{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,17]],"date-time":"2026-08-17T18:56:52Z","timestamp":1786993012072,"version":"build-2736575974"},"reference-count":21,"publisher":"Elsevier BV","issue":"1-2","content-domain":{"domain":["jns-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of the Neurological Sciences"],"published-print":{"date-parts":[[2013,1]]},"DOI":"10.1016\/j.jns.2012.09.030","type":"journal-article","created":{"date-parts":[[2012,10,18]],"date-time":"2012-10-18T00:49:12Z","timestamp":1350521352000},"page":"176-178","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":21,"title":["The unique co-occurrence of spinocerebellar ataxia type 10 (SCA10) and Huntington disease"],"prefix":"10.1016","volume":"324","author":[{"given":"Richard H.","family":"Roxburgh","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Corrie O.","family":"Smith","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jung G.","family":"Lim","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"David F.","family":"Bachman","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Erica","family":"Byrd","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Thomas D.","family":"Bird","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jns.2012.09.030_bb0005","doi-asserted-by":"crossref","first-page":"407","DOI":"10.1002\/1531-8249(199903)45:3<407::AID-ANA21>3.0.CO;2-D","article-title":"Mapping of the gene for a novel spinocerebellar ataxia with pure cerebellar signs and epilepsy","volume":"45","author":"Matsuura","year":"1999","journal-title":"Ann Neurol"},{"issue":"5","key":"10.1016\/j.jns.2012.09.030_bb0010","doi-asserted-by":"crossref","first-page":"1423","DOI":"10.1212\/WNL.51.5.1423","article-title":"Clinical and genetic analysis of a distinct autosomal dominant spinocerebellar ataxia","volume":"51","author":"Grewal","year":"1998","journal-title":"Neurology"},{"issue":"8","key":"10.1016\/j.jns.2012.09.030_bb0015","doi-asserted-by":"crossref","first-page":"1509","DOI":"10.1212\/01.WNL.0000142109.62056.57","article-title":"Clinical phenotype of Brazilian families with spinocerebellar ataxia 10","volume":"63","author":"Teive","year":"2004","journal-title":"Neurology"},{"key":"10.1016\/j.jns.2012.09.030_bb0020","doi-asserted-by":"crossref","first-page":"216e8","DOI":"10.1212\/01.wnl.0000265596.72492.89","article-title":"Ethnic origin and extrapyramidal signs in an Argentinean spinocerebellar ataxia type 10 family","volume":"69","author":"Gatto","year":"2007","journal-title":"Neurology"},{"issue":"Suppl. 1","key":"10.1016\/j.jns.2012.09.030_bb0025","first-page":"S12","article-title":"Clinical characterization of a Venezuelan family with spinocerebellar ataxia type 10","volume":"24","author":"Gallardo","year":"2009","journal-title":"Mov Disord"},{"issue":"9","key":"10.1016\/j.jns.2012.09.030_bb0030","doi-asserted-by":"crossref","first-page":"655","DOI":"10.1016\/j.parkreldis.2011.04.001","article-title":"Spinocerebellar ataxia type 10 \u2014 a review","volume":"17","author":"Teive","year":"2011","journal-title":"Parkinsonism Relat Disord"},{"key":"10.1016\/j.jns.2012.09.030_bb0035","doi-asserted-by":"crossref","first-page":"191","DOI":"10.1038\/79911","article-title":"Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10","volume":"26","author":"Matsuura","year":"2000","journal-title":"Nat Genet"},{"issue":"6","key":"10.1016\/j.jns.2012.09.030_bb0040","doi-asserted-by":"crossref","first-page":"e1000984","DOI":"10.1371\/journal.pgen.1000984","article-title":"Inactivation of hnRNP K by expanded intronic AUUCU repeat induces apoptosis via translocation of PKCdelta to mitochondria in spinocerebellar ataxia 10","volume":"6","author":"White","year":"2010","journal-title":"PLoS Genet"},{"key":"10.1016\/j.jns.2012.09.030_bb0045","doi-asserted-by":"crossref","first-page":"83","DOI":"10.1016\/S1474-4422(10)70245-3","article-title":"Huntington's disease: from molecular pathogenesis to clinical treatment","volume":"10","author":"Ross","year":"2011","journal-title":"Lancet Neurol"},{"key":"10.1016\/j.jns.2012.09.030_bb0050","doi-asserted-by":"crossref","first-page":"e4553","DOI":"10.1371\/journal.pone.0004553","article-title":"Ancestral origin of the ATTCT repeat expansion in spinocerebellar ataxia type 10 (SCA10)","volume":"4","author":"Almeida","year":"2009","journal-title":"PLoS One"},{"key":"10.1016\/j.jns.2012.09.030_bb0055","unstructured":"Cloud L, Rosenblatt A, Margolis R, Ross C, Pillai J, Corey-Bloom J, et al. Seizures in juvenile Huntington disease: a large multi-center cohort. Mov Disord in press."