Epilepsy Research Centre

OrgUnit's Researchers
(Persons)

Results 1-5 of 13 (Search time: 0.004 seconds).

FullnameTranslated NameEmail
Archer, John Sjarcher@unimelb.edu.au
Bennett, Mark F
Berkovic, Samuel FSamuel.BERKOVIC@austin.org.au
Cameron, Jillian Mjill.cameron@austin.org.au
Hildebrand, Michael Smichael.hildebrand@unimelb.edu.au

OrgUnit's Researchers publications
(Dept/Workgroup Publication)

Results 541-560 of 636 (Search time: 0.016 seconds).

Publication YearTitleAuthor(s)
541Feb-2020SCN1A variants in vaccine-related febrile seizures: a prospective study.Damiano, John A; Deng, Lucy; Li, Wenhui; Burgess, Rosemary; Schneider, Amy L ; Crawford, Nigel W; Buttery, Jim; Gold, Michael; Richmond, Peter; Macartney, Kristine K; Hildebrand, Michael S ; Scheffer, Ingrid E ; Wood, Nicholas; Berkovic, Samuel F 
542Dec-2019SCN1A-related phenotypes: Epilepsy and beyond.Scheffer, Ingrid E ; Nabbout, Rima
543Jul-2016SCN8A encephalopathy: Research progress and prospects.Meisler, Miriam H; Helman, Guy; Hammer, Michael F; Fureman, Brandy E; Gaillard, William D; Goldin, Alan L; Hirose, Shinichi; Ishii, Atsushi; Kroner, Barbara L; Lossin, Christoph; Mefford, Heather C; Parent, Jack M; Patel, Manoj; Schreiber, John; Stewart, Randall; Whittemore, Vicky; Wilcox, Karen; Wagnon, Jacy L; Pearl, Phillip L; Vanderver, Adeline; Scheffer, Ingrid E 
5441-Oct-2001Seizure outcome after temporal lobectomy: current research practice and findings.McIntosh, A M; Wilson, Sarah J; Berkovic, Samuel F 
5451-Jan-1994Seizure outcome and pathological findings following temporal lobectomy in patients with complex partial seizures and foreign tissue lesions seen only on MRI.Murphy, M A; Fabinyi, Gavin C ; Berkovic, Samuel F ; Kalnins, Renate M; Bladin, Peter F 
5461-May-2002Seizure-associated hippocampal volume loss: a longitudinal magnetic resonance study of temporal lobe epilepsy.Briellmann, Regula S; Berkovic, Samuel F ; Syngeniotis, Ari; King, Mark A; Jackson, Graeme D 
54712-Mar-2015Seizures are regulated by ubiquitin-specific peptidase 9 X-linked (USP9X), a de-ubiquitinase.Paemka, Lily; Mahajan, Vinit B; Ehaideb, Salleh N; Skeie, Jessica M; Tan, Men Chee; Wu, Shu; Cox, Allison J; Sowers, Levi P; Gecz, Jozef; Jolly, Lachlan; Ferguson, Polly J; Darbro, Benjamin W; Schneider, Amy; Scheffer, Ingrid E ; Carvill, Gemma L; Mefford, Heather C; El-Shanti, Hatem; Wood, Stephen A; Manak, J Robert; Bassuk, Alexander G
548Apr-2016Seizures as presenting and prominent symptom in chorea-acanthocytosis with c.2343del VPS13A gene mutationBenninger, Felix; Afawi, Zaid; Korczyn, Amos D; Oliver, Karen L; Pendziwiat, Manuela; Masayuki, Nakamura; Sano, Akira; Helbig, Ingo; Berkovic, Samuel F ; Blatt, Ilan
54927-Nov-2001Seizures in family members of patients with hippocampal sclerosis.Briellmann, Regula S; Torn-Broers, Y; Jackson, Graeme D ; Berkovic, Samuel F 
5502021Seizures in Sotos syndrome: Phenotyping in 49 patients.Fortin, Olivier; Vincelette, Christian; Khan, Afsheen Q; Berrahmoune, Saoussen; Dassi, Christelle; Karimi, Mitra; Scheffer, Ingrid E ; Lu, Jun; Davis, Kellie; Myers, Kenneth A
551Jan-2021Self-limited focal epilepsy and childhood apraxia of speech with WAC pathogenic variants.Alawadhi, Abdulla; Morgan, Angela T; Mucha, Bettina E; Scheffer, Ingrid E ; Myers, Kenneth A
55221-Mar-2022Self-reported impact of developmental stuttering across the lifespan.Boyce, Jessica O; Jackson, Victoria E; van Reyk, Olivia; Parker, Richard; Vogel, Adam P; Eising, Else; Horton, Sarah E; Gillespie, Nathan A; Scheffer, Ingrid E ; Amor, David J; Hildebrand, Michael S ; Fisher, Simon E; Martin, Nicholas G; Reilly, Sheena; Bahlo, Melanie; Morgan, Angela T
