Zobrazeno 1 - 10
of 73
pro vyhledávání: '"André Rolim, Belisário"'
Autor:
Érica Louback Oliveira, André Rolim Belisário, Natiely Pereira Silva, Paulo Val Rezende, Maristela Braga Muniz, Larissa Maira Moura Oliveira, Cibele Velloso-Rodrigues, Marcos Borato Viana
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss 2, Pp 167-175 (2024)
Introduction: Hemoglobinopathy Sβ-thalassemia (HbSβ-thal) has a wide range of clinical and laboratory severity. There is limited information on the natural history of HbSβ-thal and its modulating factors. We described the molecular, hematological,
Externí odkaz:
https://doaj.org/article/16fa5354517c4d65bff05b35282ba520
Autor:
Domício Antônio Costa-Júnior, Thaisa N. Souza Valente, André Rolim Belisário, Gisele Queiroz Carvalho, Miguel Madeira, Cibele Velloso-Rodrigues
Publikováno v:
Molecular Genetics and Metabolism Reports, Vol 39, Iss , Pp 101086- (2024)
Objectives: Our study evaluated the association of the polymorphism rs724016 in the ZBTB38 gene, previously associated with height in other populations, with predictors of height, clinical outcomes, and laboratory parameters in sickle cell anemia (SC
Externí odkaz:
https://doaj.org/article/c9faf8bdbd6b46c8a3c90c04394ebe2b
Autor:
André Rolim Belisário, Franciane Mendes-Oliveira, Valquíria Reis de Souza, Eduarda Bolina-Santos, Fabíola Gomes Mendes, Elizabeth Castro Moreno, Alice Timponi Franca, Ester Cerdeira Sabino, Dayane Andriotti Otta, Elaine Speziali de Faria, Jordana Grazziela Alves Coelho-dos-Reis, Olindo Assis Martins-Filho, Anna Bárbara Carneiro-Proietti
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 44, Iss 2, Pp 169-176 (2022)
Introduction: Leg ulcers (LUs) are relatively common in patients with sickle cell anemia (SCA). The role of inflammation and nitric oxide (NO) pathways in the pathophysiology of the LU is not understood. Objective: The aim of this study was to verify
Externí odkaz:
https://doaj.org/article/4293074a7eb54c25be6d18a97c67d7c9
Autor:
André Rolim Belisário, Paula F. Blatyta, Diana Vivanco, Claudia Di Lorenzo Oliveira, Anna Bárbara Carneiro-Proietti, Ester Cerdeira Sabino, Cesar de Almeida-Neto, Paula Loureiro, Cláudia Máximo, Sheila de Oliveira Garcia Mateos, Miriam V. Flor-Park, Daniela de Oliveira Werneck Rodrigues, Rosimere Afonso Mota, Thelma T. Gonçalez, Thomas J. Hoffmann, Shannon Kelly, Brian Custer, for the Recipient Epidemiology and Donor Evaluation Study-III (REDS-III) International Component Brazil
Publikováno v:
BMC Infectious Diseases, Vol 20, Iss 1, Pp 1-11 (2020)
Abstract Background Sickle cell disease (SCD) is a multisystem disorder characterized by a wide spectrum of clinical manifestations and severity. Studies investigating potential effects of co-morbid human immunodeficiency virus (HIV) and SCD have pro
Externí odkaz:
https://doaj.org/article/d7062ca698a44f63b699b8505170f440
Autor:
Cristina Botelho Barra, Thais Ramos Villela, Nedstâni de Freitas Soares, Enrico Antônio Colosimo, André Rolim Belisário, Ana Cristina Simões E Silva, Ivani Novato Silva
Publikováno v:
PLoS ONE, Vol 17, Iss 12, p e0279298 (2022)
Glucocorticoids (GC) replacement are the mainstay treatment for 21-hydroxylase deficiency (21-OHD), the most common cause of congenital adrenal hyperplasia (CAH), in its classical form. There are novel insights into the genetic basis of the GC action
Externí odkaz:
https://doaj.org/article/3c976e99af1b427ea0e80c472a5ebc02
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 40, Iss 2, Pp 166-181 (2018)
Cerebrovascular disease, particularly stroke, is one of the most severe clinical complications associated with sickle cell disease and is a significant cause of morbidity in both children and adults. Over the past two decades, considerable advances h
Externí odkaz:
https://doaj.org/article/bd3f7c3ddd394c37893068bf6bd2624e
Autor:
André Rolim Belisário, Elimiramá V. C. Benfica, Luciana de Almeida de Costa, Maurício Colombini Martins, Roberta Kelly de Andradre, Paula Renata Machado Passos Pederzoli, Karen de Lima de Prata
Publikováno v:
Transfusion. 63:269-271
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9d6b564607310fa4120998ce60c4b2cd
https://doi.org/10.1111/trf.17194
https://doi.org/10.1111/trf.17194
Autor:
Pedro Antunes Pousa, Tamires Sara Campos Mendonça, Larissa Marques Fonseca, Eduardo Araújo Oliveira, André Rolim Belisário, Ana Cristina Simões e Silva
Publikováno v:
Molecular Biology Reports. 49:4341-4347
Congenital Anomalies of the Kidney and the Urinary Tract (CAKUT) are defined as a heterogeneous group of anomalies that resulted from defects in kidney and urinary tract embryogenesis. CAKUT have a complex etiology. Genetic, epigenetic and environmen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a2485396ed1a6c51168fcc1cf71b2784
https://doi.org/10.1007/s11033-022-07269-5
https://doi.org/10.1007/s11033-022-07269-5
Publikováno v:
Revista Brasileira de Hematologia e Hemoterapia, Vol 37, Iss 3, Pp 198-201 (2015)
Externí odkaz:
https://doaj.org/article/4b4acfdef4d64cf8ab287df342696ca9
Autor:
Jéssica Alves de Almeida, Roberta da Silva Filha, Paulo V. Rezende, Ana Cs E Silva, André Rolim Belisário, Fabíola Gomes Mendes, Érica Lm Vieira
Publikováno v:
Biomarkers in Medicine. 15:999-1009
Aim: The aim of this study was to compare novel kidney injury biomarkers in sickle cell anemia (SCA) children with and without albuminuria or glomerular hyperfiltration. Materials & methods: A total of 358 Brazilian children with SCA were studied. Fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e07548257b0735efbbd75ed5ca49c7e7
https://doi.org/10.2217/bmm-2020-0769
https://doi.org/10.2217/bmm-2020-0769