{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,22]],"date-time":"2026-01-22T23:08:13Z","timestamp":1769123293425,"version":"3.49.0"},"reference-count":12,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2020,2,1]],"date-time":"2020-02-01T00:00:00Z","timestamp":1580515200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2020,2,1]],"date-time":"2020-02-01T00:00:00Z","timestamp":1580515200000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","prd-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Parkinsonism &amp; Related Disorders"],"published-print":{"date-parts":[[2020,2]]},"DOI":"10.1016\/j.parkreldis.2020.01.008","type":"journal-article","created":{"date-parts":[[2020,1,16]],"date-time":"2020-01-16T19:16:45Z","timestamp":1579202205000},"page":"46-48","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":12,"special_numbering":"C","title":["Huntington disease like 2 (HDL-2) with parkinsonism and abnormal DAT-SPECT \u2013 A novel observation"],"prefix":"10.1016","volume":"71","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-0823-8916","authenticated-orcid":false,"given":"Eoin","family":"Mulroy","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Anna","family":"Latorre","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Elisa","family":"Menozzi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Pei Chiek","family":"Teh","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Francesca","family":"Magrinelli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kailash P.","family":"Bhatia","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.parkreldis.2020.01.008_bib1","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1038\/ng760","article-title":"A repeat expansion in the gene encoding junctophilin-3 is associated with Huntington Disease-like 2","volume":"29","author":"Holmes","year":"2001","journal-title":"Nat. Genet."},{"issue":"1","key":"10.1016\/j.parkreldis.2020.01.008_bib2","doi-asserted-by":"crossref","first-page":"37","DOI":"10.3233\/JHD-160232","article-title":"A systematic review of the huntington disease-like 2 phenotype","volume":"6","author":"Anderson","year":"2017","journal-title":"J Huntingtons Dis"},{"key":"10.1016\/j.parkreldis.2020.01.008_bib3","series-title":"GeneReviews\u00ae [Internet]","article-title":"Huntington disease-like 2. 2004 jan 30 [updated 2019 jun 27]","author":"Anderson","year":"1993"},{"key":"10.1016\/j.parkreldis.2020.01.008_bib4","doi-asserted-by":"crossref","first-page":"1527","DOI":"10.1002\/mds.10587","article-title":"Phenotypic features of Huntington's disease-like 2","volume":"18","author":"Walker","year":"2003","journal-title":"Mov. Disord."},{"key":"10.1016\/j.parkreldis.2020.01.008_bib5","doi-asserted-by":"crossref","first-page":"2083","DOI":"10.1002\/mds.21672","article-title":"A South African mixed ancestry family with Huntington disease-like 2: clinical and genetic features","volume":"22","author":"Bardien","year":"2007","journal-title":"Mov. Disord."},{"key":"10.1016\/j.parkreldis.2020.01.008_bib6","series-title":"Huntington Disease-like 2","author":"Margolis","year":"2012"},{"issue":"7","key":"10.1016\/j.parkreldis.2020.01.008_bib7","doi-asserted-by":"crossref","first-page":"573","DOI":"10.1002\/ajmg.b.32332","article-title":"Junctophilin 3 (JPH3) expansion mutations causing Huntington disease like 2 (HDL2) are common in South African patients with African ancestry and a Huntington disease phenotype","volume":"168","author":"Krause","year":"2015","journal-title":"Am J Med Genet B Neuropsychiatr Genet"},{"issue":"10","key":"10.1016\/j.parkreldis.2020.01.008_bib8","doi-asserted-by":"crossref","first-page":"870","DOI":"10.1016\/j.clineuro.2010.07.014","article-title":"Does reduced [(123)I]-FP-CIT binding in Huntington's disease suggest pre-synaptic dopaminergic involvement?","volume":"112","author":"Gamez","year":"2010","journal-title":"Clin. Neurol. Neurosurg."},{"issue":"4","key":"10.1016\/j.parkreldis.2020.01.008_bib9","doi-asserted-by":"crossref","first-page":"366","DOI":"10.1097\/NEN.0b013e31816b4aee","article-title":"A comparison of huntington disease and huntington disease-like 2 neuropathology","volume":"67","author":"Rudnicki","year":"2008","journal-title":"J. Neuropathol. Exp. Neurol."},{"issue":"2","key":"10.1016\/j.parkreldis.2020.01.008_bib10","doi-asserted-by":"crossref","first-page":"192","DOI":"10.1111\/j.1552-6569.2011.00671.x","article-title":"SPECT study of the nigrostriatal dopaminergic system in Huntington's disease","volume":"23","author":"Hwang","year":"2013","journal-title":"J. Neuroimaging"},{"issue":"15","key":"10.1016\/j.parkreldis.2020.01.008_bib11","doi-asserted-by":"crossref","first-page":"3164","DOI":"10.1093\/hmg\/ddw166","article-title":"A Drosophila model of Huntington disease-like 2 exhibits nuclear toxicity and distinct pathogenic mechanisms from Huntington disease","volume":"25","author":"Krench","year":"2016","journal-title":"Hum. Mol. Genet."},{"issue":"1","key":"10.1016\/j.parkreldis.2020.01.008_bib12","doi-asserted-by":"crossref","first-page":"141","DOI":"10.1016\/0006-8993(87)91506-X","article-title":"Tyrosine hydroxylase-like immunoreactivity is distributed in the matrix compartment of normal human and Huntington's disease striatum","volume":"416","author":"Ferrante","year":"1987","journal-title":"Brain Res."}],"container-title":["Parkinsonism &amp; Related Disorders"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S135380202030016X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S135380202030016X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,23]],"date-time":"2025-10-23T00:17:47Z","timestamp":1761178667000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S135380202030016X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2020,2]]},"references-count":12,"alternative-id":["S135380202030016X"],"URL":"https:\/\/doi.org\/10.1016\/j.parkreldis.2020.01.008","relation":{},"ISSN":["1353-8020"],"issn-type":[{"value":"1353-8020","type":"print"}],"subject":[],"published":{"date-parts":[[2020,2]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Huntington disease like 2 (HDL-2) with parkinsonism and abnormal DAT-SPECT \u2013 A novel observation","name":"articletitle","label":"Article Title"},{"value":"Parkinsonism & Related Disorders","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.parkreldis.2020.01.008","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"simple-article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2020 Elsevier Ltd. All rights reserved.","name":"copyright","label":"Copyright"}]}}