Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Miriam V. Flor Park"'
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:
Kelly Nunes, Vitor R. C. Aguiar, Márcio Silva, Alexandre C. Sena, Danielli C. M. de Oliveira, Carla L. Dinardo, Fernanda S. G. Kehdy, Eduardo Tarazona-Santos, Vanderson G. Rocha, Anna Barbara F. Carneiro-Proietti, Paula Loureiro, Miriam V. Flor-Park, Claudia Maximo, Shannon Kelly, Brian Custer, Bruce S. Weir, Ester C. Sabino, Luís Cristóvão Porto, Diogo Meyer
Publikováno v:
Frontiers in Immunology, Vol 11 (2020)
A match of HLA loci between patients and donors is critical for successful hematopoietic stem cell transplantation. However, the extreme polymorphism of HLA loci – an outcome of millions of years of natural selection – reduces the chances that tw
Externí odkaz:
https://doaj.org/article/7135c23b854d4ea48891ccb520ebe641
Autor:
Kambe Banda, David N. Adjei, Uzima Chirwa, Obiageli E Nnodu, Assaf P. Oron, Isaac Nyanor, Upendo Masamu, Gaston K. Mazandu, Patience Kuona, Victoria Nembaware, Andre Pascal Kengne, Andrew D. Campbell, Daima Bukini, Jade Hotchkiss, Julie Makani, Nchangwi Syntia Munung, Mario Jonas, Catherine Chunda-Liyoka, Vivian Painstil, Jean-Michel Serufuri, Jill Kent, Kevin K Esoh, Miriam V Flor-Park, Malula Nkanyemka, Deogratias Munube, Ambroise Wonkam, Chandré Oosterwyk, Valentina Josiane Ngo Bitoungui, Annette Uwineza, Bamidele O. Tayo, Arthemon Nguweneza, Khuthala Mnika, Jack Morrice, Nicola Mulder, Nathan Edward Siebu, Kofi A. Anie, Agnes Jonathan
Publikováno v:
OMICS : a Journal of Integrative Biology
Sickle cell disease (SCD) is one of the most common blood disorders impacting planetary health. Over 300,000 newborns are diagnosed with SCD each year globally, with an increasing trend. The sickle cell disease ontology (SCDO) is the most comprehensi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6e6e0dfe8e4ec166e4347eaa9657d6d
http://europepmc.org/articles/PMC7549008
http://europepmc.org/articles/PMC7549008
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, 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:
Miriam V. Flor-Park, Mina Cintho Ozahata, Isabel Cristina Gomes Moura, Paula Blatyta, Shannon Kelly, Claudia di Lorenzo Oliveira, Ligia Capuani, André Rolim Belisário, Anna B.F. Carneiro-Proietti, Aderson S. Araujo, Paula Loureiro, Claudia Maximo, Daniela O.W. Rodrigues, Rosimere A. Mota, Ester Sabino, Brian Custer, Vanderson Rocha
Publikováno v:
Transplantation and Cellular Therapy. 28:708.e1-708.e8
Manifestations of sickle cell disease (SCD) begin early in childhood and cause morbidity and decreased life expectancy. Hematopoietic stem cell transplantation (HSCT) is curative but associated with risk of mortality attributable to the transplant. T
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6d5cf0122b21e75a8631a3611198715
https://doi.org/10.1016/j.jtct.2022.06.024
https://doi.org/10.1016/j.jtct.2022.06.024
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:
Cecilia Salete Alencar, Yuelong Guo, Donald Brambilla, João Eduardo Ferreira, Grier P. Page, Michael P. Busch, Miriam V Flor-Park, Claudia Maximo, Rosimere Afonso Mota, Thelma T Gonçalez, Daniela de Oliveira Werneck Rodrigues, Mina Cintho Ozahata, Ligia Capuani, Shannon Kelly, Carolina Miranda Teixeira, Paula Loureiro, Tassila P Salomon Silva, Anna Bárbara F. Carneiro-Proietti, Clarisse Lopes de Castro Lobo, Aderson S Araujo, Ester Cerdeira Sabino, Carolyn Hoppe, Brian Custer, Liliana Preiss
Publikováno v:
Repositório Institucional da USP (Biblioteca Digital da Produção Intelectual)
Universidade de São Paulo (USP)
instacron:USP
Br J Haematol
Universidade de São Paulo (USP)
instacron:USP
Br J Haematol
Approximately 3,500 children with Sickle Cell Disease (SCD) are born in Brazil each year, but the burden of SCD morbidity is not fully characterised. A large, multi-centre cohort was established to characterise clinical outcomes in the Brazilian SCD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3506df52b09d83333563cb9bd5cf64e8
https://doi.org/10.1111/bjh.15462
https://doi.org/10.1111/bjh.15462