Utilize este identificador para referenciar este registo: http://hdl.handle.net/10451/53156
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degois.publication.titleJournal of Neurologypt_PT
dc.relation.publisherversionhttps://www.springer.com/journal/415pt_PT
dc.contributor.authorCoelho, Pedro-
dc.contributor.authorPaula, André-
dc.contributor.authorMartins, Isabel Vidal-
dc.contributor.authorFalcão De Campos, Catarina-
dc.contributor.authorFerreira, João-
dc.contributor.authorAntunes, Ana Patrícia-
dc.contributor.authorAlbuquerque, Luísa-
dc.date.accessioned2022-05-24T14:06:07Z-
dc.date.available2022-05-24T14:06:07Z-
dc.date.issued2022-
dc.identifier.citationJ Neurol. 2022 May 18;1-5pt_PT
dc.identifier.issn0340-5354-
dc.identifier.urihttp://hdl.handle.net/10451/53156-
dc.description© The Author(s), under exclusive licence to Springer-Verlag GmbH Germany 2022.pt_PT
dc.description.abstractCombined central and peripheral demyelination (CCPD) is a rare neurological entity that afects both the central and peripheral nervous system with demyelinating lesions. The pattern of involvement of the central nervous system (CNS) includes frequent bilateral optical neuritis, involvement of grey matter and occasional longitudinally extensive transverse myelitis (LETM) in the absence of oligoclonal bands (OCB) or antibodies such as antiaquaporin-4 (AQP4) and anti-myelin oligodendrocyte glycoprotein (MOG). Peripheral nervous system (PNS) involvement occurs mainly as a chronic infammatory demyelinating polyneuropathy (CIDP)-like disease. Infections and vaccinations are known triggers. CCPD typically evolves aggressively with progressive cumulative neurological impairment despite immunosuppression.pt_PT
dc.language.isoengpt_PT
dc.publisherSpringer Naturept_PT
dc.rightsrestrictedAccesspt_PT
dc.titleCombined central and peripheral demyelination after COVID-19 vaccinationpt_PT
dc.typearticlept_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.peerreviewedyespt_PT
dc.identifier.doi10.1007/s00415-022-11188-7pt_PT
dc.identifier.eissn1432-1459-
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