-H, Dibbens, L, Bearden, D R, Møller, R S & Rubboli, G 2021, ' KCNT1-related epilepsies and epileptic encephalopathies : phenotypic and mutational spectrum ', Brain : a journal of neurology, vol. 144, no. 12, pp. 3635-3650 . https://doi.org/10.1093/brain/awab219
Brain, Vol. 144, No 12 (2021) pp. 3635-3650
Brain
Bonardi, C M, Heyne, H O, Fiannacca, M, Fitzgerald, M P, Gardella, E,
Academic Journal
Stamberger, Hannah; Hammer, Trine B; Gardella, Elena; Vlaskamp, Danique R M; Bertelsen, Birgitte; Mandelstam, Simone; de Lange, Iris; Zhang, Jing; Myers, Candace T; Fenger, Christina; Afawi, Zaid; Almanza Fuerte, Edith P; Andrade, Danielle M; Balcik, Yunus; Ben Zeev, Bruria; Bennett, Mark F; Berkovic, Samuel F; Isidor, Bertrand; Bouman, Arjan; Brilstra, Eva; Busk, Øyvind L; Cairns, Anita; Caumes, Roseline; Chatron, Nicolas; Dale, Russell C; de Geus, Christa; Edery, Patrick; Gill, Deepak; Granild-Jensen, Jacob Bie; Gunderson, Lauren; Gunning, Boudewijn; Heimer, Gali; Helle, Johan R; Hildebrand, Michael S; Hollingsworth, Georgie; Kharytonov, Volodymyr; Klee, Eric W; Koeleman, Bobby P C; Koolen, David A; Korff, Christian; Küry, Sébastien; Lesca, Gaetan; Lev, Dorit; Leventer, Richard J; Mackay, Mark T; Macke, Erica L; McEntagart, Meriel; Mohammad, Shekeeb S; Monin, Pauline; Montomoli, Martino; Morava, Eva; Moutton, Sebastien; Muir, Alison M; Parrini, Elena; Procopis, Peter; Ranza, Emmanuelle Nathalie; Reed, Laura; Reif, Philipp S; Rosenow, Felix; Rossi, Massimiliano; Sadleir, Lynette G; Sadoway, Tara; Schelhaas, Helenius J; Schneider, Amy L; Shah, Krati; Shalev, Ruth; Sisodiya, Sanjay M; Smol, Thomas; Stumpel, Connie T R M; Stuurman, Kyra; Symonds, Joseph D; Mau-Them, Frederic Tran; Verbeek, Nienke; Verhoeven, Judith S; Wallace, Geoffrey; Yosovich, Keren; Zarate, Yuri A; Zerem, Ayelet; Zuberi, Sameer M; Guerrini, Renzo; Mefford, Heather C; Patel, Chirag; Zhang, Yue-Hua; Møller, Rikke S; Scheffer, Ingrid E
Genetics in Medicine, 23, 2, pp. 363-373
Genetics in Medicine, Vol. 23, No 2 (2021) pp. 363-373
Genetics in medicine
Stamberger, H, Hammer, T B, Gardella, E, Vlaskamp, D R M, Bertelsen, B, Mandelstam, S, de Lange, I, Zhang, J, Myers, C T, Fenger, C, Afawi, Z, Almanza Fuerte, E P, Andrade, D M, Balcik, Y, Ben Zeev, B, Bennett, M F, Berkovic, S F, Isidor, B, Bouman, A, Brilstra, E, Busk, Ø L, Cairns, A, Caumes, R, Chatron, N, Dale, R C, de Geus, C, Edery, P, Gill, D, Granild-Jensen, J B, Gunderson, L,Gunning , B, Heimer, G, Helle, J R, Hildebrand, M S, Hollingsworth, G, Kharytonov, V, Klee, E W, Koeleman, B P C, Koolen, D A, Korff, C, Küry, S, Lesca, G, Lev, D, Leventer, R J, Mackay, M T, Macke, E L, McEntagart, M, Mohammad, S