dc.creatorGrotto H.Z.
dc.creatorCosta F.F.
dc.date1992
dc.date2015-06-30T14:22:35Z
dc.date2015-11-26T14:43:25Z
dc.date2015-06-30T14:22:35Z
dc.date2015-11-26T14:43:25Z
dc.date.accessioned2018-03-28T21:51:31Z
dc.date.available2018-03-28T21:51:31Z
dc.identifier
dc.identifierRevista Paulista De Medicina. , v. 110, n. 6, p. 262 - 266, 1992.
dc.identifier350362
dc.identifier
dc.identifierhttp://www.scopus.com/inward/record.url?eid=2-s2.0-0026942601&partnerID=40&md5=e8ba8114c2dc5795ceab00de3075b309
dc.identifierhttp://www.repositorio.unicamp.br/handle/REPOSIP/99631
dc.identifierhttp://repositorio.unicamp.br/jspui/handle/REPOSIP/99631
dc.identifier2-s2.0-0026942601
dc.identifier.urihttp://repositorioslatinoamericanos.uchile.cl/handle/2250/1251669
dc.descriptionThe splenic function measured by the counts of "pitted" erythrocytes has been assessed in 87 patients with sickle cell disease (59 homozygotes for hemoglobin S (SS), 14 double heterozygotes for Hb S and beta zero thalassemia (S/beta zero thal), 4 S/beta+ thal and 10 SC patients) in Southeast Brazil. Results showed a progressive increase in pit counts according to age. The reduction pattern in the splenic function was similar for the SS, S/beta zero thal and S/beta+ thal patients, and over the age of 12 almost all patients presented counts compatible with severe splenic hypofunction. Patients with SC hemoglobinopathy presented slower development of hyposplenism and lower levels of pit counts even in advanced ages. Except for S/beta+ thal patients, the developmental pattern of hyposplenism was not different from that reported among patients in the United States and Jamaica.
dc.description110
dc.description6
dc.description262
dc.description266
dc.languageen
dc.publisher
dc.relationRevista Paulista de Medicina
dc.rightsfechado
dc.sourceScopus
dc.titlePattern Of Splenic Phagocytic Function In Brazilian Patients With Sickle Cell Disease.
dc.typeArtículos de revistas


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