Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/19074
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dc.contributor.authorFisher, Robert S-
dc.contributor.authorCross, J Helen-
dc.contributor.authorD'Souza, Carol-
dc.contributor.authorFrench, Jacqueline A-
dc.contributor.authorHaut, Sheryl R-
dc.contributor.authorHigurashi, Norimichi-
dc.contributor.authorHirsch, Edouard-
dc.contributor.authorJansen, Floor E-
dc.contributor.authorLagae, Lieven-
dc.contributor.authorMoshé, Solomon L-
dc.contributor.authorPeltola, Jukka-
dc.contributor.authorRoulet Perez, Eliane-
dc.contributor.authorScheffer, Ingrid E-
dc.contributor.authorSchulze-Bonhage, Andreas-
dc.contributor.authorSomerville, Ernest-
dc.contributor.authorSperling, Michael-
dc.contributor.authorYacubian, Elza Márcia-
dc.contributor.authorZuberi, Sameer M-
dc.date2017-03-08-
dc.date.accessioned2018-09-13T00:14:47Z-
dc.date.available2018-09-13T00:14:47Z-
dc.date.issued2017-04-
dc.identifier.citationEpilepsia 2017; 58(4): 531-542-
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/19074-
dc.description.abstractThis companion paper to the introduction of the International League Against Epilepsy (ILAE) 2017 classification of seizure types provides guidance on how to employ the classification. Illustration of the classification is enacted by tables, a glossary of relevant terms, mapping of old to new terms, suggested abbreviations, and examples. Basic and extended versions of the classification are available, depending on the desired degree of detail. Key signs and symptoms of seizures (semiology) are used as a basis for categories of seizures that are focal or generalized from onset or with unknown onset. Any focal seizure can further be optionally characterized by whether awareness is retained or impaired. Impaired awareness during any segment of the seizure renders it a focal impaired awareness seizure. Focal seizures are further optionally characterized by motor onset signs and symptoms: atonic, automatisms, clonic, epileptic spasms, or hyperkinetic, myoclonic, or tonic activity. Nonmotor-onset seizures can manifest as autonomic, behavior arrest, cognitive, emotional, or sensory dysfunction. The earliest prominent manifestation defines the seizure type, which might then progress to other signs and symptoms. Focal seizures can become bilateral tonic-clonic. Generalized seizures engage bilateral networks from onset. Generalized motor seizure characteristics comprise atonic, clonic, epileptic spasms, myoclonic, myoclonic-atonic, myoclonic-tonic-clonic, tonic, or tonic-clonic. Nonmotor (absence) seizures are typical or atypical, or seizures that present prominent myoclonic activity or eyelid myoclonia. Seizures of unknown onset may have features that can still be classified as motor, nonmotor, tonic-clonic, epileptic spasms, or behavior arrest. This "users' manual" for the ILAE 2017 seizure classification will assist the adoption of the new system.-
dc.language.isoeng-
dc.subjectClassification-
dc.subjectEpilepsy (taxonomy)-
dc.subjectFocal-
dc.subjectGeneralized-
dc.subjectSeizures-
dc.titleInstruction manual for the ILAE 2017 operational classification of seizure types.-
dc.typeJournal Article-
dc.identifier.journaltitleEpilepsia-
dc.identifier.affiliationCollege of Medicine, Veterinary & Life Sciences, University of Glasgow, Glasgow, United Kingdomen
dc.identifier.affiliationDepartment of Pediatric Neurology, Brain Center Rudolf Magnus, University Medical Center, Utrecht, The Netherlandsen
dc.identifier.affiliationUnite Francis Rohmer, Strasbourg, Franceen
dc.identifier.affiliationDepartment of Pediatrics, Jikei University School of Medicine, Tokyo, Japanen
dc.identifier.affiliationMontefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York, New York, U.S.Aen
dc.identifier.affiliationUCL-Institute of Child Health, Great Ormond Street Hospital for Children, London, United Kingdomen
dc.identifier.affiliationBombay Epilepsy Society, Mumbai, Indiaen
dc.identifier.affiliationDepartment of Neurology, NYU Langone School of Medicine, New York, New York, U.S.Aen
dc.identifier.affiliationAustin Health, Heidelberg, Victoria, Australiaen
dc.identifier.affiliationPediatric Neurorehabilitation Unit, CHUV, LaUSAnne, Switzerlanden
dc.identifier.affiliationDepartment of Neurology, Jefferson Comprehensive Epilepsy Center, Thomas Jefferson University, Philadelphia, Pennsylvania, U.S.Aen
dc.identifier.affiliationThe Paediatric Neurosciences Research Group, Royal Hospital for Children, Glasgow, United Kingdomen
dc.identifier.affiliationPediatric Neurology, University Hospitals KU Leuven, Leuven, Belgiumen
dc.identifier.affiliationSaul R. Korey Department of Neurology, Department of Pediatrics and Dominick P. Purpura Department Neuroscience, Montefiore Medical Center, Bronx, New York, U.S.Aen
dc.identifier.affiliationDepartment of Neurology, Tampere University Hospital, Tampere, Finlanden
dc.identifier.affiliationFlorey Institute and University of Melbourne, Royal Children's Hospital, Melbourne, Victoria, Australiaen
dc.identifier.affiliationEpilepsy Center, University Medical Center Freiburg, Freiburg, Germanyen
dc.identifier.affiliationFaculty of Medicine, Prince of Wales Clinical School, University of New South Wales, Sydney, New South Wales, Australiaen
dc.identifier.affiliationDepartment of Neurology and Neurosurgery, Epilepsy Research and Treatment Unit, São Paulo, Brazilen
dc.identifier.affiliationStanford Department of Neurology & Neurological Sciences, Stanford, California, U.S.Aen
dc.identifier.doi10.1111/epi.13671-
dc.identifier.orcid0000-0002-2311-2174-
dc.identifier.pubmedid28276064-
dc.type.austinJournal Article-
dc.type.austinResearch Support, N.I.H., Extramural-
dc.type.austinResearch Support, Non-U.S. Gov't-
local.name.researcherScheffer, Ingrid E
item.cerifentitytypePublications-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.fulltextNo Fulltext-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.languageiso639-1en-
crisitem.author.deptEpilepsy Research Centre-
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