M. M. Aleluia

发表

Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients

B. Andrade, V. Borges, C. C. Guarda, 2019, Scientific Reports.

Hydroxyurea in the management of sickle cell disease: pharmacogenomics and enzymatic metabolism

S. C. M. A. Yahouédéhou, Rayra P Santiago, M. M. Aleluia, 2018, The Pharmacogenomics Journal.

Transforming Growth Factor Beta Receptor 3 Haplotypes in Sickle Cell Disease Are Associated with Lipid Profile and Clinical Manifestations

C. C. Guarda, S. C. M. A. Yahouédéhou, Rayra P Santiago, 2020, Mediators of inflammation.

Heme-mediated cell activation: the inflammatory puzzle of sickle cell anemia

C. C. Guarda, S. C. M. A. Yahouédéhou, Rayra P Santiago, 2017, Expert review of hematology.

Laboratory and Genetic Biomarkers Associated with Cerebral Blood Flow Velocity in Hemoglobin SC Disease

C. C. Guarda, Rayra P Santiago, M. M. Aleluia, 2017, Disease markers.

Leptin − 2548 G > A gene polymorphism is associated with lipids metabolism and TGF-β alteration in sickle cell disease

C. C. Guarda, Rayra P Santiago, M. M. Aleluia, 2016 .

Priapism in sickle cell disease: Associations between NOS3 and EDN1 genetic polymorphisms and laboratory biomarkers

S. C. M. A. Yahouédéhou, Rayra P Santiago, M. M. Aleluia, 2021, PloS one.

Association of laboratory markers and cerebral blood flow among sickle cell anemia children

S. C. M. A. Yahouédéhou, Rayra P Santiago, M. M. Aleluia, 2022, Frontiers in Pediatrics.

Association of classical markers and establishment of the dyslipidemic sub-phenotype of sickle cell anemia

Rayra P Santiago, M. M. Aleluia, Luciana M Fiuza, 2017, Lipids in Health and Disease.

Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC)

S. C. M. A. Yahouédéhou, Rayra P Santiago, M. M. Aleluia, 2020, PloS one.

Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients

C. C. Guarda, S. C. M. A. Yahouédéhou, Rayra P Santiago, 2021, Mediators of inflammation.

Genetic Polymorphisms Associated with Environmental Exposure to Polycyclic Derivatives in African Children

S. C. M. A. Yahouédéhou, Rayra P Santiago, M. M. Aleluia, 2018, Disease markers.

Sickle Cell Anemia Patients in Use of Hydroxyurea: Association between Polymorphisms in Genes Encoding Metabolizing Drug Enzymes and Laboratory Parameters

S. C. M. A. Yahouédéhou, Rayra P Santiago, M. M. Aleluia, 2018, Disease markers.

Evaluation of Cardiometabolic Parameters among Obese Women Using Oral Contraceptives

Rayra P Santiago, M. M. Aleluia, M. Gonçalves, 2017, Front. Endocrinol..

Investigation of Lipid Profile and Clinical Manifestations in SCA Children

S. C. M. A. Yahouédéhou, Rayra P Santiago, M. M. Aleluia, 2020, Disease markers.

Leg Ulcers in Sickle Cell Disease: A Multifactorial Analysis Highlights the Hemolytic Profile

C. C. Guarda, S. C. M. A. Yahouédéhou, Rayra P Santiago, 2023, Hematology reports.

A Description of the Hemolytic Component in Sickle Leg Ulcer: The Role of Circulating miR-199a-5p, miR-144, and miR-126

C. C. Guarda, S. C. M. A. Yahouédéhou, Rayra P Santiago, 2022, Biomolecules.

Comparative study of sickle cell anemia and hemoglobin SC disease: clinical characterization, laboratory biomarkers and genetic profiles

Rayra P Santiago, M. M. Aleluia, M. Gonçalves, 2017, BMC Hematology.

Effect of lysed and non-lysed sickle red cells on the activation of NLRP3 inflammasome and LTB4 production by mononuclear cells

C. C. Guarda, Rayra P Santiago, M. M. Aleluia, 2021, Inflammation Research.

Circulating MicroRNAs as Novel Potential Diagnostic Biomarkers for Osteosarcoma: A Systematic Review

M. M. Aleluia, C. Kaneto, G. Borges, 2021, Biomolecules.

TGFBR3 Polymorphisms (rs1805110 and rs7526590) Are Associated with Laboratory Biomarkers and Clinical Manifestations in Sickle Cell Anemia

C. C. Guarda, S. C. M. A. Yahouédéhou, Rayra P Santiago, 2020, Disease markers.

The origin of HTLV-1 in southern Bahia by phylogenetic, mtDNA and β-globin analysis

L. Alcântara, M. M. Aleluia, M. Gonçalves, 2015 .

The origin of HTLV-1 in southern Bahia by b , go b , phylogenetic , mtDNA and β-globin analysis

L. Alcântara, M. M. Aleluia, M. Gonçalves, 2015 .

Serum haptoglobin and hemopexin levels are depleted in pediatric sickle cell disease patients.

G. Vercellotti, C. C. Guarda, Rayra P Santiago, 2018, Blood cells, molecules & diseases.

Serum Haptoglobin and Hemopexin Levels in Pediatric SS and SC Disease Patients: Biomarker of Hemolysis and Inflammation

G. Vercellotti, C. C. Guarda, Rayra P Santiago, 2016 .

Association of classical markers and establishment of the dyslipidemic sub-phenotype of sickle cell anemia

Rayra P Santiago, M. M. Aleluia, Luciana M Fiuza, 2017, Lipids in Health and Disease.

Genetic modulation of fetal hemoglobin in hydroxyurea‐treated sickle cell anemia

M. Steinberg, S. C. M. A. Yahouédéhou, Rayra P Santiago, 2017, American journal of hematology.

Association of the clinical profile and overall survival of pediatric patients with acute lymphoblastic leukemia

M. M. Aleluia, C. D. da Guarda, T. Fonseca, 2023, Frontiers in Pediatrics.

Hydroxyurea in the management of sickle cell disease: pharmacogenomics and enzymatic metabolism

S. C. M. A. Yahouédéhou, Rayra P Santiago, M. M. Aleluia, 2018, The Pharmacogenomics Journal.