Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Aderson S. Araújo"'
Autor:
Matheus F. Bezerra, Bruna R. Larrazábal, Aleide S. Lima, Mariana R. Mello, Raphael F. Pimentel, Isabel Weinhäuser, Fernando F. Costa, Kleber Y. Fertrin, Aderson S. Araújo, Cíntia G. Machado, Marcos A. Bezerra, Antonio R. Lucena-Araujo
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss 3, Pp 328-331 (2022)
Introduction: One of the most critical complications in myelodysplastic syndromes (MDS) is the progression to acute myeloid leukemia (AML). The dynamics of clonal evolution in MDS and how acquired mutations can be used as biomarkers to track disease
Externí odkaz:
https://doaj.org/article/e5ed6b5297b44c6382c8a6bc32345e6b
Autor:
Diego A. Pereira-Martins, Igor F. Domingos, Edis Belini-Junior, Juan L. Coelho-Silva, Isabel Weinhäuser, Aderson S. Araújo, Clarisse L. Lobo, Claudia R. Bonini-Domingos, Marcos A. Bezerra, Antonio R. Lucena-Araujo
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 3, Pp 243-248 (2021)
Introduction: Sickle cell anemia (SCA) is a Mendelian disorder with a heterogeneous clinical course. The reasons for this phenotypic diversity are not entirely established, but it is known that high fetal hemoglobin levels lead to a milder course of
Externí odkaz:
https://doaj.org/article/b4f7b9e9364742d191c10f93c9d5a4c7
Autor:
Flávia M. G. C. Bandeira, Marcos A. C. Bezerra, Magnun N. N. Santos, Yara M. Gomes, Aderson S. Araújo, Frederico G. C. Abath
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 29, Iss 2, Pp 179-184 (2007)
A anemia falciforme caracteriza-se como quadro hemolítico hereditário que evolui cronicamente causando danos físicos e emocionais às pessoas acometidas. Até o presente momento não se dispõe de tratamento curativo, a não ser o transplante de m
Externí odkaz:
https://doaj.org/article/ea58909372364127a9eb6becc53f4433
Autor:
Flavia M. G. C. Bandeira, Jaqueline C. Peres, Eduardo J. Carvalho, Ivane Bezerra, Aderson S. Araújo, Mariana R. B. Mello, Cíntia Machado
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 26, Iss 3, Pp 189-194 (2004)
O uso de hidroxiuréia promove a elevação dos níveis de hemoglobina fetal (Hb F) em pacientes portadores de síndromes falciformes (SF) e o medicamento vem sendo estudado em vários grupos de pacientes, incluindo adultos e crianças. O presente tr
Externí odkaz:
https://doaj.org/article/41117f98fb4740759b33df0ac7249e36
Autor:
Maria L. Salustiano-Bandeira, Amanda Moreira-Aguiar, Diego A. Pereira-Martins, Juan L. Coelho-Silva, Isabel Weinhäuser, Pedro L. França-Neto, Aleide S. Lima, Ana S. Lima, Anemari R. Baccarin, Fernanda B. Silva, Manuela A. de Melo, Fernanda S. Niemann, Luciana Nardinelli, César A. Ortiz Rojas, Bruno K. Duarte, Aderson S. Araujo, Elisa A. Azevedo, Clarice N. Morais, Lorena L. Figueiredo-Pontes, Jan J. Schuringa, Gerwin Huls, Israel Bendit, Eduardo M. Rego, Sara T. Olalla Saad, Fabiola Traina, Marcos A. Bezerra, Antonio R. Lucena-Araujo
Publikováno v:
Blood Cancer Journal, Vol 14, Iss 1, Pp 1-3 (2024)
Externí odkaz:
https://doaj.org/article/67ef150b7ee54451934361d769848375
Autor:
Ariani Impieri de Souza, Marina L.G. Dias, Ana Laura Carneiro Gomes Ferreira, Manuela Freire Hazin-Costa, Aderson S. Araújo, Flavia Anchielle Carvalho da Silva
Publikováno v:
International journal of gynaecology and obstetrics: the official organ of the International Federation of Gynaecology and Obstetrics. 143(1)
OBJECTIVE To compare clinical and obstetric adverse events among pregnant women with sickle cell disease (SCD) according to genotype. METHODS The present cross-sectional study enrolled women aged 15-49 years with SCD and prior pregnancy attending a h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bcc0d2a76e24fafa33fb83bc16a745d3
https://pubmed.ncbi.nlm.nih.gov/30030929
https://pubmed.ncbi.nlm.nih.gov/30030929
Autor:
Tiago Eugênio Faria e Arantes, Silvio B. Campos, Thayze T. Martins, João Lins de Andrade Neto, Vasco Bravo-Filho, Fabiana Brasileiro, Aderson S. Araújo
Publikováno v:
Retina. 35:257-263
To assess peripapillary retinal nerve fiber layer, macular ganglion cell complex, and total macular thicknesses using spectral domain optical coherence tomography on sickle cell disease patients with and without sickle retinopathy.Nineteen eyes of 11
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be600ec5a7c4a4cebce8d0e3b8370adc
https://doi.org/10.1097/iae.0000000000000309
https://doi.org/10.1097/iae.0000000000000309
Autor:
Bidossessi Wilfried Hounkpe, Francine Chenou, Igor de Farias Domingos, Evilazio Cunha Cardoso, Marcondes José de Vasconcelos Costa Sobreira, Aderson S. Araujo, Antonio Roberto Lucena‐Araújo, Pedro Vieira da Silva Neto, Adriana Malheiro, Nelson Abrahim Fraiji, Fernando Ferreira Costa, Marcos André C. Bezerra, Magnun Nueldo Nunes Santos, Erich Vinicius De Paula
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 5, Iss 1, Pp 204-210 (2021)
Abstract Background Recent evidence suggests that generation of neutrophil extracellular traps (NETosis), one of the components of immunothrombosis, is associated with the pathogenesis of both venous thromboembolism and sickle cell disease (SCD). NET
Externí odkaz:
https://doaj.org/article/7a2ac59c8d2740c2896aa4fa58dc8a97