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| | Publication Year | Title | Author(s) |
| 321 | 19-Mar-2021 | EXPRESS: International Stroke Genetics Consortium Recommendations for Studies of Genetics of Stroke Outcome and Recovery. | Lindgren, Arne; Braun, Robynne; Majersik, Jennifer J; Clatworthy, Philip; Mainali, Shraddha; Derdeyn, Colin P; Maguire, Jane Margaret; Jern, Christina; Rosand, Jonathan; Cole, John W; Lee, Jin-Moo; Khatri, Pooja; Nyquist, Paul A; Debette, Stà Phanie; Keat Wei, Loo; Rundek, Tatjana; Leifer, Dana; Thijs, Vincent N ; Lemmens, Robin; Heitsch, Laura; Prasad, Kameshwar; Jimenez-Conde, Jordi; Dichgans, Martin; Rost, Natalia S; Cramer, Steven C; Bernhardt, Julie; Worrall, Bradford B; Cadenas, Israel |
| 322 | 26-May-2021 | EXPRESS: Protocol of a randomised controlled trial investigating the effectiveness of Recovery-focused Community support to Avoid readmissions and improve Participation after Stroke (ReCAPS). | Cadilhac, Dominique; Cameron, Jan; Kilkenny, Monique F; Andrew, Nadine Elizabeth; Harris, Dawn; Ellery, Fiona; Thrift, Amanda G; Purvis, Tara; Kneebone, Ian; Dewey, Helen; Drummond, Avril; Hackett, Maree L; Grimley, Rohan; Middleton, Sandy; Thijs, Vincent N ; Cloud, Geoffrey; Carey, Mariko L; Butler, Ernest; Ma, Henry; Churilov, Leonid ; Hankey, Graeme J; English, Coralie Kym; Lannin, Natasha A |
| 323 | 26-Apr-2013 | Expression of the transmembrane lysosomal protein SCARB2/Limp-2 in renin secretory granules controls renin release. | Lee, D ; Desmond, Michael J; Fraser, S A; Katerelos, M ; Gleich, Kurt; Berkovic, Samuel F ; Power, David Anthony |
| 324 | 2023 | Extended follow-up after anterior temporal lobectomy demonstrates seizure recurrence 20+ years post-surgery. | McIntosh, Anne M ; Wynd, Alex W ; Berkovic, Samuel F |
| 325 | Jul-2019 | Extending thrombolysis to 4·5-9 h and wake-up stroke using perfusion imaging: a systematic review and meta-analysis of individual patient data. | Campbell, Bruce C V; Ma, Henry; Ringleb, Peter A; Parsons, Mark W; Churilov, Leonid ; Bendszus, Martin; Levi, Christopher R; Hsu, Chung; Kleinig, Timothy J; Fatar, Marc; Leys, Didier; Molina, Carlos; Wijeratne, Tissa; Curtze, Sami; Dewey, Helen M; Barber, P Alan; Butcher, Kenneth S; De Silva, Deidre A; Bladin, Christopher F; Yassi, Nawaf; Pfaff, Johannes A R; Sharma, Gagan; Bivard, Andrew; Desmond, Patricia M; Schwab, Stefan; Schellinger, Peter D; Yan, Bernard; Mitchell, Peter J; Serena, Joaquín; Toni, Danilo; Thijs, Vincent N ; Hacke, Werner; Davis, Stephen M; Donnan, Geoffrey A |
| 326 | 4-Feb-2021 | Extent of FLAIR Hyperintense Vessels May Modify Treatment Effect of Thrombolysis: A Post hoc Analysis of the WAKE-UP Trial. | Grosch, Anne Sophie; Kufner, Anna; Boutitie, Florent; Cheng, Bastian; Ebinger, Martin; Endres, Matthias; Fiebach, Jochen B; Fiehler, Jens; Königsberg, Alina; Lemmens, Robin; Muir, Keith W; Nighoghossian, Norbert; Pedraza, Salvador; Siemonsen, Claus Z; Thijs, Vincent ; Wouters, Anke; Gerloff, Christian; Thomalla, Götz; Galinovic, Ivana |
| 327 | 2022 | Factors associated with paid employment 12 months after stroke in A Very Early Rehabilitation Trial (AVERT). | Cain, Stephen; Churilov, Leonid ; Collier, Janice M; Carvalho, Lilian B; Borschmann, Karen ; Moodie, Marj; Thijs, Vincent N ; Bernhardt, Julie |
| 328 | Jul-2020 | Familial adult myoclonic epilepsy type 1 SAMD12 TTTCA repeat expansion arose 17,000 years ago and is present in Sri Lankan and Indian families. | Bennett, Mark F ; Oliver, Karen L; Regan, Brigid M; Bellows, Susannah T; Schneider, Amy L ; Rafehi, Haloom; Sikta, Neblina; Crompton, Douglas E; Coleman, Matthew; Hildebrand, Michael S ; Corbett, Mark A; Kroes, Thessa; Gecz, Jozef; Scheffer, Ingrid E ; Berkovic, Samuel F ; Bahlo, Melanie |
| 329 | 2000 | Familial epilepsies: quality of life issues in genetic research. | Berkovic, Samuel F |
