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Outbreak of Guillain-Barre syndrome in Perú
dc.contributor.author | Díaz-Soto, S. | |
dc.contributor.author | Chavez, Karen | |
dc.contributor.author | Chaca, Alex | |
dc.contributor.author | Alanya, Joseff | |
dc.contributor.author | Tirado-Hurtado, Indira | |
dc.date.accessioned | 2020-03-27T20:03:05Z | |
dc.date.available | 2020-03-27T20:03:05Z | |
dc.date.issued | 2019 | |
dc.identifier.uri | https://hdl.handle.net/20.500.14308/2637 | |
dc.description.abstract | Guillain-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.format | application/pdf | es_PE |
dc.language.iso | eng | es_PE |
dc.publisher | eNeurologicalSci. Elsevier | es_PE |
dc.rights | info:eu-repo/semantics/openAccess | es_PE |
dc.rights | Attribution-NonCommercial-NoDerivs 3.0 United States | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/3.0/us/ | * |
dc.source | Universidad Privada San Juan Bautista | es_PE |
dc.source | Repositorio institucional - UPSJB | es_PE |
dc.subject | Síndorme de Guillain-Barré | es_PE |
dc.subject | Neuropatía paralítica aguda | es_PE |
dc.subject | Brote | es_PE |
dc.subject | Enterovirus | es_PE |
dc.title | Outbreak of Guillain-Barre syndrome in Perú | es_PE |
dc.type | info:eu-repo/semantics/article | es_PE |
dc.publisher.country | PE |