{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2023,9,25]],"date-time":"2023-09-25T12:24:21Z","timestamp":1695644661953},"reference-count":13,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2015,5,1]],"date-time":"2015-05-01T00:00:00Z","timestamp":1430438400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["ejpn-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["European Journal of Paediatric Neurology"],"published-print":{"date-parts":[[2015,5]]},"DOI":"10.1016\/j.ejpn.2014.12.001","type":"journal-article","created":{"date-parts":[[2014,12,24]],"date-time":"2014-12-24T05:36:20Z","timestamp":1419399380000},"page":"364-366","update-policy":"http:\/\/dx.doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":5,"title":["Posterior fossa syndrome in a patient with an\u00a0ornithine transcarbamylase deficiency"],"prefix":"10.1016","volume":"19","author":[{"given":"S.C.M.","family":"Nedermeijer","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"J.","family":"van den Hout","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Geleijns","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H.","family":"de Klerk","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.E.","family":"Catsman-Berrevoets","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"issue":"1","key":"10.1016\/j.ejpn.2014.12.001_bib1","doi-asserted-by":"crossref","first-page":"50","DOI":"10.1542\/peds.49.1.50","article-title":"Normal pressure hydrocephalus: complication of posterior fossa surgery in children","volume":"49","author":"Stein","year":"1972","journal-title":"Pediatrics"},{"issue":"8","key":"10.1016\/j.ejpn.2014.12.001_bib2","doi-asserted-by":"crossref","first-page":"763","DOI":"10.1016\/j.clineuro.2008.05.013","article-title":"Cerebellar neurocognition: insights into the bottom of the brain","volume":"110","author":"Baillieux","year":"2008","journal-title":"Clin Neurol Neurosurg"},{"issue":"3","key":"10.1016\/j.ejpn.2014.12.001_bib3","doi-asserted-by":"crossref","first-page":"355","DOI":"10.1007\/s00381-010-1328-2","article-title":"Cerebellar mutism: review of the literature","volume":"27","author":"Gudrunardottir","year":"2011","journal-title":"Childs Nerv Syst"},{"issue":"5","key":"10.1016\/j.ejpn.2014.12.001_bib4","doi-asserted-by":"crossref","first-page":"434","DOI":"10.1016\/j.ejpn.2011.12.013","article-title":"Auditory-perceptual speech analysis in children with cerebellar tumours: a long-term follow-up study","volume":"16","author":"De Smet","year":"2012","journal-title":"Eur J Paediatr Neurol"},{"issue":"4","key":"10.1016\/j.ejpn.2014.12.001_bib5","doi-asserted-by":"crossref","first-page":"193","DOI":"10.1016\/j.ejpn.2007.01.007","article-title":"Postoperative motor speech production in children with the syndrome of 'cerebellar' mutism and subsequent dysarthria: a critical review of the literature","volume":"11","author":"De Smet","year":"2007","journal-title":"Eur J Paediatr Neurol"},{"issue":"1","key":"10.1016\/j.ejpn.2014.12.001_bib6","doi-asserted-by":"crossref","first-page":"49","DOI":"10.1016\/j.pediatrneurol.2009.01.013","article-title":"Transient mutism and pathologic laughter in the course of cerebellitis","volume":"41","author":"Dimova","year":"2009","journal-title":"Pediatr Neurol"},{"issue":"Suppl. 1","key":"10.1016\/j.ejpn.2014.12.001_bib7","doi-asserted-by":"crossref","first-page":"151","DOI":"10.1023\/A:1005374027693","article-title":"Neurodevelopmental outcome of long-term therapy of urea cycle disorders in Japan","volume":"21","author":"Uchino","year":"1998","journal-title":"J Inherit Metab Dis"},{"issue":"3","key":"10.1016\/j.ejpn.2014.12.001_bib8","doi-asserted-by":"crossref","first-page":"115","DOI":"10.1016\/S1090-3798(03)00040-0","article-title":"Ornithine transcarbamylase deficiency: a urea cycle defect","volume":"7","author":"Gordon","year":"2003","journal-title":"Eur J Paediatr Neurol"},{"issue":"10","key":"10.1016\/j.ejpn.2014.12.001_bib9","doi-asserted-by":"crossref","first-page":"1420","DOI":"10.1111\/j.1651-2227.2008.00952.x","article-title":"Diagnosis, symptoms, frequency and mortality of 260 patients with urea cycle disorders from a 21-year, multicentre study of acute hyperammonaemic episodes","volume":"97","author":"Summar","year":"2008","journal-title":"Acta Paediatr"},{"issue":"1","key":"10.1016\/j.ejpn.2014.12.001_bib11","doi-asserted-by":"crossref","first-page":"54","DOI":"10.1136\/adc.86.1.54","article-title":"Neurological outcome of patients with ornithine carbamoyltransferase deficiency","volume":"86","author":"Nicolaides","year":"2002","journal-title":"Arch Dis Child"},{"issue":"4","key":"10.1016\/j.ejpn.2014.12.001_bib12","doi-asserted-by":"crossref","first-page":"455","DOI":"10.1007\/s00247-011-2253-6","article-title":"Urea cycle disorders: brain MRI and neurological outcome","volume":"42","author":"Bireley","year":"2012","journal-title":"Pediatr Radiol"},{"issue":"3","key":"10.1016\/j.ejpn.2014.12.001_bib13","doi-asserted-by":"crossref","first-page":"423","DOI":"10.1016\/S0022-3476(05)83432-8","article-title":"Ornithine transcarbamylase deficiency presenting with strokelike episodes","volume":"122","author":"Christodoulou","year":"1993","journal-title":"J Pediatr"},{"issue":"4","key":"10.1016\/j.ejpn.2014.12.001_bib14","doi-asserted-by":"crossref","first-page":"259","DOI":"10.1007\/s00431-002-1135-1","article-title":"Acute extrapyramidal syndrome in mild ornithine transcarbamylase deficiency: metabolic stroke involving the caudate and putamen without metabolic decompensation","volume":"162","author":"Keegan","year":"2003","journal-title":"Eur J Pediatr"}],"container-title":["European Journal of Paediatric Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1090379814002025?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1090379814002025?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2022,4,25]],"date-time":"2022-04-25T08:30:05Z","timestamp":1650875405000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1090379814002025"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,5]]},"references-count":13,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2015,5]]}},"alternative-id":["S1090379814002025"],"URL":"https:\/\/doi.org\/10.1016\/j.ejpn.2014.12.001","relation":{},"ISSN":["1090-3798"],"issn-type":[{"value":"1090-3798","type":"print"}],"subject":[],"published":{"date-parts":[[2015,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Posterior fossa syndrome in a patient with an\u00a0ornithine transcarbamylase deficiency","name":"articletitle","label":"Article Title"},{"value":"European Journal of Paediatric Neurology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ejpn.2014.12.001","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2014 European Paediatric Neurology Society. Published by Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}