Search Results - "Aleluia, Milena"

Sickle cell disease: A distinction of two most frequent genotypes (HbSS and HbSC) by da Guarda, Caroline Conceição, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Santiago, Rayra Pereira, Neres, Joelma Santana Dos Santos, Fernandes, Camila Felix de Lima, Aleluia, Milena Magalhães, Figueiredo, Camylla Vilas Boas, Fiuza, Luciana Magalhães, Carvalho, Suellen Pinheiro, Oliveira, Rodrigo Mota de, Fonseca, Cleverson Alves, Ndidi, Uche Samuel, Nascimento, Valma Maria Lopes, Rocha, Larissa Carneiro, Goncalves, Marilda Souza

“…Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present highly variable clinical manifestations. Sickle cell anemia…”
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Priapism in sickle cell disease: Associations between NOS3 and EDN1 genetic polymorphisms and laboratory biomarkers by Figueiredo, Camylla Vilas Boas, Santiago, Rayra Pereira, da Guarda, Caroline Conceição, Oliveira, Rodrigo Mota, Fiuza, Luciana Magalhães, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Carvalho, Suéllen Pinheiro, Neres, Joelma Santana Dos Santos, Oliveira, Antonio Mateus de Jesus, Fonseca, Cleverson Alves, Nascimento, Valma Maria Lopes, Lyra, Isa Menezes, Aleluia, Milena Magalhães, Goncalves, Marilda Souza

“…Priapism is a urologic emergency characterized by an uncontrolled, persistent and painful erection in the absence of sexual stimulation, which can lead to…”
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Hydroxyurea in the management of sickle cell disease: pharmacogenomics and enzymatic metabolism by Yahouédéhou, Sètondji Cocou Modeste Alexandre, Adorno, Elisângela Vitória, da Guarda, Caroline Conceição, Ndidi, Uche Samuel, Carvalho, Suellen Pinheiro, Santiago, Rayra Pereira, Aleluia, Milena Magalhães, de Oliveira, Rodrigo Mota, Gonçalves, Marilda de Souza

“…Hydroxyurea (HU) was approved to be used in the treatment of sickle cell disease (SCD) because of its anti-sickling potential. However, there is variability in…”
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Circulating MicroRNAs as Novel Potential Diagnostic Biomarkers for Osteosarcoma: A Systematic Review by Gally, Thaís Borges, Aleluia, Milena Magalhães, Borges, Grasiely Faccin, Kaneto, Carla Martins

“…Osteosarcoma (OS) is a fast-progressing bone tumor with high incidence in children and adolescents. The main diagnostic methods for OS are imaging exams and…”
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Serum haptoglobin and hemopexin levels are depleted in pediatric sickle cell disease patients by Santiago, Rayra Pereira, Guarda, Caroline Conceição, Figueiredo, Camylla Vilas Boas, Fiuza, Luciana Magalhaes, Aleluia, Milena Magalhães, Adanho, Corynne Stephanie Ahouefa, Carvalho, Magda Oliveira Seixas, Pitanga, Thassila Nogueira, Zanette, Dalila Luciola, Lyra, Isa Menezes, Nascimento, Valma Maria Lopes, Vercellotti, Gregory M., Belcher, John D., Goncalves, Marilda Souza

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Hydroxyurea alters circulating monocyte subsets and dampens its inflammatory potential in sickle cell anemia patients by Guarda, Caroline C., Silveira-Mattos, Paulo S. M., Yahouédéhou, Sètondji C. M. A., Santiago, Rayra P., Aleluia, Milena M., Figueiredo, Camylla V. B., Fiuza, Luciana M., Carvalho, Suellen P., Oliveira, Rodrigo M., Nascimento, Valma M. L., Luz, Nívea F., Borges, Valéria M., Andrade, Bruno B., Gonçalves, Marilda S.

“…Sickle cell anemia (SCA) is a hemolytic disease in which vaso-occlusion is an important pathophysiological mechanism. The treatment is based on hydroxyurea…”
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Association of the clinical profile and overall survival of pediatric patients with acute lymphoblastic leukemia by Correa, Bruno Terra, Silva, Gabriela Sales Serra, Mendes, Webert Joaquim Silva, Maia, Amanda de Moraes, Aleluia, Augusto Cezar Magalhães, Fonseca, Teresa Cristina Cardoso, da Guarda, Caroline Conceição, Gonçalves, Marilda de Souza, Aleluia, Milena Magalhães

“…IntroductionThe clarification of etiopathology, the improvement of chemotherapy regimens and their risk stratifications, and the improvement in treatment…”
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Associations between TGF-β1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients by Santiago, Rayra P., Carvalho, Magda O. S., Figueiredo, Camylla V. B., Fiuza, Luciana M., Oliveira, Rodrigo M., Yahouédéhou, Sètondji C. M. A., Nascimento, Valma M. L., Lyra, Isa M., Araujo-Santos, Théo, Luz, Nívea F., Aleluia, Milena M., Guarda, Caroline C., Borges, Valéria M., Goncalves, Marilda S.

