{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,22]],"date-time":"2026-03-22T09:58:38Z","timestamp":1774173518022,"version":"3.50.1"},"reference-count":13,"publisher":"Elsevier BV","issue":"8","license":[{"start":{"date-parts":[[2014,8,1]],"date-time":"2014-08-01T00:00:00Z","timestamp":1406851200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","prd-journal.com","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Parkinsonism &amp; Related Disorders"],"published-print":{"date-parts":[[2014,8]]},"DOI":"10.1016\/j.parkreldis.2014.05.004","type":"journal-article","created":{"date-parts":[[2014,5,13]],"date-time":"2014-05-13T18:05:06Z","timestamp":1400004306000},"page":"884-888","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":26,"title":["Three families with Perry syndrome from distinct parts of the world"],"prefix":"10.1016","volume":"20","author":[{"given":"Pawel","family":"Tacik","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Fabienne C.","family":"Fiesel","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-9901-9008","authenticated-orcid":false,"given":"Shinsuke","family":"Fujioka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Owen A.","family":"Ross","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Felipe","family":"Pretelt","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Camilo","family":"Casta\u00f1eda Cardona","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alexa","family":"Kidd","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael","family":"Hlavac","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anthony","family":"Raizis","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Michael S.","family":"Okun","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Sharleen","family":"Traynor","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Audrey J.","family":"Strongosky","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Wolfdieter","family":"Springer","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Zbigniew K.","family":"Wszolek","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.parkreldis.2014.05.004_bib1","doi-asserted-by":"crossref","first-page":"108","DOI":"10.1001\/archneur.1975.00490440058009","article-title":"Hereditary mental depression and Parkinsonism with taurine deficiency","volume":"32","author":"Perry","year":"1975","journal-title":"Arch Neurol"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib2","doi-asserted-by":"crossref","first-page":"149","DOI":"10.1016\/j.jns.2009.08.044","article-title":"Elucidating the genetics and pathology of Perry syndrome","volume":"289","author":"Wider","year":"2010","journal-title":"J\u00a0Neurol Sci"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib3","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1016\/j.jns.2013.04.008","article-title":"Perry syndrome: a disorder to consider in the differential diagnosis of Parkinsonism","volume":"330","author":"Aji","year":"2013","journal-title":"J\u00a0Neurol Sci"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib4","doi-asserted-by":"crossref","first-page":"163","DOI":"10.1038\/ng.293","article-title":"DCTN1 mutations in Perry syndrome","volume":"412","author":"Farrer","year":"2009","journal-title":"Nat Genet"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib5","first-page":"620","article-title":"Latin America's first case of Perry syndrome and a new treatment option for respiratory insufficiency","volume":"26","author":"Pretelt","year":"2014","journal-title":"J\u00a0Neurol"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib6","doi-asserted-by":"crossref","first-page":"388","DOI":"10.1016\/j.parkreldis.2014.01.010","article-title":"Expansion of the clinicopathological and mutational spectrum of Perry syndrome","volume":"20","author":"Chung","year":"2014","journal-title":"Parkinsonism Relat Disord"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib7","doi-asserted-by":"crossref","first-page":"208","DOI":"10.1001\/jamaneurol.2013.5100","article-title":"DCTN1 mutation analysis in families with progressive supranuclear palsy-like phenotypes","volume":"71","author":"Caroppo","year":"2014","journal-title":"JAMA Neurol"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib8","doi-asserted-by":"crossref","first-page":"767","DOI":"10.1002\/mds.22950","article-title":"Perry syndrome due to the DCTN1 G71R mutation: a distinctive levodopa responsive disorder with behavioral syndrome, vertical gaze palsy, and respiratory failure","volume":"25","author":"Newsway","year":"2010","journal-title":"Mov Disord"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib9","doi-asserted-by":"crossref","DOI":"10.1002\/mds.25833","article-title":"A\u00a0novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy","author":"Araki","year":"2014","journal-title":"Mov Disord"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib10","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1016\/j.parkreldis.2007.07.014","article-title":"Rapidly progressive familial parkinsonism with central hypoventilation, depression and weight loss (Perry syndrome) \u2013 a literature review","volume":"14","author":"Wider","year":"2008","journal-title":"Parkinsonism Relat Disord"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib11","doi-asserted-by":"crossref","first-page":"759","DOI":"10.1146\/annurev.cellbio.20.012103.094623","article-title":"Dynactin","volume":"20","author":"Schroer","year":"2004","journal-title":"Annu Rev Cell Dev Biol"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib12","doi-asserted-by":"crossref","first-page":"344","DOI":"10.1016\/j.neuron.2012.02.026","article-title":"The p150(Glued) CAP-Gly domain regulates initiation of retrograde transport at synaptic termini","volume":"74","author":"Lloyd","year":"2012","journal-title":"Neuron"},{"key":"10.1016\/j.parkreldis.2014.05.004_bib13","doi-asserted-by":"crossref","first-page":"331","DOI":"10.1016\/j.neuron.2012.02.025","article-title":"Dynactin is required for transport initiation from the distal axon","volume":"74","author":"Moughamian","year":"2012","journal-title":"Neuron"}],"container-title":["Parkinsonism &amp; Related Disorders"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1353802014001904?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1353802014001904?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,10,4]],"date-time":"2018-10-04T02:03:34Z","timestamp":1538618614000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1353802014001904"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,8]]},"references-count":13,"journal-issue":{"issue":"8","published-print":{"date-parts":[[2014,8]]}},"alternative-id":["S1353802014001904"],"URL":"https:\/\/doi.org\/10.1016\/j.parkreldis.2014.05.004","relation":{},"ISSN":["1353-8020"],"issn-type":[{"value":"1353-8020","type":"print"}],"subject":[],"published":{"date-parts":[[2014,8]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Three families with Perry syndrome from distinct parts of the world","name":"articletitle","label":"Article Title"},{"value":"Parkinsonism & Related Disorders","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.parkreldis.2014.05.004","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2014 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}