Aderson Da Silva Araujo

Recife, PE, Brazil

Last Updated: 09/26/2026

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Found 13 publications

Sickle Cell Disease in Brazil: Current Management.

Sickle Cell Disease in Brazil: Current Management.

Journal: Hemoglobin

Published: April 25, 2024

The endocannabinoid system's genetic polymorphisms in sickle cell anemia patients.

The endocannabinoid system's genetic polymorphisms in sickle cell anemia patients.

Journal: Scientific reports

Published: April 03, 2024

Polymorphisms and gene expression of metalloproteinases and their inhibitors associated with cerebral ischemic stroke in young patients with sickle cell anemia.

Polymorphisms and gene expression of metalloproteinases and their inhibitors associated with cerebral ischemic stroke in young patients with sickle cell anemia.

Journal: Molecular biology reports

Published: November 18, 2022

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

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

Journal: Annals of hematology

Published: August 28, 2020

Whole-exome sequencing indicates FLG2 variant associated with leg ulcers in Brazilian sickle cell anemia patients.

Whole-exome sequencing indicates FLG2 variant associated with leg ulcers in Brazilian sickle cell anemia patients.

Journal: Experimental biology and medicine (Maywood, N.J.)

Published: May 14, 2019

Global gene expression reveals an increase of HMGB1 and APEX1 proteins and their involvement in oxidative stress, apoptosis and inflammation pathways among beta-thalassaemia intermedia and major phenotypes.

Global gene expression reveals an increase of HMGB1 and APEX1 proteins and their involvement in oxidative stress, apoptosis and inflammation pathways among beta-thalassaemia intermedia and major phenotypes.

Journal: British journal of haematology

Published: January 26, 2019

Chemokines in pregnant women with sickle cell disease.

Chemokines in pregnant women with sickle cell disease.

Journal: Cytokine

Published: January 03, 2018

Association of the SOD2 Polymorphism (Val16Ala) and SOD Activity with Vaso-occlusive Crisis and Acute Splenic Sequestration in Children with Sickle Cell Anemia.

Association of the SOD2 Polymorphism (Val16Ala) and SOD Activity with Vaso-occlusive Crisis and Acute Splenic Sequestration in Children with Sickle Cell Anemia.

Journal: Mediterranean journal of hematology and infectious diseases

Published: September 13, 2017

Guidelines on the treatment of anemia of chronic renal failure using recombinant human erythropoietin: Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Guidelines Project: Associação Médica Brasileira - 2014.

Guidelines on the treatment of anemia of chronic renal failure using recombinant human erythropoietin: Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Guidelines Project: Associação Médica Brasileira - 2014.

Journal: Revista brasileira de hematologia e hemoterapia

Published: August 11, 2014

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.

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.

Journal: American journal of hematology

Published: May 27, 2014

Evaluation of CD4(+)CD25(+)FoxP3(+) T cell populations, IL-10 production, and their correlation with clinical and biochemical parameters in sickle cell anemia patients with leg ulcers.

Evaluation of CD4(+)CD25(+)FoxP3(+) T cell populations, IL-10 production, and their correlation with clinical and biochemical parameters in sickle cell anemia patients with leg ulcers.

Journal: Cytokine

Published: March 25, 2014

Evaluation of Th17 related cytokines associated with clinical and laboratorial parameters in sickle cell anemia patients with leg ulcers.

Evaluation of Th17 related cytokines associated with clinical and laboratorial parameters in sickle cell anemia patients with leg ulcers.

Journal: Cytokine

Published: March 04, 2013

Showing 1-12 of 13

Last Updated: 09/26/2026