{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,7,17]],"date-time":"2026-07-17T10:01:18Z","timestamp":1784282478225,"version":"3.55.0"},"reference-count":16,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2019,3,1]],"date-time":"2019-03-01T00:00:00Z","timestamp":1551398400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"funder":[{"DOI":"10.13039\/100008914","name":"Ontario Brain Institute","doi-asserted-by":"publisher","id":[{"id":"10.13039\/100008914","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["epilepsybehavior.com","clinicalkey.jp","clinicalkey.com","clinicalkey.es","clinicalkey.fr","clinicalkey.com.au","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Epilepsy &amp; Behavior"],"published-print":{"date-parts":[[2019,3]]},"DOI":"10.1016\/j.yebeh.2018.12.018","type":"journal-article","created":{"date-parts":[[2019,1,14]],"date-time":"2019-01-14T23:52:44Z","timestamp":1547509964000},"page":"121-124","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":22,"special_numbering":"C","title":["STXBP1 encephalopathy is associated with awake bruxism"],"prefix":"10.1016","volume":"92","author":[{"given":"Arezoo","family":"Rezazadeh","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Mohammed","family":"Uddin","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"suffix":"III","given":"O. Carter","family":"Snead","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Victor","family":"Lira","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0003-3954-7284","authenticated-orcid":false,"given":"Alexandra","family":"Silberberg","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shelly","family":"Weiss","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Elizabeth J.","family":"Donner","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Maria","family":"Zak","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Laura","family":"Bradbury","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Stephen W.","family":"Scherer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Alfonso","family":"Fasano","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Danielle M.","family":"Andrade","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.yebeh.2018.12.018_bb0005","doi-asserted-by":"crossref","first-page":"782","DOI":"10.1038\/ng.150","article-title":"De novo mutations in the gene encoding STXBP1 (MUNC18-1) cause early infantile epileptic encephalopathy","volume":"40","author":"Saitsu","year":"2008","journal-title":"Nat Genet"},{"key":"10.1016\/j.yebeh.2018.12.018_bb0010","doi-asserted-by":"crossref","first-page":"748","DOI":"10.1002\/ana.21625","article-title":"De novo STXBP1 mutations in mental retardation and nonsyndromic epilepsy","volume":"65","author":"Hamdan","year":"2009","journal-title":"Ann Neurol"},{"key":"10.1016\/j.yebeh.2018.12.018_bb0015","doi-asserted-by":"crossref","first-page":"607","DOI":"10.1038\/ejhg.2010.183","article-title":"Intellectual disability without epilepsy associated with STX BP1 disruption","volume":"19","author":"Hamdan","year":"2011","journal-title":"Eur J Hum Genet"},{"issue":"10","key":"10.1016\/j.yebeh.2018.12.018_bb0020","doi-asserted-by":"crossref","first-page":"954","DOI":"10.1212\/WNL.0000000000002457","article-title":"STXBP1 encephalopathy: a neurodevelopmental disorder including epilepsy","volume":"86","author":"Stamberger","year":"2016","journal-title":"Neurology"},{"key":"10.1016\/j.yebeh.2018.12.018_bb0025","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1007\/s10048-014-0431-z","article-title":"A novel de novo STXBP1 mutation is associated with mitochondrial complex I deficiency and late-onset juvenile-onset parkinsonism","volume":"16","author":"Keogh","year":"2015","journal-title":"Neurogenetics"},{"issue":"7","key":"10.1016\/j.yebeh.2018.12.018_bb0030","doi-asserted-by":"crossref","first-page":"599","DOI":"10.1111\/jopr.12479","article-title":"Bruxism in movement disorders: a comprehensive review","volume":"26","author":"Ella","year":"2017","journal-title":"J Prosthodont"},{"issue":"10","key":"10.1016\/j.yebeh.2018.12.018_bb0035","doi-asserted-by":"crossref","first-page":"1384","DOI":"10.1002\/mds.22115","article-title":"Movement