{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,12,19]],"date-time":"2025-12-19T15:14:26Z","timestamp":1766157266156},"reference-count":22,"publisher":"FapUNIFESP (SciELO)","issue":"2b","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Arq. Neuro-Psiquiatr."],"published-print":{"date-parts":[[2007,6]]},"abstract":"<jats:p>We describe seven patients with genetically confirmed Huntington's disease (HD) who had non-choreic movement disorders as presenting symptoms or signs. Patients with movement disorders other than chorea in the early stages tended to have larger CAG trinucleotide repeat expansion in comparison with more \"typical\" HD patients.<\/jats:p>","DOI":"10.1590\/s0004-282x2007000300007","type":"journal-article","created":{"date-parts":[[2007,9,28]],"date-time":"2007-09-28T03:01:13Z","timestamp":1190948473000},"page":"402-405","source":"Crossref","is-referenced-by-count":16,"title":["Non-choreic movement disorders as initial manifestations of Huntington's disease"],"prefix":"10.1590","volume":"65","author":[{"given":"Nilson","family":"Becker","sequence":"first","affiliation":[{"name":"Federal University of Paran\u00e1, Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Renato P.","family":"Munhoz","sequence":"additional","affiliation":[{"name":"Federal University of Paran\u00e1, Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Salmo","family":"Raskin","sequence":"additional","affiliation":[{"name":"Federal University of Paran\u00e1, Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lineu C\u00e9sar","family":"Werneck","sequence":"additional","affiliation":[{"name":"Federal University of Paran\u00e1, Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"H\u00e9lio A.G.","family":"Teive","sequence":"additional","affiliation":[{"name":"Federal University of Paran\u00e1, Brazil"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"530","reference":[{"key":"ref1","doi-asserted-by":"crossref","first-page":"142","DOI":"10.1016\/S1566-2772(00)00014-1","article-title":"Huntington's disease","volume":"1","author":"Ross CA","year":"2001","journal-title":"Clin Neurosci Res"},{"key":"ref2","doi-asserted-by":"crossref","first-page":"958","DOI":"10.1038\/sj.embor.7400250","article-title":"Huntingtin and the molecular pathogenesis of Huntington's disease: Fourth in Molecular Medicine Review Series","volume":"5","author":"Landles C","year":"2004","journal-title":"EMBO Rep"},{"key":"ref3","doi-asserted-by":"crossref","first-page":"971","DOI":"10.1016\/0092-8674(93)90585-E","article-title":"A novel gene containing a trinucleotide repeat that is expanded and unstable on Huntington's disease chromosomes","volume":"72","year":"1993","journal-title":"Cell","ISSN":"http:\/\/id.crossref.org\/issn\/0092-8674","issn-type":"print"},{"key":"ref4","doi-asserted-by":"crossref","first-page":"S2","DOI":"10.1038\/nm1067","article-title":"Molecular pathways to neurodegeneration","volume":"10","author":"Bossy-Wetzel E","year":"2004","journal-title":"Nat Med","ISSN":"http:\/\/id.crossref.org\/issn\/1078-8956","issn-type":"print"},{"key":"ref5","doi-asserted-by":"crossref","first-page":"414","DOI":"10.1016\/j.molmed.2003.08.006","article-title":"Huntington's disease: a synaptopathy?","volume":"9","author":"Li J-Y","year":"2003","journal-title":"Trends Mol Med"},{"key":"ref6","doi-asserted-by":"crossref","first-page":"305","DOI":"10.1097\/00005792-199709000-00001","article-title":"Huntington disease and the related disorder, dentatorubral-pallidoluysian atrophy (DRPLA)","volume":"76","author":"Ross CA","year":"1997","journal-title":"Medicine","ISSN":"http:\/\/id.crossref.org\/issn\/0025-7974","issn-type":"print"},{"key":"ref7","doi-asserted-by":"crossref","first-page":"50","DOI":"10.1034\/j.1399-0004.2000.580108.x","article-title":"Atypical movement disorders in the early stages of Huntington's disease","volume":"58","author":"Squitieri F","year":"2000","journal-title":"Clin Genet","ISSN":"http:\/\/id.crossref.org\/issn\/0009-9163","issn-type":"print"},{"key":"ref8","series-title":"Movement disorders: neurologic principles & practice","first-page":"3","volume-title":"Approach to the patient with a movement disorder and overview of movement disorders","author":"Kumar A","year":"2004","edition":"2. Ed."