S, Monin, P, Montomoli, M, Morava, E, Moutton, S, Muir, A M, Parrini, E, Procopis, P, Ranza, E, Reed, L, Reif, P S, Rosenow, F, Rossi, M, Sadleir, L G, Sadoway, T, Schelhaas, H J, Schneider, A L, Shah, K, Shalev, R, Sisodiya, S M, Smol, T, Stumpel, C T R M, Stuurman, K, Symonds, J D, Mau-Them, F T, Verbeek, N, Verhoeven, J S, Wallace, G, Yosovich, K, Zarate, Y A, Zerem, A, Zuberi, S M, Guerrini, R, Mefford, H C, Patel, C, Zhang, Y H, Møller, R S & Scheffer, I E 2021, ' NEXMIF encephalopathy : an X-linked disorder with male and female phenotypic patterns ', Genetics in Medicine, vol. 23, no. 2, pp. 363-373 . https://doi.org/10.1038/s41436-020-00988-9
Stamberger, H, Hammer, T B, Gardella, E, Vlaskamp, D R M, Bertelsen, B, Mandelstam, S, de Lange, I, Zhang, J, Myers, C T, Fenger, C, Afawi, Z, Almanza Fuerte, E P, Andrade, D M, Balcik, Y, Ben Zeev, B, Bennett, M F, Berkovic, S F, Isidor, B, Bouman, A, Brilstra, E, Busk, Ø L, Cairns, A, Caumes, R, Chatron, N, Dale, R C, de Geus, C, Edery, P, Gill, D, Granild-Jensen, J B, Gunderson, L,Gunning , B, Heimer, G, Helle, J R, Hildebrand, M S, Hollingsworth, G, Kharytonov, V, Klee, E W, Koeleman, B P C, Koolen, D A, Korff, C, Küry, S, Lesca, G, Lev, D, Leventer, R J, Mackay, M T, Macke, E L, McEntagart, M, Mohammad, S S, Monin, P, Montomoli, M, Morava, E, Moutton, S, Muir, A M, Parrini, E, Procopis, P, Ranza, E, Reed, L, Reif, P S, Rosenow, F, Rossi, M, Sadleir, L G, Sadoway, T, Schelhaas, H J, Schneider, A L, Shah, K, Shalev, R, Sisodiya, S M, Smol, T, Stumpel, C T R M, Stuurman, K, Symonds, J D, Mau-Them, F T, Verbeek, N, Verhoeven, J S, Wallace, G, Yosovich, K, Zarate, Y A, Zerem, A, Zuberi, S M, Guerrini, R, Mefford, H C, Patel, C, Zhang, Y-H, Møller, R S & Scheffer, I E 2021, 'NEXMIF encephalopathy : an X-linked disorder with male and female phenotypic patterns', Genetics in medicine : official journal of the American College of Medical Genetics, vol. 23, no. 2, pp. 363-373. https://doi.org/10.1038/s41436-020-00988-9
Genetics in Medicine, Vol. 23, No 2 (2021) pp. 363-373
Genetics in medicine
Stamberger, H, Hammer, T B, Gardella, E, Vlaskamp, D R M, Bertelsen, B, Mandelstam, S, de Lange, I, Zhang, J, Myers, C T, Fenger, C, Afawi, Z, Almanza Fuerte, E P, Andrade, D M, Balcik, Y, Ben Zeev, B, Bennett, M F, Berkovic, S F, Isidor, B, Bouman, A, Brilstra, E, Busk, Ø L, Cairns, A, Caumes, R, Chatron, N, Dale, R C, de Geus, C, Edery, P, Gill, D, Granild-Jensen, J B, Gunderson, L,
Stamberger, H, Hammer, T B, Gardella, E, Vlaskamp, D R M, Bertelsen, B, Mandelstam, S, de Lange, I, Zhang, J, Myers, C T, Fenger, C, Afawi, Z, Almanza Fuerte, E P, Andrade, D M, Balcik, Y, Ben Zeev, B, Bennett, M F, Berkovic, S F, Isidor, B, Bouman, A, Brilstra, E, Busk, Ø L, Cairns, A, Caumes, R, Chatron, N, Dale, R C, de Geus, C, Edery, P, Gill, D, Granild-Jensen, J B, Gunderson, L,
