Zobrazeno 1 - 10
of 204
pro vyhledávání: '"Maria Stella, Figueiredo"'
Autor:
Karina Moura Sawada, Niele Silva de Moraes, Lara Miguel Quirino Araújo, Fernanda Martins Gazoni, Marise Lazaretti-Castro, Maysa Seabra Cendoroglo, John P. Bilezikian, Maria Stella Figueiredo, Fania Cristina dos Santos
Publikováno v:
Einstein (São Paulo), Vol 22 (2024)
Objective: To investigating the relationship between α-Klotho and FGF-23 with bone biochemical markers and bone density findings in extremely aged individuals. Methods: A total of 55 individuals with a mean age of 85.6 years were subjected to clinic
Externí odkaz:
https://doaj.org/article/c80c7106f1a846ec85c04bd7f5ec3fa1
Autor:
Clarisse Lobo, Aderson Araújo, Alexandre de Albuquerque Antunes, Ana Cristina Silva Pinto, Ariadne Carvalho Godinho, Cassia Silvestre Mariano Pires, Cinthia Cristina Matheus, Xerez de Albuquerque, Daniele Campos Fontes Neves, Fábio de Lima Moreno, Giorgio Baldanzi, Grazziella Curado Siufi, Heloisa Helena Pereira Miranda, Jane Hankins, Joice Aragão, Josefina Aparecida Pellegrini Braga, Juliana Touguinha Neves Martins, Luciana Campos Costa Machado de Souza, Maria Stella Figueiredo, Mirella Rodrigues Oliveira, Patricia Santos Resende Cardoso, Patricia Costa Alves Pinto, Patricia Gomes Moura, Rodolfo Delfini Cançado, Paulo Ivo Cortez de Araujo, Sara Olalla Saad, Sandra Regina Loggetto, Teresa Cristina Cardoso Fonseca
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss 1, Pp 67-71 (2024)
To date, hydroxyurea is the only effective and safe drug that significantly reduces morbidity and mortality of individuals with Sickle cell disease. Twenty years of real-life experience has demonstrated that hydroxyurea reduces pain attacks, vaso-occ
Externí odkaz:
https://doaj.org/article/a32acf3cc33942eaa75b50704759457d
Autor:
Fernanda Souza Angotti Carrara, Daniela Gerent Petry Piotto, Ilana Izidoro Silva, Claudio Arnaldo Len, Gleice Clemente Souza Russo, Sonia Mayumi Chiba, Vera Lucia Sdepanian, Josefina Aparecida Pellegrini Braga, Maria Stella Figueiredo, Maria Cristina Andrade, Marta Liliane de Almeida Maia, Ana Lúcia Abreu, Celia Maria Camelo Silva, Maria Teresa Terreri
Publikováno v:
Jornal de Pediatria, Vol 99, Iss 3, Pp 254-262 (2023)
Objective: Advances in medicine have increased the life expectancy of pediatric patients with chronic illnesses, and challenges with the guided transition of adolescents and young adults from pediatric clinics to adult clinics have grown. The aim of
Externí odkaz:
https://doaj.org/article/bb63906110e7422e99190533dc015136
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 45, Iss 1, Pp 45-51 (2023)
Introduction: Sickle cell anemia is a monogenic disorder caused by a mutation in the β-hemoglobin gene, resulting in sickle hemoglobin that can polymerize. Presentation and clinical course have significant inter-individual variability and classifyin
Externí odkaz:
https://doaj.org/article/96847aeb60a64709aa988ce52ad83cc6
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:
Caio Cesar Justino, Felipe Favorette Campanharo, Marina Nobrega Augusto, Stela Cezarino de Morais, Maria Stella Figueiredo
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss 3, Pp 212-214 (2020)
Externí odkaz:
https://doaj.org/article/918a4fe3619e48b69bca9192b3c2d47a
Autor:
Elmutaz M. Shaikho, John J. Farrell, Abdulrahman Alsultan, Hatem Qutub, Amein K. Al-Ali, Maria Stella Figueiredo, David H.K. Chui, Lindsay A. Farrer, George J. Murphy, Gustavo Mostoslavsky, Paola Sebastiani, Martin H. Steinberg
Publikováno v:
BMC Genomics, Vol 18, Iss 1, Pp 1-7 (2017)
Abstract Background Sickle cell anemia causes severe complications and premature death. Five common β-globin gene cluster haplotypes are each associated with characteristic fetal hemoglobin (HbF) levels. As HbF is the major modulator of disease seve
Externí odkaz:
https://doaj.org/article/6916a1fd4f2f428e9450ecfe0629af1c
Autor:
Seonmi Park, Andreia Gianotti-Sommer, Francisco Javier Molina-Estevez, Kim Vanuytsel, Nick Skvir, Amy Leung, Sarah S. Rozelle, Elmutaz Mohammed Shaikho, Isabelle Weir, Zhihua Jiang, Hong-Yuan Luo, David H.K. Chui, Maria Stella Figueiredo, Abdulraham Alsultan, Amein Al-Ali, Paola Sebastiani, Martin H. Steinberg, Gustavo Mostoslavsky, George J. Murphy
Publikováno v:
Stem Cell Reports, Vol 8, Iss 4, Pp 1076-1085 (2017)
Summary: Sickle cell anemia affects millions of people worldwide and is an emerging global health burden. As part of a large NIH-funded NextGen Consortium, we generated a diverse, comprehensive, and fully characterized library of sickle-cell-disease-
Externí odkaz:
https://doaj.org/article/52d22f01919b4214b5dcc432e367860c
Autor:
Bruna Spinella Pierrot-Gallo, Perla Vicari, Sandra Satiko Matsuda, Samuel Ademola Adegoke, Grazielle Mecabo, Maria Stella Figueiredo
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 37, Iss 5, Pp 329-335 (2015)
BACKGROUND: Haptoglobin genotypes, and interleukin-6 and -8 participate in the pathophysiology of sickle cell anemia. The expression of cytokines is regulated by genetic mechanisms however the effect of haptoglobin polymorphisms on these cytokines is
Externí odkaz:
https://doaj.org/article/5b1dcd261a7348e5a7782e1cf40a20de
Autor:
Fernanda souza Angotti Carrara Bafi, Daniela Gerent Petry Piotto, Nathalia Oliveira Batista, Ilana Izidoro, Claudio Arnaldo Len, Gleice Clemente, Sonia Mayumi Chiba, Vera Lucia Sdepanian, Josefina Braga, Maria Stella Figueiredo, Maria Cristina Andrade, Marta Maia, Celia Camelo Silva, Maria Teresa Terreri
Publikováno v:
XXXIX Congresso Brasileiro de Reumatologia.