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The Lancet (British edition), 2018-03, Vol.391 (10125), p.1085-1096
- Thiele, Elizabeth A
- Marsh, Eric D
- French, Jacqueline A
- Mazurkiewicz-Beldzinska, Maria
- Benbadis, Selim R
- Joshi, Charuta
- Lyons, Paul D
- Taylor, Adam
- Roberts, Claire
- Sommerville, Kenneth
- Gunning, Boudewjin
- Gawlowicz, Jacek
- Lisewski, Pawel
- Mazurkiewicz Beldzinska, Maria
- Mitosek Szewczyk, Krystyna
- Steinborn, Barbara
- Zolnowska, Marta
- Hughes, Elaine
- McLellan, Ailsa
- Benbadis, Selim
- Ciliberto, Michael
- Clark, Gary
- Dlugos, Dennis
- Filloux, Francis
- Flamini, Robert
- French, Jacqueline
- Frost, Michael
- Haut, Sheryl
- Kapoor, Siddarth
- Kessler, Sudha
- Laux, Linda
- Lyons, Paul
- Marsh, Eric
- Moore, David
- Morse, Richard
- Nagaraddi, Venkatesh
- Rosenfeld, William
- Seltzer, Laurie
- Shellhaas, Renée
- Sullivan, Joseph
- Thiele, Elizabeth
- Thio, Liu Lin
- Wang, David
- Wilfong, Angus
2018
Link zum Volltext
The New England journal of medicine, 2017-05, Vol.376 (21), p.2011-2020
2017
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Current opinion in neurology, 2019-04, Vol.32 (2), p.220
2019
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Brain (London, England : 1878), 2020-02, Vol.143 (2), p.554-569
2020
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Neurotherapeutics, 2021-07, Vol.18 (3), p.1458-1467
2021
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Journal of child neurology, 2017-01, Vol.32 (1), p.35-40
2017
Link zum Volltext
American journal of human genetics, 2016-10, Vol.99 (4), p.802-816
- Li, Dong
- Yuan, Hongjie
- Ortiz-Gonzalez, Xilma R.
- Marsh, Eric D.
- Tian, Lifeng
- McCormick, Elizabeth M.
- Kosobucki, Gabrielle J.
- Chen, Wenjuan
- Schulien, Anthony J.
- Chiavacci, Rosetta
- Tankovic, Anel
- Naase, Claudia
- Brueckner, Frieder
- von Stülpnagel-Steinbeis, Celina
- Hu, Chun
- Kusumoto, Hirofumi
- Hedrich, Ulrike B.S.
- Elsen, Gina
- Hörtnagel, Konstanze
- Aizenman, Elias
- Lemke, Johannes R.
- Hakonarson, Hakon
- Traynelis, Stephen F.
- Falk, Marni J.
2016
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Nature medicine, 2023-06, Vol.29 (6), p.1468-1475
2023
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Journal of autism and developmental disorders, 2023-05
2023
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Nature communications, 2019-06, Vol.10 (1), p.2655-14, Article 2655
2019
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Lancet neurology, 2016-03, Vol.15 (3), p.270-278
- Devinsky, Orrin, Dr Prof
- Marsh, Eric, MD
- Friedman, Daniel, MD
- Thiele, Elizabeth, Prof
- Laux, Linda, MD
- Sullivan, Joseph, MD
- Miller, Ian, MD
- Flamini, Robert, MD
- Wilfong, Angus, MD
- Filloux, Francis, MD
- Wong, Matthew, MD
- Tilton, Nicole, CRNP
- Bruno, Patricia, RN
- Bluvstein, Judith, MD
- Hedlund, Julie, RN
- Kamens, Rebecca
- Maclean, Jane, MD
- Nangia, Srishti, MD
- Singhal, Nilika Shah, MD
- Wilson, Carey A, MD
- Patel, Anup, MD
- Cilio, Maria Roberta, Prof
2016
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Epilepsia (Copenhagen), 2017-03, Vol.58 (3), p.402-411
2017
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Epilepsy research, 2019-08, Vol.154, p.13-20
2019
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Proceedings of the National Academy of Sciences - PNAS, 2012-12, Vol.109 (52), p.21516-21521
2012
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Brain (London, England : 1878), 2020-01, Vol.143 (1), p.191-209
2020
Link zum Volltext
Neurobiology of disease, 2021-01, Vol.148, p.105176-105176, Article 105176
2021
Link zum Volltext
Neuroscience, 2018-08, Vol.384, p.350-360
2018
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Comparison of Core Features in Four Developmental Encephalopathies in the Rett Natural History Study
2020
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CNS drugs, 2022-06, Vol.36 (6), p.591-604
2022
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Lancet neurology, 2022-05, Vol.21 (5), p.417-427
- Knight, Elia M Pestana
- Amin, Sam
- Bahi-Buisson, Nadia
- Benke, Tim A
- Cross, J Helen
- Demarest, Scott T
- Olson, Heather E
- Specchio, Nicola
- Fleming, Thomas R
- Aimetti, Alex A
- Gasior, Maciej
- Devinsky, Orrin
- Belousova, Elena
- Belyaev, Oleg
- Ben-Zeev, Bruria
- Brunklaus, Andreas
- Ciliberto, Michael A.
