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pro vyhledávání: '"Menezes Neto, Osvaldo Alves de"'
Publikováno v:
Repositório Institucional da UFSUniversidade Federal de SergipeUFS.
Sickle cell anemia (SCA) is the result of a mutation in the beta globin chain gene, resulting in the production of an abnormal hemoglobin, Hb S. Losing oxygen, Hb S decreases its solubility, suffering aggregation and polymerization, which hardens and
Externí odkaz:
https://ri.ufs.br/handle/riufs/3892
Publikováno v:
Repositório Institucional da UFS
Universidade Federal de Sergipe (UFS)
instacron:UFS
Universidade Federal de Sergipe (UFS)
instacron:UFS
Introduction: Sickle cell anemia (SCA) is a genetic disease responsible for the production of hemoglobin S (HbS) and has a wide variety of clinical presentations. One of the most widespread therapies is transfusion, which, while offering clinical ben
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::b9fff559136b38841bbb4164600956f4
http://ri.ufs.br/jspui/handle/riufs/13080
http://ri.ufs.br/jspui/handle/riufs/13080
Publikováno v:
Repositório Institucional da UFS
Universidade Federal de Sergipe (UFS)
instacron:UFS
Universidade Federal de Sergipe (UFS)
instacron:UFS
Sickle cell anemia (SCA) is the result of a mutation in the beta globin chain gene, resulting in the production of an abnormal hemoglobin, Hb S. Losing oxygen, Hb S decreases its solubility, suffering aggregation and polymerization, which hardens and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3056::ee3ab957f9818d7980821dd1a2d5a402
https://ri.ufs.br/handle/riufs/3892
https://ri.ufs.br/handle/riufs/3892
Autor:
Araújo, Jerônimo Gonçalves, Araújo-Melo, Carlos André, Menezes-Neto, Osvaldo Alves de, Silveira, Diego Fernandes Chagas da, Correia, Jailson Barros, Cipolotti, Rosana
Publikováno v:
Journal of Pediatric Hematology / Oncology; August 2011, Vol. 33 Issue: 6 p421-423, 3p