S
Saide Maria Sarmento Trindade
Publications - 3
Citations - 48
Saide Maria Sarmento Trindade is an academic researcher. The author has contributed to research in topics: Sickle cell anemia & Population. The author has an hindex of 2, co-authored 2 publications receiving 43 citations.
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DNA polymorphisms at BCL11A, HBS1L-MYB and Xmn1-HBG2 site loci associated with fetal hemoglobin levels in sickle cell anemia patients from Northern Brazil.
Greice de Lemos Cardoso,Isabela Guerreiro Diniz,Aylla N L M Silva,Daniele Almeida Cunha,Josivaldo Soares da Silva Junior,Camila Tavares Carvalho Uchôa,Sidney Santos,Saide Maria Sarmento Trindade,Maria do Socorro de Oliveira Cardoso,João Farias Guerreiro +9 more
TL;DR: The results showed that high levels of HbF were primarily influenced by alleles of BCL11A and HMIP and to a lesser extent by rs748214 Gγ-globin (HBG2) gene promoter, and reinforce the suggestion that studies of association between genetic modifiers and clinical and laboratory manifestations in Brazil must be controlled by ancestry.
Journal ArticleDOI
The Spectrum of β-Thalassemia Mutations in a Population from the Brazilian Amazon.
Aylla N L M Silva,Greice de Lemos Cardoso,Daniele Almeida Cunha,Isabela Guerreiro Diniz,Sidney Santos,Gabriela Barreto Andrade,Saide Maria Sarmento Trindade,Maria do Socorro de Oliveira Cardoso,Larissa T V M Francês,João Farias Guerreiro +9 more
TL;DR: The profile of β-thal mutations found in northern Brazil is different from those described in other regions of the country, and the European contribution in the southeast and south was largely made up of immigrants of other nationalities, such as Italian and Spanish, in addition to Portuguese.
Journal ArticleDOI
Cerebral Vasculopathy in Children With Sickle Cell Disease in an Amazonian Population
Felipe Lima Alcolumbre Tobelem,Guilherme Augusto Lira Ribeiro de Andrade,Joelma Karin Sagica Fernandes Paschoal,Maria do Socorro de Oliveira Cardoso,Saide Maria Sarmento Trindade,Eric Homero Albuquerque Paschoal,Fernando M. Paschoal-Jr,E. Bor Seng Shu +7 more
TL;DR: Complementary examinations should be performed in all patients with changes on transcranial Doppler to confirm cerebral vasculopathy in children with sickle cell disease, according to an epidemiologic, descriptive, and cross-sectional study.