dc.creatorDe Oliveira C.C.
dc.creatorCiasca S.M.
dc.creatorMoura-Ribeiro M.V.L.
dc.date2008
dc.date2015-06-30T19:17:35Z
dc.date2015-11-26T14:41:32Z
dc.date2015-06-30T19:17:35Z
dc.date2015-11-26T14:41:32Z
dc.date.accessioned2018-03-28T21:48:31Z
dc.date.available2018-03-28T21:48:31Z
dc.identifier
dc.identifierArquivos De Neuro-psiquiatria. , v. 66, n. 1, p. 30 - 33, 2008.
dc.identifier0004282X
dc.identifier10.1590/S0004-282X2008000100008
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-42049118965&partnerID=40&md5=0e3892919b97ad6ef0284bd0f0c3b049
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/105616
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/105616
dc.identifier2-s2.0-42049118965
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1250882
dc.descriptionThe aim of this study was to characterize a group of patients (n=8) with sickle cell disease (SCD) and ischemic stroke concerning the clinical, neurological, imaging and progressive aspects. Data were collected from records and completed with an interview of patients and their parents. In this study there were 8 patients with ages ranging from 10 to 23 years old; SCD diagnosis was given between one and two years of age with clinical features of fatigue and anemia. The stroke was ischemic in all individuals and the first cerebrovascular event occurred before 6 years of age; 3 patients had recurrence of stroke despite prophylactic blood transfusion therapy and both cerebral hemispheres were affected in 4 patients. Clinical and neurological current features observed were: acute pain crises, sialorrhea, mouth breathing, motor, and neuropsychological impairments resulting from cortical-subcortical structure lesions.
dc.description66
dc.description1
dc.description30
dc.description33
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dc.languageen
dc.publisher
dc.relationArquivos de Neuro-Psiquiatria
dc.rightsaberto
dc.sourceScopus
dc.titleStroke In Patients With Sickle Cell Disease: Clinical And Neurological Aspects
dc.typeArtículos de revistas


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