{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T05:51:14Z","timestamp":1790833874764,"version":"4.1.0"},"reference-count":18,"publisher":"Spandidos Publications","issue":"2","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2015,2]]},"DOI":"10.3892\/etm.2014.2136","type":"journal-article","created":{"date-parts":[[2014,12,16]],"date-time":"2014-12-16T03:04:25Z","timestamp":1418699065000},"page":"417-420","source":"Crossref","is-referenced-by-count":11,"title":["Spinocerebellar ataxia type 3\/Machado-Joseph disease manifested as spastic paraplegia: A clinical and genetic study"],"prefix":"10.3892","volume":"9","author":[{"given":"YANMIN","family":"SONG","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"YUNHAI","family":"LIU","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"NING","family":"ZHANG","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"LILI","family":"LONG","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"2249","published-online":{"date-parts":[[2014,12,16]]},"reference":[{"key":"key20180108130150_b1-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"43","DOI":"10.1136\/jnnp.72.1.43","article-title":"The prevalence of \u2018pure\u2019 autosomal dominant hereditary spastic paraparesis in the island of Ireland","volume":"72","author":"McMonagle","year":"2002","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"key20180108130150_b2-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"1377","DOI":"10.1016\/S0895-4356(97)00202-3","article-title":"Hereditary ataxias and spastic paraplegias: methodological aspects of a prevalence study in Portugal","volume":"50","author":"Silva","year":"1997","journal-title":"J Clin Epidemiol"},{"key":"key20180108130150_b3-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"65","DOI":"10.1007\/s11910-996-0011-1","article-title":"Hereditary spastic paraplegia","volume":"6","author":"Fink","year":"2006","journal-title":"Curr Neurol Neurosci Rep"},{"key":"key20180108130150_b4-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"746","DOI":"10.1001\/jamaneurol.2013.1707","article-title":"Hereditary ataxia and spastic paraplegia in Portugal: a population-based prevalence study","volume":"70","author":"Coutinho","year":"2013","journal-title":"JAMA Neurol"},{"key":"key20180108130150_b5-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"437","DOI":"10.1016\/B978-0-444-51892-7.00027-9","article-title":"Machado-Joseph disease\/spinocerebellar ataxia type 3","volume":"103","author":"Paulson","year":"2012","journal-title":"Handb Clin Neurol"},{"key":"key20180108130150_b6-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"25","DOI":"10.1016\/j.jns.2005.04.009","article-title":"Spinocerebellar ataxia type 6 in Mainland China: molecular and clinical features in four families","volume":"236","author":"Jiang","year":"2005","journal-title":"J Neurol Sci"},{"key":"key20180108130150_b7-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"1151","DOI":"10.1016\/S0140-6736(83)92879-9","article-title":"Classification of the hereditary ataxias and paraplegias","volume":"21","author":"Harding","year":"1983","journal-title":"Lancet"},{"key":"key20180108130150_b8-etm-09-02-0417","first-page":"1122","article-title":"Clinical features and zygosity diagnosis of hereditary spastic paraplegia in identical twins","volume":"5","author":"Li","year":"2006","journal-title":"Zhoghua Shenjing Yixue Zazhi"},{"key":"key20180108130150_b9-etm-09-02-0417","article-title":"Aids to the Examination of the Peripheral Nervous System","volume-title":"Memorandum no. 45","author":"Medical Research Council","year":"1976"},{"key":"key20180108130150_b10-etm-09-02-0417","first-page":"1519","article-title":"Susceptibility gene for stroke or cerebral infarction in the Han population in Hunan Province of China","volume":"8","author":"Mo","year":"2013","journal-title":"Neural Regen Res"},{"key":"key20180108130150_b11-etm-09-02-0417","first-page":"520","article-title":"The clinical features and genomic diagnosis of hereditary spinocerebellar ataxia type 1","volume":"5","author":"Han","year":"2006","journal-title":"Cuzhong Yu Shenjing Jibing"},{"key":"key20180108130150_b12-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"935","DOI":"10.1212\/WNL.46.4.935","article-title":"Fatal familial insomnia: behavioral and cognitive feaures","volume":"46","author":"Gallassi","year":"1996","journal-title":"Neurology"},{"key":"key20180108130150_b13-etm-09-02-0417","first-page":"673","article-title":"Inherited prion diseases","volume-title":"Prion Biology and Diseases","author":"Kong","year":"2004","edition":"2nd edition"},{"key":"key20180108130150_b14-etm-09-02-0417","first-page":"846","article-title":"Machado-Joseph disease: A proposal of spastic paraplegic subtype","volume":"46","author":"Sakai","year":"1996","journal-title":"Neurology"},{"key":"key20180108130150_b15-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"338","DOI":"10.1016\/j.parkreldis.2011.01.015","article-title":"Relative contribution of SCA2, SCA3 and SCA17 in Korean patients with parkinsonism and ataxia","volume":"17","author":"Yun","year":"2011","journal-title":"Parkinsonism Relat Disord"},{"key":"key20180108130150_b16-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"131","DOI":"10.1186\/1471-2377-11-131","article-title":"Parkinsonian phenotype in Machado-Joseph disease (MJD\/SCA3): a two-case report","volume":"11","author":"Bettencourt","year":"2011","journal-title":"BMC Neurol"},{"key":"key20180108130150_b17-etm-09-02-0417","doi-asserted-by":"crossref","first-page":"578","DOI":"10.1002\/ajmg.10514","article-title":"Difference in disease-free survival curve and regional distribution according to subtype of spinocerebellar ataxia: a study of 1,286 Japanese patients","volume":"114","author":"Maruyama","year":"2002","journal-title":"Am J Med Genet"},{"key":"key20180108130150_b18-etm-09-02-0417","first-page":"54","article-title":"Correlation between CAG repeat length and clinical features in Machado-Joseph disease","volume":"57","author":"Maciel","year":"1995","journal-title":"Am J Hum Genet"}],"container-title":["Experimental and Therapeutic Medicine"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/spandidos-publications.com\/10.3892\/etm.2014.2136\/download","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2018,1,8]],"date-time":"2018-01-08T17:53:19Z","timestamp":1515433999000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.spandidos-publications.com\/10.3892\/etm.2014.2136"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,12,16]]},"references-count":18,"journal-issue":{"issue":"2","published-online":{"date-parts":[[2014,12,16]]},"published-print":{"date-parts":[[2015,2]]}},"alternative-id":["10.3892\/etm.2014.2136"],"URL":"https:\/\/doi.org\/10.3892\/etm.2014.2136","relation":{},"ISSN":["1792-0981","1792-1015"],"issn-type":[{"value":"1792-0981","type":"print"},{"value":"1792-1015","type":"electronic"}],"subject":[],"published":{"date-parts":[[2014,12,16]]}}}