},{"key":"ref9","doi-asserted-by":"crossref","first-page":"977","DOI":"10.1590\/S0004-282X2000000600001","article-title":"Huntington disease: DNA analysis in Brazilian population","volume":"58","author":"Raskin S","year":"2000","journal-title":"Arq Neuropsiquiatr","ISSN":"http:\/\/id.crossref.org\/issn\/0004-282X","issn-type":"print"},{"key":"ref10","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1097\/00004850-200403000-00001","article-title":"Huntington's disease: present treatments and future therapeutic modalities","volume":"19","author":"Bonelli RM","year":"2004","journal-title":"Int Clin Psychopharmacol","ISSN":"http:\/\/id.crossref.org\/issn\/0268-1315","issn-type":"print"},{"key":"ref11","doi-asserted-by":"crossref","first-page":"128","DOI":"10.1602\/neurorx.1.1.128","article-title":"The paradigma of Huntington's disease: therapeutic opportunities in neurodegeneration","volume":"1","author":"Leegwater-Kim J","year":"2004","journal-title":"NeuroRx"},{"key":"ref12","series-title":"Huntington's disease","first-page":"28","volume-title":"Clinical neurology of Huntington's disease","author":"Kremer B","year":"2002","edition":"3. Ed."},{"key":"ref13","doi-asserted-by":"crossref","first-page":"1326","DOI":"10.1001\/archneur.57.9.1326","article-title":"Dystonia-predominant adult-onset Huntington disease: association between motor phenotype and age of onset in adults","volume":"57","author":"Louis ED","year":"2000","journal-title":"Arch Neurol","ISSN":"http:\/\/id.crossref.org\/issn\/0003-9942","issn-type":"print"},{"key":"ref14","first-page":"363","article-title":"Repetitive belching, aerophagia, and torticollis in Huntington's disease: a case report","volume":"13","author":"Hu MTM","year":"1998","journal-title":"Mov Disord","ISSN":"http:\/\/id.crossref.org\/issn\/0855-3185","issn-type":"print"},{"key":"ref15","first-page":"103","article-title":"Tourettism associated with Huntington's disease","volume":"10","author":"Jankovic J","year":"1995","journal-title":"Mov Disord","ISSN":"http:\/\/id.crossref.org\/issn\/0855-3185","issn-type":"print"},{"key":"ref16","doi-asserted-by":"crossref","first-page":"1","DOI":"10.1002\/ajmg.1320390102","article-title":"Huntington's disease and childhood onset Tourette syndrome","volume":"39","author":"Kerbeshian J","year":"1991","journal-title":"Am J Med Genet","ISSN":"http:\/\/id.crossref.org\/issn\/0148-7299","issn-type":"print"},{"key":"ref17","first-page":"927","article-title":"Huntington's disease mimicking Tourette syndrome","volume":"39","author":"Alonso H","year":"2004","journal-title":"Rev Neurol","ISSN":"http:\/\/id.crossref.org\/issn\/0210-0010","issn-type":"print"},{"key":"ref18","doi-asserted-by":"crossref","first-page":"383","DOI":"10.1007\/BF02341787","article-title":"Tourettism as clinical presentation of Huntington's disease with onset in childhood","volume":"19","author":"Angelini L","year":"1998","journal-title":"Ital J Neurol Sci","ISSN":"http:\/\/id.crossref.org\/issn\/0392-0461","issn-type":"print"},{"key":"ref19","series-title":"Neurogenetics","first-page":"25","volume-title":"Molecular genetic tools","author":"Pulst SM","year":"2000"},{"key":"ref20","doi-asserted-by":"crossref","first-page":"2385","DOI":"10.1093\/brain\/awh278","article-title":"Trinucleotide repeats and neurodegenerative disease","volume":"127","author":"Everett CM","year":"2004","journal-title":"Brain","ISSN":"http:\/\/id.crossref.org\/issn\/0006-8950","issn-type":"print"},{"key":"ref21","doi-asserted-by":"crossref","first-page":"527","DOI":"10.1136\/pgmj.2004.019356","article-title":"Chorea and related disorders","volume":"80","author":"Bhidayasiri R","year":"2004","journal-title":"Postgrad Med J","ISSN":"http:\/\/id.crossref.org\/issn\/0032-5473","issn-type":"print"},{"key":"ref22","doi-asserted-by":"crossref","first-page":"1016","DOI":"10.1212\/01.wnl.0000204230.16619.d9","article-title":"The association of CAG repeat length with clinical progression in Huntington disease","volume":"66","author":"Rosenblatt A","year":"2006","journal-title":"Neurology","ISSN":"http:\/\/id.crossref.org\/issn\/0028-3878","issn-type":"print"}],"container-title":["Arquivos de Neuro-Psiquiatria"],"original-title":[],"link":[{"URL":"http:\/\/www.scielo.br\/pdf\/anp\/v65n2b\/07.pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2019,5,3]],"date-time":"2019-05-03T10:04:30Z","timestamp":1556877870000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.scielo.br\/scielo.php?script=sci_arttext&pid=S0004-282X2007000300007&lng=en&tlng=en"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2007,6]]},"references-count":22,"journal-issue":{"issue":"2b","published-print":{"date-parts":[[2007,6]]}},"alternative-id":["S0004-282X2007000300007"],"URL":"https:\/\/doi.org\/10.1590\/s0004-282x2007000300007","relation":{},"ISSN":["0004-282X"],"issn-type":[{"value":"0004-282X","type":"electronic"}],"subject":[],"published":{"date-parts":[[2007,6]]}}}