{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,14]],"date-time":"2026-09-14T10:49:42Z","timestamp":1789382982039,"version":"build-2803163510"},"reference-count":24,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2016,11,1]],"date-time":"2016-11-01T00:00:00Z","timestamp":1477958400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["epilepsybehavior.com","clinicalkey.jp","clinicalkey.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Epilepsy &amp; Behavior"],"published-print":{"date-parts":[[2016,11]]},"DOI":"10.1016\/j.yebeh.2016.08.023","type":"journal-article","created":{"date-parts":[[2016,10,19]],"date-time":"2016-10-19T19:01:51Z","timestamp":1476903711000},"page":"242-247","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":21,"special_numbering":"PA","title":["Epilepsy with myoclonic absences: Electroclinical characteristics in a distinctive pediatric epilepsy phenotype"],"prefix":"10.1016","volume":"64","author":[{"given":"Paresh","family":"Zanzmera","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ramshekhar N.","family":"Menon","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kalyani","family":"Karkare","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Himanshu","family":"Soni","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sujit","family":"Jagtap","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ashalatha","family":"Radhakrishnan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.yebeh.2016.08.023_bb0005","first-page":"379","article-title":"Etude des de'charges de pointes ondes chez l'homme. II: Les aspects cliniquesee'lectroence'phalographiques des absences myocloniques","volume":"121","author":"Tassinari","year":"1969","journal-title":"Rev Neurol"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0010","doi-asserted-by":"crossref","first-page":"389","DOI":"10.1111\/j.1528-1157.1989.tb05316.x","article-title":"Proposal for revised classification of epilepsies and epileptic syndromes","volume":"30","author":"Commission on Classification and Terminology of the International League Against Epilepsy","year":"1989","journal-title":"Epilepsia"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0015","series-title":"Epileptic syndromes in infancy, childhood and adolescence","first-page":"151","article-title":"Epilepsy with myoclonic absences","author":"Tassinari","year":"1992"},{"issue":"Suppl. 3","key":"10.1016\/j.yebeh.2016.08.023_bb0020","first-page":"S42","article-title":"The absence epilepsies","volume":"34","author":"Porter","year":"1993","journal-title":"Epilepsia"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0025","doi-asserted-by":"crossref","first-page":"288","DOI":"10.1136\/adc.70.4.288","article-title":"Epilepsy with myoclonic absences","volume":"70","author":"Manonmani","year":"1994","journal-title":"Arch Dis Child"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0030","first-page":"81","article-title":"Myoclonic absences in the first three years of lBioflel","volume":"91\u201392","author":"Fontana","year":"1995","journal-title":"Lega It Epil"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0035","doi-asserted-by":"crossref","first-page":"746","DOI":"10.1177\/088307389901401112","article-title":"Epilepsy with myoclonic absences with early onset: a follow-up study","volume":"14","author":"Verrotti","year":"1999","journal-title":"J Child Neurol"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0040","unstructured":"Malin Rev Fr Dr. A.J. Vineland Social Maturity Scale and Manual. Indian Adaption. Ed. Bharata J. Mysore, Swayam Sidha Prakashan, 1992."},{"key":"10.1016\/j.yebeh.2016.08.023_bb0045","doi-asserted-by":"crossref","DOI":"10.1212\/WNL.0b013e31821e54c9","article-title":"Teaching video neuroimages: epilepsy with myoclonic absences: a distinct electroclinical syndrome","volume":"76","author":"Menon","year":"2011","journal-title":"Neurology"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0050","series-title":"Evolution and prognosis of epilepsy","first-page":"2","article-title":"Evolution and prognosis of primary generalized epilepsies of the petit mal absence type","author":"Lugaresi","year":"1973"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0055","first-page":"242","article-title":"Epilepsy with myoclonic absences","volume":"5","author":"Salas Puig","year":"1990","journal-title":"Neurologia"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0060","doi-asserted-by":"crossref","first-page":"660","DOI":"10.1111\/j.1528-1157.1998.tb01435.x","article-title":"Myoclonus absence-like