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Transfusion|August 4, 2025
Alloanti-D in a DBT pregnant woman responsible for hemolytic disease of the fetus and newborn: Molecular study and genetic counselingCarolina Trucco Boggione, Caroline Bénech, María José Pigozzi, et al.Transfusion|September 3, 2011
Comprehensive analysis of RHD alleles in Argentineans with variant D phenotypesMelina E Luján Brajovich, Carolina Trucco Boggione, Claudia S Biondi, et al.Blood Transfusion = Trasfusione Del Sangue|May 3, 2016
Genotyping approach for non-invasive foetal RHD detection in an admixed populationCarolina Trucco Boggione, Melina E Luján Brajovich, Stella M Mattaloni, et al.Transfusion|May 14, 2014
Molecular structures identified in serologically D- samples of an admixed populationCarolina Trucco Boggione, Melina E Luján Brajovich, Marcel Tarragó, et al.Vox Sanguinis|October 12, 2025
A para-Bombay phenotype due to compound heterozygosity involving a novel FUT1 variantMelina Luján Brajovich, Cecilia González, Cintia Principi, et al.Transfusion|September 11, 2019
Characterization of RHD locus polymorphism in D negative and D variant donors from Northwestern ArgentinaCarolina Trucco Boggione, Núria Nogués, Cecilia González-Santesteban, 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|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.Pageof 1