{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,9,8]],"date-time":"2026-09-08T12:48:10Z","timestamp":1788871690990,"version":"build-2803163510"},"reference-count":23,"publisher":"Elsevier BV","issue":"1-2","license":[{"start":{"date-parts":[[2014,11,1]],"date-time":"2014-11-01T00:00:00Z","timestamp":1414800000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2014,11,1]],"date-time":"2014-11-01T00:00:00Z","timestamp":1414800000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"DOI":"10.13039\/501100001700","name":"Ministry of Education, Culture, Sports, Science and Technology","doi-asserted-by":"crossref","id":[{"id":"10.13039\/501100001700","id-type":"DOI","asserted-by":"crossref"}]},{"name":"Amyloidosis Research Committee"},{"DOI":"10.13039\/501100003478","name":"Ministry of Health, Labour and Welfare, Japan","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100003478","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["clinicalkey.com","clinicalkey.com.au","clinicalkey.es","clinicalkey.fr","clinicalkey.jp","jns-journal.com","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Journal of the Neurological Sciences"],"published-print":{"date-parts":[[2014,11]]},"DOI":"10.1016\/j.jns.2014.08.009","type":"journal-article","created":{"date-parts":[[2014,8,13]],"date-time":"2014-08-13T11:34:56Z","timestamp":1407929696000},"page":"133-137","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":10,"title":["Clinical features of Japanese patients with inclusion body myositis"],"prefix":"10.1016","volume":"346","author":[{"given":"Hiroko","family":"Hori","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Satoshi","family":"Yamashita","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nozomu","family":"Tawara","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tomoo","family":"Hirahara","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Kensuke","family":"Kawakami","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Tomo","family":"Nishikami","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yasushi","family":"Maeda","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yukio","family":"Ando","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.jns.2014.08.009_bb0005","doi-asserted-by":"crossref","first-page":"554","DOI":"10.1007\/s00415-011-6185-8","article-title":"Increase in number of sporadic inclusion body myositis (sIBM) in Japan","volume":"259","author":"Suzuki","year":"2011","journal-title":"J Neurol"},{"key":"10.1016\/j.jns.2014.08.009_bb0010","doi-asserted-by":"crossref","first-page":"333","DOI":"10.2169\/internalmedicine.52.8910","article-title":"Demographic features of Japanese patients with sporadic inclusion body myositis: a single-center referral experience","volume":"52","author":"Nakanishi","year":"2013","journal-title":"Intern Med"},{"key":"10.1016\/j.jns.2014.08.009_bb0015","doi-asserted-by":"crossref","first-page":"1253","DOI":"10.1001\/archneur.58.8.1253","article-title":"Inclusion body myositis mimicking motor neuron disease","volume":"58","author":"Dabby","year":"2001","journal-title":"Arch Neurol"},{"key":"10.1016\/j.jns.2014.08.009_bb0020","doi-asserted-by":"crossref","first-page":"949","DOI":"10.1002\/mus.880131010","article-title":"Electrophysiological spectrum of inclusion body myositis","volume":"13","author":"Joy","year":"1990","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.jns.2014.08.009_bb0025","doi-asserted-by":"crossref","first-page":"327","DOI":"10.1016\/0022-510X(90)90167-L","article-title":"Inclusion body myositis: peripheral nerve involvement. Combined morphological and electrophysiological studies on peripheral nerves","volume":"99","author":"Lindberg","year":"1990","journal-title":"J Neurol Sci"},{"key":"10.1016\/j.jns.2014.08.009_bb0030","doi-asserted-by":"crossref","first-page":"142","DOI":"10.1016\/j.nmd.2009.11.003","article-title":"Inclusion body myositis: MRC Centre for Neuromuscular Diseases, IBM workshop, London, 13 June 2008","volume":"20","author":"Hilton-Jones","year":"2010","journal-title":"Neuromuscul Disord"},{"key":"10.1016\/j.jns.2014.08.009_bb0035","doi-asserted-by":"crossref","first-page":"473","DOI":"10.1002\/mus.20958","article-title":"Inclusion body myositis functional rating scale: a reliable and valid measure of disease severity","volume":"37","author":"Jackson","year":"2008","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.jns.2014.08.009_bb0040","doi-asserted-by":"crossref","first-page":"1154","DOI":"10.1001\/archneur.1987.00520230042011","article-title":"Spectrum of inclusion body myositis","volume":"44","author":"Ringel","year":"1987","journal-title":"Arch Neurol"},{"issue":"Pt 3","key":"10.1016\/j.jns.2014.08.009_bb0045","doi-asserted-by":"crossref","first-page":"727","DOI":"10.1093\/brain\/112.3.727","article-title":"Inclusion body myositis. Observations in 40 patients","volume":"112","author":"Lotz","year":"1989","journal-title":"Brain"},{"key":"10.1016\/j.jns.2014.08.009_bb0050","first-page":"1385","article-title":"Inclusion body myositis: analysis of 32 cases","volume":"19","author":"Sayers","year":"1992","journal-title":"J