Search Results - "Cerqueira, Bruno A. V."

Arginase levels and their association with Th17-related cytokines, soluble adhesion molecules (sICAM-1 and sVCAM-1) and hemolysis markers among steady-state sickle cell anemia patients by Vilas-Boas, Wendell, Cerqueira, Bruno A. V, Zanette, Angela M. D, Reis, Mitermayer G, Barral-Netto, Manoel, Goncalves, Marilda S

“…Sickle cell anemia (SCA) is characterized by a marked endothelial dysfunction, owing to many factors. Arginine metabolism can be related to the inflammatory…”
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Increased concentrations of IL-18 and uric acid in sickle cell anemia: Contribution of hemolysis, endothelial activation and the inflammasome by Cerqueira, Bruno A.V., Boas, Wendell V., Zanette, Angela D., Reis, Mitermayer G., Goncalves, Marilda S.

“…► We observed a positive correlation between IL-18 and uric acid. ► Classical markers of prognosis were associated with IL-18 and uric acid. ► The inflammasome…”
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Endothelial Nitric Oxide Synthase (-786T＞C) and Endothelin-1 (5665G＞T) Gene Polymorphisms as Vascular Dysfunction Risk Factors in Sickle Cell Anemia by Vilas-Boas, Wendell, Figueiredo, Camylla V. B., Pitanga, Thassila N., Carvalho, Magda O. S., Santiago, Rayra P., Santana, Sânzio S., Guarda, Caroline C., Zanette, Angela M. D., Cerqueira, Bruno A. V., Gonçalves, Marilda S.

“…Sickle cell anemia (SCA) patients have vascular complications, and polymorphisms in endothelin-1 (ET-1) and endothelial nitric oxide synthase (eNOS) genes were…”
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Inflammatory mediators in sickle cell anaemia highlight the difference between steady state and crisis in paediatric patients by Carvalho, Magda O. S., Araujo‐Santos, Théo, Reis, João H. O., Rocha, Larissa C., Cerqueira, Bruno A. V., Luz, Nívea F., Lyra, Isa M., Lopes, Valma M., Barbosa, Cynara G., Fiuza, Luciana M., Santiago, Rayra P., Figueiredo, Camylla V. B., Guarda, Caroline C., Barral Neto, Manoel, Borges, Valéria M., Gonçalves, Marilda S.

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Outcome of B-Cell Acute Lymphoblastic Leukemia in Brazilian Children: Immunophenotypical, Hematological, and Clinical Evaluation by Cézar, Rodrigo S, Cerqueira, Bruno A V, da Paz, Silvana de Souza, Barbosa, Cynara G, de Moura Neto, José P, Barreto, José H de S, Goncalves, Marilda de S

“…The aim of this study is to investigate the clinical, hematological, and immunophenotypic characteristics of Brazilian children with B-cell acute lymphoblastic…”
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Expression Of Nitric Oxide Synthase, Vascular Cell Adhesion Molecule and C- Reactive Protein Receptor In Sickle Cell Leucocytes: Relationship With Chronic Inflammation by Boas, Wendell Vilas, Cerqueira, Bruno A.V., Pitanga, Thassila Nogueira, Santana, Sanzio Silva, Reis, Joao Oliveira, Goncalves, Marilda Souza

“…Chronic and acute inflammatory phenomenon's can contribute to activate several cells types and may play important role in the steady- and crisis-states of…”
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Nitrite Levels Are Associated To Fetal Hemoglobin Concentration In Patients With Sickle Cell Anemia: Implications In Inflammatory Process by Pitanga, Thassila Nogueira, Cerqueira, Bruno A.V., Boas, Wendell Vilas, Santana, Sanzio S., Reis, João O., Goncalves, Marilda Souza

“…Sickle cell anemia (SCA) is a genetical hemolytic disorder defined as chronic inflammatory disease. Nitrite (NO-2) in SCA (HbSS) patients may be associated…”
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Soluble Vascular Cell Adhesion Molecule Levels, Endothelin-1 and Endothelial Nitric Oxide Synthase Gene Polymorphisms: Association with Clinical Symptoms in Sickle Cell Anemia by Vilas-Boas, Wendell, Figueiredo, Camylla Vilas Boas, Cerqueira, Bruno A.V., Pitanga, Thassila, Zanette, Angela, Reis, Mitermayer, Goncalves, Marilda

