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Issue DateTitleAuthor(s)
2018High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotypeDEZAN, Marcia Regina; OLIVEIRA, Valeria B.; GOMES, Carolina Nunes; LUZ, Fabio; GALLUCCI, Antonio J.; BONIFACIO, Silvia L.; ALENCAR, Cecilia Salete; SABINO, Ester C.; PEREIRA, Alexandre C.; KRIEGER, Jose E.; ROCHA, Vanderson; MENDRONE-JUNIOR, Alfredo; DINARDO, Carla L.
2017-318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patientsOLIVEIRA, V. B.; DEZAN, M. R.; GOMES, F. C. A.; GUALANDRO, S. F. Menosi; KRIEGER, J. E.; PEREIRA, A. C.; MARSIGLIA, J. D.; LEVI, J. E.; ROCHA, V.; MENDRONE-JUNIOR, A.; SABINO, E. C.; DINARDO, C. L.
2020Fc gamma R2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patientsCOSTA NETO, Abel; SANTOS, Flavia; RIBEIRO, Ingrid; OLIVEIRA, Valeria; DEZAN, Marcia; KASHIMA, Simone; COVAS, Dimas; PEREIRA, Alexandre; FONSECA, Guilherme; MOREIRA, Frederico; KRIEGER, Jose; GUALANDRO, Sandra; ROCHA, Vanderson; MENDRONE JR., Alfredo; DINARDO, Carla L.
2019Prevalence and laboratorial determinants of the clinical relevance of antibodies of undetermined specificityCONRADO, Marina Cavalcanti de Albuquerque da Veiga; CARDOSO, Regina A.; DEZAN, Marcia Regina; OLIVEIRA, Valeria Brito; NETO, Abel da Costa; ZIZA, Karen Chinoca; KRIEGER, Jose Eduardo; PEREIRA, Alexandre Costa; SABINO, Ester Cerdeira; ROCHA, Vanderson; MENDRONE-JUNIOR, Alfredo; DINARDO, Carla Luana
2021Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed ProgramDINARDO, Carla L.; OLIVEIRA, Theo G. M.; KELLY, Shannon; ASHLEY-KOCH, Allison; TELEN, Marilyn; SCHMIDT, Luciana C.; CASTILHO, Shirley; MELO, Karla; DEZAN, Marcia R.; WHEELER, Marsha M.; JOHNSEN, Jill M.; NICKERSON, Deborah A.; JAIN, Deepti; CUSTER, Brian; PEREIRA, Alexandre C.; SABINO, Ester C.
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