Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Magnun Nueldo Nunes, Santos"'
Autor:
Adekunle Emmanuel Alagbe, Gisele Audrei Pedroso, Beatriz Benedetti de Oliveira, Edivilson da Costa, Gisélia Aparecida Freire Maia, Bruna Facanali Piellusch, Susan Elisabeth Domingues Costa Jorge, Fernando Ferreira Costa, José Luiz Proença Modena, Angelica Zaninelli Schreiber, Maria de Fátima Sonati, Magnun Nueldo Nunes Santos
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss 1, Pp 14-21 (2024)
Introduction: The hemogram and hemogram-derivative ratios (HDRs) are becoming markers of the severity and mortality of COVID-19. We evaluated the hemograms and serial weekly HDRs [neutrophil-lymphocyte ratio (NLR), monocyte-lymphocyte ratio (MLR), pl
Externí odkaz:
https://doaj.org/article/5ae5a371a1b94ac59205079d3c6eada3
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
Autor:
Elza Miyuki Kimura, Denise Madureira Oliveira, Susan Elisabeth Jorge, Daniela Maria Ribeiro, Tânia Regina Zaccariotto, Magnun Nueldo Nunes Santos, Vanessa Almeida, Dulcinéia Martins Albuquerque, Fernando Ferreira Costa, Maria de Fátima Sonati
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 37, Iss 2, Pp 103-108 (2015)
Background: Brazil has a multiethnic population with a high diversity of hemoglobinopathies. While screenings for beta-globin mutations are far more common, alterations affecting alpha-globin genes are usually more silent and less well known. The aim
Externí odkaz:
https://doaj.org/article/26ced1cda486421d92d57652b39af210
Autor:
Bidossessi Wilfried Hounkpe, Carla Roberta Peachazepi Moraes, Carolina Lanaro, Magnun Nueldo Nunes Santos, Fernando Ferreira Costa, Erich Vinicius De Paula
Publikováno v:
Exp Biol Med (Maywood)
Hemolytic diseases such as Sickle Cell Disease (SCD) are characterized by a natural propensity for both arterial and venous thrombosis. The ability of heme to induce tissue factor (TF) activation has been shown both in animal models of SCD, and in hu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca5942125f247af9cd66472ce41b2d05
https://europepmc.org/articles/PMC9554166/
https://europepmc.org/articles/PMC9554166/
Autor:
Adekunle Emmanuel Alagbe, Gisele Audrei Pedroso, Beatriz Benedetti de Oliveira, Edivilson da Costa, Gisélia Aparecida Freire Maia, Bruna Facanali Piellusch, Susan Elisabeth Domingues Costa Jorge, Fernando Ferreira Costa, José Luiz Proença Modena, Angelica Zaninelli Schreiber, Maria de Fátima Sonati, Magnun Nueldo Nunes Santos
Publikováno v:
Hematology, transfusion and cell therapy.
The hemogram and hemogram-derivative ratios (HDRs) are becoming markers of the severity and mortality of COVID-19. We evaluated the hemograms and serial weekly HDRs [neutrophil-lymphocyte ratio (NLR), monocyte-lymphocyte ratio (MLR), platelet-lymphoc
Autor:
Flavia Miranda Gomes C Bandeira, Magnun Nueldo Nunes Santos, Marcos André M Bezerra, Yara M Gomes, Aderson Silva Araujo, Maria Cynthia Braga, Wayner Vieira Souza, Frederico G C Abath
Publikováno v:
Revista de Saúde Pública, Vol 42, Iss 2, Pp 234-241 (2008)
OBJETIVO: Estimar o incremento no número adicional de afetados com base na prevalência de síndromes falciformes em familiares de casos-índice. MÉTODOS: Estudo transversal em familiares de amostra aleatória dos casos-índice identificados por pr
Externí odkaz:
https://doaj.org/article/b9e6222ee2e64cb9bca66658075c2cf8
Autor:
Betânia Lucena Domingues, Hatzlhofer, Diego Antonio, Pereira-Martins, Igor, de Farias Domingos, Gabriela da Silva, Arcanjo, Isabel, Weinhäuser, Diego Arruda, Falcão, Isabela Cristina Cordeiro, Farias, Jéssica Vitória Gadelha, de Freitas Batista, Luana Priscilla Laranjeira, Prado, Jéssica Maria Florencio, Oliveira, Thais Helena Chaves, Batista, Marcondes José de Vasconcelos Costa, Sobreira, Rodrigo Marcionilo, de Santana, Amanda Bezerra de Sá, Araújo, Manuela Albuquerque, de Melo, Bruna Vasconcelos, de Ancântara, Juan Luiz, Coelho-Silva, Ana Beatriz Lucas, de Moura Rafael, Danízia Menezes, de Lima Silva, Flávia Peixoto, Albuquerque, Magnun Nueldo Nunes, Santos, Ana Cláudia, Dos Anjos, Fernando Ferreira, Costa, Aderson, da Silva Araújo, Antonio Roberto, Lucena-Araújo, Marcos André Cavalcanti, Bezerra
Publikováno v:
Annals of hematology. 100(4)
Alpha thalassemia and beta-globin haplotype are considered classical genetic disease modifiers in sickle cell anemia (SCA) causing clinical heterogeneity. Nevertheless, their functional impact on SCA disease emergence and progression remains elusive.
Autor:
Oladele Simeon, Olatunya, Dulcineia Martins, Albuquerque, Magnun Nueldo Nunes, Santos, Tolorunju Segun, Kayode, Adekunle, Adekile, Fernando Ferreira, Costa
Publikováno v:
The Application of Clinical Genetics
Purpose To determine the various haptoglobin genotypes and their influence on the clinico-laboratory manifestations among young Nigerian sickle cell anemia (SCA) patients. Patients and Methods A total of 101 SCA patients and 64 controls were studied.