Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Aderson da Silva Araújo"'
Autor:
Rodolfo D. Cançado, Aderson da Silva Araújo, Alex Freire Sandes, Celso Arrais, Clarisse Lopes de Castro Lobo, Maria Stella Figueiredo, Sandra Fátima Menosi Gualandro, Sara Teresinha Olalla Saad, Fernando Ferreira Costa
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 3, Pp 341-348 (2021)
Paroxysmal nocturnal hemoglobinuria is a chronic, multi-systemic, progressive and life-threatening disease characterized by intravascular hemolysis, thrombotic events, serious infections and bone marrow failure. Paroxysmal nocturnal hemoglobinuria re
Externí odkaz:
https://doaj.org/article/d0c651cc3b40439ba8584c9d32114b52
Autor:
Okeke Chinedu, Wouitchékpo Vincent Tonassé, Dulcinéia Martins Albuquerque, Igor de Farias Domingos, Aderson da Silva Araújo, Marcos André Cavalcanti Bezerra, Maria de Fátima Sonati, Magnun Nueldo Nunes dos Santos
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss 2, Pp 165-170 (2021)
Introduction: Mutations affecting genes involved in oxidative and signaling pathways may be associated with kidney disease in sickle cell anemia. We determined the allele and genotype frequencies of some polymorphisms in the promoter regions of the H
Externí odkaz:
https://doaj.org/article/874eebcef95940afb6c1fe7c4b2627a6
Autor:
Manuela Freire Hazin Costa, Leuridan Cavalcante Torres, Marina Cadena da Matta, Aderson da Silva Araújo, Ariani Impieri Souza
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 41, Iss 4, Pp 298-302 (2019)
Background: Despite advances in health care for sickle cell disease patients, as well as in the improvement in reproductive issues mainly in women with the disease, pregnancy is still a challenge, both for the mother and the child, with high rates of
Externí odkaz:
https://doaj.org/article/b683f280a44b4f37854ec4777ca7cb9d
Autor:
Vanessa Araujo Gomes Santaterra, Maiara Marx Luz Fiusa, Bidossessi Wilfried Hounkpe, Francine Chenou, Wouitchekpo Vincent Tonasse, Loredana Nilkenes Gomes da Costa, Diego Garcia-Weber, Igor de Farias Domingos, Franciele de Lima, Ivanio Teixeira Borba-Junior, Aderson da Silva Araújo, Antonio Roberto Lucena-Araújo, Marcos André Cavalcante Bezerra, Magnun Nueldo Nunes dos Santos, Fernando Ferreira Costa, Jaime Millán, Erich Vinicius De Paula
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Free extracellular heme has been shown to activate several compartments of innate immunity, acting as a danger-associated molecular pattern (DAMP) in hemolytic diseases. Although localized endothelial barrier (EB) disruption is an important part of i
Externí odkaz:
https://doaj.org/article/68ef82d31e9d4903aea19036d7c741a4
Autor:
Fernanda Silva Medeiros, Taciana Furtado de Mendonça, Katiuscia Araújo de Miranda Lopes, Laís Medeiros da Câmara França, Andreia Soares da Silva, Luydson Richardson Silva Vasconcelos, Maria do Carmo Valgueiro Costa de Oliveira, Ana Cláudia Mendonça dos Anjos, Betânia Lucena Domingues Hatzlhofer, Marcos André Cavalcanti Bezerra, Aderson da Silva Araújo, Patrícia Moura, Maria do Socorro de Mendonça Cavalcanti
Publikováno v:
Genetics and Molecular Biology, Vol 40, Iss 3, Pp 600-603 (2017)
Abstract Sickle cell anemia (SCA) presents heterogenous clinical manifestations that cannot be explained solely by alterations to hemoglobin (Hb); other components such as endothelial adhesion, thrombosis and inflammation may be involved. The mannose