Academic Journal
Fitzgerald, Mark; Fiannacca, Martina; Smith, Douglas; Gertler, Tracy; Gunning, Boudewijn; Syrbe, Steffen; Verbeek, Nienke; Stamberger, Hannah; Weckhuysen, Sarah; Ceulemans, Berten; Schoonjans, An-Sofie; Rossi, Massimiliano; Demarquay, Geneviève; Lesca, Gaetan; Olofsson, Kern; Koolen, D.A.; Hornemann, Frauke; Baulac, Stephanie; Rubboli, Guido; Minks, Kelly; Lee, Bohoon; Helbig, Ingo; Dlugos, Dennis; Møller, Rikke; Bearden, David
Neurotherapeutics, 16, 3, pp. 848-857
Neurotherapeutics
Fitzgerald, M P, Fiannacca, M, Smith, D M, Gertler, T S,Gunning , B, Syrbe, S, Verbeek, N, Stamberger, H, Weckhuysen, S, Ceulemans, B, Schoonjans, A S, Rossi, M, Demarquay, G, Lesca, G, Olofsson, K, Koolen, D A, Hornemann, F, Baulac, S, Rubboli, G, Minks, K Q, Lee, B, Helbig, I, Dlugos, D, Møller, R S & Bearden, D 2019, ' Treatment Responsiveness in KCNT1-Related Epilepsy ', Neurotherapeutics, vol. 16, no. 3, pp. 848-857 . https://doi.org/10.1007/s13311-019-00739-y
Neurotherapeutics
Fitzgerald, M P, Fiannacca, M, Smith, D M, Gertler, T S,
Academic Journal
Sharon Shmuely; Rainer Surges; Robert M. Helling; W. Boudewijn Gunning; Eva H. Brilstra; Judith S. Verhoeven; J. Helen Cross; Sanjay M. Sisodiya; Hanno L. Tan; Josemir W. Sander; Roland D. Thijs
Annals of Clinical and Translational Neurology, Vol 7, Iss 4, Pp 462-473 (2020)
Academic Journal
Baldassari, Sara ; Picard, Fabienne ; Verbeek, Nienke E. ; van Kempen, Marjan ; Brilstra, Eva H. ; Lesca, Gaetan ; Conti, Valerio ; Guerrini, Renzo ; Bisulli, Francesca ; Licchetta, Laura ; Pippucci, Tommaso ; Tinuper, Paolo ; Hirsch, Edouard ; de Saint Martin, Anne ; Chelly, Jamel ; Rudolf, Gabrielle ; Chipaux, Mathilde ; Ferrand-Sorbets, Sarah ; Dorfmüller, Georg ; Sisodiya, Sanjay ; Balestrini, Simona ; Schoeler, Natasha ; Hernandez-Hernandez, Laura ; Krithika, S. ; Oegema, Renske ; Hagebeuk, Eveline ; Gunning, Boudewijn ; Deckers, Charles ; Berghuis, Bianca ; Wegner, Ilse ; Niks, Erik ; Jansen, Floor E. ; Braun, Kees ; de Jong, Daniëlle ; Rubboli, Guido ; Talvik, Inga ; Sander, Valentin ; Uldall, Peter ; Jacquemont, Marie-Line ; Nava, Caroline ; Leguern, Eric ; Julia, Sophie ; Gambardella, Antonio ; d’Orsi, Giuseppe ; Crichiutti, Giovanni ; Faivre, Laurence ; Darmency, Veronique ; Benova, Barbora ; Krsek, Pavel ; Biraben, Arnaud ; Lebre, Anne-Sophie ; Jennesson, Mélanie ; Sattar, Shifteh ; Marchal, Cécile ; Nordli, Douglas R, Jr ; Lindstrom, Kristin ; Striano, Pasquale ; Lomax, Lysa Boissé ; Kiss, Courtney ; Bartolomei, Fabrice ; Lepine, Anne