Browsing by Author "Fiuza, Luciana Magalhães"
Now showing items 1-17 of 17
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Association of classical markers and establishment of the dyslipidemic sub-phenotype of sickle cell anemia
Aleluia, Milena Magalhães et al. | Date Issued: 2017 -
CAT -21A>T variant alters hydroxyurea pharmacokinetic parameters in Brazilian children with sickle cell anemia
Yahouédéhou, Sètondji Cocou Modeste Alexandre et al. | Date Issued: 2022 -
A description of the hemolytic component in sickle leg ulcer: the role of circulating miR-199a-5p, miR-144, and miR-126
Santos, Edvan do Carmo et al. | Date Issued: 2022 -
Genetic Polymorphisms Associated with Environmental Exposure to Polycyclic Derivatives in African Children
Oliveira, Rodrigo Mota de et al. | Date Issued: 2018 -
Heme-mediated cell activation: the inflammatory puzzle of sickle cell anemia
Guarda, Caroline Conceição da et al. | Date Issued: 2017 -
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 -
Inflammatory mediators in sickle cell anaemia highlight the difference between steady state and crisis in paediatric patients
Carvalho, Magda Oliveira Seixas et al. | Date Issued: 2017 -
Investigation of Lipid Profile and Clinical Manifestations in SCA Children
Guarda, Caroline Conceição da et al. | Date Issued: 2020 -
Laboratory and Genetic Biomarkers Associated with Cerebral Blood Flow Velocity in Hemoglobin SC Disease
Santiago, Rayra Pereira et al. | Date Issued: 2017 -
Leg ulcers in sickle cell disease: a multifactorial analysis highlights the hemolytic profile
Santos, Edvan do Carmo et al. | Date Issued: 2023 -
Leptin − 2548 G > A gene polymorphism is associated with lipids metabolism and TGF-β alteration in sickle cell disease
Figueiredo, Camylla Vilas Boas et al. | Date Issued: 2016 -
Polimorfismos em genes de citocinas inflamatórias associados ao Acidente Vascular Cerebral na anemia falciforme
Fiuza, Luciana Magalhães | Date Issued: 2020INTRODUÇÃO: Pacientes com anemia falciforme (AF) apresentam variabilidade fenotípica elevada, podendo apresentar diversas manifestações clínicas, incluindo o Acidente Vascular Cerebral (AVC). No contexto da AF, o comprometimento ... -
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 -
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