Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Marcondes José de Vasconcelos Costa Sobreira"'
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:
Marcondes José de Vasconcelos Costa Sobreira, Aderson S Araujo, Antonio R. Lucena-Araujo, Flávia Peixoto Albuquerque, Isabela Cristina Cordeiro Farias, Danízia Menezes de Lima Silva, Diego A Pereira-Martins, Manuela Albuquerque de Melo, Bruna Vasconcelos de Ancântara, Gabriela da Silva Arcanjo, Diego Arruda Falcão, Ana Claudia Mendonça dos Anjos, A. S. Araújo, Magnun N. N. Santos, Rodrigo Marcionilo Santana, Thais Helena Chaves Batista, Isabel Weinhäuser, Jéssica Vitória Gadelha de Freitas Batista, Betânia Lucena Domingues Hatzlhofer, Ana Beatriz Lucas de Moura Rafael, Luana Priscilla Laranjeira Prado, Igor de Farias Domingos, Fernando Ferreira Costa, Marcos André Cavalcanti Bezerra, Juan L Coelho-Silva, Jéssica Maria Florencio Oliveira
Publikováno v:
Annals of Hematology. 100:921-931
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:
Gabriela da Silva Arcanjo, Antonio R. Lucena-Araujo, Marcondes José de Vasconcelos Costa Sobreira, Jéssica Vitória Gadelha de Freitas Batista, Aderson S Araujo, Igor de Farias Domingos, A. S. Araújo, Magnun N. N. Santos, Thais Helena Chaves Batista, Jéssica Maricelly Deodato de Oliveira, Marcos André Cavalcanti Bezerra, Fernanda Silva Medeiros, Diego A Pereira-Martins, Diego Arruda Falcão, Flávia Peixoto Albuquerque, Ana Claudia Mendonça dos Anjos, Manuela F. Hazin, Dulcineia M. Albuquerque, Luana Priscilla Morais Laranjeira, Betânia Lucena Domingues Hatzlhofer, Fernando Ferreira Costa, Rodrigo Marcionilo Santana
Publikováno v:
Annals of Hematology. 100:903-911
Hyperbilirubinemia in patients with sickle cell anemia (SCA) as a result of enhanced erythrocyte destruction, lead to cholelithiasis development in a subset of patients. Evidence suggests that hyperbilirubinemia may be related to genetic variations,
Autor:
Adriana Malheiro, Nelson Abrahim Fraiji, Marcos André Cavalcanti Bezerra, Magnun N. N. Santos, Pedro Vieira da Silva Neto, Evilazio Cunha Cardoso, Marcondes José de Vasconcelos Costa Sobreira, Aderson S Araujo, Bidossessi Wilfried Hounkpe, Francine Chenou, Antonio R. Lucena-Araujo, Erich Vinicius De Paula, Fernando Ferreira Costa, Igor de Farias Domingos
Publikováno v:
Research and Practice in Thrombosis and Haemostasis, Vol 5, Iss 1, Pp 204-210 (2021)
Research and Practice in Thrombosis and Haemostasis
Research and Practice in Thrombosis and Haemostasis
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). NETosis is a
Autor:
Antonio R. Lucena-Araujo, Thais Helena Chaves Batista, Camila Mabel de Albuquerque Ramos, Gabriela da Silva Arcanjo, Rodrigo Marcionilo Santana, Ana Cláudia Mendeonça dos Anjos, Fernando Ferreira Costa, Marcondes José de Vasconcelos Costa Sobreira, Aderson S Araujo, Marcos André Cavalcanti Bezerra, Dulcineia M. Albuquerque
Publikováno v:
Hematology, Transfusion and Cell Therapy
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:
Dulcineia M. Albuquerque, Marcondes José de Vasconcelos Costa Sobreira, Maria de Fátima Sonati, Antonio R. Lucena-Araujo, Maria Heloisa Souza Lima Blotta, Aderson S Araujo, Adekunle Emmanuel Alagbe, Igor de Farias Domingos, Fernando Ferreira Costa, Marcos André Cavalcanti Bezerra, Magnun N. N. Santos, Rômulo Tadeu Dias de Oliveira, Carolina Lanaro, Diego A Pereira-Martins
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Universidade de São Paulo (USP)
instacron:USP
Sickle cell anemia (SCA) pathophysiology is characterized by the activation of sickle red blood cells, reticulocytes, leukocytes, platelets, and endothelial cells, and with the expression of several inflammatory molecules. Therefore, it is conceivabl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7f17128bee53a2840a28c5256b341995
Autor:
Luydson Richardson Silva Vasconcelos, Mario J.A. Saad, Marcondes José de Vasconcelos Costa Sobreira, Aderson S Araujo, Antonio R. Lucena-Araujo, Diego A Pereira-Martins, Diego Arruda Falcão, Gabriela da Silva Arcanjo, Thais Helena Chaves Batista, Fernando Ferreira Costa, Bruno M. Carvalho, Marcos André Cavalcanti Bezerra, Rodrigo Marcionilo Santana
Publikováno v:
Blood. 134:975-975
Introduction: Leg ulcers (LUs) are a cutaneous complication of sickle cell anemia (SCA), whose etiology is considered multifactorial. In the search for new candidates for modulators of SCA clinical events, recent evidence suggests the significant rol
Autor:
Evilazio Cunha Cardoso, Nelson Abrahim Fraiji, Marcos André Cavalcanti Bezerra, Igor de Farias Domingos, Marcondes José de Vasconcelos Costa Sobreira, Adriana Malheiro, Aderson S Araujo, Magnun N. N. Santos, Fernando Ferreira Costa, Erich Vinicius De Paula, Bidossessi Wilfried Hounkpe, Francine Chenou, Antonio R. Lucena-Araujo, Pedro Vieira da Silva Neto
Publikováno v:
Blood. 134:2257-2257
Introduction: Recent evidence suggests that coagulation activation is involved in the pathogenesis of progressive organ failure in Sickle Cell Anemia (SCA). In addition, generation of neutrophil extracellular traps (NETosis), one of the components of