| 330 | Aug-2017 | Familial epilepsy with anterior polymicrogyria as a presentation of COL18A1 mutations. | Corbett, Mark A; Turner, Samantha J; Gardner, Alison; Silver, Jeremy; Stankovich, Jim; Leventer, Richard J; Derry, Christopher P; Carroll, Renée; Ha, Thuong; Scheffer, Ingrid E ; Bahlo, Melanie; Jackson, Graeme D ; Mackey, David A; Berkovic, Samuel F ; Gecz, Jozef |
| 331 | 10-Jul-2012 | Familial focal epilepsy with variable foci mapped to chromosome 22q12: expansion of the phenotypic spectrum. | Klein, Karl Martin; O'Brien, Terence J; Praveen, Kavita; Heron, Sarah E; Mulley, John C; Foote, Simon; Berkovic, Samuel F ; Scheffer, Ingrid E |
| 332 | 1-Sep-2010 | Familial Lennox-Gastaut syndrome in male siblings with a novel DCX mutation and anterior pachygyria. | Lawrence, Kate M; Mei, Davide; Newton, Mark R; Leventer, Richard J; Guerrini, Renzo; Berkovic, Samuel F |
| 333 | Aug-2017 | Familial mesial temporal lobe epilepsy and the borderland of déjà vu | Perucca, Piero ; Crompton, Douglas E; Bellows, Susannah T; McIntosh, Anne M ; Kalincik, Tomas; Newton, Mark R; Vajda, Frank JE; Scheffer, Ingrid E ; Kwan, Patrick; O'Brien, Terence J; Tan, K Meng; Berkovic, Samuel F |
| 334 | 23-Sep-2010 | Familial mesial temporal lobe epilepsy: a benign epilepsy syndrome showing complex inheritance. | Crompton, Douglas E; Scheffer, Ingrid E ; Taylor, Isabella; Cook, Mark J; McKelvie, Penelope A; Vears, Danya F; Lawrence, Kate M; McMahon, Jacinta M; Grinton, Bronwyn E; McIntosh, Anne M ; Berkovic, Samuel F |
| 335 | Nov-2023 | Familial mesial temporal lobe epilepsy: clinical spectrum and genetic evidence for a polygenic architecture. | Harris, Rebekah V; Oliver, Karen L; Perucca, Piero ; Striano, Pasquale; Labate, Angelo; Riva, Antonella; Grinton, Bronwyn E; Reid, Joshua; Hutton, Jessica; Todaro, Marian; O'Brien, Terence J; Kwan, Patrick; Sadleir, Lynette G; Mullen, Saul A ; Dazzo, Emanuela; Crompton, Douglas E; Scheffer, Ingrid E ; Bahlo, Melanie; Nobile, Carlo; Gambardella, Antonio; Berkovic, Samuel F |
| 336 | 1-Dec-1998 | Familial partial epilepsy with variable foci: a new partial epilepsy syndrome with suggestion of linkage to chromosome 2. | Scheffer, Ingrid E ; Phillips, H A; O'Brien, C E; Saling, Michael M ; Wrennall, J A; Wallace, Robyn H; Mulley, John C; Berkovic, Samuel F |
| 337 | 1-Sep-2004 | Familial partial epilepsy with variable foci: clinical features and linkage to chromosome 22q12. | Berkovic, Samuel F ; Serratosa, Jose M; Phillips, Hilary A; Xiong, Lan; Andermann, Eva; Díaz-Otero, Fernando; Gómez-Garre, Pilar; Martín, Mercedes; Fernández-Bullido, Yolanda; Andermann, Frederick; Lopes-Cendes, Iscia; Dubeau, Francois; Desbiens, Richard; Scheffer, Ingrid E ; Wallace, Robyn H; Mulley, John C; Pandolfo, Massimo |
| 338 | 1-Dec-2020 | The feasibility of delivering first suspected seizure care using telehealth: A mixed methods controlled study. | Lewis, Annie K; Harding, Katherine E; Taylor, Nicholas F; O'Brien, Terence J; Carney, Patrick W |
| 339 | Apr-2021 | Feasibility trial of metformin XR in people with pre-diabetes and stroke (MIPPS)-randomised open blinded endpoint controlled trial. | Tabesh, Marjan; Hachem, Mariam; Lau, Lik-Hui; Borschmann, Karen ; Churilov, Leonid ; Price, Sarah A L; Sumithran, Priya ; Donnan, Geoffrey A ; Zajac, Jeffrey D ; Thijs, Vincent N ; Ekinci, Elif I |
| 340 | Nov-2020 | Features of intracranial hemorrhage in cerebral venous thrombosis. | Afifi, K; Bellanger, G; Buyck, P J; Zuurbier, S M; Esperon, C G; Barboza, M A; Costa, P; Escudero, I; Renard, D; Lemmens, R; Hinteregger, N; Fazekas, F; Conde, J Jimenez; Giralt-Steinhauer, E; Hiltunen, S; Arauz, A; Pezzini, A; Montaner, J; Putaala, J; Weimar, C; Schlamann, Marc; Gattringer, T; Tatlisumak, T; Coutinho, J M; Demaerel, P; Thijs, Vincent N |