seizures and chromosome abnormality syndromes","volume":"39","author":"Elia","year":"1998","journal-title":"Epilepsia"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0065","doi-asserted-by":"crossref","first-page":"57","DOI":"10.1684\/j.1950-6945.2001.tb00471.x","article-title":"A clinical spectrum of the myoclonic manifestations associated with typical absences in childhood absence epilepsy: a video-polygraphic study","volume":"3","author":"Capovilla","year":"2001","journal-title":"Epileptic Disord"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0070","doi-asserted-by":"crossref","first-page":"178","DOI":"10.1016\/j.braindev.2004.01.008","article-title":"Epilepsy with myoclonic absences","volume":"27","author":"Bureau","year":"2005","journal-title":"Brain Dev"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0075","doi-asserted-by":"crossref","first-page":"757","DOI":"10.1016\/j.ncl.2009.04.002","article-title":"Pathophysiology and treatment of myoclonus","volume":"27","author":"Caviness","year":"2009","journal-title":"Neurol Clin"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0080","series-title":"Epileptic syndromes in infancy, childhood and adolescence","first-page":"305","article-title":"The syndrome of myoclonic absences","author":"Bureau","year":"2002"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0085","series-title":"Typical absences and related epileptic syndromes","first-page":"187","article-title":"Myoclonic absence epilepsy","author":"Tassinari","year":"1995"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0090","doi-asserted-by":"crossref","first-page":"180","DOI":"10.1136\/adc.71.2.180","article-title":"Epilepsy with myoclonic absences","volume":"71","author":"Appleton","year":"1994","journal-title":"Arch Dis Child"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0095","doi-asserted-by":"crossref","first-page":"369","DOI":"10.1111\/j.1469-8749.1992.tb11445.x","article-title":"Lamotrigine for intractable childhood epilepsy: a preliminary communication","volume":"34","author":"Gibbs","year":"1992","journal-title":"Dev Med Child Neurol"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0100","series-title":"The treatment of epilepsy: principles and practice","first-page":"624","article-title":"Less common epileptic syndromes","author":"Roger","year":"1993"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0105","series-title":"The treatment of epilepsy","first-page":"247","article-title":"Treatment of epilepsies with myoclonia","author":"Genton","year":"1996"},{"key":"10.1016\/j.yebeh.2016.08.023_bb0110","doi-asserted-by":"crossref","first-page":"147","DOI":"10.1016\/S0920-1211(97)00080-6","article-title":"Myoclonus and epilepsy in childhood: a review of treatment with valproate, ethosuximide, lamotrigine and zonisamide","volume":"29","author":"Wallace","year":"1998","journal-title":"Epilepsy Res"},{"issue":"Suppl. 1","key":"10.1016\/j.yebeh.2016.08.023_bb0115","first-page":"S95","article-title":"Add-on lamotrigine in pediatric patients with treatment-resistant epilepsy","volume":"32","author":"Dulac","year":"1991","journal-title":"Epilepsia"},{"issue":"Suppl. 3","key":"10.1016\/j.yebeh.2016.08.023_bb0120","first-page":"S82","article-title":"Lamotrigine (Lamictal) as add-on therapy in pediatric patients with treatment-resistant epilepsy: an overview","volume":"33","author":"Yuen","year":"1992","journal-title":"Epilepsia"}],"container-title":["Epilepsy &amp; Behavior"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1525505016301925?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1525505016301925?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2024,6,20]],"date-time":"2024-06-20T01:50:26Z","timestamp":1718848226000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1525505016301925"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2016,11]]},"references-count":24,"alternative-id":["S1525505016301925"],"URL":"https:\/\/doi.org\/10.1016\/j.yebeh.2016.08.023","relation":{},"ISSN":["1525-5050"],"issn-type":[{"value":"1525-5050","type":"print"}],"subject":[],"published":{"date-parts":[[2016,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Epilepsy with myoclonic absences: Electroclinical characteristics in a distinctive pediatric epilepsy phenotype","name":"articletitle","label":"Article Title"},{"value":"Epilepsy & Behavior","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.yebeh.2016.08.023","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2016 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}