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dc.contributor.authorDíaz-Soto, S.
dc.contributor.authorChavez, Karen
dc.contributor.authorChaca, Alex
dc.contributor.authorAlanya, Joseff
dc.contributor.authorTirado-Hurtado, Indira
dc.date.accessioned2020-03-27T20:03:05Z
dc.date.available2020-03-27T20:03:05Z
dc.date.issued2019
dc.identifier.urihttps://hdl.handle.net/20.500.14308/2637
dc.description.abstractGuillain-Barre syndrome (GBS) is the most common and most severe acute paralytic neuropathy with an annual incidence of 0.5 to 2 per 100, 000 inhabitants. It can affect people of all ages, but it is more frequent in adults and in males [1,2]. The specific cause of GBS is still unknown; however, its development is associated with previous respiratory or gastrointestinal infections or another pathology in which the immune system attacks the peripheral nerves [2]. GBS has no cure, but an adequate treatment can improve symptoms and shorten its duration (more than 90% of patients can recover completely one year after the onset of the disease); whereas few cases are fatal (mortality rate of 3–7%) [2,3].es_PE
dc.formatapplication/pdfes_PE
dc.language.isoenges_PE
dc.publishereNeurologicalSci. Elsevieres_PE
dc.rightsinfo:eu-repo/semantics/openAccesses_PE
dc.rightsAttribution-NonCommercial-NoDerivs 3.0 United States*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/3.0/us/*
dc.sourceUniversidad Privada San Juan Bautistaes_PE
dc.sourceRepositorio institucional - UPSJBes_PE
dc.subjectSíndorme de Guillain-Barrées_PE
dc.subjectNeuropatía paralítica agudaes_PE
dc.subjectBrotees_PE
dc.subjectEnteroviruses_PE
dc.titleOutbreak of Guillain-Barre syndrome in Perúes_PE
dc.typeinfo:eu-repo/semantics/articlees_PE
dc.publisher.countryPE


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