{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,5,20]],"date-time":"2026-05-20T04:15:04Z","timestamp":1779250504032,"version":"3.51.4"},"reference-count":17,"publisher":"Elsevier BV","issue":"3","license":[{"start":{"date-parts":[[2011,5,1]],"date-time":"2011-05-01T00:00:00Z","timestamp":1304208000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"},{"start":{"date-parts":[[2011,5,1]],"date-time":"2011-05-01T00:00:00Z","timestamp":1304208000000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/legal\/tdmrep-license"}],"funder":[{"DOI":"10.13039\/501100003593","name":"Conselho Nacional de Desenvolvimento Cient\u00edfico e Tecnol\u00f3gico","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100003593","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100002322","name":"Coordena\u00e7\u00e3o de Aperfei\u00e7oamento de Pessoal de N\u00edvel Superior","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100002322","id-type":"DOI","asserted-by":"publisher"}]},{"DOI":"10.13039\/501100004612","name":"Funda\u00e7\u00e3o Arauc\u00e1ria","doi-asserted-by":"publisher","id":[{"id":"10.13039\/501100004612","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["Mitochondrion"],"published-print":{"date-parts":[[2011,5]]},"DOI":"10.1016\/j.mito.2011.01.003","type":"journal-article","created":{"date-parts":[[2011,2,7]],"date-time":"2011-02-07T04:11:30Z","timestamp":1297051890000},"page":"528-532","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":30,"title":["MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients"],"prefix":"10.1016","volume":"11","author":[{"given":"Paulo Jos\u00e9","family":"Lorenzoni","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Rosana H.","family":"Scola","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Cl\u00e1udia S. Kamoi","family":"Kay","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Raquel C.","family":"Arndt","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Carlos E.","family":"Silvado","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Lineu C.","family":"Werneck","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.mito.2011.01.003_bb0005","doi-asserted-by":"crossref","first-page":"457","DOI":"10.1038\/290457a0","article-title":"Sequence and organization of the human mitochondrial genome","volume":"290","author":"Anderson","year":"1981","journal-title":"Nature"},{"key":"10.1016\/j.mito.2011.01.003_bb0010","doi-asserted-by":"crossref","first-page":"32","DOI":"10.1590\/S0004-282X1990000100006","article-title":"Mitochondrial myopathy and myoclonic epilepsy","volume":"48","author":"Arruda","year":"1990","journal-title":"Arq. Neuropsiquiatr."},{"key":"10.1016\/j.mito.2011.01.003_bb0015","doi-asserted-by":"crossref","first-page":"441","DOI":"10.1016\/j.mito.2004.07.036","article-title":"Pathology of skeletal muscle in mitochondrial disorders","volume":"4","author":"Bourgeois","year":"2004","journal-title":"Mitochondrion"},{"key":"10.1016\/j.mito.2011.01.003_bb0020","doi-asserted-by":"crossref","first-page":"409","DOI":"10.1002\/mus.20465","article-title":"Pure neural leprosy: diagnostic value of the polymerase chain reaction","volume":"33","author":"Cunha","year":"2006","journal-title":"Muscle Nerve"},{"key":"10.1016\/j.mito.2011.01.003_bb0025","first-page":"217","article-title":"Clinical features and genetics of myoclonic epilepsy with ragged red fibers","volume":"89","author":"DiMauro","year":"2002","journal-title":"Adv. Neurol."},{"key":"10.1016\/j.mito.2011.01.003_bb0030","doi-asserted-by":"crossref","first-page":"S90","DOI":"10.1002\/mus.880181419","article-title":"Clinicopathological features of MERRF","volume":"3","author":"Fukuhara","year":"1995","journal-title":"Muscle Nerve Suppl."},{"key":"10.1016\/j.mito.2011.01.003_bb0035","doi-asserted-by":"crossref","first-page":"117","DOI":"10.1016\/0022-510X(80)90031-3","article-title":"Myoclonus epilepsy associated with ragged-red fibers (mitochondrial abnormalities): disease entity or a syndrome?","volume":"47","author":"Fukuhara","year":"1980","journal-title":"J. Neurol. Sci."