The endocannabinoid system's genetic polymorphisms in sickle cell anemia patients.

Authors: Berti, Amanda Cristina Meneguetti, de Castro, Vanessa da Silveira Ramos, Arcanjo, Gabriela Silva, da Silva Araujo, Aderson, Lucena-Araujo, Antonio Roberto, Bezerra, Marcos André Cavalcanti, Gazarini, Lucas, da Silva, Danilo Grünig Humberto, Belini-Júnior, Edis

Source: Scientific Reports; 12/30/2024, Vol. 14 Issue 1, p1-9, 9p

Subject Terms: SICKLE cell anemia, SINGLE nucleotide polymorphisms, CANNABINOID receptors, BLOOD diseases, GENETIC polymorphisms, BLOOD platelet aggregation

Chemokines in pregnant women with sickle cell disease

Authors: Hazin-Costa, Manuela Freire, da Silva Aráujo, Aderson, Guerra, Glaucia Lins, da Matta, Marina Cadena, Torres, Leuridan Cavalcante, Souza, Ariani Impieri

Source: In Cytokine January 2019 113:195-199

Evaluation of CD4+CD25+FoxP3+ T cell populations, IL-10 production, and their correlation with clinical and biochemical parameters in sickle cell anemia patients with leg ulcers

Authors: Rêgo, Moacyr Jesus Barreto Melo, da Silva, Rafael Ramos, Pereira, Michelly Cristiny, da Silva Araújo, Aderson, Pitta, Ivan da Rocha, Falcão, Diego Arruda, Bezerra, Marcos André Cavalcanti, Pitta, Maira Galdino da Rocha

Source: In Cytokine October 2015 75(2):310-315

Guidelines on the treatment of anemia of chronic renal failure using recombinant human erythropoietin: Associação Brasileira de Hematologia, Hemoterapia e Terapia Celular Guidelines Project: Associação Médica Brasileira – 2014

Authors: da Silva Araújo, Aderson, de Castro Lobo, Clarisse Lopes, Covas, Dimas Tadeu, Costa, Fernando Ferreira, Medeiros, Letícia, Cançado, Rodolfo Delfini, Gualandro, Sandra Fátima Menosi, Saad, Sara Teresinha Olalla

Source: In Revista Brasileira de Hematologia e Hemoterapia November-December 2014 36(6):450-453

Evaluation of Th17 related cytokines associated with clinical and laboratorial parameters in sickle cell anemia patients with leg ulcers

Authors: da Silva, Rafael Ramos, Pereira, Michelly Cristiny, Melo Rêgo, Moacyr Jesus Barreto, Domingues Hatzlhofer, Betania Lucena, da Silva Araújo, Aderson, Cavalcanti Bezerra, Marcos André, da Rocha Pitta, Ivan, da Rocha Pitta, Maira Galdino

Source: In Cytokine February 2014 65(2):143-147

Association between the genetic polymorphisms of glutathione S-transferase (GSTM1 and GSTT1) and the clinical manifestations in sickle cell anemia

Authors: de Oliveira Filho, Romério Alencar, Silva, Géssyka Jerônimo, de Farias Domingos, Igor, Hatzlhofer, Betânia Lucena Domingues, da Silva Araújo, Aderson, de Lima Filho, José Luiz, Bezerra, Marcos André Cavalcanti, Martins, Danyelly Bruneska Gondim, de Araújo, Rosângela Ferreira Frade

Source: In Blood Cells, Molecules and Diseases August 2013 51(2):76-79

Polymorphisms and gene expression of metalloproteinases and their inhibitors associated with cerebral ischemic stroke in young patients with sickle cell anemia.

Authors: do Kleyton Palmeira, Ó., da Silva Freire, Ana Karla, de Nóbrega, Débora Nascimento, dos Santos Souza, Roberta, Farias, Isabela Cristina Cordeiro, de Mendonça Belmont, Taciana Furtado, da Silva, Andreia Soares, da Silva Arcanjo, Gabriela, da Silva Araujo, Aderson, dos Anjos, Ana Cláudia Mendonça, de Araujo, Antônio Roberto Lucena, Bezerra, Marcos André Cavalcanti, de Moura, Patricia Muniz Mendes Freire, do Socorro Mendonça Cavalcanti, Maria, Vasconcelos, Luydson Richardson Silva

Source: Molecular Biology Reports; Apr2023, Vol. 50 Issue 4, p3341-3353, 13p

Brazilian Thalassemia Association protocol for iron chelation therapy in patients under regular transfusion.

Authors: de Almeida Veríssimo, Monica Pinheiro, Loggetto, Sandra Regina, Fabron Junior, Antonio, Roberto Baldanzi, Giorgio, Hamerschlak, Nelson, Fernandes, Juliano Lara, da Silva Araujo, Aderson, de Castro Lobo, Clarisse Lopes, Yotsumoto Fertrin, Kleber, Antonios Berdoukas, Vasilios, Galanello, Renzo

Source: Brazilian Journal of Hematology & Hemotherapy / Revista Brasileira de Hematologia e Hemoterapia; 2013, Vol. 35 Issue 6, p428-434, 7p

Subject Terms: CHELATION therapy, BETA-Thalassemia