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Revista Brasileira De Hematologia E Hemoterapia|June 7, 2013
An easy and efficient strategy for KEL genotyping in a multiethnic populationCarine Prisco Arnoni, Janaína Guinhem Muniz, Tatiane Aparecida de Paula, et al.
Hematology, Transfusion and Cell Therapy|November 13, 2020
Duffy phenotyping and FY*B-67T/C genotyping as screening test for benign constitutional neutropeniaMaria E S F Barreto, Mariana E Lipay, Leandro D Santos, et al.
Blood Transfusion = Trasfusione Del Sangue|March 9, 2018
SMIM1 polymorphisms in a donor population from southeast Brazil and their correlation with VEL expressionCarine Prisco Arnoni, Tatiane A De Paula Vendrame, Janaína Guilhem Muniz, et al.
Vox Sanguinis|February 22, 2026
Integrated serological and molecular investigation of ABO subgroups underlying atypical ABO typing in southeastern BrazilCarine Prisco Arnoni, Tatiane Aparecida Paula de Vendrame, Nayara Morais Silva, et al.
Immunohematology|February 5, 2021
Identification of rare blood types in southern Brazil: impact on transfusion supportCristiane da Silva Rodrigues de Araújo, Bruna A Machado, Cristiana D Reche, et al.
Vox Sanguinis|May 8, 2026
Molecular characterization of D variants in Brazilian blood donors and their association with RhCE and Duffy phenotypesThamy C S Silva, Marcia R Dezan, Sidneia Costa, et al.
Transfusion Medicine and Hemotherapy : Offizielles Organ Der Deutschen Gesellschaft Fur Transfusionsmedizin Und Immunhamatologie|March 10, 2017
Clinical Significance of an Alloantibody against the Kell Blood Group GlycoproteinStella Maris Mattaloni, Carine Arnoni, Rosario Céspedes, et al.
Transfusion|December 2, 2008
Murine monoclonal anti-s and other anti-glycophorin B antibodies resulting from immunizations with a GPB.s peptideGregory R Halverson, Edith Tossas, Randall W Velliquette, et al.
Human Biology|October 14, 2006
Frequencies of ABO, MNSs, and Duffy phenotypes among blood donors and malaria patients from four Brazilian Amazon areasCarlos Eugênio Cavasini, Luiz Carlos De Mattos, Renata Tomé Alves, et al.
Transfusion|May 8, 2020
Extensive clinical, serologic and molecular studies lead to the first reported Rhmod phenotype in ArgentinaNicolás Mufarrege, Noelia Franco, Carolina Trucco Boggione, et al.
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