Fabienne ; Schoonjans, An-Sofie ; Stouffs, Katrien ; Jansen, Anna ; Panagiotakaki, Eleni ; Ricard-Mousnier, Brigitte ; Thevenon, Julien ; de Bellescize, Julitta ; Catenoix, Hélène ; Dorn, Thomas ; Zenker, Martin ; Müller-Schlüter, Karen ; Brandt, Christian ; Krey, Ilona ; Polster, Tilman ; Wolff, Markus ; Balci, Meral ; Rostasy, Kevin ; Achaz, Guillaume ; Zacher, Pia ; Becher, Thomas ; Cloppenborg, Thomas ; Yuskaitis, Christopher J. ; Weckhuysen, Sarah ; Poduri, Annapurna ; Lemke, Johannes R. ; Møller, Rikke S. ; Baulac, Stéphanie
In Genetics in Medicine February 2019 21(2):398-408
Academic Journal
de Lange, Iris M. ; Gunning, Boudewijn ; Sonsma, Anja C.M. ; van Gemert, Lisette ; van Kempen, Marjan ; Verbeek, Nienke E. ; Sinoo, Claudia ; Nicolai, Joost ; Knoers, Nine V.A.M. ; Koeleman, Bobby P.C. ; Brilstra, Eva H.
In Epilepsy & Behavior January 2019 90:252-259
Academic Journal
Ben-Menachem, Elinor; Gunning, Boudewijn; Arenas Cabrera, Carmen María; VanLandingham, Kevan; Crockett, Julie; Critchley, David; Wray, Louise; Tayo, Bola; Morrison, Gilmour; Toledo, Manuel
CNS Drugs. :1-12
Academic Journal
Helbig, Katherine; Lauerer, Robert; Bahr, Jacqueline; Souza, Ivana; Myers, Candace; Uysal, Betül; Schwarz, Niklas; Gandini, Maria; Huang, Sun; Keren, Boris; Mignot, Cyril; Afenjar, Alexandra; Billette de Villemeur, Thierry; Héron, Delphine; Nava, Caroline; Valence, Stéphanie; Buratti, Julien; Fagerberg, Christina; Soerensen, Kristina; Kibaek, Maria; Kamsteeg, Erik-Jan; Koolen, David; Gunning, Boudewijn; Schelhaas, H Jurgen; Kruer, Michael; Fox, Jordana; Bakhtiari, Somayeh; Jarrar, Randa; Padilla-Lopez, Sergio; Lindstrom, Kristin; Jin, Sheng Chih; Zeng, Xue; Bilguvar, Kaya; Papavasileiou, Antigone; Xing, Qinghe; Zhu, Changlian; Boysen, Katja; Vairo, Filippo; Lanpher, Brendan; Klee, Eric; Tillema, Jan-Mendelt; Payne, Eric; Cousin, Margot; Kruisselbrink, Teresa; Wick, Myra; Baker, Joshua; Haan, Eric; Smith, Nicholas; Sadeghpour, Azita; Davis, Erica; Katsanis, Nicholas; Corbett, Mark; Maclennan, Alastair; Gecz, Jozef; Biskup, Saskia; Goldmann, Eva; Rodan, Lance; Kichula, Elizabeth; Segal, Eric; Jackson, Kelly; Asamoah, Alexander; Dimmock, David; Mccarrier, Julie; Botto, Lorenzo; Filloux, Francis; Tvrdik, Tatiana; Cascino, Gregory; Klingerman, Sherry; Neumann, Catherine; Wang, Raymond; Jacobsen, Jessie; Nolan, Melinda; Snell, Russell; Lehnert, Klaus; Sadleir, Lynette; Anderlid, Britt-Marie; Kvarnung, Malin; Guerrini, Renzo; Friez, Michael; Lyons, Michael; Leonhard, Jennifer; Kringlen, Gabriel; Casas, Kari; El Achkar, Christelle; Smith, Lacey; Rotenberg, Alexander; Poduri, Annapurna; Sanchis-Juan, Alba; Carss, Keren; Rankin, Julia; Zeman, Adam; Raymond, F