“…Abstract 2118 Vascular occlusions trigger most of the acute and chronic sickle cell anemia (HbSS) clinical complications and have been associated with high…”
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Biomarkers of Hemolysis and Inflammation in Sickle Cell Disease Children: Association with Nasopharynx and Oropharynx Bacteria colonization by Rocha, Larissa, Seixas, Magda, Cerqueira, Bruno A.V., Lopes, Valma, Reis, Mitermayer, Goncalves, Marilda

“…Abstract 2140 Nasopharynx and oropharynx bacterium colonization can be considered as initiation factor for local or systemic disease. The Streptococcus…”
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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 by Cerqueira, Bruno A.V., Boas, Wendell Vilas, Fonseca, Teresa Cristina, Souza, Regiana Q., Aleluia, Milena Magalhães, Cunha, Bruna A., Pimenta, Felipe A., Pitanga, Thassila Nogueira, Reis, João Oliveira, Santana, Sanzio Silva, Goncalves, Marilda Souza

“…Sickle cell anemia is a severe monogenic disorder characterized by the homozygous state of a single beta globin gene mutation, with heterogeneous clinic…”
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Lymphocyte Surface Molecule Expression on Basal State and After Challenge: Association of Clinical Profile, Inflammation, Hematological and Biochemical Markers in Sickle Cell Anemia Patients by Cerqueira, Bruno A.V., Vilas-Boas, Wendell, Zanette, Angela, Clarencio, Jorge, Salvino, Marco, Cezar, Rodrigo, Andrade, Daniela, Reis, Mitermayer, Goncalves, Marilda

“…Abstract 2146 Sickle cell anemia (SCA) is a common, severe monogenetic disorder characterized by chronic hemolysis, frequent infections, chronic inflammatory…”
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The Interferon Gamma Gene Polymorphism In Acquired Aplastic Anemia and Its Association With HLA by Salvino, Marco Aurelio, Goncalves, Marilda Souza, Cerqueira, Bruno A.V., Medeiros, Larissa A, Lins, Flavio, Solla, Davi, Alcantara, Adriano, Marques, Marinho, Moura, Alessandro, Santos, Herbert Henrique, Souza, Lais Guimaraes, Andrade, Juliana, Alencar, Dora Marcia, Dourado, Daniela, Scheinberg, Phillip, Meyer, Roberto

“…Idiopathic acquired aplastic anemia (AAA) is a rare and life-threatening disease, characterized by pancytopenia. Its immune-mediated physiopathology is not yet…”
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HLA and Aplastic Anemia: associations In Large Brazilian Cohorts by Salvino, Marco Aurelio, Medeiros, Larissa A, Moura, Alessandro, Batista, Marianna, Goncalves, Marilda Souza, Mezes, Eliane, Santos, Luciano, Arruda, Gloria Bomfim, Pereira, Noemi Farah, Cerqueira, Bruno A.V., Schittini, Anelisa, Botura, Monica, Fernandes Schriefer, Ana Luzia, Oliveira, Michel M, Funke, Vaneuza A M, Pasquini, Ricardo, Scheinberg, Phillip, Meyer, Roberto

“…Aplastic anemia (AA) is perceived as an immune mediated disease where T-lymphocytes recognize and destroy bone marrow elements leading to varying degrees of…”
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CD32, CD18, CD11b and CD62L Expression on Monocyte without and After Lipopolysaccharide (LPS) Challenge: Association with Inflammatory and Hemolysis Markers In Sickle Cell Anemia by Cerqueira, Bruno A.V., Vilas-Boas, Wendell, Neto, Jose Moura, Clarencio, Jorge, Andrade, Daniela, Cezar, Rodrigo, Zanette, Angela, Reis, Mitermayer, Goncalves, Marilda

“…Abstract 1655 Vaso-occlusive episodes (VOE) in sickle cell anemia, homozygous form of hemoglobin S (HB S), involve interactions between sickle red blood cells…”
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Endothelial nitric oxide synthase gene polymorphisms as vascular dysfunction risk factors in sickle cell anemia by Vilas-Boas, Wendell, Figueiredo, Camylla V. B, Pitanga, Thassila N, Carvalho, Magda O. S, Santiago, Rayra P, Santana, Sanzio S, Guarda, Caroline C, Zanette, Angela M. D, Cerqueira, Bruno A. V, Goncalves, Marilda S

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