“…Transforming growth factor beta (TGF-β) is a cytokine with important involvement in biological processes related to the pathogenesis of sickle cell disease…”
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Effect of lysed and non-lysed sickle red cells on the activation of NLRP3 inflammasome and LTB4 production by mononuclear cells by Pitanga, Thassila N., Santana, Sânzio S., Zanette, Dalila L., Guarda, Caroline C., Santiago, Rayra P., Maffili, Vitor V., Lima, Jonilson B., Carvalho, Graziele Q., Filho, Jaime R., Ferreira, Junia R. D., Aleluia, Milena M., Nascimento, Valma M. L., Carvalho, Magda O. S., Lyra, Isa M., Borges, Valéria M., Oliveira, Ricardo R., Goncalves, Marilda S.

“…Objective and design This study tested the hypothesis that sickle red blood cell (SS-RBC) can induce inflammasome NLRP3 components gene expression in…”
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TGFBR3 Polymorphisms (rs1805110 and rs7526590) Are Associated with Laboratory Biomarkers and Clinical Manifestations in Sickle Cell Anemia by Rocha, Larissa Carneiro, Guarda, Caroline Conceição, Gonçalves, Marilda Souza, Fonseca, Cleverson Alves, Carvalho, Suellen Pinheiro, Aleluia, Milena Magalhães, Oliveira, Rodrigo Mota, Yahouédéhou, Sétondji Cocou Modeste Alexandre, Fiuza, Luciana Magalhães, Figueiredo, Camylla Vilas Boas, Santiago, Rayra Pereira, Nascimento, Valma Maria Lopes

“…Individuals with sickle cell anemia (SCA) present chronic anemia, hemolysis, an exacerbated inflammatory response, and heterogeneous clinical complications,…”
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Sickle Cell Anemia Patients in Use of Hydroxyurea: Association between Polymorphisms in Genes Encoding Metabolizing Drug Enzymes and Laboratory Parameters by Goncalves, Marilda Souza, Adorno, Elisângela Vitoria, Ferreira, Junia Raquel Dutra, Carvalho, Suellen Pinheiro, Guarda, Caroline Conceição, Santiago, Rayra Pereira, Oliveira, Rodrigo Mota, Carvalho, Magda Oliveira Seixas, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Aleluia, Milena Magalhães

“…This study investigated associations between SNPs in genes encoding metabolizing drug enzymes and laboratory parameters in sickle cell anemia patients under…”
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Transforming Growth Factor Beta Receptor 3 Haplotypes in Sickle Cell Disease Are Associated with Lipid Profile and Clinical Manifestations by Rocha, Larissa C., Guarda, Caroline Conceição, Gonçalves, Marilda Souza, Fonseca, Cleverson A., Carvalho, Suellen P., Aleluia, Milena M., Oliveira, Rodrigo M., Yahouédéhou, Sètondji C. M. A., Fiuza, Luciana M., Figueiredo, Camylla V. B., Santiago, Rayra P., Nascimento, Valma M. L.

“…Individuals with sickle cell disease (SCD) present both chronic and acute inflammatory events. The TGF-β pathway is known to play a role in immune response,…”
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Associations between TGF- β 1 Levels and Markers of Hemolysis, Inflammation, and Tissue Remodeling in Pediatric Sickle Cell Patients by Santiago, Rayra P, Carvalho, Magda O S, Figueiredo, Camylla V B, Fiuza, Luciana M, Oliveira, Rodrigo M, Yahouédéhou, Sètondji C M A, Nascimento, Valma M L, Lyra, Isa M, Araujo-Santos, Théo, Luz, Nívea F, Aleluia, Milena M, Guarda, Caroline C, Borges, Valéria M, Goncalves, Marilda S

“…Transforming growth factor beta (TGF- ) is a cytokine with important involvement in biological processes related to the pathogenesis of sickle cell disease…”
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A Description of the Hemolytic Component in Sickle Leg Ulcer: The Role of Circulating miR-199a-5p, miR-144, and miR-126 by Santos, Edvan do Carmo, Melo, Gabriela Imbassahy Valentim, Santana, Paulo Vinícius Bispo, Quadros, Idaiara Graziele Silva, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Guarda, Caroline Conceição da, Santiago, Rayra Pereira, Fiuza, Luciana Magalhães, Carvalho, Suéllen Pinheiro, Adorno, Elisângela Vitória, Kaneto, Carla Martins, Fonseca, Teresa Cristina Cardoso, Goncalves, Marilda Souza, Aleluia, Milena Magalhães