Lucy; Blyth, Moira; Kerr, Bronwyn; Ruiz, Karla; Urquhart, Jill; Hughes, Imelda; Banka, Siddharth; Hedrich, Ulrike; Scheffer, Ingrid; Helbig, Ingo; Zamponi, Gerald; Lerche, Holger; Mefford, Heather; Allori, Alexander; Angrist, Misha; Ashley, Patricia; Bidegain, Margarita; Boyd, Brita; Chambers, Eileen; Cope, Heidi; Cotten, C. Michael; Curington, Theresa; Ellestad, Sarah; Fisher, Kimberley; French, Amanda; Gallentine, William; Goldberg, Ronald; Hill, Kevin; Kansagra, Sujay; Katsanis, Sara; Kurtzberg, Joanne; Marcus, Jeffrey; Mcdonald, Marie; Mikati, Mohammed; Miller, Stephen; Murtha, Amy; Perilla, Yezmin; Pizoli, Carolyn; Purves, Todd; Ross, Sherry; Smith, Edward; Wiener, John
American Journal of Human Genetics, 103, 5, pp. 666-678
Deciphering Developmental Disorders Study 2018, ' De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias ', American Journal of Human Genetics, vol. 103, no. 5, pp. 666-678 . https://doi.org/10.1016/j.ajhg.2018.09.006
Deciphering Developmental Disorders Study, Task Force for Neonatal Genomics, Helbig, KL, Lauerer, RJ, Bahr, JC, Souza, IA, Myers, CT, Uysal, B, Schwarz, N, Gandini, MA, Huang, S, Keren, B, Mignot, C, Afenjar, A, Billette, D V T, Héron, D, Nava, C, Valence, S, Buratti, J, Fagerberg, C R, Soerensen, K P, Kibaek, M, Kamsteeg, E-J, Koolen, D A,Gunning , B, Schelhaas, H J, Kruer, M C, Fox, J, Bakhtiari, S, Jarrar, R, Padilla-Lopez, S, Lindstrom, K, Jin, S C, Zeng, X, Bilguvar, K, Papavasileiou, A, Xing, Q, Zhu, C, Boysen, K, Vairo, F, Lanpher, B C, Klee, E W, Tillema, J-M, Payne, E T, Cousin, M A, Kruisselbrink, T M, Wick, M J, Baker, J, Haan, E, Kerr, B, Hughes, I & Banka, S 2019, 'Correction : De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias', American Journal of Human Genetics, vol. 104, no. 3, pp. P562. https://doi.org/10.1016/j.ajhg.2019.02.015
Deciphering Developmental Disorders Study 2018, 'De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias', American Journal of Human Genetics, vol. 103, no. 5, pp. 666-678. https://doi.org/10.1016/j.ajhg.2018.09.006
American Journal of Human Genetics, vol 103, iss 5
Deciphering Developmental Disorders Study 2018, ' De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias ', American Journal of Human Genetics, vol. 103, no. 5, pp. 666-678 . https://doi.org/10.1016/j.ajhg.2018.09.006
Deciphering Developmental Disorders Study, Task Force for Neonatal Genomics, Helbig, KL, Lauerer, RJ, Bahr, JC, Souza, IA, Myers, CT, Uysal, B, Schwarz, N, Gandini, MA, Huang, S, Keren, B, Mignot, C, Afenjar, A, Billette, D V T, Héron, D, Nava, C, Valence, S, Buratti, J, Fagerberg, C R, Soerensen, K P, Kibaek, M, Kamsteeg, E-J, Koolen, D A,
