Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Joelma Santana Dos Santos Neres"'
Autor:
Joelma Santana dos Santos Neres, Sètondji Cocou Modeste Alexandre Yahouédéhou, Marilda Souza Goncalves
Publikováno v:
Pharmaceuticals, Vol 16, Iss 6, p 857 (2023)
Inconsistent therapeutic responses have been observed among patients with sickle cell anemia (SCA) undergoing hydroxyurea (HU) following the adoption of the standardized protocol. Moreover, this treatment regimen necessitates a prolonged period to re
Externí odkaz:
https://doaj.org/article/982c6b2130074231b328d2832e8e0914
Autor:
Camylla Vilas Boas Figueiredo, Rayra Pereira Santiago, Caroline Conceição da Guarda, Rodrigo Mota Oliveira, Luciana Magalhães Fiuza, Sètondji Cocou Modeste Alexandre Yahouédéhou, Suéllen Pinheiro Carvalho, Joelma Santana Dos Santos Neres, Antonio Mateus de Jesus Oliveira, Cleverson Alves Fonseca, Valma Maria Lopes Nascimento, Isa Menezes Lyra, Milena Magalhães Aleluia, Marilda Souza Goncalves
Publikováno v:
PLoS ONE, Vol 16, Iss 2, p e0246067 (2021)
Priapism is a urologic emergency characterized by an uncontrolled, persistent and painful erection in the absence of sexual stimulation, which can lead to penile fibrosis and impotence. It is highly frequent in sickle cell disease (SCD) associated wi
Externí odkaz:
https://doaj.org/article/6de39a391e37471c8497f9ff44f767b3
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:
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, Isa Menezes Lyra, Antonio Mateus de Jesus Oliveira, Camylla Vilas Boas Figueiredo, Rodrigo Mota de Oliveira, Rayra Pereira Santiago, Cleverson Alves Fonseca, Caroline Conceição da Guarda, Suellen Pinheiro Carvalho, Sètondji Cocou Modeste Alexandre Yahouédéhou, Milena Magalhães Aleluia, Joelma Santana dos Santos Neres, Marilda Souza Goncalves
Publikováno v:
PLoS ONE, Vol 16, Iss 2, p e0246067 (2021)
PLoS ONE
PLoS ONE
Priapism is a urologic emergency characterized by an uncontrolled, persistent and painful erection in the absence of sexual stimulation, which can lead to penile fibrosis and impotence. It is highly frequent in sickle cell disease (SCD) associated wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8371d495f8f70f37b3767de50d42006c
https://doaj.org/article/6de39a391e37471c8497f9ff44f767b3
https://doaj.org/article/6de39a391e37471c8497f9ff44f767b3
Autor:
Eugênia Terra Granado Pina, Marilda Souza Goncalves, Sânzio Silva Santana, Elisângela Vitória Adorno, Isa Menezes Lyra, Cynara Gomes Barbosa, Ivana Paula Ribeiro Leite, Thassila Nogueira Pitanga, Jaime Ribeiro-Filho, Joelma Santana dos Santos Neres, J Ferreira, Sètondji Cocou Modeste Alexandre Yahouédéhou
Publikováno v:
Expert review of hematology. 13(10)
Ticagrelor is an antiplatelet agent approved for the treatment of patients with an acute coronary syndrome or a history of myocardial infarction. Considering the evidence demonstrating that ticagrelor-mediated inhibition of platelet activation and ag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2bb62f2a8f34486481acc0520165f938
https://pubmed.ncbi.nlm.nih.gov/32972255
https://pubmed.ncbi.nlm.nih.gov/32972255
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