{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T16:51:16Z","timestamp":1786985476441,"version":"build-2736575974"},"reference-count":27,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2017,3,1]],"date-time":"2017-03-01T00:00:00Z","timestamp":1488326400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","brainanddevelopment.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Brain and Development"],"published-print":{"date-parts":[[2017,3]]},"DOI":"10.1016\/j.braindev.2016.09.014","type":"journal-article","created":{"date-parts":[[2016,10,22]],"date-time":"2016-10-22T08:17:08Z","timestamp":1477124228000},"page":"243-247","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":20,"title":["\u201cSymptomatic\u201d infection-associated acute encephalopathy in children with underlying neurological disorders"],"prefix":"10.1016","volume":"39","author":[{"given":"Yoshimichi","family":"Hirayama","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshiaki","family":"Saito","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yoshihiro","family":"Maegaki","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.braindev.2016.09.014_b0005","doi-asserted-by":"crossref","first-page":"337","DOI":"10.1016\/j.braindev.2011.07.012","article-title":"Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes","volume":"34","author":"Hoshino","year":"2012","journal-title":"Brain Dev"},{"key":"10.1016\/j.braindev.2016.09.014_b0010","doi-asserted-by":"crossref","first-page":"45","DOI":"10.1111\/j.1600-0404.2007.00809.x","article-title":"Acute encephalopathy associated with influenza and other viral infections","volume":"186","author":"Mizuguchi","year":"2007","journal-title":"Acta Neurol Scand Suppl"},{"key":"10.1016\/j.braindev.2016.09.014_b0015","doi-asserted-by":"crossref","first-page":"132","DOI":"10.3174\/ajnr.A1247","article-title":"Excitotoxicity in acute encephalopathy with biphasic seizures and late reduced diffusion","volume":"30","author":"Takanashi","year":"2009","journal-title":"AJNR Am J Neuroradiol"},{"key":"10.1016\/j.braindev.2016.09.014_b0020","doi-asserted-by":"crossref","first-page":"1163","DOI":"10.1007\/s00234-015-1573-x","article-title":"Disrupted glutamate-glutamine cycle in acute encephalopathy with biphasic seizures and late reduced diffusion","volume":"57","author":"Takanashi","year":"2015","journal-title":"Neuroradiology"},{"key":"10.1016\/j.braindev.2016.09.014_b0025","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1016\/j.ejpn.2015.01.011","article-title":"Mild encephalopathy with reversible splenial lesion: an important differential of encephalitis","volume":"19","author":"Ka","year":"2015","journal-title":"Eur J Paediatr Neurol"},{"key":"10.1016\/j.braindev.2016.09.014_b0030","doi-asserted-by":"crossref","first-page":"512","DOI":"10.1016\/j.braindev.2010.09.002","article-title":"Carnitine palmitoyl transferase II polymorphism is associated with multiple syndromes of acute encephalopathy with various infectious diseases","volume":"33","author":"Shinohara","year":"2011","journal-title":"Brain Dev"},{"key":"10.1016\/j.braindev.2016.09.014_b0035","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.eplepsyres.2015.08.001","article-title":"Missense mutations in sodium channel SCN1A and SCN2A predispose children to encephalopathy with severe febrile seizures","volume":"117","author":"Saitoh","year":"2015","journal-title":"Epilepsy Res"},{"key":"10.1016\/j.braindev.2016.09.014_b0040","doi-asserted-by":"crossref","first-page":"2158","DOI":"10.1111\/j.1528-1167.2009.02175.x","article-title":"Hemiconvulsion-hemiplegia syndrome in a patient with severe myoclonic epilepsy in