- Darra, Francesca
- Davis, Ronald
- De Giorgis, Valentina
- Doronina, Olga
- Fahey, Michael
- Guerrini, Renzo
- Heydemann, Peter
- Khaletskaya, Olga
- Lisewski, Pawel
- Marsh, Eric D.
- Moosa, Ahsan N.
- Perry, Scott
- Philip, Sunny
- Rajaraman, Rajsekar R.
- Renfroe, Ben
- Saneto, Russell P.
- Scheffer, Ingrid E.
- Sogawa, Yoshimi
- Suter, Bernhardt
- Sweney, Matthew T.
- Tarquinio, Daniel
- Veggiotti, Pierangelo
- Wallace, Geoff
- Weisenberg, Judy
- Wilfong, Angus
- Wirrell, Elaine C.
- Zafar, Muhammad
- Zolnowska, Marta
2022
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European journal of human genetics : EJHG, 2023-02, Vol.31 (2), p.169-178
2023
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American journal of medical genetics. Part A, 2022-09, Vol.188 (9), p.2617-2626
2022
Link zum Volltext
Annals of neurology, 2017-03, Vol.81 (3), p.419-429
- Olson, Heather E.
- Kelly, McKenna
- LaCoursiere, Christopher M.
- Pinsky, Rebecca
- Tambunan, Dimira
- Shain, Catherine
- Ramgopal, Sriram
- Takeoka, Masanori
- Libenson, Mark H.
- Julich, Kristina
- Loddenkemper, Tobias
- Marsh, Eric D.
- Segal, Devorah
- Koh, Susan
- Salman, Michael S.
- Paciorkowski, Alex R.
- Yang, Edward
- Bergin, Ann M.
- Sheidley, Beth Rosen
- Poduri, Annapurna
2017
Link zum Volltext
Annals of neurology, 2019-12, Vol.86 (6), p.899-912
- Kang, Seok Kyu
- Vanoye, Carlos G.
- Misra, Sunita N.
- Echevarria, Dennis M.
- Calhoun, Jeffrey D.
- O'Connor, John B.
- Fabre, Katarina L.
- McKnight, Dianalee
- Demmer, Laurie
- Goldenberg, Paula
- Grote, Lauren E.
- Thiffault, Isabelle
- Saunders, Carol
- Strauss, Kevin A.
- Torkamani, Ali
- der Smagt, Jasper
- Gassen, Koen
- Carson, Robert P.
- Diaz, Jullianne
- Leon, Eyby
- Jacher, Joseph E.
- Hannibal, Mark C.
- Litwin, Jessica
- Friedman, Neil R.
- Schreiber, Allison
- Lynch, Bryan
- Poduri, Annapurna
- Marsh, Eric D.
- Goldberg, Ethan M.
- Millichap, John J.
- George, Alfred L.
- Kearney, Jennifer A.
2019
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An mtDNA mutant mouse demonstrates that mitochondrial deficiency can result in autism endophenotypes
2021
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