{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,20]],"date-time":"2026-01-20T05:18:07Z","timestamp":1768886287443,"version":"3.49.0"},"reference-count":20,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"2","content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2012,12]]},"abstract":"<jats:sec>\n            <jats:title>Abstract<\/jats:title>\n            <jats:p>Inclusion body myositis is the most common idiopathic inflammatory myopathy in elderly individuals. It typically causes proximal and distal limb weakness with forearm flexors and quadriceps being the most severely affected muscles. Axial musculature is infrequently involved. Here, we report an 80-year-old man who presented with an 18-month history of progressive truncal weakness causing stooped posture while standing and walking. Neurologic examination revealed no limb weakness. magnetic resonance imaging studies showed atrophy and findings, suggesting fatty replacement of paraspinal muscles. Needle electromyography confirmed the presence of an axial myopathy. Thoracic paraspinal muscle biopsy showed canonical features of inclusion body myositis. The current patient broadens the clinical presentation of inclusion body myositis.<\/jats:p>\n          <\/jats:sec>","DOI":"10.1097\/cnd.0b013e3182650718","type":"journal-article","created":{"date-parts":[[2012,11,21]],"date-time":"2012-11-21T09:12:29Z","timestamp":1353489149000},"page":"78-81","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":17,"title":["Camptocormia Due to Inclusion Body Myositis"],"prefix":"10.1097","volume":"14","author":[{"given":"Brent P.","family":"Goodman","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Teerin","family":"Liewluck","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Brian A.","family":"Crum","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Robert J.","family":"Spinner","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"276","reference":[{"key":"R1-5-20240808","doi-asserted-by":"crossref","first-page":"1186","DOI":"10.1136\/jnnp.2009.173823","article-title":"Inclusion body myositis: old and new concepts.","volume":"80","author":"Amato","year":"2009","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"R4-5-20240808","doi-asserted-by":"crossref","first-page":"355","DOI":"10.1212\/01.wnl.0000171857.09079.9f","article-title":"Camptocormia: pathogenesis, classification, and response to therapy.","volume":"65","author":"Azher","year":"2005","journal-title":"Neurology"},{"key":"R5-5-20240808","doi-asserted-by":"crossref","first-page":"51","DOI":"10.1136\/jnnp.60.1.51","article-title":"Bent spine syndrome.","volume":"60","author":"Serratice","year":"1996","journal-title":"J Neurol Neurosurg Psychiatry"},{"key":"R6-5-20240808","doi-asserted-by":"crossref","first-page":"730","DOI":"10.1007\/s00415-002-0701-9","article-title":". Axial myopathyan unrecognized entity.","volume":"249","author":"Mahjneh","year":"2002","journal-title":"J Neurol"},{"key":"R7-5-20240808","first-page":"829","article-title":". Myopathie tardive localisee aux muscles spinaux: une cause de cyphose lombaire acquise de ladulte.","volume":"58","author":"Laroche","year":"1991","journal-title":"Rev Rhum Mal Osteoartic"},{"key":"R8-5-20240808","first-page":"1011","article-title":"Aziza R, et al..","volume":"20","author":"Laroche","year":"1995","journal-title":"Is camptocormia a primary muscle disease Spine"},{"key":"R9-5-20240808","doi-asserted-by":"crossref","first-page":"189","DOI":"10.1002\/mus.10016","article-title":". Bent spine syndrome: computed tomographic study and isokinetic evaluation.","volume":"25","author":"Laroche","year":"2002","journal-title":"Muscle Nerve"},{"key":"R10-5-20240808","doi-asserted-by":"crossref","first-page":"542","DOI":"10.1002\/mus.20777","article-title":". Axial myopathy due to primary amyloidosis.","volume":"36","author":"Friedman","year":"2007","journal-title":"Muscle Nerve"},{"key":"R11-5-20240808","doi-asserted-by":"crossref","first-page":"824","DOI":"10.1002\/mus.20506","article-title":". Response of the dropped headbent spine syndrome to treatment with intravenous immunoglobulin.","volume":"33","author":"Dominick","year":"2006","journal-title":"Muscle Nerve"},{"key":"R12-5-20240808","doi-asserted-by":"crossref","first-page":"162","DOI":"10.1016\/j.jns.2007.09.042","article-title":". Dropped-head syndrome due steroid responsive focal myositis: a case report and review of the literature.","volume":"267","author":"Kastrup","year":"2008","journal-title":"J Neurol Sci"},{"key":"R13-5-20240808","doi-asserted-by":"crossref","first-page":"769","DOI":"10.1002\/(SICI)1097-4598(199906)22:6<769::AID-MUS15>3.0.CO;2-D","article-title":". Focal steroid responsive myositis causing dropped head syndrome.","volume":"22","author":"Biran","year":"1999","journal-title":"Muscle Nerve"},{"key":"R14-5-20240808","doi-asserted-by":"crossref","first-page":"110","DOI":"10.1007\/s00256-005-0011-2","article-title":". Dropped-head syndrome due to isolated myositis of neck extensor muscles: MRI findings.","volume":"35","author":"Gaeta","year":"2006","journal-title":"Skeletal Radiol"},{"key":"R15-5-20240808","doi-asserted-by":"crossref","first-page":"2023","DOI":"10.1097\/00007632-199609010-00020","article-title":". Cervical kyphosis after resolution of myopathic head drop. A case report.","volume":"21","author":"Jaster","year":"1996","journal-title":"Spine"},{"key":"R16-5-20240808","doi-asserted-by":"crossref","first-page":"598","DOI":"10.1002\/mds.10110","article-title":". Camptocormia in Parkinsons disease mimicked by focal myositis of the paraspinal muscles.","volume":"17","author":"Wunderlich","year":"2002","journal-title":"Mov Disord"},{"key":"R17-5-20240808","doi-asserted-by":"crossref","first-page":"993","DOI":"10.1212\/WNL.45.5.993","article-title":". Inclusion body myositis presenting with isolated erector spinae paresis.","volume":"45","author":"Hund","year":"1995","journal-title":"Neurology"},{"key":"R18-5-20240808","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":"R19-5-20240808","doi-asserted-by":"crossref","first-page":"727","DOI":"10.1093\/brain\/112.3.727","article-title":". Inclusion body myositis: observation in 40 patients.","volume":"112","author":"Lotz","year":"1989","journal-title":"Brain"},{"key":"R20-5-20240808","doi-asserted-by":"crossref","first-page":"705","DOI":"10.1002\/ana.410380504","article-title":". Inclusion body myositis and myopathies.","volume":"38","author":"Griggs","year":"1995","journal-title":"Ann Neurol"},{"key":"R21-5-20240808","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":"R22-5-20240808","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"}],"container-title":["Journal of Clinical Neuromuscular Disease"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/journals.lww.com\/00131402-201212000-00005","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,8,8]],"date-time":"2024-08-08T23:23:27Z","timestamp":1723159407000},"score":1,"resource":{"primary":{"URL":"https:\/\/journals.lww.com\/00131402-201212000-00005"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2012,12]]},"references-count":20,"journal-issue":{"issue":"2","published-print":{"date-parts":[[2012]]}},"URL":"https:\/\/doi.org\/10.1097\/cnd.0b013e3182650718","relation":{},"ISSN":["1522-0443"],"issn-type":[{"value":"1522-0443","type":"print"}],"subject":[],"published":{"date-parts":[[2012,12]]}}}