Valéria Brito Oliveira

Author

Fundação Pró-Sangue Hemocentro de São Paulo ORCID

Also Known As

V. B. Oliveira, V. Oliveira, V.B. Oliveira, VCC Oliveira, VICTOR MACHADO SALVADOR DE OLIVEIRA, Valeria B. Oliveira, Valeria Brito Oliveira, Valeria Oliveira, Valmira Barbosa de Oliveira, Valmira Oliveira

Publications

171

Citations

H-Index

Concepts

All Affiliations

Fundação Pró-Sangue Hemocentro de São Paulo Universidade de São Paulo

About

Valéria Brito Oliveira is an author at Fundação Pró-Sangue Hemocentro de São Paulo specializing in medicine, blood transplantation, and immunohematology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	2	2	51
2	Public Health	1	1	15
3	Blood Transplantation	1	1	15
4	Epidemiology	1	1	15
5	Immunology	1	1	15

Valéria Brito Oliveira

Publications

105

Citations

H-Index

Page 1

	Year	Citations
RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients Marcia Regina Dezan, Ingrid Helena Ribeiro, Valéria Brito Oliveira, Blood Cells Molecules and Diseases SequencingMedicineGeneticsNext-generation SequencingPathology	2017	36
‐318C/T polymorphism of the <i><scp>CTLA</scp>‐4</i> gene is an independent risk factor for <scp>RBC</scp> alloimmunization among sickle cell disease patients Valéria Brito Oliveira, Marcia Regina Dezan, Francisco C. A. Gomes, International Journal of Immunogenetics	2017	21
Effectiveness of a red cell antigen‐matching transfusion protocol in sickle cell disease patients Marcia Regina Dezan, Valéria Brito Oliveira, J. V. S. Bianchi, ISBT Science Series ImmunohematologyAntibody DevelopmentScp SImmunologyTransplantation Medicine	2016	15
Defining the clinical relevance of red blood cell autoantibodies by Monocyte Monolayer Assay Marina C. A. V. Conrado, Amanda N. D'Avila, Juliana Borges Vieira, Journal of Clinical Laboratory Analysis	2017	12
Evaluation of the applicability and effectiveness of a molecular strategy for identifying weak D and DEL phenotype among D– blood donors of mixed origin exhibiting high frequency of <i>RHD*Ψ</i> Marcia Regina Dezan, Luis Giovani Oliveira Guardalini, Elaine Pessoa, Transfusion	2017	11
High frequency of variant <i><scp>RHD</scp></i> genotypes among donors and patients of mixed origin with serologic weak‐D phenotype Marcia Regina Dezan, Valéria Brito Oliveira, Carolina Gomes, Journal of Clinical Laboratory Analysis	2018	10

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