},{"key":"10.1016\/j.jns.2012.09.030_bb0060","doi-asserted-by":"crossref","first-page":"267","DOI":"10.1111\/j.1399-0004.2004.00241.x","article-title":"International Huntington's Disease Collaborative Group; a new model for prediction of the age of onset and penetrance for Huntington's disease based on CAG length","volume":"65","author":"Langbehn","year":"2004","journal-title":"Clin Genet"},{"issue":"8","key":"10.1016\/j.jns.2012.09.030_bb0065","doi-asserted-by":"crossref","first-page":"1285","DOI":"10.1001\/archneur.59.8.1285","article-title":"Clinical features and ATTCT repeat expansion in spinocerebellar ataxia type 10","volume":"59","author":"Grewal","year":"2002","journal-title":"Arch Neurol"},{"issue":"5","key":"10.1016\/j.jns.2012.09.030_bb0070","doi-asserted-by":"crossref","first-page":"443","DOI":"10.6061\/clinics\/2012(05)07","article-title":"Spinocerebellar ataxias: genotype\u2013phenotype correlations in 104 Brazilian families","volume":"67","author":"Teive","year":"2012","journal-title":"Clinics (Sao Paulo)"},{"key":"10.1016\/j.jns.2012.09.030_bb0075","doi-asserted-by":"crossref","first-page":"437","DOI":"10.1034\/j.1399-0004.2002.610607.x","article-title":"Homozygosity in Huntington's disease: new ethical dilemma caused by molecular diagnosis","volume":"61","author":"Alonso","year":"2002","journal-title":"Clin Genet"},{"key":"10.1016\/j.jns.2012.09.030_bb0080","first-page":"172","article-title":"Homozygosity in Huntington's disease","volume":"36","author":"Durr","year":"1999","journal-title":"J Med Genet"},{"issue":"4","key":"10.1016\/j.jns.2012.09.030_bb0085","doi-asserted-by":"crossref","first-page":"440","DOI":"10.1212\/WNL.31.4.440","article-title":"Myotonic dystrophy associated with Down syndrome (trisomy 21)","volume":"31","author":"Bird","year":"1981","journal-title":"Neurology"},{"issue":"1\u20132","key":"10.1016\/j.jns.2012.09.030_bb0090","doi-asserted-by":"crossref","first-page":"91","DOI":"10.1016\/j.jns.2004.02.009","article-title":"Coexistence of tuberous sclerosis and Friedreich ataxia","volume":"221","author":"Walker","year":"2004","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.jns.2012.09.030_bb0095","doi-asserted-by":"crossref","first-page":"112","DOI":"10.1001\/archneur.63.1.112","article-title":"Double trouble in hereditary neuropathy: concomitant mutation in the PMP-22 gene and another gene produce novel phenotypes","volume":"63","author":"Hodapp","year":"2006","journal-title":"Arch Neurol"},{"issue":"3","key":"10.1016\/j.jns.2012.09.030_bb0100","doi-asserted-by":"crossref","first-page":"415","DOI":"10.3233\/JAD-2011-101890","article-title":"PSEN1 and PRNP gene mutations: co-occurrence makes onset very early in a family with FTD phenotype","volume":"24","author":"Bernardi","year":"2011","journal-title":"J Alzheimers Dis"},{"issue":"9","key":"10.1016\/j.jns.2012.09.030_bb0105","doi-asserted-by":"crossref","first-page":"1200","DOI":"10.1001\/archneurol.2011.3044","article-title":"Two in one: report of a patient with spinocerebellar ataxia types 2 and 10","volume":"69","author":"Kapur","year":"2012","journal-title":"Arch Neurol"}],"container-title":["Journal of the Neurological Sciences"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X12005369?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X12005369?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2019,7,4]],"date-time":"2019-07-04T16:01:15Z","timestamp":1562256075000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022510X12005369"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2013,1]]},"references-count":21,"journal-issue":{"issue":"1-2","published-print":{"date-parts":[[2013,1]]}},"alternative-id":["S0022510X12005369"],"URL":"https:\/\/doi.org\/10.1016\/j.jns.2012.09.030","relation":{},"ISSN":["0022-510X"],"issn-type":[{"value":"0022-510X","type":"print"}],"subject":[],"published":{"date-parts":[[2013,1]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"The unique co-occurrence of spinocerebellar ataxia type 10 (SCA10) and Huntington disease","name":"articletitle","label":"Article Title"},{"value":"Journal of the Neurological Sciences","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jns.2012.09.030","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2012 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}