Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Elisângela Vitória Adorno"'
Autor:
Joelma Figueiredo Menezes, Magda Oliveira Seixas Carvalho, Larissa Carneiro Rocha, Felipe Miranda dos Santos, Elisângela Vitória Adorno, Cyntia Cajado de Souza, Rayra Pereira Santiago, Caroline Conceição da Guarda, Rodrigo Mota de Oliveira, Camylla Vilas Boas Figueiredo, Suéllen Pinheiro Carvalho, Sètondji Cocou Modeste Alexandre Yahouédéhou, Luciana Magalhães Fiuza, Corynne Stéphanie Ahouefa Adanho, Thassila Nogueira Pitanga, Isa Menezes Lyra, Valma Maria Lopes Nascimento, Alberto Augusto Noronha-Dutra, Marilda Souza Goncalves
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-10 (2023)
Abstract Sickle cell disease (SCD) patients often exhibit a dyslipidemic sub-phenotype. Paraoxonase 1 (PON 1) is a serum glycoprotein associated with the high-density lipoproteins cholesterol (HDL-C), and variability in PON1 activity depends on the P
Externí odkaz:
https://doaj.org/article/d3ca186186fb49ce9f36b6457163e292
Autor:
Edvan do Carmo Santos, Paulo Vinícius Bispo Santana, Laíne Lopes Silva de Jesus, Gabriela Imbassahy Valentim Melo, Sètondji Cocou Modeste Alexandre Yahouédéhou, Caroline Conceição da Guarda, Rayra Pereira Santiago, Luciana Magalhães Fiuza, Suéllen Pinheiro Carvalho, Liz Oliveira dos Santos, Elisângela Vitória Adorno, Augusto Cezar Magalhães Aleluia, Luciene Cristina Gastalho Campos Luiz, Teresa Cristina Cardoso Fonseca, Marilda de Souza Gonçalves, Milena Magalhães Aleluia
Publikováno v:
Hematology Reports, Vol 15, Iss 1, Pp 119-129 (2023)
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 the double heterozygous of HbS and HbC (HbSC) is defined as SC hemoglobinopathy. The patho
Externí odkaz:
https://doaj.org/article/7b6fd16d69e34155add7f5c83a6fb970
Autor:
Sètondji Cocou Modeste Alexandre Yahouédéhou, Joelma Santana dos Santos Neres, Caroline Conceição da Guarda, Suellen Pinheiro Carvalho, Rayra Pereira Santiago, Camylla Vilas Boas Figueiredo, Luciana Magalhães Fiuza, Uche Samuel Ndidi, Rodrigo Mota de Oliveira, Cleverson Alves Fonseca, Valma Maria Lopes Nascimento, Larissa Carneiro Rocha, Corynne Stéphanie Ahouéfa Adanho, Tiago Santos Carvalho da Rocha, Elisângela Vitória Adorno, Marilda Souza Goncalves
Publikováno v:
Frontiers in Pharmacology, Vol 11 (2020)
Differences in hydroxyurea response in sickle cell anemia may arise due to a series of factors with genetic factors appearing to be predominant. This study aims to investigate the effects of single nucleotide polymorphisms in genes encoding drug-meta
Externí odkaz:
https://doaj.org/article/3400dd841545442395b4388443304024
Autor:
Edvan do Carmo Santos, Gabriela Imbassahy Valentim Melo, Paulo Vinícius Bispo Santana, Idaiara Graziele Silva Quadros, Sètondji Cocou Modeste Alexandre Yahouédéhou, Caroline Conceição da Guarda, Rayra Pereira Santiago, Luciana Magalhães Fiuza, Suéllen Pinheiro Carvalho, Elisângela Vitória Adorno, Carla Martins Kaneto, Teresa Cristina Cardoso Fonseca, Marilda Souza Goncalves, Milena Magalhães Aleluia
Publikováno v:
Biomolecules, Vol 12, Iss 2, p 317 (2022)
Sickle leg ulcers (SLU) are malleoli lesions with exuberant hemolytic pathophysiology. The microRNAs are potential genetic biomarkers for several pathologies. Thereby, we aimed to assess the expression of circulating miR-199a-5p, miR-144, and miR-126
Externí odkaz:
https://doaj.org/article/b88c870c3ae942d883d74d07733352bb
Autor:
Milena Magalhães Aleluia, Caroline Conceição da Guarda, Rayra Pereira Santiago, Teresa Cristina Cardoso Fonseca, Fábia Idalina Neves, Regiana Quinto de Souza, Larissa Alves Farias, Felipe Araújo Pimenta, Luciana Magalhães Fiuza, Thassila Nogueira Pitanga, Júnia Raquel Dutra Ferreira, Elisângela Vitória Adorno, Bruno Antônio Veloso Cerqueira, Marilda de Souza Gonçalves
