Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Rosimere Afonso Mota"'
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:
Camila Cruz de Martino, Cecilia Salete Alencar, Paula Loureiro, Anna Barbara de Freitas Carneiro-Proietti, Claudia de Alvarenga Máximo, Rosimere Afonso Mota, Daniela Oliveira Werneck Rodrigues, Nelson Gaburo Junior, Shannon Kelly, Ester Cerdeira Sabino, International Component of the NHLBI Recipient Epidemiology and Donor Evaluation Study (REDS-III)
Publikováno v:
PLoS ONE, Vol 14, Iss 12, p e0216020 (2019)
BackgroundThe diagnosis of sickle cell disease (SCD) is made by hemoglobin assays such as high-performance liquid chromatography (HPLC), isoelectric focusing and cellulose acetate or citrate agar electrophoresis. These assays are easy to perform and
Externí odkaz:
https://doaj.org/article/a4ddfe9d23244790bc7c680f7f73be67
Autor:
Claudia Maximo, Recipient Epidemiology, Rosimere Afonso Mota, Isabel Cristina Gomes Moura, Aderson S Araujo, Ester Cerdeira Sabino, Mina Cintho Ozahata, Anna Bárbara F. Carneiro-Proietti, Shannon Kelly, Daniela de Oliveira Werneck Rodrigues, André Rolim Belisário, Miriam V Flor-Park, Christopher McClure, Paula Loureiro, Brian Custer
Publikováno v:
Hemoglobin. 44:1-9
We described the clinical, laboratory and molecular characteristics of individuals with Hb S (HBB: c.20A>T)/β-thalassemia (Hb S/β-thal) participating in the Recipient Epidemiology and Donor Evaluation Study (REDS-III) Brazil Sickle Cell Disease coh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3680e7c00e0f762a29d090b3414558fc
https://doi.org/10.1080/03630269.2020.1731530
https://doi.org/10.1080/03630269.2020.1731530
Autor:
Paula Loureiro, Franciane Mendes, Anna Bárbara F. Carneiro-Proietti, Paula Fraiman Blatyta, Thelma T Gonçalez, Liliana Preiss, Rosimere Afonso Mota, Daniela de Oliveira Werneck Rodrigues, Miriam Park, Shannon Kelly, Ester Cerdeira Sabino, Cesar de Almeida Neto, Claudia Maximo, Brian Custer, Alfredo Mendrone-Jr
Publikováno v:
Transfusion. 60:343-350
BACKGROUND Patients with sickle cell disease (SCD) often require red blood cell (RBC) transfusion for clinical complications, so may be exposed to transfusion-transmitted infections (TTIs). The prevalence of markers for human immunodeficiency virus (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3d882c400b25735dc93ce106d9840dc4
https://doi.org/10.1111/trf.15619
https://doi.org/10.1111/trf.15619
Autor:
Paula Loureiro, Rosimere Afonso Mota, Claudia Maximo, Miriam V Flor-Park, Brian Custer, Mina Cintho Ozahata, Ester Cerdeira Sabino, Shannon Kelly, AB Carneiro-Proietti, Icg Moura, André Rolim Belisário, Dow Rodrigues, Acse Silva, Carla Luana Dinardo
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 43, Iss, Pp S18-S19 (2021)
Aim Chronic kidney disease (CKD) has a significant impact on sickle cell disease (SCD) morbidity and mortality. Early identification of individuals at highest risk of developing CKD may allow therapeutic intervention to prevent worse outcomes. This s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e36a365eb0b7302342efd40e08eeff5c
http://www.sciencedirect.com/science/article/pii/S2531137921001802
http://www.sciencedirect.com/science/article/pii/S2531137921001802
Autor:
Alessa Assis Guimarães Silvério, Arthur Macedo Goulart Silva, Leandro de Freitas Teles, Larissa Caires Gonzaga, Rosimere Afonso Mota, Ronaldo Urias Mendonça Júnior, Anne Carolline Amaral Batista Ramos, Elaine Veloso Rocha Urias