infancy","volume":"50","author":"Sakakibara","year":"2009","journal-title":"Epilepsia"},{"key":"10.1016\/j.braindev.2016.09.014_b0045","doi-asserted-by":"crossref","first-page":"1571","DOI":"10.1212\/WNL.0b013e31828f18d8","article-title":"ADORA2A polymorphism predisposes children to encephalopathy with febrile status epilepticus","volume":"80","author":"Shinohara","year":"2013","journal-title":"Neurology"},{"key":"10.1016\/j.braindev.2016.09.014_b0050","doi-asserted-by":"crossref","first-page":"830","DOI":"10.1017\/S0012162205001751","article-title":"Atypical case of hemiconvulsions-hemiplegia-epilepsy syndrome revealing contralateral focal cortical dysplasia","volume":"47","author":"Bahi-Buisson","year":"2005","journal-title":"Dev Med Child Neurol"},{"key":"10.1016\/j.braindev.2016.09.014_b0055","doi-asserted-by":"crossref","first-page":"186","DOI":"10.1002\/ajmg.a.36198","article-title":"Hemiconvulsion-hemiplegia-epilepsy syndrome with 1q44 microdeletion: causal or chance association","volume":"164A","author":"Gupta","year":"2014","journal-title":"Am J Med Genet A"},{"key":"10.1016\/j.braindev.2016.09.014_b0060","doi-asserted-by":"crossref","first-page":"472","DOI":"10.1016\/j.braindev.2009.09.012","article-title":"Clustered subclinical seizures in a patient with acute encephalopathy with biphasic seizures and late reduced diffusion","volume":"32","author":"Komatsu","year":"2010","journal-title":"Brain Dev"},{"key":"10.1016\/j.braindev.2016.09.014_b0065","doi-asserted-by":"crossref","first-page":"1886","DOI":"10.1111\/j.1528-1167.2010.02600.x","article-title":"Acute encephalopathy with a truncation mutation in the SCN1A gene: a case report","volume":"51","author":"Takayanagi","year":"2010","journal-title":"Epilepsia"},{"key":"10.1016\/j.braindev.2016.09.014_b0070","doi-asserted-by":"crossref","first-page":"558","DOI":"10.1111\/j.1528-1167.2011.03402.x","article-title":"Mutations of the SCN1A gene in acute encephalopathy","volume":"53","author":"Saitoh","year":"2012","journal-title":"Epilepsia"},{"issue":"221\u20137","key":"10.1016\/j.braindev.2016.09.014_b0075","first-page":"e2","article-title":"Serial MRI and neurodevelopmental outcome in 9- to 10-year-old children with neonatal encephalopathy","volume":"157","author":"van Kooij","year":"2010","journal-title":"J Pediatr"},{"key":"10.1016\/j.braindev.2016.09.014_b0080","doi-asserted-by":"crossref","first-page":"64","DOI":"10.1016\/j.braindev.2008.04.001","article-title":"Development of epilepsy in newborns with moderate hypoxic-ischemic encephalopathy and neonatal seizures","volume":"31","author":"Pisani","year":"2009","journal-title":"Brain Dev"},{"key":"10.1016\/j.braindev.2016.09.014_b0085","doi-asserted-by":"crossref","first-page":"e102","DOI":"10.1111\/j.1528-1167.2012.03418.x","article-title":"Seizures and epilepsy in Sotos syndrome: analysis of 19 Caucasian patients with long-term follow-up","volume":"53","author":"Nicita","year":"2012","journal-title":"Epilepsia"},{"key":"10.1016\/j.braindev.2016.09.014_b0090","doi-asserted-by":"crossref","first-page":"495","DOI":"10.1017\/S0012162206001058","article-title":"Tuberous sclerosis complex: clinical features, diagnosis, and prevalence within Northern Ireland","volume":"48","author":"Devlin","year":"2006","journal-title":"Dev Med Child Neurol"},{"key":"10.1016\/j.braindev.2016.09.014_b0095","doi-asserted-by":"crossref","first-page":"420","DOI":"10.1016\/j.braindev.2007.12.004","article-title":"Epilepsy in patients with congenital cytomegalovirus infection","volume":"30","author":"Suzuki","year":"2008","journal-title":"Brain Dev"},{"key":"10.1016\/j.braindev.2016.09.014_b0100","doi-asserted-by":"crossref","first-page":"17864","DOI":"10.1523\/JNEUROSCI.3179-11.2011","article-title":"Chronic perinatal hypoxia reduces