Publikováno v:
Lipids in Health and Disease, Vol 16, Iss 1, Pp 1-9 (2017)
Abstract Background Sickle cell anemia (SCA) patients exhibit sub-phenotypes associated to hemolysis and vaso-occlusion. The disease has a chronic inflammatory nature that has been also associated to alterations in the lipid profile. This study aims
Externí odkaz:
https://doaj.org/article/ed208174616147b98497bfe5fbf4bacb
Autor:
Sètondji Cocou Modeste Alexandre Yahouédéhou, Caroline Conceição da Guarda, Camylla Vilas Boas Figueiredo, Rayra Pereira Santiago, Suellen Pinheiro Carvalho, Luciana Magalhães Fiuza, Uche Samuel Ndidi, Rodrigo Mota Oliveira, Magda Oliveira Seixas Carvalho, Valma Maria Lopes Nascimento, Larissa Carneiro Rocha, Isa Menezes Lyra, Elisângela Vitória Adorno, Marilda Souza Goncalves
Publikováno v:
PLoS ONE, Vol 14, Iss 7, p e0218040 (2019)
This study investigated the effects of hydroxyurea (HU) on hematological, biochemical and inflammatory parameters in children with sickle cell anemia (SCA) in association with βS haplotype and α-thalassemia. We included 22 children with SCA who wer
Externí odkaz:
https://doaj.org/article/75c771f077224792836bb5f6109ca140
Autor:
Júnia Raquel Dutra Ferreira, Milena Magalhães Aleluia, Camylla Vilas Boas Figueiredo, Larissa Castro de Lima Vieira, Rayra Pereira Santiago, Caroline Conceição da Guarda, Cynara Gomes Barbosa, Ricardo Riccio Oliveira, Elisângela Vitória Adorno, Marilda de Souza Gonçalves
Publikováno v:
Frontiers in Endocrinology, Vol 8 (2017)
BackgroundCombined oral contraceptive (COC) use has been associated with an unfavorable impact on carbohydrate and lipid metabolism in diverse populations of normal weight and obese women. The present study aimed to evaluate the cardiometabolic and i
Externí odkaz:
https://doaj.org/article/ab1451a58dae47f4a9763008a1286f95
Autor:
Elisângela Vitória Adorno, Ângela Zanette, Isa Lyra, Magda Oliveira Seixas, Mitermayer Galvão Reis, Marilda Souza Gonçalves
Publikováno v:
Genetics and Molecular Biology, Vol 31, Iss 3, Pp 621-625 (2008)
Beta S-globin gene (βS-globin) haplotypes, markers for severe sickle cell anemia (SCA), and the alpha-thalassemia 2 gene 3.7 kb deletion (-α2(3.7 kb) thal) along with demographic and clinical data were investigated in SCA outpatients (n = 125, 63 f
Externí odkaz:
https://doaj.org/article/0c6e7317bbf349f98d7a52ac9c5d0507
Autor:
Fábio David Couto, Elisângela Vitória Adorno, Joelma Figueiredo Menezes, José Pereira Moura Neto, Marco Antônio Vasconcelos Rêgo, Mitermayer Galvão dos Reis, Marilda Souza Gonçalves
Publikováno v:
Cadernos de Saúde Pública, Vol 20, Iss 2, Pp 529-533 (2004)
The C677T polymorphism in the methylenetetrahydrofolate reductase gene (MTHFR) is associated with an increase in total homocysteine serum levels (tHcy), described as a risk factor for cardiovascular disease. Eight hundred forty-three neonates from tw
Externí odkaz:
https://doaj.org/article/efe8703bf72d4798a576fe53e3015c99
Autor:
Fábio David Couto, Elisângela Vitória Adorno, Joelma Figueiredo Menezes, José Pereira Moura Neto, Marco Antônio Vasconcelos Rêgo, Mitermayer Galvão dos Reis, Marilda Souza Gonçalves
Publikováno v:
Cadernos de Saúde Pública, Vol 20, Iss 2, Pp 529-533
The C677T polymorphism in the methylenetetrahydrofolate reductase gene (MTHFR) is associated with an increase in total homocysteine serum levels (tHcy), described as a risk factor for cardiovascular disease. Eight hundred forty-three neonates from tw
Externí odkaz:
https://doaj.org/article/c34d2f32b85d4cdfbd31af29ad6aca11