Publikováno v:
Research, Society and Development. 11:e359111335638
A hemofilia é uma doença hemorrágica hereditária e um dos principais desafios do seu tratamento é o desenvolvimento de inibidores. O objetivo desse trabalho foi discutir a literatura que trata da presença de inibidores face à abordagem diagnó
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::52e9a0ddc658124d058f691ce40d949d
https://doi.org/10.33448/rsd-v11i13.35638
https://doi.org/10.33448/rsd-v11i13.35638
Autor:
Rosimere Afonso Mota, Shannon Kelly, João Eduardo Ferreira, André Rolim Belisário, Miriam V Flor-Park, Claudia Maximo, Paula Loureiro, Yuelong Guo, Grier P. Page, Brian Custer, Mina Cintho Ozahata, Anna Bárbara F. Carneiro-Proietti, Ester Cerdeira Sabino, Carla Luana Dinardo, Daniela de Oliveira Werneck Rodrigues
Publikováno v:
J Sex Med
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Introduction Priapism is the persistent and painful erection of the penis and is a common sickle cell disease (SCD) complication. Aim The goal of this study was to characterize clinical and genetic factors associated with priapism within a large mult
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8b2601d032e901653723004a99874810
https://doi.org/10.1016/j.jsxm.2019.09.012
https://doi.org/10.1016/j.jsxm.2019.09.012
Autor:
Rosimere Afonso Mota, Anna Bárbara F. Carneiro-Proietti, Miriam V Flor-Park, Aderson S Araujo, Ester Cerdeira Sabino, Vanderson Rocha, Claudia Maximo, Paula Loureiro, Shannon Kelly, Daniela de Oliveira Werneck Rodrigues, Liliana Preiss, Brian Custer
Publikováno v:
Biology of Blood and Marrow Transplantation. 25:2103-2109
Sickle cell disease (SCD) is associated with significant morbidity, and allogeneic hematopoietic stem cell transplantation (HSCT) remains the primary curative treatment. Recently, the Brazilian Ministry of Health released a regulation that required t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1516c945f7fde1b2249abb7dd431db7
https://doi.org/10.1016/j.bbmt.2019.06.013
https://doi.org/10.1016/j.bbmt.2019.06.013
Autor:
André R, Belisário, Anna B, Carneiro-Proietti, Ester Cerdeira, Sabino, Aderson, Araújo, Paula, Loureiro, Cláudia, Máximo, Miriam V, Flor-Park, Daniela D O W, Rodrigues, Mina Cintho, Ozahata, Christopher, McClure, Rosimere Afonso, Mota, Isabel C, Gomes Moura, Brian, Custer, Shannon, Kelly
Publikováno v:
Hemoglobin
We described the clinical, laboratory and molecular characteristics of individuals with Hb S (HBB: c.20A>T)/β-thalassemia (Hb S/β-thal) participating in the Recipient Epidemiology and Donor Evaluation Study (REDS-III) Brazil Sickle Cell Disease coh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::fab0e20d268e2c7e2b30a6dce3f70130
https://pubmed.ncbi.nlm.nih.gov/32172616
https://pubmed.ncbi.nlm.nih.gov/32172616
Autor:
Belisário, André R., Carneiro-Proietti, Anna B., Sabino, Ester Cerdeira, Aderson Araújo, Loureiro, Paula, Máximo, Cláudia, Flor-Park, Miriam V., Rodrigues, Daniela D.O.W., Ozahata, Mina Cintho, McClure, Christopher, Rosimere Afonso Mota, Moura, Isabel C. Gomes, Custer, Brian, Kelly, Shannon
We described the clinical, laboratory and molecular characteristics of individuals with Hb S (HBB: c.20A>T)/β-thalassemia (Hb S/β-thal) participating in the Recipient Epidemiology and Donor Evaluation Study (REDS-III) Brazil Sickle Cell Disease coh
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54877df9de01e377675a930dedbce7f1
