Please use this identifier to cite or link to this item: https://repositorio.unifesp.br/handle/11600/30293
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dc.contributor.authorFelicio, Andre C. [UNIFESP]
dc.contributor.authorGodelro-Junior, Clecio [UNIFESP]
dc.contributor.authorAlberto, Lucianna G. [UNIFESP]
dc.contributor.authorPinto, Aline P. M. [UNIFESP]
dc.contributor.authorSallum, Juliana M. F. [UNIFESP]
dc.contributor.authorTelve, Helio G.
dc.contributor.authorBarsottini, Orlando G. P. [UNIFESP]
dc.date.accessioned2016-01-24T13:49:23Z-
dc.date.available2016-01-24T13:49:23Z-
dc.date.issued2008-01-01
dc.identifierhttp://dx.doi.org/10.1016/j.parkreldis.2007.08.008
dc.identifier.citationParkinsonism & Related Disorders. Oxford: Elsevier B.V., v. 14, n. 4, p. 370-372, 2008.
dc.identifier.issn1353-8020
dc.identifier.urihttp://repositorio.unifesp.br/handle/11600/30293-
dc.description.abstractBehr syndrome is an autosomal recessive disease characterized by early-onset ataxia, optic atrophy and other signs such as pyramidal tract dysfunction. Autosomal dominant inheritance has also been described. in this case report we present a family pedigree of patients with an inherited autosomal dominant Behr syndrome-like phenotype emphasizing their clinical and neuroimaging features. (c) 2007 Elsevier B.V. All rights reserved.en
dc.format.extent370-372
dc.language.isoeng
dc.publisherElsevier B.V.
dc.relation.ispartofParkinsonism & Related Disorders
dc.rightsAcesso restrito
dc.subjectBehr syndromeen
dc.subjectcerebellar ataxiaen
dc.subjectoptic atrophyen
dc.subjectautosomal dominanten
dc.titleFamilial Behr syndrome-like phenotype with autosomal dominant inheritanceen
dc.typeArtigo
dc.rights.licensehttp://www.elsevier.com/about/open-access/open-access-policies/article-posting-policy
dc.contributor.institutionUniversidade Federal de São Paulo (UNIFESP)
dc.contributor.institutionUniv Fed Parana
dc.description.affiliationUniversidade Federal de São Paulo, Dept Neurol & Neurosurg, São Paulo, Brazil
dc.description.affiliationUniversidade Federal de São Paulo, Dept Ophthalmol, São Paulo, Brazil
dc.description.affiliationUniv Fed Parana, Movement Disorder Unit, BR-80060000 Curitiba, Parana, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Dept Neurol & Neurosurg, São Paulo, Brazil
dc.description.affiliationUnifespUniversidade Federal de São Paulo, Dept Ophthalmol, São Paulo, Brazil
dc.identifier.doi10.1016/j.parkreldis.2007.08.008
dc.description.sourceWeb of Science
dc.identifier.wosWOS:000257646500022
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