Zobrazeno 1 - 10
of 57
pro vyhledávání: '"Belinda P. Simões"'
Autor:
Mariana L. C. Silveira, Wilma T. Anselmo-Lima, Francesca M. Faria, Danielle L. C. Queiroz, Rodrigo L. Nogueira, Marcelo G. J. Leite, Ricardo M. Lessa, Belinda P. Simões, Edwin Tamashiro, Fabiana C. P. Valera
Publikováno v:
BMC Infectious Diseases, Vol 19, Iss 1, Pp 1-6 (2019)
Abstract Background Early diagnosis of acute invasive fungal rhinosinusitis (AIFRS) is vital to improving outcomes in immunocompromised patients. This study evaluated the impact of a systematic protocol with nasal endoscopy and biopsies to early dete
Externí odkaz:
https://doaj.org/article/2162a50a536441b7886ec150cf4caeb6
Autor:
Karina Tozatto-Maio, Robert Girot, Indou Deme Ly, Ana Cristina Silva Pinto, Vanderson Rocha, Francisco Fernandes, Ibrahima Diagne, Yahia Benzerara, Carla L. Dinardo, Julia Pavan Soler, Simone Kashima, Itauá Leston Araujo, Chantal Kenzey, Guilherme H. H. Fonseca, Evandra S. Rodrigues, Fernanda Volt, Luciana Jarduli, Annalisa Ruggeri, Christina Mariaselvam, Sandra F. M. Gualandro, Hanadi Rafii, Barbara Cappelli, Felipe Melo Nogueira, Graziana Maria Scigliuolo, Renato Luiz Guerino-Cunha, Kelen Cristina Ribeiro Malmegrim, Belinda P. Simões, Eliane Gluckman, Ryad Tamouza
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
Sickle cell disease (SCD), the most common monogenic disease worldwide, is marked by a phenotypic variability that is, to date, only partially understood. Because inflammation plays a major role in SCD pathophysiology, we hypothesized that single nuc
Externí odkaz:
https://doaj.org/article/67cb8a7ed9504d0aaebc582eaf5a2b7d
Autor:
Lucas C.M. Arruda, Kelen C.R. Malmegrim, João R. Lima-Júnior, Emmanuel Clave, Juliana B.E. Dias, Daniela A. Moraes, Corinne Douay, Isabelle Fournier, Hélène Moins-Teisserenc, Antônio José Alberdi, Dimas T. Covas, Belinda P. Simões, Pauline Lansiaux, Antoine Toubert, Maria Carolina Oliveira
Publikováno v:
Blood Advances, Vol 2, Iss 2, Pp 126-141 (2018)
Abstract: To evaluate the immunological mechanisms associated with clinical outcomes after autologous hematopoietic stem cell transplantation (AHSCT), focusing on regulatory T- (Treg) and B- (Breg) cell immune reconstitution, 31 systemic sclerosis (S
Externí odkaz:
https://doaj.org/article/9767335330294441b6144d475820254c
Autor:
Jaquellyne G. Penaforte-Saboia, Renan M. Montenegro, Carlos E. Couri, Livia A. Batista, Ana Paula D. R. Montenegro, Virginia O. Fernandes, Hussain Akhtar, Carlos A. Negrato, Kelen Cristina Ribeiro Malmegrim, Daniela Aparecida Moraes, Juliana B. E. Dias, Belinda P. Simões, Marilia Brito Gomes, Maria Carolina Oliveira
Publikováno v:
Frontiers in Endocrinology, Vol 8 (2017)
ObjectiveTo explore the impact on microvascular complications, long-term preservation of residual B-cell function and glycemic control of patients with type 1 diabetes treated with autologous nonmyeloablative hematopoietic stem-cell transplantation (
Externí odkaz:
https://doaj.org/article/1a40998c5f0f45528b0094c5965950b2
Autor:
Fernanda M.B. Trigo, Marcelo R. Luizon, Hélio S. Dutra, Ângelo Maiolino, Márcio Nucci, Belinda P. Simões
Publikováno v:
Leukemia Research Reports, Vol 3, Iss 2, Pp 76-78 (2014)
Stem cell transplantation affects patient׳s vulnerability to infections due to immunological changes related to chemotherapy. Multiple myeloma is characterized by susceptibility to infections, and IL-6 and TNF-α increased levels affect immune respo
Externí odkaz:
https://doaj.org/article/72587d43ebfc4cb5a6bcfd9ee8465b6a
Autor:
Belinda P. Simões, Fabiano Pieroni, George M. N. Barros, Clarisse L. Machado, Rodolfo D. Cançado, Marco Aurélio Salvino, Ivan Angulo, Julio Cesar Voltarelli
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 32, Pp 46-53 (2010)
Os distúrbios hereditários das hemoglobinas são as doenças genéticas mais frequentes do homem e mais difundidas no mundo, abrangendo sobretudo continentes como África, Américas, Europa e extensas regiões da Ásia. Estima-se que haja 270 milh
Externí odkaz:
https://doaj.org/article/8fda25a33497453ba957b83f31198007
Autor:
Ana Paula Mastropietro, Érika A. Oliveira-Cardoso, Belinda P. Simões, Júlio César Voltarelli, Manoel Antônio Santos
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 32, Iss 2, Pp 102-107 (2010)
Embora a literatura aponte a necessidade de avaliação das condições de trabalho, suporte social e familiar dos pacientes submetidos ao transplante de medula óssea (TMO), são poucas as pesquisas nacionais acerca da influência do perfil socioeco
Externí odkaz:
https://doaj.org/article/dce861c5a0f84bea9c3ded446eae6ba2
Autor:
Julio C. Voltarelli, Carlos E. B. Couri, Maria Carolina Rodrigues, Daniela A. Moraes, Ana Beatriz P. L. Stracieri, Fabiano Pieroni, George Navarro, Maria Isabel A. Madeira, Belinda P. Simões
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 31, Pp 149-156 (2009)
Nesta revisão são discutidas várias alternativas de regeneração do conjunto de células produtoras de insulina do pâncreas, usando células-tronco embrionárias do cordão umbilical e adultas, e o trabalho que está sendo realizado em nosso gru
Externí odkaz:
https://doaj.org/article/b2836c5b74a644d7a7d5261bbfca9ffe
Autor:
Júlio C. Voltarelli, Carlos Eduardo B. Couri, Maria Carolina Rodrigues, Ana Beatriz P. L. Stracieri, Daniela A. Moraes, Fabiano Pieroni, George Navarro, Maria Isabel A. Madeira, Belinda P. Simões
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 30, Pp 55-59 (2008)
In this review, we present 1) scientific basis for the use of high dose immunosuppression followed by autologous peripheral blood hematopoietic stem cell transplantation for newly diagnosed type 1 diabetes mellitus, 2) an update of clinical and labor
Externí odkaz:
https://doaj.org/article/d5c215a70e1b4e60b51b735005e96789
Autor:
Rony Schaffel, Belinda P. Simões
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 30, Pp 52-58 (2008)
O cromossomo Filadélfia (Ph1) é a alteração citogenética mais comum da Leucemia Linfoblástica Aguda do adulto (LLA). Esta alteração citogenética predomina nos adultos com mais de 50 anos e na LLA de origem na célula B, principalmente CD10 p
Externí odkaz:
https://doaj.org/article/dd8ad995bbf0488fa874a19edf657c89