Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Mariana R. B. Mello"'
Autor:
Flavia M. G. C. Bandeira, Jaqueline C. Peres, Eduardo J. Carvalho, Ivane Bezerra, Aderson S. Araújo, Mariana R. B. Mello, Cíntia Machado
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 26, Iss 3, Pp 189-194 (2004)
O uso de hidroxiuréia promove a elevação dos níveis de hemoglobina fetal (Hb F) em pacientes portadores de síndromes falciformes (SF) e o medicamento vem sendo estudado em vários grupos de pacientes, incluindo adultos e crianças. O presente tr
Externí odkaz:
https://doaj.org/article/41117f98fb4740759b33df0ac7249e36
Autor:
Kleber Yotsumoto Fertrin, Isabel Weinhäuser, Fernando Ferreira Costa, Raphael Ferreira Pimentel, Aleide S. Lima, Antonio R. Lucena-Araujo, Cíntia G. F. Machado, Matheus F Bezerra, Mariana R. B. Mello, Bruna R. Larrazábal, Marcos André Cavalcanti Bezerra, Aderson S Araujo
Publikováno v:
Hematology, transfusion and cell therapy. 44(3)
Introduction One of the most critical complications in myelodysplastic syndromes (MDS) is the progression to acute myeloid leukemia (AML). The dynamics of clonal evolution in MDS and how acquired mutations can be used as biomarkers to track disease p
Autor:
Kleber Yotsumoto Fertrin, Betania Lucena Domingues Hatzlhofer, Aderson S Araujo, Dulcineia M. Albuquerque, Sara Terezinha Olalla Saad, Marcos André Cavalcanti Bezerra, Carolina Lanaro, Carla F. Franco-Penteado, Flavia Rubia Pallis, Mark Westerman, Mariana R. B. Mello, Fernando Ferreira Costa, Gordana Olbina
Publikováno v:
American Journal of Hematology. 89:385-390
Growth differentiation factor 15 (GDF-15) is a bone marrow-derived cytokine whose ability to suppress iron regulator hepcidin in vitro and increased concentrations found in patients with ineffective erythropoiesis (IE)suggest that hepcidin deficiency
Autor:
Fernando Ferreira Costa, Katia B Pagnano, Mariana R. B. Mello, Fernanda Gonçalves Pereira-Cunha, Dulcineia M. Albuquerque, Krizzia Borges Albanez, Irene Lorand-Metze, Konradin Metze
Publikováno v:
Diagnostic Pathology, Vol 7, Iss 1, p 75 (2012)
Diagnostic Pathology
Diagnostic Pathology
Background Acute promyelocytic leukemia is a cytogenetically well defined entity. Nevertheless, some features observed at diagnosis are related to a worse outcome of the patients. Methods In a prospective study, we analyzed peripheral (PB) leukocyte
Autor:
Sara T.O. Saad, Vanessa Tonin Garrido, Venina Marcela Dominical, Aderson S Araujo, Nicola Conran, Fernando Ferreira Costa, Marcos André Cavalcanti Bezerra, Renata Proença-Ferreira, Marina Pereira Colella, Mariana R. B. Mello, Fabiola Traina
Publikováno v:
British journal of haematology. 158(6)
Chronic vascular inflammation and endothelial activation may initiate vaso-occlusion in sickle cell disease (SCD). TNFSF14 (CD258; LIGHT), a recently-identified pro-thrombotic and pro-inflammatory tumour necrosis factor (TNF)-superfamily cytokine, ha
Autor:
Mariana R B, Mello, Konradin, Metze, Randall L, Adam, Fernanda G, Pereira, Micheline G, Magalhães, Cíntia G F, Machado, Irene, Lorand-Metze
Publikováno v:
Analytical and quantitative cytology and histology. 30(2)
To determine if phenotypic subtypes of acute lymphoblastic leukemia (ALL) are associated with different nuclear textures.In 49 newly diagnosed patients, diagnostic work-up was made by routinely Giemsa-stained smears and immunophenotyping. B-precursor
Autor:
Mariana R. B. Mello, Kleber Yotsumoto Fertrin, Dulcineia M. Albuquerque, Fernando Ferreira Costa, Aderson S Araujo, Carolina Lanaro, Carla F. Franco-Penteado, Betania Lucena Domingues Hatzlhofer, Marcos André Cavalcanti Bezerra
Publikováno v:
Blood. 124:4058-4058
The pathophysiology of sickle cell anemia (SCA) involves hemolysis, vaso-occlusion and a chronic inflammatory state. Iron overload secondary to blood transfusions is a frequent complication in these patients, but cannot be adequately estimated by ser
Autor:
Luana Priscilla Laranjeira Prado, Marcos André Cavalcanti Bezerra, Isabela Cristina Farias, Igor de Farias Domingos, Taciana Furtado de Mendonça, Maria do Socorro Cavalcanti, PatrÃcia Moura, Luydson Richardson Silva Vasconcelos, Diego Arruda Falcão, Mariana R. B. Mello, Aderson S Araujo, Kleber Yotsumoto Fertrin, A.R.L. Araújo, Fernando Ferreira Costa
Publikováno v:
Blood. 124:4912-4912
Leg ulcers are the most common clinical manifestations of sickle cell anemia (SCA), a monogenic disease with huge clinical diversity among patients. They affect 8% to 10% of SCA patients, reaching a percentage greater than 50% in patients residing in
Autor:
Flávia M. G. C. Bandeira, Mariana R. B. Mello, Eduardo J. Carvalho, Aderson S Araujo, Jaqueline C. Peres, Ivane Bezerra, Cíntia G. F. Machado
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia v.26 n.3 2004
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: 26, Issue: 3, Pages: 189-194, Published: 2004
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: 26, Issue: 3, Pages: 189-194, Published: 2004
O uso de hidroxiuréia promove a elevação dos níveis de hemoglobina fetal (Hb F) em pacientes portadores de síndromes falciformes (SF) e o medicamento vem sendo estudado em vários grupos de pacientes, incluindo adultos e crianças. O presente tr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3036b413854c776cc28e22b980e87e5c
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842004000300008
http://old.scielo.br/scielo.php?script=sci_arttext&pid=S1516-84842004000300008
Autor:
Marcos André Cavalcanti Bezerra, Betania Lucena Borges Tavares Domingues, Fernando Ferreira Costa, Dulcineia M. Albuquerque, Mariana R. B. Mello, Sara Teresinha Olalla Saad, Gordana Olbina, Mark Westerman, Aderson S Araujo, Kleber Yotsumoto Fertrin, Carolina Lanaro, Carla F. Franco-Penteado
Publikováno v:
Blood. 118:346-346
Abstract 346 Background and Aims: Ineffective erythropoiesis in thalassemias and congenital dyserythropoietic anemia has been associated with hepcidin deficiency and spontaneous iron overload, potentially mediated by an abnormally high production of