Zobrazeno 1 - 10
of 24
pro vyhledávání: '"Larissa Carneiro Rocha"'
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:
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:
Caroline Conceição da Guarda, Sètondji Cocou Modeste Alexandre Yahouédéhou, Rayra Pereira Santiago, Joelma Santana Dos Santos Neres, Camila Felix de Lima Fernandes, Milena Magalhães Aleluia, Camylla Vilas Boas Figueiredo, Luciana Magalhães Fiuza, Suellen Pinheiro Carvalho, Rodrigo Mota de Oliveira, Cleverson Alves Fonseca, Uche Samuel Ndidi, Valma Maria Lopes Nascimento, Larissa Carneiro Rocha, Marilda Souza Goncalves
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0228399 (2020)
Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present highly variable clinical manifestations. Sickle cell anemia (SCA) is the most severe form, while SC hemoglobinopathy (HbSC) is thought to be milder. Thus
Externí odkaz:
https://doaj.org/article/f8190f50a51a4031937210902d2562a8
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:
Magda Oliveira Seixas Carvalho, André Luís Carvalho Santos Souza, Mauricio Batista Carvalho, Ana Paula Almeida Souza Pacheco, Larissa Carneiro Rocha, Valma Maria Lopes do Nascimento, Camylla Vilas Boas Figueiredo, Caroline Conceição Guarda, Rayra Pereira Santiago, Adekunle Adekile, Marilda de Souza Goncalves
Publikováno v:
Frontiers in Immunology, Vol 8 (2017)
Alpha-1 antitrypsin (AAT) is an inhibitor of neutrophil elastase and a member of the serine proteinase inhibitor (serpin) superfamily, and little is known about its activity in sickle cell disease (SCD). We hypothesize that AAT may undergo changes in
Externí odkaz:
https://doaj.org/article/9085d13e4a4646f1bcf962433de67878
Autor:
Rayra Pereira Santiago, Sètondji Cocou Modeste Alexandre Yahouédéhou, Valma Maria Lopes Nascimento, Marilda Souza Goncalves, Rodrigo Mota de Oliveira, Cleverson Alves Fonseca, Caroline Conceição da Guarda, Camylla V. B. Figueiredo, Larissa Carneiro Rocha, Suellen Pinheiro Carvalho, Milena Magalhães Aleluia, Luciana Magalhães Fiuza
Publikováno v:
Mediators of Inflammation
Mediators of Inflammation, Vol 2020 (2020)
Mediators of Inflammation, Vol 2020 (2020)
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, angiogenesis, inflammation, hematopoiesis, vascular inflammation, and cell proliferation. Po
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::124f1289d91ce7ef468644ac1fbe816b
https://doi.org/10.1155/2020/3185015
https://doi.org/10.1155/2020/3185015
Autor:
Rayra Pereira Santiago, Rodrigo Mota de Oliveira, Cleverson Alves Fonseca, Milena Magalhães Aleluia, Camylla Vilas Boas Figueiredo, Larissa Carneiro Rocha, Marilda Souza Goncalves, Caroline Conceição da Guarda, Joelma Santana dos Santos Neres, Valma Maria Lopes Nascimento, Suellen Pinheiro Carvalho, Luciana Magalhães Fiuza, Sètondji Cocou Modeste Alexandre Yahouédéhou, Antonio Mateus de Jesus Oliveira, Camila Felix de Lima Fernandes
Publikováno v:
Disease Markers, Vol 2020 (2020)
Disease Markers
Disease Markers
Introduction. Clinical complications in sickle cell anemia (SCA) are heterogeneous and involve several molecules. It has been suggested that SCA individuals present a dyslipidemic phenotype and that lipid parameters are associated with severe clinica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe905f3e94977b3d198c5f69f0b83236
https://doi.org/10.1155/2020/8842362
https://doi.org/10.1155/2020/8842362
Autor:
Valma Maria Lopes Nascimento, Luciana Magalhães Fiuza, Rayra Pereira Santiago, Larissa Carneiro Rocha, Camila Felix de Lima Fernandes, Rodrigo Mota de Oliveira, Uche Samuel Ndidi, Marilda Souza Goncalves, Cleverson Alves Fonseca, Camylla Vilas Boas Figueiredo, Sètondji Cocou Modeste Alexandre Yahouédéhou, Caroline Conceição da Guarda, Milena Magalhães Aleluia, Joelma Santana dos Santos Neres, Suellen Pinheiro Carvalho
Publikováno v:
PLoS ONE, Vol 15, Iss 1, p e0228399 (2020)
PLoS ONE
PLoS ONE
Sickle cell disease (SCD) consists of a group of hemoglobinopathies in which individuals present highly variable clinical manifestations. Sickle cell anemia (SCA) is the most severe form, while SC hemoglobinopathy (HbSC) is thought to be milder. Thus
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::887870d13d032adacf8f51cac6d764df
https://doaj.org/article/f8190f50a51a4031937210902d2562a8
https://doaj.org/article/f8190f50a51a4031937210902d2562a8
Autor:
Luciana Magalhães Fiuza, Valma Maria Lopes Nascimento, Milena Magalhães Aleluia, Marilda Souza Goncalves, Rayra Pereira Santiago, Caroline Conceição da Guarda, Larissa Carneiro Rocha, Suellen Pinheiro Carvalho, Rodrigo Mota de Oliveira, Cleverson Alves Fonseca, Sètondji Cocou Modeste Alexandre Yahouédéhou, Camylla Vilas Boas Figueiredo
Publikováno v:
Disease Markers, Vol 2020 (2020)
Disease Markers
Disease Markers
Individuals with sickle cell anemia (SCA) present chronic anemia, hemolysis, an exacerbated inflammatory response, and heterogeneous clinical complications, which may be modulated by the transforming growth factor beta (TGF-β) pathway. Thus, we aime
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87e5eb3001214751a11754b75affcd95
https://doaj.org/article/b356b85522df4d88a65eeb8be0e16a6f
https://doaj.org/article/b356b85522df4d88a65eeb8be0e16a6f
Autor:
Caroline Conceição da Guarda, Isa Menezes Lyra, Larissa Carneiro Rocha, Marilda Souza Goncalves, Camylla V. B. Figueiredo, Rayra Pereira Santiago, Théo Araújo-Santos, Manoel Barral Neto, Valéria M. Borges, Magda Oliveira Seixas Carvalho, Nívea F. Luz, Joao Oliveira Reis, Valma Maria Lopes, Bruno A. V. Cerqueira, Luciana Magalhães Fiuza, Cynara Gomes Barbosa
Publikováno v:
British Journal of Haematology. 182:933-936
Instituto Gonc alo Moniz- Fundacao Oswaldo Cruz (IGM-FIOCRUZ) and the Hospital da Crianc a das Obras Sociais Irma Dulce (HCOSID) approved this study, with protocol number 0016.0.225.000-09.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6c759ea10f295cc1113d67872e13c0d
https://doi.org/10.1111/bjh.14896
https://doi.org/10.1111/bjh.14896