disorders in Rett syndrome: an analysis of 60 patients with detected MECP2 mutation and correlation with mutation type","volume":"23","author":"Temudo","year":"2008","journal-title":"Mov Disord"},{"key":"10.1016\/j.yebeh.2018.12.018_bb0040","doi-asserted-by":"crossref","first-page":"1753","DOI":"10.1212\/WNL.41.11.1753","article-title":"Altered neurochemical markers in Rett's syndrome","volume":"41","author":"Wenk","year":"1991","journal-title":"Neurology"},{"issue":"3","key":"10.1016\/j.yebeh.2018.12.018_bb0045","doi-asserted-by":"crossref","first-page":"e44","DOI":"10.1111\/epi.13692","article-title":"Adult motor phenotype differentiates Dravet syndrome from Lennox\u2013Gastaut syndrome and links SCN1A to early onset parkinsonian features","volume":"58","author":"Aljaafari","year":"2017","journal-title":"Epilepsia"},{"key":"10.1016\/j.yebeh.2018.12.018_bb0050","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1006\/geno.1997.5202","article-title":"Identification and characterization of the human ortholog of rat STXBP1, a protein implicated in vesicle trafficking and neurotransmitter release","volume":"48","author":"Swanson","year":"1998","journal-title":"Genomics"},{"key":"10.1016\/j.yebeh.2018.12.018_bb0055","doi-asserted-by":"crossref","first-page":"251","DOI":"10.1016\/S0168-0102(02)00041-X","article-title":"Alteration of methamphetamine-induced striatal dopamine release in mint-1 knockout mice","volume":"43","author":"Mori","year":"2002","journal-title":"Neurosci Res"},{"issue":"1","key":"10.1016\/j.yebeh.2018.12.018_bb0060","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1007\/s00784-017-2117-z","article-title":"Single nucleotide polymorphisms in genes of dopaminergic pathways are associated with bruxism","volume":"22","author":"Oporto","year":"2018","journal-title":"Clin Oral Investig"},{"key":"10.1016\/j.yebeh.2018.12.018_bb0065","doi-asserted-by":"crossref","first-page":"73","DOI":"10.1002\/mds.870120113","article-title":"The effect of catecholamine precursor l-dopa on sleep bruxism: a controlled clinical trial","volume":"12","author":"Lobbezoo","year":"1997","journal-title":"Mov Disord"},{"key":"10.1016\/j.yebeh.2018.12.018_bb0070","doi-asserted-by":"crossref","first-page":"1610","DOI":"10.1177\/00220345970760091401","article-title":"Effects of the D2 receptor agonist bromocriptine on sleep bruxism: report of two single-patient clinical trials","volume":"76","author":"Lobbezoo","year":"1997","journal-title":"J Dent Res"},{"key":"10.1016\/j.yebeh.2018.12.018_bb0075","doi-asserted-by":"crossref","first-page":"315","DOI":"10.1097\/00002826-199308000-00003","article-title":"Bruxism secondary to chronic antidopaminergic drug exposure","volume":"16","author":"Micheli","year":"1993","journal-title":"Clin Neuropharmacol"},{"issue":"2","key":"10.1016\/j.yebeh.2018.12.018_bb0080","doi-asserted-by":"crossref","first-page":"10","DOI":"10.1007\/s11940-016-0396-3","article-title":"Current treatments of bruxism","volume":"18","author":"Guaita","year":"2016","journal-title":"Curr Treat Options Neurol"}],"container-title":["Epilepsy &amp; Behavior"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1525505018309582?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1525505018309582?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,8,7]],"date-time":"2019-08-07T21:45:25Z","timestamp":1565214325000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1525505018309582"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2019,3]]},"references-count":16,"alternative-id":["S1525505018309582"],"URL":"https:\/\/doi.org\/10.1016\/j.yebeh.2018.12.018","relation":{},"ISSN":["1525-5050"],"issn-type":[{"value":"1525-5050","type":"print"}],"subject":[],"published":{"date-parts":[[2019,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"STXBP1 encephalopathy is associated with awake bruxism","name":"articletitle","label":"Article Title"},{"value":"Epilepsy & Behavior","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.yebeh.2018.12.018","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2018 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}