{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2025,10,28]],"date-time":"2025-10-28T14:48:43Z","timestamp":1761662923884},"reference-count":33,"publisher":"Japanese Society of Internal Medicine","issue":"22","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":["Intern. Med."],"published-print":{"date-parts":[[2010]]},"DOI":"10.2169\/internalmedicine.49.4025","type":"journal-article","created":{"date-parts":[[2010,11,15]],"date-time":"2010-11-15T06:12:15Z","timestamp":1289801535000},"page":"2409-2414","source":"Crossref","is-referenced-by-count":4,"title":["Prevalence of Autosomal Dominant Cerebellar Ataxia in Aomori, the Northernmost Prefecture of Honshu, Japan"],"prefix":"10.2169","volume":"49","author":[{"given":"Yukiko","family":"Yamamoto-Watanabe","sequence":"first","affiliation":[{"name":"Department of Neurology, Hirosaki University Graduate School of Medicine"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mitsunori","family":"Watanabe","sequence":"additional","affiliation":[{"name":"Department of Neurology, Hirosaki University Graduate School of Medicine"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Motofumi","family":"Hikichi","sequence":"additional","affiliation":[{"name":"Hikichi Clinic"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yoshio","family":"Ikeda","sequence":"additional","affiliation":[{"name":"Department of Neurology, Graduate School of Medicine, Dentistry and Pharmaceutical Sciences"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mandy","family":"Jackson","sequence":"additional","affiliation":[{"name":"Centre for Integrative Physiology, University of Edinburgh"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yasuhito","family":"Wakasaya","sequence":"additional","affiliation":[{"name":"Department of Neurology, Hirosaki University Graduate School of Medicine"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Etsuro","family":"Matsubara","sequence":"additional","affiliation":[{"name":"Department of Neurology, Hirosaki University Graduate School of Medicine"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Takeshi","family":"Kawarabayashi","sequence":"additional","affiliation":[{"name":"Department of Neurology, Hirosaki University Graduate School of Medicine"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Kazuya","family":"Kannari","sequence":"additional","affiliation":[{"name":"Department of Physical Therapy, Faculty of Health Sciences, Aomori University of Health and Welfare"}],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Mikio","family":"Shoji","sequence":"additional","affiliation":[{"name":"Department of Neurology, Hirosaki University Graduate School of Medicine"}],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"962","reference":[{"key":"1","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1097\/WNO0b013e3181b416de","volume":"29","author":"Paulson HL","year":"2009","journal-title":"J Neuroophthalmology","ISSN":"http:\/\/id.crossref.org\/issn\/0165-8107","issn-type":"print"},{"key":"2","doi-asserted-by":"publisher","DOI":"10.1212\/01.wnl.0000324625.00404.15"},{"key":"3","doi-asserted-by":"publisher","DOI":"10.1038\/ng0793-221"},{"key":"4","doi-asserted-by":"publisher","DOI":"10.1038\/ng1196-285"},{"key":"5","doi-asserted-by":"publisher","DOI":"10.1038\/ng1194-221"},{"key":"6","doi-asserted-by":"publisher","DOI":"10.1038\/ng0197-62"},{"key":"7","doi-asserted-by":"publisher","DOI":"10.1038\/ng0997-65"},{"key":"8","doi-asserted-by":"publisher","DOI":"10.1038\/7710"},{"key":"9","doi-asserted-by":"crossref","unstructured":"9. Koide R, Kobayashi S, Shimohata T, et al. A neurological disease caused by an expanded CAG trinucleotide repeat in the TATA-binding protein gene: a new polyglutamine disease? Human Molecular Genetics 8: 2047-2053, 1999.","DOI":"10.1093\/hmg\/8.11.2047"},{"key":"10","doi-asserted-by":"publisher","DOI":"10.1038\/ng0194-9"},{"key":"11","doi-asserted-by":"publisher","DOI":"10.1038\/ng0194-14"},{"key":"12","doi-asserted-by":"publisher","DOI":"10.1016\/j.ajhg.2009.09.019"},{"key":"13","doi-asserted-by":"crossref","first-page":"950","DOI":"10.1212\/WNL.54.4.950","volume":"54","author":"Ikeda Y, Shizuka M, Watanabe M, Oka","year":"2000","journal-title":"Neurology","ISSN":"http:\/\/id.crossref.org\/issn\/0028-3878","issn-type":"print"},{"key":"14","doi-asserted-by":"crossref","unstructured":"14. Fujigasaki H, Martin JJ, De Deyn PP, et al. CAG repeat expansion in the TATA box-binding protein gene causes autosomal dominant cerebellar ataxia. Brain 124: 1939-1947, 2001.","DOI":"10.1093\/brain\/124.10.1939"},{"key":"15","doi-asserted-by":"crossref","first-page":"280","DOI":"10.1086\/432518","volume":"77","author":"Ishikawa K, Toru S, Tsunemi T, et a","year":"2005","journal-title":"American Journal of Human