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Results 1-4 of 4 (Search time: 0.005 seconds).
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.
2017RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patientsDEZAN, Marcia R.; RIBEIRO, Ingrid Helena; OLIVEIRA, Valeria B.; VIEIRA, Juliana B.; GOMES, Francisco C.; FRANCO, Lucas A. M.; VARUZZA, Leonardo; RIBEIRO, Roberto; CHINOCA, Karen Ziza; LEVI, Jose Eduardo; KRIEGER, Jose Eduardo; PEREIRA, Alexandre Costa; GUALANDRO, Sandra F. M.; ROCHA, Vanderson G.; MENDRONE-JUNIOR, Alfredo; SABINO, Ester Cerdeira; DINARDO, Carla Luana
2019A Toll-like receptor 2 genetic variant modulates occurrence of bacterial infections in patients with sickle cell diseaseTOZATTO-MAIO, Karina; GIROT, Robert; LY, Indou D.; ROCHA, Vanderson; PINTO, Ana C. Silva; DIAGNE, Ibrahima; BENZERARA, Yahia; DINARDO, Carla L.; KASHIMA, Simone; LESTON-ARAUJO, Itaua; KENZEY, Chantal; FONSECA, Guilherme H. H.; RODRIGUES, Evandra S.; VOLT, Fernanda; JARDULI, Luciana R.; RUGGERI, Annalisa; MARIASELVAM, Christina M.; GUALANDRO, Sandra F. M.; ELAYOUBI, Hanadi; CUNHA, Renato; CAPPELLI, Barbara; MALMEGRIM, Kelen C. R.; SIMOES, Belinda P.; GLUCKMAN, Eliane; TAMOUZA, Ryad
2020Effectiveness of strategies to screen for blood donors with RH variants in a mixed populationALMEIDA, Fabio Augusto Abreu de; DEZAN, Marcia Regina; OLIVEIRA, Valeria Brito; ALENCAR, Cecilia Salete; LUZ, Fabio; KRIEGER, Jose Eduardo; PEREIRA, Alexandre Costa; SABINO, Ester Cerdeira; ROCHA, Vanderson; MENDRONE-JUNIOR, Alfredo; DINARDO, Carla Luana
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