{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,20]],"date-time":"2026-09-20T00:45:46Z","timestamp":1789865146962,"version":"4.0.1"},"reference-count":11,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2019,1,1]],"date-time":"2019-01-01T00:00:00Z","timestamp":1546300800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2019,1,1]],"date-time":"2019-01-01T00:00:00Z","timestamp":1546300800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2019,7,3]],"date-time":"2019-07-03T00:00:00Z","timestamp":1562112000000},"content-version":"vor","delay-in-days":183,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0\/"}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Epilepsy &amp; Behavior Reports"],"published-print":{"date-parts":[[2019]]},"DOI":"10.1016\/j.ebr.2019.100329","type":"journal-article","created":{"date-parts":[[2019,7,22]],"date-time":"2019-07-22T11:30:56Z","timestamp":1563795056000},"page":"100329","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":2,"special_numbering":"C","title":["Adolescent-onset absence epilepsy years after resolution of childhood epilepsy with myoclonic-atonic seizures"],"prefix":"10.1016","volume":"12","author":[{"given":"Sarah H.","family":"Berth","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Eric H.","family":"Kossoff","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.ebr.2019.100329_bb0005","doi-asserted-by":"crossref","first-page":"1303","DOI":"10.1111\/j.1528-1167.2012.03581.x","article-title":"Dissecting the genetic basis of myoclonic-astatic epilepsy","volume":"53","author":"Tang","year":"2012","journal-title":"Epilepsia"},{"key":"10.1016\/j.ebr.2019.100329_bb0010","doi-asserted-by":"crossref","first-page":"14","DOI":"10.1016\/j.eplepsyres.2018.04.010","article-title":"How do we diagnose and treat epilepsy with myoclonic-atonic seizures (Doose syndrome)? Results of the pediatric epilepsy research consortium survey","volume":"144","author":"Nickels","year":"2018","journal-title":"Epilepsy Res"},{"key":"10.1016\/j.ebr.2019.100329_bb0015","doi-asserted-by":"crossref","first-page":"988","DOI":"10.1111\/j.1469-8749.2010.03744.x","article-title":"Doose syndrome (myoclonic-astatic epilepsy): 40 years of progress","volume":"52","author":"Kelley","year":"2010","journal-title":"Dev Med Child Neurol"},{"key":"10.1016\/j.ebr.2019.100329_bb0020","doi-asserted-by":"crossref","first-page":"15","DOI":"10.1016\/S0920-1211(99)00021-2","article-title":"Delineation of cryptogenic Lennox-Gastaut syndrome and myoclonic astatic epilepsy using multiple correspondence analysis","volume":"36","author":"Kaminska","year":"1999","journal-title":"Epilepsy Res"},{"key":"10.1016\/j.ebr.2019.100329_bb0025","doi-asserted-by":"crossref","first-page":"122","DOI":"10.1055\/s-2002-33675","article-title":"Treatment and long-term prognosis of myoclonic-astatic epilepsy of early childhood","volume":"33","author":"Oguni","year":"2002","journal-title":"Neuropediatrics."},{"key":"10.1016\/j.ebr.2019.100329_bb0030","doi-asserted-by":"crossref","first-page":"2048","DOI":"10.1111\/epi.13916","article-title":"Intractable seizures after a lengthy remission in childhood-onset epilepsy","volume":"58","author":"Camfield","year":"2017","journal-title":"Epilepsia."},{"key":"10.1016\/j.ebr.2019.100329_bb0035","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1017\/cjn.2018.364","article-title":"Co-existence of Rolandic and 3 Hz spike-wave discharges on EEG in children with epilepsy","volume":"46","author":"Datta","year":"2019","journal-title":"Can J Neurol Sci"},{"key":"10.1016\/j.ebr.2019.100329_bb0040","doi-asserted-by":"crossref","first-page":"428","DOI":"10.1016\/j.pediatrneurol.2009.07.004","article-title":"Childhood absence epilepsy in patients with benign focal epileptiform discharges","volume":"41","author":"Sarkis","year":"2009","journal-title":"Pediatr Neurol"},{"key":"10.1016\/j.ebr.2019.100329_bb0045","doi-asserted-by":"crossref","first-page":"212","DOI":"10.1016\/0387-7604(95)00133-6","article-title":"Sequential occurrence of benign partial epilepsy and childhood absence epilepsy in three patients","volume":"18","author":"Gambardella","year":"1996","journal-title":"Brain Dev"},{"key":"10.1016\/j.ebr.2019.100329_bb0050","doi-asserted-by":"crossref","first-page":"838","DOI":"10.1177\/08830738020170111601","article-title":"Coincidence of Rolandic and absence features: rare, but not impossible","volume":"17","author":"Dimova","year":"2002","journal-title":"J Child Neurol"},{"issue":"Suppl. 2","key":"10.1016\/j.ebr.2019.100329_bb0055","doi-asserted-by":"crossref","first-page":"53","DOI":"10.1111\/j.1528-1167.2006.00690.x","article-title":"The natural history of myoclonic astatic epilepsy (Doose syndrome) and Lennox Gastaut syndrome","volume":"47","author":"Stephani","year":"2006","journal-title":"Epilepsia."}],"container-title":["Epilepsy &amp; Behavior Reports"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S258998641930084X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S258998641930084X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,11,12]],"date-time":"2025-11-12T00:06:59Z","timestamp":1762906019000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S258998641930084X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019]]},"references-count":11,"alternative-id":["S258998641930084X"],"URL":"https:\/\/doi.org\/10.1016\/j.ebr.2019.100329","relation":{},"ISSN":["2589-9864"],"issn-type":[{"value":"2589-9864","type":"print"}],"subject":[],"published":{"date-parts":[[2019]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Adolescent-onset absence epilepsy years after resolution of childhood epilepsy with myoclonic-atonic seizures","name":"articletitle","label":"Article Title"},{"value":"Epilepsy & Behavior Reports","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ebr.2019.100329","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2019 The Authors. Published by Elsevier Inc.","name":"copyright","label":"Copyright"}],"article-number":"100329"}}