{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,16]],"date-time":"2026-05-16T09:46:46Z","timestamp":1778924806258,"version":"3.51.4"},"reference-count":5,"publisher":"Elsevier BV","issue":"1","license":[{"start":{"date-parts":[[2015,1,1]],"date-time":"2015-01-01T00:00:00Z","timestamp":1420070400000},"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":[[2015,1]]},"DOI":"10.1016\/j.ejpn.2014.10.005","type":"journal-article","created":{"date-parts":[[2014,11,3]],"date-time":"2014-11-03T07:56:33Z","timestamp":1415001393000},"page":"72-74","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":20,"title":["Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine"],"prefix":"10.1016","volume":"19","author":[{"given":"S.","family":"Kinder","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"C.","family":"Ossig","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Wienecke","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Beyer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"von der Hagen","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"A.","family":"Storch","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"M.","family":"Smitka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.ejpn.2014.10.005_bib1","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1016\/j.nurt.2007.01.014","article-title":"Brandt T Episodic ataxia type 2","volume":"4","author":"Strupp","year":"2007","journal-title":"Neurother J Am Soc Exp Neurother"},{"key":"10.1016\/j.ejpn.2014.10.005_bib2","doi-asserted-by":"crossref","first-page":"162","DOI":"10.1111\/j.1749-6632.2011.06149.x","article-title":"The role of regularity and synchrony of cerebellar Purkinje cells for pathological nystagmus","volume":"1233","author":"Glasauer","year":"2011","journal-title":"Ann N Y Acad Sci"},{"key":"10.1016\/j.ejpn.2014.10.005_bib3","doi-asserted-by":"crossref","first-page":"17","DOI":"10.1212\/01.WNL.0000101675.61074.50","article-title":"Clinical spectrum of episodic ataxia type 2","volume":"62","author":"Jen","year":"2004","journal-title":"Neurology"},{"key":"10.1016\/j.ejpn.2014.10.005_bib4","doi-asserted-by":"crossref","first-page":"114","DOI":"10.1159\/000315145","article-title":"Phenotypic variability of episodic ataxia type 2 mutations: a family study","volume":"64","author":"Jung","year":"2010","journal-title":"Eur Neurol"},{"key":"10.1016\/j.ejpn.2014.10.005_bib5","doi-asserted-by":"crossref","first-page":"1289","DOI":"10.1136\/jnnp.2008.159103","article-title":"Episodic ataxia type 2: unusual aspects in clinical and genetic presentation. Special emphasis in childhood","volume":"80","author":"Bertholon","year":"2009","journal-title":"J Neurol Neurosurg Psychiatr"}],"container-title":["European Journal of Paediatric Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1090379814001743?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1090379814001743?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,9,28]],"date-time":"2018-09-28T02:20:11Z","timestamp":1538101211000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1090379814001743"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2015,1]]},"references-count":5,"journal-issue":{"issue":"1","published-print":{"date-parts":[[2015,1]]}},"alternative-id":["S1090379814001743"],"URL":"https:\/\/doi.org\/10.1016\/j.ejpn.2014.10.005","relation":{},"ISSN":["1090-3798"],"issn-type":[{"value":"1090-3798","type":"print"}],"subject":[],"published":{"date-parts":[[2015,1]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Novel frameshift mutation in the CACNA1A gene causing a mixed phenotype of episodic ataxia and familiar hemiplegic migraine","name":"articletitle","label":"Article Title"},{"value":"European Journal of Paediatric Neurology","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.ejpn.2014.10.005","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2014 Published by Elsevier Ltd.","name":"copyright","label":"Copyright"}]}}