Valma L. Nascimento
Salvador, BA, Brazil
Last Updated: 09/26/2026
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Found 15 publications
Role of paraoxonase 1 activity and PON1 gene polymorphisms in sickle cell disease.
Journal: Scientific reports
Published: August 23, 2022
TGFBR3 Polymorphisms (rs1805110 and rs7526590) Are Associated with Laboratory Biomarkers and Clinical Manifestations in Sickle Cell Anemia.
Journal: Disease markers
Published: August 03, 2020
Effect of lysed and non-lysed sickle red cells on the activation of NLRP3 inflammasome and LTB4 production by mononuclear cells.
Journal: Inflammation research : official journal of the European Histamine Research Society ... [et al.]
Published: June 19, 2020
Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients.
Journal: Mediators of inflammation
Published: June 09, 2020
Transforming Growth Factor Beta Receptor 3 Haplotypes in Sickle Cell Disease Are Associated with Lipid Profile and Clinical Manifestations.
Journal: Mediators of inflammation
Published: May 24, 2020
Sickle Cell Anemia: Variants in the CYP2D6, CAT, and SLC14A1 Genes Are Associated With Improved Hydroxyurea Response.
Journal: Frontiers in pharmacology
Published: April 17, 2020
Investigation of Lipid Profile and Clinical Manifestations in SCA Children.
Journal: Disease markers
Published: April 07, 2020
Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC).
Journal: PloS one
Published: October 21, 2019
Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia.
Journal: PloS one
Published: January 05, 2019
Serum haptoglobin and hemopexin levels are depleted in pediatric sickle cell disease patients.
Journal: Blood cells, molecules & diseases
Published: June 22, 2018
Last Updated: 09/26/2026