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Betânia Lucena Domingues Hatzlhofer

Federal University of Pernambuco

22

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110

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Influence of UGT1A1 promoter polymorphism, α-thalassemia and βs haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.

2021 Annals of Hematology
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Alpha thalassemia, but not βS-globin haplotypes, influence sickle cell anemia clinical outcome in a large, single-center Brazilian cohort.

2021 Annals of Hematology
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Association of the SOD2 polymorphism (Val6Ala) and SOD activity with vaso-occlusive crisis and acute splenic sequestration in children with sickle cell anemia

2018 Mediterranean Journal of Hematology and Infectious Diseases
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Combined genotypes of the MBL2 gene related to low mannose-binding lectin levels are associated with vaso-occlusive events in children with sickle cell anemia

2017 Genetics and Molecular Biology
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Single Nucleotide Polymorphisms at +191 and +292 of Galectin-3 Gene (LGALS3) Related to Lower GAL-3 Serum Levels Are Associated with Frequent Respiratory Tract Infection and Vaso-Occlusive Crisis in Children with Sickle Cell Anemia

2016 PLOS ONE
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Lack of association between the Duffy antigen receptor for chemokines (DARC) expression and clinical outcome of children with sickle cell anemia.

2015 Immunology Letters
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Prevalence and molecular defect characterization of glucose‐6‐phosphate dehydrogenase deficiency in Brazilian blood donors

2015 International Journal of Laboratory Hematology
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THE REDUCTION OF PEROXIREDOXINS ACTIVITY ARE CORELATED WITH THE INCREASE OF REACTIVE OXYGEN SPECIES (ROS) AND CELL HEMOLYSIS OBSERVED IN PATIENTS WITH HEMOLITIC ANEMIAS

2014 Haematologica
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Follow-up of children with hemoglobinopathies diagnosed by the Brazilian Neonatal Screening Program in the State of Pernambuco.

2014 Revista Brasileira De Hematologia E Hemoterapia
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Erythropoiesis-driven regulation of hepcidin in human red cell disorders is better reflected through concentrations of soluble transferrin receptor rather than growth differentiation factor 15

2014 American Journal of Hematology
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