Externí odkaz:
https://doaj.org/article/8d6b488b9ac8486bbb5511d9e9285af2
Autor:
Aderson da Silva Araújo, Clarisse Lopes de Castro Lobo, Dimas Tadeu Covas, Fernando Ferreira Costa, Letícia Medeiros, Rodolfo Delfini Cançado, Sandra Fátima Menosi Gualandro, Sara Teresinha Olalla Saad
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 36, Iss 6, Pp 450-453 (2014)
Externí odkaz:
https://doaj.org/article/0aafd72eb63f4bb3ac19a8dacbb5786d
Autor:
Taciana Furtado de Mendonça Belmont, Kleyton Palmeira do Ó, Andreia Soares da Silva, Kamila de Melo Vilar, Fernanda Silva Medeiros, Luydson Richardson Silva Vasconcelos, Ana Claudia Mendonça Dos Anjos, Betânia Lucena Domingues Hatzlhofer, Maíra Galdino da Rocha Pitta, Marcos André Cavalcanti Bezerra, Aderson da Silva Araújo, Moacyr Jesus Barreto de Melo Rego, Patrícia Moura, Maria do Socorro Mendonça Cavalcanti
Publikováno v:
PLoS ONE, Vol 11, Iss 9, p e0162297 (2016)
INTRODUCTION:Patients with sickle cell anemia (SCA) may present chronic hemolytic anemia, vaso-occlusion and respiratory tract infection (RTI) episodes. Galectin-3 (GAL-3) is a multifunctional protein involved in inflammation, apoptosis, adhesion and
Externí odkaz:
https://doaj.org/article/b76fc6fdf9364d74b98985bbdfab4927
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:
Eduardo Cerello Chapchap, Murilo Marques Almeida Silva, Reijane Alves de Assis, Lucila Nassif Kerbauy, Michelli da Silva Diniz, Laércio Alberto Rosemberg, Sandra Regina Loggetto, Aderson da Silva Araujo, Antonio Fabron Junior, Monica Pinheiro de Almeida Verissimo, Giorgio Roberto Baldanzi, Breno Pannia Esposito, Fernando Tricta, Merula Emmanoel Anargyrou Steagall, Claudia Ângela Galleni Di Sessa Vellozo, Kleber Yotsumoto Fertrin, Ronaldo Hueb Baroni, Nelson Hamerschlak
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss 1, Pp 7-15 (2023)
Introduction: Magnetic resonance imaging (MRI) T2* technique is used to assess iron overload in the heart, liver and pancreas of thalassaemic patients. Optimal iron chelation and expected tissue iron response rates remain under investigation. The obj
Externí odkaz:
https://doaj.org/article/c8ed232d608c4a8084c62faf3ad93cdb
Autor:
Clarisse Lopes de Castro Lobo, Letícia Medeiros, Sara Teresinha Olalla Saad, Aderson da Silva Araújo, Rodolfo D. Cançado, Sandra Fátima Menosi Gualandro, Dimas Tadeu Covas, Fernando Ferreira Costa
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia
Revista Brasileira de Hematologia e Hemoterapia, Volume: 36, Issue: 6, Pages: 450-453, Published: DEC 2014
Revista Brasileira de Hematologia e Hemoterapia, Vol 36, Iss 6, Pp 450-453 (2014)
Revista Brasileira de Hematologia e Hemoterapia v.36 n.6 2014
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
Revista Brasileira de Hematologia e Hemoterapia, Volume: 36, Issue: 6, Pages: 450-453, Published: DEC 2014
Revista Brasileira de Hematologia e Hemoterapia, Vol 36, Iss 6, Pp 450-453 (2014)
Revista Brasileira de Hematologia e Hemoterapia v.36 n.6 2014
Revista brasileira de hematologia e hemoterapia
Associação Brasileira de Hematologia e Hemoterapia e Terapia Celular (ABHHTC)
instacron:ABHHTC
pecial article uidelines on the treatment of anemia of chronic enal failure using recombinant human rythropoietin: Associacao Brasileira de ematologia, Hemoterapia e Terapia Celular uidelines Project: Associacao Medica Brasileira – 014 derson da Si