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Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/31884
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dc.contributor.authorPerucca, Piero-
dc.contributor.authorStanley, Kate-
dc.contributor.authorHarris, Natasha-
dc.contributor.authorMcIntosh, Anne M-
dc.contributor.authorAsadi-Pooya, Ali A-
dc.contributor.authorMikati, Mohamad A-
dc.contributor.authorAndrade, Danielle M-
dc.contributor.authorDugan, Patricia-
dc.contributor.authorDepondt, Chantal-
dc.contributor.authorChoi, Hyunmi-
dc.contributor.authorHeinzen, Erin L-
dc.contributor.authorCavalleri, Gianpiero L-
dc.contributor.authorBuono, Russell J-
dc.contributor.authorDevinsky, Orrin-
dc.contributor.authorSperling, Michael R-
dc.contributor.authorBerkovic, Samuel F-
dc.contributor.authorDelanty, Norman-
dc.contributor.authorGoldstein, David B-
dc.contributor.authorO'Brien, Terence J-
dc.date2022-
dc.date.accessioned2023-01-12T04:58:01Z-
dc.date.available2023-01-12T04:58:01Z-
dc.date.issued2022-12-19-
dc.identifier.citationAnnals of Neurology 2022en_US
dc.identifier.issn1531-8249-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/31884-
dc.description.abstractGenetic factors have long been debated as a cause of failure of surgery for mesial temporal lobe epilepsy (MTLE). We investigated whether rare genetic variation influences seizure outcomes of MTLE surgery.en_US
dc.language.isoeng-
dc.titleRare Genetic Variation and Outcome of Surgery for Mesial Temporal Lobe Epilepsy.en_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleAnnals of Neurologyen_US
dc.identifier.affiliationEpilepsy Research Centreen_US
dc.identifier.affiliationInstitute for Genomic Medicine, Columbia University, New York, New York, USA.en_US
dc.identifier.affiliationJefferson Comprehensive Epilepsy Center, Department of Neurology, Thomas Jefferson University, Philadelphia, Pennsylvania, USA.en_US
dc.identifier.affiliationDivision of Pediatric Neurology and Developmental Medicine, Department of Pediatrics, Duke University, Durham, North Carolina, USA.en_US
dc.identifier.affiliationDivision of Neurology, University of Toronto, Toronto, Ontario, Canada.en_US
dc.identifier.affiliationDepartment of Neurology, New York University Langone Medical Center, New York, New York, USA.en_US
dc.identifier.affiliationDepartment of Neurology, Hôpital Universitaire de Bruxelles, Hôpital Erasme, Université Libre de Bruxelles, Brussels, Belgium.en_US
dc.identifier.affiliationDepartment of Neurology, Columbia University, New York, New York, USA.en_US
dc.identifier.affiliationDivision of Pharmacotherapy and Experimental Therapeutics, Eshelman School of Pharmacy, University of North Carolina, Chapel Hill, North Carolina, USA.en_US
dc.identifier.affiliationFutureNeuro Research Centre, Royal College of Surgeons in Ireland, Dublin, Ireland.en_US
dc.identifier.affiliationDepartment of Biomedical Science, Cooper Medical School of Rowan University, Camden, New Jersey, USA.en_US
dc.identifier.affiliationFutureNeuro Research Centre, Royal College of Surgeons in Ireland, Dublin, Ireland.en_US
dc.identifier.affiliationInstitute for Genomic Medicine, Columbia University, New York, New York, USA.en_US
dc.identifier.affiliationDepartment of Neuroscience, Central Clinical School, Monash University, Melbourne, Victoria, Australia.en_US
dc.identifier.doi10.1002/ana.26581en_US
dc.type.contentTexten_US
dc.identifier.orcid0000-0002-7855-7066en_US
dc.identifier.orcid0000-0002-2598-7601en_US
dc.identifier.orcid0000-0003-0044-4632en_US
dc.identifier.orcid0000-0003-4580-841Xen_US
dc.identifier.pubmedid36534060-
local.name.researcherBerkovic, Samuel F
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptNeurology-
crisitem.author.deptComprehensive Epilepsy Program-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptEpilepsy Research Centre-
crisitem.author.deptNeurology-
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