Search Results - "da Guarda, Caroline"

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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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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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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Hydroxyurea alters hematological, biochemical and inflammatory biomarkers in Brazilian children with SCA: Investigating associations with βS haplotype and α-thalassemia by Yahouédéhou, Sètondji Cocou Modeste Alexandre, da Guarda, Caroline Conceição, Figueiredo, Camylla Vilas Boas, Santiago, Rayra Pereira, Carvalho, Suellen Pinheiro, Fiuza, Luciana Magalhães, Ndidi, Uche Samuel, Oliveira, Rodrigo Mota, Carvalho, Magda Oliveira Seixas, Nascimento, Valma Maria Lopes, Rocha, Larissa Carneiro, Lyra, Isa Menezes, Adorno, Elisângela Vitória, Goncalves, Marilda Souza

“…This study investigated the effects of hydroxyurea (HU) on hematological, biochemical and inflammatory parameters in children with sickle cell anemia (SCA) in…”
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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 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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Genetic Polymorphisms Associated with Environmental Exposure to Polycyclic Derivatives in African Children by Guarda, Caroline Conceição, Aleluia, Milena Magalhães, Barbosa, Cynara Gomes, Adorno, Elisângela Vitoria, Goncalves, Marilda Souza, de Miranda, Fernando Nunes, Fiuza, Luciana Magalhães, da Paz, Silvana Souza, Carvalho, Suellen Pinheiro, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Santiago, Rayra Pereira, Figueiredo, Camylla Vilas Boas, Oliveira, Rodrigo Mota, Fonseca, Cleverson Alves

“…Background. The nonracial leukopenia may be a result of exposure to polycyclic derivatives (benzene-toluene-xylene (BTX)) and may arise from a possible change…”
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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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Evaluation of Cardiometabolic Parameters among Obese Women Using Oral Contraceptives by Ferreira, Júnia Raquel Dutra, Aleluia, Milena Magalhães, Figueiredo, Camylla Vilas Boas, Vieira, Larissa Castro de Lima, Santiago, Rayra Pereira, da Guarda, Caroline Conceição, Barbosa, Cynara Gomes, Oliveira, Ricardo Riccio, Adorno, Elisângela Vitória, Gonçalves, Marilda de Souza

“…Combined oral contraceptive (COC) use has been associated with an unfavorable impact on carbohydrate and lipid metabolism in diverse populations of normal…”
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Comparative study of sickle cell anemia and hemoglobin SC disease: clinical characterization, laboratory biomarkers and genetic profiles by Aleluia, Milena Magalhães, Fonseca, Teresa Cristina Cardoso, Souza, Regiana Quinto, Neves, Fábia Idalina, da Guarda, Caroline Conceição, Santiago, Rayra Pereira, Cunha, Bruna Laís Almeida, Figueiredo, Camylla Villas Boas, Santana, Sânzio Silva, da Paz, Silvana Sousa, Ferreira, Júnia Raquel Dutra, Cerqueira, Bruno Antônio Veloso, Gonçalves, Marilda de Souza

“…In this study, we evaluate the association of different clinical profiles, laboratory and genetic biomarkers in patients with sickle cell anemia (SCA) and…”
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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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Leg Ulcers in Sickle Cell Disease: A Multifactorial Analysis Highlights the Hemolytic Profile by Santos, Edvan do Carmo, Santana, Paulo Vinícius Bispo, Jesus, Laíne Lopes Silva de, Melo, Gabriela Imbassahy Valentim, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Guarda, Caroline Conceição da, Santiago, Rayra Pereira, Fiuza, Luciana Magalhães, Carvalho, Suéllen Pinheiro, Santos, Liz Oliveira Dos, Adorno, Elisângela Vitória, Aleluia, Augusto Cezar Magalhães, Luiz, Luciene Cristina Gastalho Campos, Fonseca, Teresa Cristina Cardoso, Gonçalves, Marilda de Souza, Aleluia, Milena Magalhães

“…Sickle cell disease (SCD) is characterized by the presence of the variant S hemoglobin (HbS). The homozygous genotype (HbSS) is sickle cell anemia (SCA), while…”
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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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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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Heme changes HIF-α, eNOS and nitrite production in HUVECs after simvastatin, HU, and ascorbic acid therapies by da Guarda, Caroline C., Santiago, Rayra P., Pitanga, Thassila N., Santana, Sanzio S., Zanette, Dalila L., Borges, Valéria M., Goncalves, Marilda S.

“…The sickle cell disease (SCD) is a hemolytic genetic anemia characterized by free heme and hemoglobin release into intravascular spaces, with endothelial…”
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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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Role of paraoxonase 1 activity and PON1 gene polymorphisms in sickle cell disease by Menezes, Joelma Figueiredo, Carvalho, Magda Oliveira Seixas, Rocha, Larissa Carneiro, dos Santos, Felipe Miranda, Adorno, Elisângela Vitória, de Souza, Cyntia Cajado, Santiago, Rayra Pereira, da Guarda, Caroline Conceição, de Oliveira, Rodrigo Mota, Figueiredo, Camylla Vilas Boas, Carvalho, Suéllen Pinheiro, Yahouédéhou, Sètondji Cocou Modeste Alexandre, Fiuza, Luciana Magalhães, Adanho, Corynne Stéphanie Ahouefa, Pitanga, Thassila Nogueira, Lyra, Isa Menezes, Nascimento, Valma Maria Lopes, Noronha-Dutra, Alberto Augusto, Goncalves, Marilda Souza

“…Sickle cell disease (SCD) patients often exhibit a dyslipidemic sub-phenotype. Paraoxonase 1 (PON 1) is a serum glycoprotein associated with the high-density…”
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Nasopharyngeal and Oropharyngeal Colonization by Staphylococcus aureus and Streptococcus pneumoniae and Prognostic Markers in Children with Sickle Cell Disease from the Northeast of Brazil by Rocha, Larissa C, Carvalho, Magda O S, Nascimento, Valma M L, Dos Santos, Milena S, Barros, Tânia F, Adorno, Elisângela V, Reis, Joice N, da Guarda, Caroline C, Santiago, Rayra P, Gonçalves, Marilda de Souza

“…We investigated the nasopharynx and oropharynx microbiota in sickle cell disease (SCD) to identify the microorganisms, antibiotic sensitivity, prevalent…”
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Association of homocysteine and inflammatory-related molecules in sickle cell anemia by Vilas-Boas, Wendell, Veloso Cerqueira, Bruno Antonio, Figueiredo, Camylla V B, Santiago, Rayra Pereira, da Guarda, Caroline C, Pitanga, Thassila Nogueira, Santana, Sanzio Silva, Dias Zanette, Angela Maria, Goncalves, Marilda de Souza

“…Investigate the role of homocysteine (Hcy), Th17-related cytokines, and adhesion molecules in the inflammatory state seen in the sickle cell anemia (SCA). We…”
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