169 results on '"Goncalves, Marilda Souza"'
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2. Role of paraoxonase 1 activity and PON1 gene polymorphisms in sickle cell disease
3. Prevalence of arboviruses in sickle cell disease patients from two different regions of Brazil, the North and Northeast
4. Association of laboratory markers and cerebral blood flow among sickle cell anemia children
5. Sickle cell disease retinopathy: characterization among pediatric and teenage patients from northeastern Brazil
6. Effectiveness of Pharmacokinetic-Guided Hydroxyurea Dose Individualization in Patients with Sickle Cell Anemia: A Mini-Review.
7. A Description of the Hemolytic Component in Sickle Leg Ulcer: The Role of Circulating miR-199a-5p, miR-144, and miR-126
8. Inclusion Complexes of Non-Steroidal Anti-Inflammatory Drugs with Cyclodextrins: A Systematic Review
9. Priapism in sickle cell disease: Associations between NOS3 and EDN1 genetic polymorphisms and laboratory biomarkers
10. Duffy Blood System and G6PD Genetic Variants In P. Vivax Malaria Patients From Manaus, Amazonas, Brazil
11. Globin haplotypes of human T-cell lymphotropic virus type I-infected individuals in Salvador, Bahia, Brazil, suggest a post-columbian african origin of this virus
12. An evaluation of ticagrelor for the treatment of sickle cell anemia
13. Sickle Cell Anemia: Variants in the CYP2D6, CAT, and SLC14A1 Genes Are Associated With Improved Hydroxyurea Response
14. Hydroxyurea Scavenges Free Radicals and Induces the Expression of Antioxidant Genes in Human Cell Cultures Treated With Hemin
15. Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC)
16. Serum haptoglobin and hemopexin levels are depleted in pediatric sickle cell disease patients
17. Effect of N(Epsilon)-(carboxymethyl)lysine on Laboratory Parameters and Its Association withβSHaplotype in Children with Sickle Cell Anemia
18. Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia
19. Differential gene expression analysis of sickle cell anemia in steady and crisis state
20. Hydroxyurea Exhibits Antioxidant Activity Via the Nrf2 Pathway- Antioxidant/Electrophile Response Element Regulated By p62/ SQSTM1
21. Laboratory and Genetic Biomarkers Associated with Cerebral Blood Flow Velocity in Hemoglobin SC Disease
22. The DAU Allele and Anti-D Alloimmunization Present With High Frequency in Brazilian Sickle Cell Disease Patients
23. Transcranial Doppler in hemoglobin SC disease
24. Laboratorial and Genetic Biomarkers Associated to Cerebral Blood Flow Velocity on Hemoglobin SC Disease
25. Influence of Hydroxyurea on Neutrophil Microparticles: A SCA Model
26. Cardiometabolic and Hemostatic Profiles of Women Carriers of Hemoglobin Variants Using Combined Oral Contraceptives
27. Toll-like Receptors Gene Expression Is Modulated By Lysed Sickle Red Blood Cells
28. Serum Haptoglobin and Hemopexin Levels in Pediatric SS and SC Disease Patients: Biomarker of Hemolysis and Inflammation
29. Genome Wide Association Study of Sickle Cell Disease Individuals with Stroke Risk
30. Effect of N(Epsilon)-(carboxymethyl)lysine on Laboratory Parameters and Its Association with βS Haplotype in Children with Sickle Cell Anemia.
31. Sickle Cell Inflammatory Environment Is Associated with Products of the Eicosanoid Synthesis Pathways
32. Heme Concentration As a Biomarker of Sickle Cell Disease Severity: Its Role in Steady-State and in Crisis Patients
33. The Host Genetic Diversity in Malaria Infection
34. Metabolism and gene polymorphisms of the folate pathway in Brazilian women with history of recurrent abortion
35. Paraoxonase 1 Activity and Pon 1 Gene Polymorphisms As a Potential Prognostic Biomarker in Sickle Cell Disease
36. Alpha-1 Antitrypsin and SERPINA1 gene Mutation As New Biomarker in Sickle Cell Disease
37. Genetics and Molecular Biology
38. Transcranial Doppler in hemoglobin SC disease.
39. Nitrite Levels Are Associated To Fetal Hemoglobin Concentration In Patients With Sickle Cell Anemia: Implications In Inflammatory Process
40. Toll Like Receptors Have mRNA Differentiated Expression In Dendritic Cells In Crisis-State Sickle Cell Anemia Patients, Suggesting a Pivotal Role Of These Molecules and Cell Type In The Maintenance Of Inflammatory Response
41. Expression Of Nitric Oxide Synthase, Vascular Cell Adhesion Molecule and C- Reactive Protein Receptor In Sickle Cell Leucocytes: Relationship With Chronic Inflammation
42. The Interferon Gamma Gene Polymorphism In Acquired Aplastic Anemia and Its Association With HLA
43. HLA and Aplastic Anemia: associations In Large Brazilian Cohorts
44. Endothelial Protein C Receptor (EPCR), Oxide Nitric Synthase (NOS) and Tissue Factor (Factor III) Gene Expression: The Role Like Promising Biomarkers In Sickle Cell Anemia
45. Alpha 1 Antitrypsin, C Reactive Protein, and Hemolysis Markers: Association With Cytokines Profile In Sickle Cell Disease Patients In Steady-State and Crisis-State
46. The Prevalence of Wheezing and its Association with Body Mass Index and Abdominal Obesity in Children
47. Cytokine profiles in sickle cell anemia: Pathways to be unraveled
48. Sickle cell disease: Only one road, but different pathways for inflammation
49. Lipoprotein Cholesterol and Triglyceride in Children with Steady-State Sickle Cell Disease.
50. ICAM-1(CD54) and Tissue Factor (CD142) Monocytes Expression Among Sickle Cell Anemia Steady-State Children: Association with VCAM-1 and ICAM-1 Soluble and Cytokines Related to Inflamossome and Th17 Response.
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