Search Results - "Mota, Rosimere A."

Clinical and genetic ancestry profile of a large multi‐centre sickle cell disease cohort in Brazil by Carneiro‐Proietti, Anna B. F., Kelly, Shannon, Miranda Teixeira, Carolina, Sabino, Ester C., Alencar, Cecilia S., Capuani, Ligia, Salomon Silva, Tassila P., Araujo, Aderson, Loureiro, Paula, Máximo, Cláudia, Lobo, Clarisse, Flor‐Park, Miriam V., Rodrigues, Daniela O. W., Mota, Rosimere A., Gonçalez, Thelma T., Hoppe, Carolyn, Ferreira, João E., Ozahata, Mina, Page, Grier P., Guo, Yuelong, Preiss, Liliana R., Brambilla, Donald, Busch, Michael P., Custer, Brian

“…Summary Approximately 3500 children with sickle cell disease (SCD) are born in Brazil each year, but the burden of SCD morbidity is not fully characterised. A…”
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Is Severity Score Associated With Indication for Hematopoietic Stem Cell Transplantation in Individuals With Sickle Cell Anemia? by Flor-Park, Miriam V., Ozahata, Mina Cintho, Moura, Isabel Cristina Gomes, Blatyta, Paula, Kelly, Shannon, Oliveira, Claudia di Lorenzo, Capuani, Ligia, Belisário, André Rolim, Carneiro-Proietti, Anna B.F., Araujo, Aderson S., Loureiro, Paula, Maximo, Claudia, Rodrigues, Daniela O.W., Mota, Rosimere A., Sabino, Ester, Custer, Brian, Rocha, Vanderson

“…Manifestations of sickle cell disease (SCD) begin early in childhood and cause morbidity and decreased life expectancy. Hematopoietic stem cell transplantation…”
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Identification and Characterization of Hematopoietic Stem Cell Transplant Candidates in a Sickle Cell Disease Cohort by Flor-Park, Miriam V., Kelly, Shannon, Preiss, Liliana, Custer, Brian, Carneiro-Proietti, Anna B.F., Araujo, Aderson S., Loureiro, Paula, Maximo, Claudia, Rodrigues, Daniela O.W., Mota, Rosimere A., Sabino, Ester C., Rocha, Vanderson

“…•Of 2064 SCA patients, 16% of children and 26% of adults had at least 1 HSCT indication.•The most common indication for transplant was stroke (11.6%).•Fifty…”
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