},{"key":"10.1016\/j.mito.2011.01.003_bb0040","doi-asserted-by":"crossref","first-page":"471","DOI":"10.1016\/j.mito.2004.07.008","article-title":"Neuroimaging of mitochondrial disorders","volume":"4","author":"Haas","year":"2004","journal-title":"Mitochondrion"},{"key":"10.1016\/j.mito.2011.01.003_bb0045","doi-asserted-by":"crossref","first-page":"S102","DOI":"10.1002\/mus.880181421","article-title":"Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas","volume":"3","author":"Larsson","year":"1995","journal-title":"Muscle Nerve Suppl."},{"key":"10.1016\/j.mito.2011.01.003_bb0050","doi-asserted-by":"crossref","first-page":"668","DOI":"10.1590\/S0004-282X2009000400018","article-title":"MELAS: clinical features, muscle biopsy and molecular genetics","volume":"67","author":"Lorenzoni","year":"2009","journal-title":"Arq. Neuropsiquiatr."},{"key":"10.1016\/j.mito.2011.01.003_bb0055","doi-asserted-by":"crossref","first-page":"483","DOI":"10.1016\/0960-8966(95)00009-C","article-title":"The 8344 mutation in mitochondrial DNA: a comparison between the proportion of mutant DNA and clinico-pathologic findings","volume":"5","author":"Ozawa","year":"1995","journal-title":"Neuromuscul. Dis."},{"key":"10.1016\/j.mito.2011.01.003_bb0060","first-page":"933","article-title":"Maternally inherited cardiomyopathy and hearing loss associated with a novel mutation in the mitochondrial DNA tRNALys gene (G8363A)","volume":"58","author":"Santorelli","year":"1996","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.mito.2011.01.003_bb0065","doi-asserted-by":"crossref","first-page":"239","DOI":"10.1016\/S1474-4422(05)70043-0","article-title":"Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects","volume":"4","author":"Shahwan","year":"2005","journal-title":"Lancet Neurol."},{"key":"10.1016\/j.mito.2011.01.003_bb0070","first-page":"1179","article-title":"Mitochondrial genetics: principles and practice","volume":"51","author":"Shoffner","year":"1992","journal-title":"Am. J. Hum. Genet."},{"key":"10.1016\/j.mito.2011.01.003_bb0075","doi-asserted-by":"crossref","first-page":"16","DOI":"10.1016\/j.jns.2006.09.021","article-title":"Progressive myoclonic epilepsy: a clinical, electrophysiological and pathological study from South India","volume":"252","author":"Sinha","year":"2007","journal-title":"J. Neurol. Sci."},{"issue":"suppl","key":"10.1016\/j.mito.2011.01.003_bb0080","first-page":"2","article-title":"The value of muscle biopsy in neurology: a study of 290 biopsies","volume":"10","author":"Werneck","year":"1981","journal-title":"Rev. Bras. Clin. Ter."},{"key":"10.1016\/j.mito.2011.01.003_bb0085","doi-asserted-by":"crossref","first-page":"2153","DOI":"10.1093\/brain\/awh259","article-title":"Mitochondrial disorders","volume":"127","author":"Zeviani","year":"2004","journal-title":"Brain"}],"container-title":["Mitochondrion"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1567724911000249?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1567724911000249?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2025,10,27]],"date-time":"2025-10-27T12:54:22Z","timestamp":1761569662000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1567724911000249"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2011,5]]},"references-count":17,"journal-issue":{"issue":"3","published-print":{"date-parts":[[2011,5]]}},"alternative-id":["S1567724911000249"],"URL":"https:\/\/doi.org\/10.1016\/j.mito.2011.01.003","relation":{},"ISSN":["1567-7249"],"issn-type":[{"value":"1567-7249","type":"print"}],"subject":[],"published":{"date-parts":[[2011,5]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"MERRF: Clinical features, muscle biopsy and molecular genetics in Brazilian patients","name":"articletitle","label":"Article Title"},{"value":"Mitochondrion","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.mito.2011.01.003","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"Copyright \u00a9 2011 Elsevier B.V. and Mitochondria Research Society. All rights reserved.","name":"copyright","label":"Copyright"}]}}