5535-Dec-2023Self-Reported Stuttering Severity Is Accurate: Informing Methods for Large-Scale Data Collection in Stuttering.Horton, Sarah; Jackson, Victoria; Boyce, Jessica; Franken, Marie-Christine; Siemers, Stephanie; John, Miya St; Hearps, Stephen; van Reyk, Olivia; Braden, Ruth; Parker, Richard; Vogel, Adam P; Eising, Else; Amor, David J; Irvine, Janelle; Fisher, Simon E; Martin, Nicholas G; Reilly, Sheena; Bahlo, Melanie; Scheffer, Ingrid E ; Morgan, Angela
554Dec-2017Sensitive quantitative detection of somatic mosaic mutation in "double cortex" syndromeDamiano, John A; Do, Hongdo; Ozturk, Ezgi; Burgess, Rosemary; Kalnins, Renate; Jones, Nigel C; Dobrovic, Alexander ; Berkovic, Samuel F ; Hildebrand, Michael S 
5555-Sep-2019Serum sodium and intracranial pressure changes after desmopressin therapy in severe traumatic brain injury patients: a multi-centre cohort study.Harrois, A; Anstey, J R; Taccone, F S; Udy, A A; Citerio, G; Duranteau, J; Ichai, C; Badenes, R; Prowle, J R; Ercole, A; Oddo, M; Schneider, A ; van der Jagt, M; Wolf, S; Helbok, R; Nelson, D W; Skrifvars, M B; Cooper, D J; Bellomo, Rinaldo 
556May-2020Severe childhood speech disorder: Gene discovery highlights transcriptional dysregulation.Hildebrand, Michael S ; Jackson, Victoria E; Scerri, Thomas S; Van Reyk, Olivia; Coleman, Matthew J; Braden, Ruth O; Turner, Samantha; Rigbye, Kristin A; Boys, Amber; Barton, Sarah; Webster, Richard; Fahey, Michael; Saunders, Kerryn; Parry-Fielder, Bronwyn; Paxton, Georgia; Hayman, Michael; Coman, David; Goel, Himanshu; Baxter, Anne; Ma, Alan; Davis, Noni; Reilly, Sheena; Delatycki, Martin; Liégeois, Frederique J; Connelly, Alan; Gecz, Jozef; Fisher, Simon E; Amor, David J; Scheffer, Ingrid E ; Bahlo, Melanie; Morgan, Angela T
5574-Dec-2023Severe Communication Delays Are Independent of Seizure Burden and Persist Despite Contemporary Treatments in SCN1A+ Dravet Syndrome: Insights from the ENVISION Natural History Study.Perry, M Scott; Scheffer, Ingrid E ; Sullivan, Joseph; Brunklaus, Andreas; Boronat, Susana; Wheless, James W; Laux, Linda; Patel, Anup D; Roberts, Colin M; Dlugos, Dennis; Holder, Deborah; Knupp, Kelly G; Lallas, Matt; Phillips, Steven; Segal, Eric; Smeyers, Patricia; Lal, Dennis; Wirrell, Elaine; Zuberi, Sameer; Brünger, Tobias; Wojnaroski, Mary; Maru, Benit; O'Donnell, Penrose; Morton, Magda; James, Emma; Vila, Maria Candida; Huang, Norman; Gofshteyn, Jacqueline S; Rico, Salvador
558Feb-2021The severe epilepsy syndromes of infancy: A population-based study.Howell, Katherine B; Freeman, Jeremy L; Mackay, Mark T; Fahey, Michael C; Archer, John S ; Berkovic, Samuel F ; Chan, Eunice; Dabscheck, Gabriel; Eggers, Stefanie; Hayman, Michael; Holberton, James; Hunt, Rodney W; Jacobs, Susan E; Kornberg, Andrew J; Leventer, Richard J; Mandelstam, Simone; McMahon, Jacinta M; Mefford, Heather C; Panetta, Julie; Riseley, Jessica; Rodriguez-Casero, Victoria; Ryan, Monique M; Schneider, Amy L ; Smith, Lindsay J; Stark, Zornitza; Wong, Flora; Yiu, Eppie M; Scheffer, Ingrid E ; Harvey, A Simon
559Jan-2018Severe infantile onset developmental and epileptic encephalopathy caused by mutations in autophagy gene WDR45.Carvill, Gemma L; Liu, Aijie; Mandelstam, Simone; Schneider, Amy; Lacroix, Amy; Zemel, Matthew; McMahon, Jacinta M; Bello-Espinosa, Luis; Mackay, Mark; Wallace, Geoffrey; Waak, Michaela; Zhang, Jing; Yang, Xiaoling; Malone, Stephen; Zhang, Yue-Hua; Mefford, Heather C; Scheffer, Ingrid E 
5601-Jul-2001Severe myoclonic epilepsy of infancy: extended spectrum of GEFS+?Singh, R; Andermann, Eva; Whitehouse, W P; Harvey, A Simon; Keene, D L; Seni, M H; Crossland, Kathryn M; Andermann, Frederick; Berkovic, Samuel F ; Scheffer, Ingrid E