Genetics","ISSN":"http:\/\/id.crossref.org\/issn\/0002-9297","issn-type":"print"},{"key":"16","doi-asserted-by":"crossref","unstructured":"16. Matsumura R, Futamura N, Ando N, Ueno S. Frequency of spinocerebellar ataxia mutations in the Kinki district of Japan. Acta Neurologica Scandinavica 107: 38-41, 2003.","DOI":"10.1034\/j.1600-0404.2003.01347.x"},{"key":"17","doi-asserted-by":"crossref","first-page":"189","DOI":"10.1007\/s12311-008-0028-x","volume":"7","author":"Tsuji S, Onodera O, Goto J, Nishiza","year":"2008","journal-title":"Cerebellum","ISSN":"http:\/\/id.crossref.org\/issn\/1473-4222","issn-type":"print"},{"key":"18","doi-asserted-by":"crossref","first-page":"857","DOI":"10.1002\/mds.21443","volume":"22","author":"Nozaki H, Ikeuchi T, Kawakami A, et","year":"2007","journal-title":"Movement Disorders","ISSN":"http:\/\/id.crossref.org\/issn\/0885-3185","issn-type":"print"},{"key":"19","doi-asserted-by":"crossref","first-page":"153","DOI":"10.1016\/S0022-510X(00)00390-7","volume":"178","author":"Onodera Y, Aoki M, Tsuda T, et al","year":"2000","journal-title":"J Neurol Sci","ISSN":"http:\/\/id.crossref.org\/issn\/0022-510X","issn-type":"print"},{"key":"20","doi-asserted-by":"publisher","DOI":"10.1016\/S0022-510X(99)00076-3"},{"key":"21","doi-asserted-by":"publisher","DOI":"10.1007\/s10038-007-0182-x"},{"issue":"7","key":"22","first-page":"763","volume":"39","author":"SUGAWARA MASAHIRO","year":"1999","journal-title":"Clinical Neurology","ISSN":"http:\/\/id.crossref.org\/issn\/0009-918X","issn-type":"print"},{"key":"23","doi-asserted-by":"publisher","DOI":"10.1620\/tjem.195.85"},{"key":"24","doi-asserted-by":"crossref","unstructured":"24. Wakisaka A, Sasaki H, Takada A, et al. Spinocerebellar ataxia 1 (SCA1) in the Japanese in Hokkaido may derive from a single common ancestry. J Med Genet 32: 590-592, 1995.","DOI":"10.1136\/jmg.32.8.590"},{"key":"25","doi-asserted-by":"crossref","first-page":"150","DOI":"10.1007\/s12311-008-0010-7","volume":"7","author":"Ikeda Y, Daughters RS, Ranum LP","year":"2008","journal-title":"Cerebellum","ISSN":"http:\/\/id.crossref.org\/issn\/1473-4222","issn-type":"print"},{"key":"26","doi-asserted-by":"crossref","first-page":"180","DOI":"10.1016\/j.jns.2006.04.009","volume":"247","author":"Ouyang Y, Sakoe K, Shimazaki H, et","year":"2006","journal-title":"J Neurol Sci","ISSN":"http:\/\/id.crossref.org\/issn\/0022-510X","issn-type":"print"},{"key":"27","doi-asserted-by":"crossref","unstructured":"27. Sakai H, Yoshida K, Shimizu Y, Morita H, Ikeda SI, Matsumoto N. Analysis of an insertion mutation in a cohort of 94 patients with spinocerebellar ataxia type 31 from Nagano, Japan. Neurogenetics 2010 Epub ahead of print.","DOI":"10.1007\/s10048-010-0245-6"},{"key":"28","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1038\/jhg.2009.44","volume":"54","author":"Hirano R, Takashima H, Okubo R, et","year":"2009","journal-title":"Journal of Human Genetics","ISSN":"http:\/\/id.crossref.org\/issn\/1434-5161","issn-type":"print"},{"key":"29","doi-asserted-by":"publisher","DOI":"10.1007\/s00234-001-0713-7"},{"key":"30","doi-asserted-by":"publisher","DOI":"10.1111\/j.1468-1331.2008.02524.x"},{"key":"31","doi-asserted-by":"crossref","first-page":"383","DOI":"10.1007\/s004150050368","volume":"246","author":"Giuffrida S, Saponara R, Restivo DA","year":"1999","journal-title":"J Neurol","ISSN":"http:\/\/id.crossref.org\/issn\/0340-5354","issn-type":"print"},{"key":"32","doi-asserted-by":"crossref","first-page":"1799","DOI":"10.1097\/00001756-200310060-00008","volume":"14","author":"Brenneis C, Bosch SM, Schocke M, We","year":"2003","journal-title":"Neuroreport","ISSN":"http:\/\/id.crossref.org\/issn\/0959-4965","issn-type":"print"},{"key":"33","doi-asserted-by":"crossref","first-page":"159","DOI":"10.1002\/mds.20656","volume":"21","author":"Brenneis C, Boesch SM, Egger KE, et","year":"2006","journal-title":"Movement Disorders","ISSN":"http:\/\/id.crossref.org\/issn\/0885-3185","issn-type":"print"}],"container-title":["Internal Medicine"],"original-title":[],"language":"en","link":[{"URL":"http:\/\/www.jstage.jst.go.jp\/article\/internalmedicine\/49\/22\/49_22_2409\/_pdf","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2021,5,19]],"date-time":"2021-05-19T17:37:39Z","timestamp":1621445859000},"score":1,"resource":{"primary":{"URL":"http:\/\/www.jstage.jst.go.jp\/article\/internalmedicine\/49\/22\/49_22_2409\/_article"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2010]]},"references-count":33,"journal-issue":{"issue":"22","published-print":{"date-parts":[[2010]]}},"URL":"https:\/\/doi.org\/10.2169\/internalmedicine.49.4025","relation":{},"ISSN":["0918-2918","1349-7235"],"issn-type":[{"value":"0918-2918","type":"print"},{"value":"1349-7235","type":"electronic"}],"subject":[],"published":{"date-parts":[[2010]]}}}