{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,11,12]],"date-time":"2025-11-12T20:18:06Z","timestamp":1762978686107,"version":"build-2065373602"},"reference-count":15,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2020,5,1]],"date-time":"2020-05-01T00:00:00Z","timestamp":1588291200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,5,1]],"date-time":"2020-05-01T00:00:00Z","timestamp":1588291200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"},{"start":{"date-parts":[[2021,5,1]],"date-time":"2021-05-01T00:00:00Z","timestamp":1619827200000},"content-version":"vor","delay-in-days":365,"URL":"http:\/\/www.elsevier.com\/open-access\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","seizure-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Seizure"],"published-print":{"date-parts":[[2020,5]]},"DOI":"10.1016\/j.seizure.2020.03.005","type":"journal-article","created":{"date-parts":[[2020,3,16]],"date-time":"2020-03-16T16:19:35Z","timestamp":1584375575000},"page":"49-52","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":6,"special_numbering":"C","title":["Vaccination management in an asymptomatic child with a novel SCN1A variant and family history of status epilepticus following vaccination: A case report on a potential new direction in personalised medicine"],"prefix":"10.1016","volume":"78","author":[{"given":"Lucy","family":"Deng","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alan","family":"Ma","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Nicholas","family":"Wood","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Simone","family":"Ardern-Holmes","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"7","key":"10.1016\/j.seizure.2020.03.005_bib0005","doi-asserted-by":"crossref","first-page":"594","DOI":"10.1212\/WNL.0b013e31820c309b","article-title":"Genotype-phenotype associations in SCN1A-related epilepsies","volume":"76","author":"Zuberi","year":"2011","journal-title":"Neurology"},{"issue":"6","key":"10.1016\/j.seizure.2020.03.005_bib0010","doi-asserted-by":"crossref","first-page":"1327","DOI":"10.1086\/320609","article-title":"De novo mutations in the sodium-channel gene SCN1A cause severe myoclonic epilepsy of infancy","volume":"68","author":"Claes","year":"2001","journal-title":"Am J Hum Genet"},{"issue":"12","key":"10.1016\/j.seizure.2020.03.005_bib0015","doi-asserted-by":"crossref","first-page":"1210","DOI":"10.1212\/WNL.0000000000004384","article-title":"Genetic epilepsy with febrile seizures plus: refining the spectrum","volume":"89","author":"Zhang","year":"2017","journal-title":"Neurology"},{"issue":"6","key":"10.1016\/j.seizure.2020.03.005_bib0020","doi-asserted-by":"crossref","first-page":"592","DOI":"10.1016\/S1474-4422(10)70107-1","article-title":"Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study","volume":"9","author":"McIntosh","year":"2010","journal-title":"Lancet Neurol"},{"issue":"5","key":"10.1016\/j.seizure.2020.03.005_bib0025","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1038\/gim.2015.30","article-title":"Standards and guidelines for the interpretation of sequence variants: a joint consensus recommendation of the American College of Medical Genetics and Genomics and the Association for Molecular Pathology","volume":"17","author":"Richards","year":"2015","journal-title":"Genet Med"},{"issue":"1","key":"10.1016\/j.seizure.2020.03.005_bib0030","doi-asserted-by":"crossref","first-page":"e5","DOI":"10.1212\/NXG.0000000000000005","article-title":"Epilepsy with auditory features: a heterogeneous clinico-molecular disease","volume":"1","author":"Pippucci","year":"2015","journal-title":"Neurol Genet"},{"key":"10.1016\/j.seizure.2020.03.005_bib0035","doi-asserted-by":"crossref","first-page":"100","DOI":"10.1016\/j.nbd.2014.12.028","article-title":"Rescuable folding defective NaV1.1 (SCN1A) mutants in epilepsy: properties, occurrence, and novel rescuing strategy with peptides targeted to the endoplasmic reticulum","volume":"75","author":"Bechi","year":"2015","journal-title":"Neurobiol Dis"},{"issue":"7616","key":"10.1016\/j.seizure.2020.03.005_bib0040","doi-asserted-by":"crossref","first-page":"285","DOI":"10.1038\/nature19057","article-title":"Analysis of protein-coding genetic variation in 60,706 humans","volume":"536","author":"Lek","year":"2016","journal-title":"Nature"},{"key":"10.1016\/j.seizure.2020.03.005_bib0045","doi-asserted-by":"crossref","first-page":"43","DOI":"10.1016\/j.eplepsyres.2016.10.006","article-title":"Mortality in dravet syndrome","volume":"128","author":"Cooper","year":"2016","journal-title":"Epilepsy Res"},{"issue":"7","key":"10.1016\/j.seizure.2020.03.005_bib0050","doi-asserted-by":"crossref","first-page":"301","DOI":"10.1007\/s11940-014-0301-x","article-title":"Management of pediatric status epilepticus","volume":"16","author":"Abend","year":"2014","journal-title":"Curr Treat Options Neurol"},{"issue":"2","key":"10.1016\/j.seizure.2020.03.005_bib0055","doi-asserted-by":"crossref","first-page":"236","DOI":"10.1086\/318454","article-title":"Neurological manifestations of enterovirus 71 infection in children during an outbreak of hand, foot, and mouth disease in Western Australia","volume":"32","author":"McMinn","year":"2001","journal-title":"Clin Infect Dis"},{"issue":"11","key":"10.1016\/j.seizure.2020.03.005_bib0060","doi-asserted-by":"crossref","first-page":"1097","DOI":"10.1016\/S1474-4422(10)70209-X","article-title":"Clinical features, diagnosis, and management of enterovirus 71","volume":"9","author":"Ooi","year":"2010","journal-title":"Lancet Neurol"},{"key":"10.1016\/j.seizure.2020.03.005_bib0065","doi-asserted-by":"crossref","first-page":"18","DOI":"10.1016\/j.pediatrneurol.2017.01.025","article-title":"Optimizing the diagnosis and management of dravet syndrome: recommendations from a North American consensus panel","volume":"68","author":"Wirrell","year":"2017","journal-title":"Pediatr Neurol"},{"key":"10.1016\/j.seizure.2020.03.005_bib0070","doi-asserted-by":"crossref","first-page":"19","DOI":"10.1055\/s-0035-1557232","article-title":"Intermittent clobazam in febrile seizures: an Indian experience","volume":"3","author":"Bajaj","year":"2005","journal-title":"J Pediatr Neurol"},{"issue":"Suppl 7","key":"10.1016\/j.seizure.2020.03.005_bib0075","doi-asserted-by":"crossref","first-page":"13","DOI":"10.1111\/epi.12306","article-title":"Epilepsy and vaccinations: Italian guidelines","volume":"54","author":"Pruna","year":"2013","journal-title":"Epilepsia"}],"container-title":["Seizure"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1059131120300716?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1059131120300716?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,21]],"date-time":"2025-10-21T01:54:37Z","timestamp":1761011677000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1059131120300716"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,5]]},"references-count":15,"alternative-id":["S1059131120300716"],"URL":"https:\/\/doi.org\/10.1016\/j.seizure.2020.03.005","relation":{},"ISSN":["1059-1311"],"issn-type":[{"type":"print","value":"1059-1311"}],"subject":[],"published":{"date-parts":[[2020,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Vaccination management in an asymptomatic child with a novel SCN1A variant and family history of status epilepticus following vaccination: A case report on a potential new direction in personalised medicine","name":"articletitle","label":"Article Title"},{"value":"Seizure","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.seizure.2020.03.005","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Crown Copyright \u00a9 2020 Published by Elsevier Ltd on behalf of British Epilepsy Association.","name":"copyright","label":"Copyright"}]}}