Deciphering Developmental Disorders Study 2018, 'De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy with Contractures, Macrocephaly, and Dyskinesias', American Journal of Human Genetics, vol. 103, no. 5, pp. 666-678. https://doi.org/10.1016/j.ajhg.2018.09.006
American Journal of Human Genetics, vol 103, iss 5
Academic Journal
Terry O’Brien; Patrick Kwan; Markus Reuber; Arjune Sen; Rhys Thomas; Lakshmi Nagarajan; Muhammad Zafar; Mark Keezer; Paul Lyons; George Morris; Andrea Andrade; David McCormick; Paolo Tinuper; Jorge Burneo; Michael Gelfand; Kristl Vonck; Yongjie Li; Kate Riney; Anto Bagic; Ryan Verner; James P Valeriano; Ricky Lee; Katarzyna Kotulska; Ellen Jespers; Maxine Dibué; Simon Harvey; Tim von Oertzen; Riem El Tahry; Andréa Julião deOliveira; Isabella D’Andrea Meira; Martin Veilleux; Kenneth Myers; GuoMing Luan; Fangcheng Li; JiWen Xu; Raja Sarma Gosala; Vrajesh Udani; Nilesh Kurwale; Michal Tzadok; Firas Fahoum; Hadassa Goldberg-Stern; Nicola Specchio; Seijiro Shimada; Tomonori Ono; Boudewijn Gunning; Louis Wagner; Rinze Neuteboom; Ewa Krzystanek; Youssef Al-Said; Mashael Omar Alkhateeb; Kasia Sieradzan; Jeffrey Cochius; Karen Keough; Marc Frost; Marie Collier; Kore Liow; Jane Boggs; Ahmed Sadek; James Wheless; James Valeriano; Linda Leary; Xiangping Zhou; Jose Ferreira; Gholam Motamedi; Masaki Iwasaki
BMJ Neurology Open, Vol 3, Iss 2 (2021)
Academic Journal
Patel, Anup D; Mazurkiewicz‐Beldzinska, Maria; Chin, Richard; Gil-Nagel, Antonio; Gunning, Boudewijn; Halford, Jonathan J.; Mitchell, Wendy; Perry, M. Scott; Thiele, Elizabeth A.; Weinstock, Arie; Dunayevich, Eduardo; Checketts, Daniel; Devinsky, Orrin
Patel, A D, Mazurkiewicz-Beldzinska, M, Chin, R, Gil-Nagel, A, Gunning , B, Halford, J J, Mitchell, W, Perry, M S, Thiele, E A, Weinstock, A, Dunayevich, E, Checketts, D & Devinsky, O 2021, ' Long-term Safety and Efficacy of Add-on Cannabidiol in Patients with Lennox-Gastaut Syndrome: Results of a Long-Term Open-Label Extension Trial : CBD long-term safety and efficacy in Lennox-Gastaut syndrome ', Epilepsia . https://doi.org/10.1111/epi.17000
Academic Journal
Johannesen, Katrine M.; Gardella, Elena; Gjerulfsen, Cathrine E.; Bayat, Allan; Rouhl, Rob P.W.; Reijnders, Margot; Whalen, Sandra; Keren, Boris; Buratti, Julien; Courtin, Thomas; Wierenga, Klaas J.; Isidor, Bertrand; Piton, Amélie; Faivre, Laurence; Garde, Aurore; Moutton, Sébastien; Tran-Mau-Them, Frédéric; Denommé-Pichon, Anne-Sophie; Coubes, Christine; Larson, Austin; Esser, Michael J.; Appendino, Juan