Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Rodolfo Delfini Cançado"'
Autor:
Gisele dos Santos Barros, Carla Vaneska Fernandes Leal, Lauro Augusto Caetano Leite, Denys Eiti Fujimoto, Rodolfo Delfini Cançado
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss 2, Pp 161-166 (2024)
Introduction: Sickle cell disease (SCD) is an inherited and multisystem blood disorder characterized by hemolytic anemia, vaso-occlusive crises (VOCs), progressive multiorgan damage and increased mortality. In Brazil, it is one of the most common mon
Externí odkaz:
https://doaj.org/article/8d1011183a9c46d5af1f77faaad1513d
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:
Aline Morgan Alvarenga, Nathália Kozikas da Silva, Rodolfo Delfini Cançado, Luís Eduardo Morato Rebouças de Carvalho, Paulo Caleb Junior Lima Santos
Publikováno v:
Einstein (São Paulo), Vol 20 (2022)
ABSTRACT Hereditary hyperferritinemia-cataract syndrome is a rare autosomal dominant disease caused by a genetic mutation in the iron responsive element in the 5’ untranslated region of the ferritin light chain gene. Hereditary hyperferritinemia-ca
Externí odkaz:
https://doaj.org/article/aca154fd7eaf47e19a9047688b2bc0be
Autor:
Sergio Augusto Buzian Brasil, Carolina Colaço, Tomas Barrese, Roberto P. Paes, Cristina Bortolheiro, Rodolfo Delfini Cançado
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss 1, Pp 93-97 (2020)
Externí odkaz:
https://doaj.org/article/f11045d27615467882c7514b7a7fe321
Autor:
Sergio Augusto Buzian Brasil, Carolina Colaço, Tomas Barrese, Roberto P. Paes, Cristina Bortolheiro, Rodolfo Delfini Cançado
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 42, Iss 2, Pp 194- (2020)
Externí odkaz:
https://doaj.org/article/0a908ee652984a0d9d0fbe8a54c6c111
Autor:
Paula Fernanda Silva Fonseca, Rodolfo Delfini Cançado, Flavio Augusto Naoum, Carla Luana Dinardo, Guilherme Henrique Hencklain Fonseca, Sandra Fatima Menosi Gualandro, José Eduardo Krieger, Alexandre Costa Pereira, Pierre Brissot, Paulo Caleb Junior Lima Santos
Publikováno v:
BMC Medical Genetics, Vol 19, Iss 1, Pp 1-5 (2018)
Abstract Background Hereditary hemochromatosis (HH) encompasses a group of autosomal recessive disorders mainly characterized by enhanced intestinal absorption of iron and its accumulation in parenchymal organs. HH diagnosis is based on iron biochemi
Externí odkaz:
https://doaj.org/article/43e123d81f7c4a6bb4f7d80d50b831ff
Autor:
Josefina Aparecida Pellegrini Braga, Mônica Pinheiro de Almeida Veríssimo, Sara Teresinha Olalla Saad, Rodolfo Delfini Cançado, Sandra Regina Loggetto
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 38, Iss 2, Pp 147-157 (2016)
Externí odkaz:
https://doaj.org/article/b5afb9cc15db47198fc2b8f6a0b09b7d
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 37, Iss 6, Pp 400-405 (2015)
ABSTRACT Nutritional iron deficiency anemia is the most common deficiency disorder, affecting more than two billion people worldwide. Oral iron supplementation is usually the first choice for the treatment of iron deficiency anemia, but in many c
Externí odkaz:
https://doaj.org/article/13f1992ca314486bbe4914c6312a2412
Autor:
Carlos Walter SOBRADO, Rodolfo Delfini CANÇADO, Lucas Faraco SOBRADO, Marcos Onofre FRUGIS, Marcel Faraco SOBRADO
Publikováno v:
Arquivos de Gastroenterologia, Vol 52, Iss 4, Pp 255-259 (2015)
Objectives - Anemia is the most common hematological alteration in patients with Crohn's disease, and is frequently related to intestinal inflammatory activity. Its cause is multifactorial and mostly associated with absolute iron deficiency (iron def
Externí odkaz:
https://doaj.org/article/ea9523c2d8714301bdbfc26b724395fa
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