glutamate-aspartate transporter function in astrocytes through the Janus kinase\/signal transducer and activator of transcription pathway","volume":"31","author":"Raymond","year":"2011","journal-title":"J Neurosci"},{"key":"10.1016\/j.braindev.2016.09.014_b0105","doi-asserted-by":"crossref","first-page":"425","DOI":"10.3389\/fncel.2014.00425","article-title":"Functional changes in glutamate transporters and astrocyte biophysical properties in a rodent model of focal cortical dysplasia","volume":"8","author":"Campbell","year":"2014","journal-title":"Front Cell Neurosci"},{"key":"10.1016\/j.braindev.2016.09.014_b0110","doi-asserted-by":"crossref","first-page":"76","DOI":"10.1177\/000992288902800204","article-title":"Extreme hyperpyrexia in childhood. Presentation similar to hemorrhagic shock and encephalopathy","volume":"28","author":"Caspe","year":"1989","journal-title":"Clin Pediatr"},{"key":"10.1016\/j.braindev.2016.09.014_b0115","doi-asserted-by":"crossref","first-page":"375","DOI":"10.1016\/S0387-7604(01)00239-X","article-title":"Seizure frequency and characteristics in children with Down syndrome","volume":"23","author":"Goldberg-Stern","year":"2001","journal-title":"Brain Dev"},{"key":"10.1016\/j.braindev.2016.09.014_b0120","doi-asserted-by":"crossref","first-page":"857","DOI":"10.1111\/dmcn.12182","article-title":"Epilepsy in Prader-Willi syndrome: experience of a national referral centre","volume":"55","author":"Gilboa","year":"2013","journal-title":"Dev Med Child Neurol"},{"key":"10.1016\/j.braindev.2016.09.014_b0125","doi-asserted-by":"crossref","first-page":"66","DOI":"10.1016\/j.pediatrneurol.2006.07.010","article-title":"Serial diffusion-weighted MRI in hemorrhagic shock and encephalopathy syndrome","volume":"36","author":"Toyoshima","year":"2007","journal-title":"Pediatr Neurol"},{"key":"10.1016\/j.braindev.2016.09.014_b0130","doi-asserted-by":"crossref","first-page":"E730","DOI":"10.1097\/BRS.0b013e3181d952fb","article-title":"Hemorrhagic shock and encephalopathy syndrome in a quadriplegic child: an argument for the triggering role of impaired thermoregulatory response","volume":"35","author":"Baugnon","year":"2010","journal-title":"Spine"},{"key":"10.1016\/j.braindev.2016.09.014_b0135","first-page":"441","article-title":"Multiorgan failure associated with hyperthermia in an infant with Prader-Willi syndrome. Case report (in Spanish)","volume":"111","author":"Donoso","year":"2013","journal-title":"Arch Argent Pediatr"}],"container-title":["Brain and Development"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0387760416301681?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0387760416301681?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,9,7]],"date-time":"2018-09-07T05:26:08Z","timestamp":1536297968000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0387760416301681"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,3]]},"references-count":27,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2017,3]]}},"alternative-id":["S0387760416301681"],"URL":"https:\/\/doi.org\/10.1016\/j.braindev.2016.09.014","relation":{},"ISSN":["0387-7604"],"issn-type":[{"value":"0387-7604","type":"print"}],"subject":[],"published":{"date-parts":[[2017,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"\u201cSymptomatic\u201d infection-associated acute encephalopathy in children with underlying neurological disorders","name":"articletitle","label":"Article Title"},{"value":"Brain and Development","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.braindev.2016.09.014","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2016 The Japanese Society of Child Neurology. Published by Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}