Rheumatol"},{"key":"10.1016\/j.jns.2014.08.009_bb0055","doi-asserted-by":"crossref","first-page":"351","DOI":"10.1007\/BF00186623","article-title":"Inclusion body myositis: clinical and histopathological features of 36 patients","volume":"71","author":"Beyenburg","year":"1993","journal-title":"Clin Investig"},{"key":"10.1016\/j.jns.2014.08.009_bb0060","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1111\/j.1600-0404.1994.tb01647.x","article-title":"Inclusion body myositis: clinical, morphological, physiological and laboratory findings in 18 cases","volume":"89","author":"Lindberg","year":"1994","journal-title":"Acta Neurol Scand"},{"key":"10.1016\/j.jns.2014.08.009_bb0065","doi-asserted-by":"crossref","first-page":"581","DOI":"10.1002\/ana.410400407","article-title":"Inclusion body myositis: clinical and pathological boundaries","volume":"40","author":"Amato","year":"1996","journal-title":"Ann Neurol"},{"key":"10.1016\/j.jns.2014.08.009_bb0070","doi-asserted-by":"crossref","first-page":"296","DOI":"10.1212\/WNL.55.2.296","article-title":"Disease progression in sporadic inclusion body myositis: observations in 78 patients","volume":"55","author":"Peng","year":"2000","journal-title":"Neurology"},{"key":"10.1016\/j.jns.2014.08.009_bb0075","doi-asserted-by":"crossref","first-page":"320","DOI":"10.1097\/00005792-200109000-00006","article-title":"Inclusion body myositis in Connecticut: observations in 35 patients during an 8-year period","volume":"80","author":"Felice","year":"2001","journal-title":"Medicine (Baltimore)"},{"key":"10.1016\/j.jns.2014.08.009_bb0080","doi-asserted-by":"crossref","first-page":"3176","DOI":"10.1093\/brain\/awr213","article-title":"Long-term observational study of sporadic inclusion body myositis","volume":"134","author":"Benveniste","year":"2011","journal-title":"Brain"},{"key":"10.1016\/j.jns.2014.08.009_bb0085","doi-asserted-by":"crossref","first-page":"1448","DOI":"10.1007\/s00415-005-0884-y","article-title":"Inclusion body myositis. Clinical features and clinical course of the disease in 64 patients","volume":"252","author":"Badrising","year":"2005","journal-title":"J Neurol"},{"key":"10.1016\/j.jns.2014.08.009_bb0090","doi-asserted-by":"crossref","first-page":"181","DOI":"10.1002\/mus.23292","article-title":"Electromyographs of the flexor digitorum profundus muscle are useful for the diagnosis of inclusion body myositis","volume":"46","author":"Hokkoku","year":"2012","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.jns.2014.08.009_bb0095","doi-asserted-by":"crossref","first-page":"377","DOI":"10.1038\/ng1332","article-title":"Inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia is caused by mutant valosin-containing protein","volume":"36","author":"Watts","year":"2004","journal-title":"Nat Genet"},{"key":"10.1016\/j.jns.2014.08.009_bb0100","doi-asserted-by":"crossref","first-page":"467","DOI":"10.1038\/nature11922","article-title":"Mutations in prion-like domains in hnRNPA2B1 and hnRNPA1 cause multisystem proteinopathy and ALS","volume":"495","author":"Kim","year":"2013","journal-title":"Nature"},{"key":"10.1016\/j.jns.2014.08.009_bb0105","first-page":"103","article-title":"Diagnostic value of markers of muscle degeneration in sporadic inclusion body myositis","volume":"30","author":"Dubourg","year":"2011","journal-title":"Acta Myol"},{"key":"10.1016\/j.jns.2014.08.009_bb0110","doi-asserted-by":"crossref","first-page":"406","DOI":"10.1111\/j.1365-2990.2012.01297.x","article-title":"Optineurin is potentially associated with TDP-43 and involved in the pathogenesis of inclusion body myositis","volume":"39","author":"Yamashita","year":"2013","journal-title":"Neuropathol Appl Neurobiol"},{"key":"10.1016\/j.jns.2014.08.009_bb0115","doi-asserted-by":"crossref","first-page":"457","DOI":"10.1097\/WCO.0b013e32834a9589","article-title":"Inflammatory myopathies: management of steroid resistance","volume":"24","author":"Dalakas","year":"2011","journal-title":"Curr Opin Neurol"}],"container-title":["Journal of the Neurological Sciences"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X1400522X?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S0022510X1400522X?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,9,20]],"date-time":"2025-09-20T15:43:25Z","timestamp":1758383005000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S0022510X1400522X"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2014,11]]},"references-count":23,"journal-issue":{"issue":"1-2","published-print":{"date-parts":[[2014,11]]}},"alternative-id":["S0022510X1400522X"],"URL":"https:\/\/doi.org\/10.1016\/j.jns.2014.08.009","relation":{},"ISSN":["0022-510X"],"issn-type":[{"value":"0022-510X","type":"print"}],"subject":[],"published":{"date-parts":[[2014,11]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Clinical features of Japanese patients with inclusion body myositis","name":"articletitle","label":"Article Title"},{"value":"Journal of the Neurological Sciences","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.jns.2014.08.009","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2014 Elsevier B.V. All rights reserved.","name":"copyright","label":"Copyright"}]}}