dc.creatorDe Lima Resende L.A.
dc.creatorKimaid P.A.T.
dc.creatorDe Lima Castro H.A.
dc.creatorFonseca R.G.
dc.creatorDal Pai V.
dc.creatorUeda A.K.
dc.creatorMontenegro M.R.G.
dc.date1998
dc.date2015-06-30T15:04:48Z
dc.date2015-11-26T15:12:51Z
dc.date2015-06-30T15:04:48Z
dc.date2015-11-26T15:12:51Z
dc.date.accessioned2018-03-28T22:22:56Z
dc.date.available2018-03-28T22:22:56Z
dc.identifier
dc.identifierRevista Brasileira De Neurologia. , v. 34, n. 2, p. 55 - 58, 1998.
dc.identifier1018469
dc.identifier
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-2542520926&partnerID=40&md5=24cd04eda0f2bf3cb1d81f2d86d73f7c
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/100491
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/100491
dc.identifier2-s2.0-2542520926
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1258483
dc.descriptionIn this paper the authors describe three cases of multicore myopathy in the same family. Case J was a white 77-year-old patient with proximal muscular atrophy and weakness, global hypotonia and global hypoactive deep tendon reflexes. Motor and sensory conduction studies were normal in all limbs. EMG examination showed a myopathic pattern with frequent spontaneous activity consisting of fibrillations and positive sharp waves. Histochemical reactions showed typical oxidative alterations of multicore myopathy. Cases 2 and 3 were the son and the daughter of case 1 respectively. They were both non-symptomatic patients with minimal EMG and histochemical alterations. These three patients illustrated the great clinical variability of this condition.
dc.description34
dc.description2
dc.description55
dc.description58
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dc.languagept
dc.publisher
dc.relationRevista Brasileira de Neurologia
dc.rightsfechado
dc.sourceScopus
dc.titleMulticore Disease: Histochemical Analysis Of A Family [miopatia Do Multicore: Análise Histoquímica De Uma Família]
dc.typeArtículos de revistas


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