Pablo; Al-Hertani, Walla; Gamboni, Beatriz; Mampel, Alejandra; Mayorga, Lía; Orsini, Alessandro; Bonuccelli, Alice; Suppiej, Agnese; Van-Gils, Julien; Vogt, Julie; Damioli, Simona; Giordano, Lucio; Moortgat, Stephanie; Wirrell, Elaine; Hicks, Sarah; Kini, Usha; Noble, Nathan; Stewart, Helen; Asakar, Shailesh; Cohen, Julie S.; Naidu, SakkuBai R.; Collier, Ashley; Brilstra, Eva H.; Li, Mindy H.; Brew, Casey; Bigoni, Stefania; Ognibene, Davide; Ballardini, Elisa; Ruivenkamp, Claudia; Faggioli, Raffaella; Afenjar, Alexandra; Rodriguez, Diana; Bick, David; Segal, Devorah; Coman, David; Gunning, Boudewijn; Devinsky, Orrin; Demmer, Laurie A.; Grebe, Theresa; Pruna, Dario; Cursio, Ida; Greenhalgh, Lynn; Graziano, Claudio; Singh, Rahul Raman; Cantalupo, Gaetano; Willems, Marjolaine; Yoganathan, Sangeetha; Góes, Fernanda; Leventer, Richard J.; Colavito, Davide; Olivotto, Sara; Scelsa, Barbara; Andrade, Andrea V.; Ratke, Kelly; Tokarz, Farha; Khan, Atiya S.; Ormieres, Clothilde; Benko, William; Keough, Karen; Keros, Sotirios; Hussain, Shanawaz; Franques, Ashlea; Varsalone, Felicia; Grønborg, Sabine; Mignot, Cyril; Heron, Delphine; Nava, Caroline; Isapof, Arnaud; Borlot, Felippe; Whitney, Robyn; Ronan, Anne; Foulds, Nicola; Somorai, Marta; Brandsema, John; Helbig, Katherine L.; Helbig, Ingo; Ortiz-González, Xilma R.; Dubbs, Holly; Vitobello, Antonio; Anderson, Mel; Spadafore, Dominic; Hunt, David; Møller, Rikke S.; Rubboli, Guido
Neurology: Genetics. Dec 01, 2021 7(6):e613-e613
Academic Journal
Arends, Johan B. ; van der Linden, Inge ; Ebus, Saskia C. ; Debeij, Mariëtte H. ; Gunning, Boudewijn W. ; Zwarts, Machiel J.
In Clinical Neurophysiology April 2017 128(4):661-666
Academic Journal
Iris M. deLange; Wout Weuring; Ruben van‘t Slot; Boudewijn Gunning; Anja C. M. Sonsma; Mark McCormack; Carolien deKovel; Lisette J. J. M. vanGemert; Flip Mulder; Marjan J. A. vanKempen; Nine V. A. M. Knoers; Eva H. Brilstra; Bobby P. C. Koeleman
Molecular Genetics & Genomic Medicine, Vol 7, Iss 7, Pp n/a-n/a (2019)
Academic Journal
Verbeek, Nienke E. ; Wassenaar, Merel ; van Campen, Jolien S. ; Sonsma, Anja ; Gunning, Boudewijn ; Knoers, Nine ; Lindhout, Dick ; Jansen, Floor E. ; Leijten, Frans ; Brilstra, Eva H. ; Kasteleijn-Nolst Trenité, Dorothée
In Epilepsy & Behavior June 2015 47:39-44
Academic Journal
Neuropsychiatric Disease and Treatment, Vol 2010, Iss Issue 1, Pp 227-231 (2010)
Academic Journal
de Lange, Iris M.; Koudijs, Marco J.; van ʼt Slot, Ruben; Gunning, Boudewijn; Sonsma, Anja C. M.; van Gemert, Lisette J. J. M.; Mulder, Flip; Carbo, Ellen C.; van Kempen, Marjan J. A.; Verbeek, Nienke E.; Nijman, Isaac J.; Ernst, Robert F.; Savelberg, Sanne M. C.; Knoers, Nine V. A. M.; Brilstra, Eva H.; Koeleman, Bobby P. C.
Epilepsia. Mar 01, 2018 59(3):690-703
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