Browsing by Author "Nascimento, Valma Maria Lopes"
Now showing items 1-9 of 9
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Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients
Guarda, Caroline Conceição da et al. | Date Issued: 2019 -
Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
Yahouédéhou, Sètondji Cocou Modeste Alexandre et al. | Date Issued: 2019 -
Investigation of Lipid Profile and Clinical Manifestations in SCA Children
Guarda, Caroline Conceição da et al. | Date Issued: 2020 -
Priapism in sickle cell disease: associations between NOS3 and EDN1 genetic polymorphisms and laboratory biomarkers
Figueiredo, Camylla Vilas Boas et al. | Date Issued: 2021 -
Role of paraoxonase 1 activity and PON1 gene polymorphisms in sickle cell disease
Menezes, Joelma Figueiredo et al. | Date Issued: 2023 -
Serum haptoglobin and hemopexin levels are depleted in pediatric sickle cell disease patients
Santiago, Rayra Pereira et al. | Date Issued: 2018 -
Sickle cell anemia: variants in the CYP2D6, CAT, and SLC14A1 genes are associated with improved hydroxyurea response
Yahouédéhou, Sètondji Cocou Modeste Alexandre et al. | Date Issued: 2020 -
Sickle cell disease: a distinction of two most frequent genotypes (HbSS and HbSC)
Guarda, Caroline Conceição da et al. | Date Issued: 2020 -
TGFBR3 Polymorphisms (rs1805110 and rs7526590) Are Associated with Laboratory Biomarkers and Clinical Manifestations in Sickle Cell Anemia
Santiago, Rayra Pereira et al. | Date Issued: 2020