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| Issue Date | Title | Author(s) |
|---|---|---|
| 2018 | High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype | DEZAN, 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 patients | OLIVEIRA, 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. |
| 2021 | Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program | DINARDO, 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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