“…Sickle leg ulcers (SLU) are malleoli lesions with exuberant hemolytic pathophysiology. The microRNAs are potential genetic biomarkers for several pathologies…”
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Association of laboratory markers and cerebral blood flow among sickle cell anemia children by Adanho, Corynne Stéphanie Ahouéfa, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Santana, Sânzio Silva, Vieira, Camilo, Santiago, Rayra Pereira, de Santana, Jeanne Machado, Pitanga, Thassila Nogueira, Aleluia, Milena Magalhães, Maffili, Vítor Valério, Leite, Ivana Paula Ribeiro, Zanette, Dalila Luciola, Lyra, Isa Menezes, Goncalves, Marilda Souza

“…BackgroundStroke is one of the highest complications of sickle-cell anemia (SCA). The Transcranial Doppler (TCD) has been adopted worldwide as a gold standard…”
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Investigation of Lipid Profile and Clinical Manifestations in SCA Children by Fonseca, Cleverson Alves, Carvalho, Suellen Pinheiro, de Oliveira, Rodrigo Mota, Nascimento, Valma Maria Lopes, Rocha, Larissa Carneiro, Gonçalves, Marilda Souza, Figueiredo, Camylla Vilas Boas, Aleluia, Milena Magalhães, Oliveira, Antonio Mateus de Jesus, Neres, Joelma Santana dos Santos, Fernandes, Camila Felix de Lima, Santiago, Rayra Pereira, Yahouédéhou, Sètondji Cocou Modeste Alexandre, da Guarda, Caroline Conceição, Fiuza, Luciana Magalhães

“…Introduction. Clinical complications in sickle cell anemia (SCA) are heterogeneous and involve several molecules. It has been suggested that SCA individuals…”
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Laboratory and Genetic Biomarkers Associated with Cerebral Blood Flow Velocity in Hemoglobin SC Disease by Ferreira, Junia Raquel Dutra, Oliveira, Rodrigo Mota, Zanette, Dalila Luciola, Lyra, Isa Menezes, Goncalves, Marilda Souza, Pitanga, Thassila Nogueira, Fiuza, Luciana Magalhães, Figueiredo, Camylla Vilas Boas, Guarda, Caroline Conceição, Santana, Sânzio Silva, Adanho, Corynne Stephanie Ahouefa, Vieira, Camilo, Santiago, Rayra Pereira, Aleluia, Milena Magalhães

“…Reference values for cerebral blood flow velocity (CBFV) in hemoglobin SC disease (HbSC) have not been established. We aimed to investigate associations…”
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Association of classical markers and establishment of the dyslipidemic sub-phenotype of sickle cell anemia by Aleluia, Milena Magalhães, da Guarda, Caroline Conceição, Santiago, Rayra Pereira, Fonseca, Teresa Cristina Cardoso, Neves, Fábia Idalina, de Souza, Regiana Quinto, Farias, Larissa Alves, Pimenta, Felipe Araújo, Fiuza, Luciana Magalhães, Pitanga, Thassila Nogueira, Ferreira, Júnia Raquel Dutra, Adorno, Elisângela Vitória, Cerqueira, Bruno Antônio Veloso, Gonçalves, Marilda de Souza

“…Sickle cell anemia (SCA) patients exhibit sub-phenotypes associated to hemolysis and vaso-occlusion. The disease has a chronic inflammatory nature that has…”
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Genetic modulation of fetal hemoglobin in hydroxyurea‐treated sickle cell anemia by Aleluia, Milena Magalhães, Santiago, Rayra Pereira, da Guarda, Caroline Conceição, Fonseca, Teresa Cristina Cardoso, Neves, Fábia Idalina, Quinto, Regiana Souza, Figueiredo, Camylla Villas Boas, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Oliveira, Rodrigo Mota, Ferreira, Júnia Raquel Dutra, Cerqueira, Bruno Antônio Veloso, Barbosa, Cynara Gomes, Milton, Jacqueline Nicole, Steinberg, Martin H., de Souza Gonçalves, Marilda

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Heme-mediated cell activation: the inflammatory puzzle of sickle cell anemia by Guarda, Caroline Conceição da, Santiago, Rayra Pereira, Fiuza, Luciana Magalhães, Aleluia, Milena Magalhães, Ferreira, Júnia Raquel Dutra, Figueiredo, Camylla Vilas Boas, Yahouedehou, Setondji Cocou Modeste Alexandre, Oliveira, Rodrigo Mota de, Lyra, Isa Menezes, Gonçalves, Marilda de Souza

“…Hemolysis triggers the onset of several clinical manifestations of sickle cell anemia (SCA). During hemolysis, heme, which is derived from hemoglobin (Hb),…”
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