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pro vyhledávání: '"KA Boy"'
Autor:
L Nascimento, NF Silva, KA Boy, R Tognon-Ribeiro, LM Mendonça, APP Santos, CV Rodrigues, RR Sales, PSAS Gerheim, MR Luizon
Publikováno v:
Hematology, Transfusion and Cell Therapy, Vol 46, Iss , Pp S39-S40 (2024)
Sickle cell disease (SCD) is an autosomal recessive monogenic disorder that modifies the adult hemoglobin and results in multiple clinical phenotypes. Increases in fetal hemoglobin (HbF) has clinical benefits by reducing the clinical severity of SCD.
Externí odkaz:
https://doaj.org/article/0cb73f11f24d485a95d1653f7477f943
Autor:
Oliveira EAM; Universidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil., Boy KA; Universidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil., Santos APP; Hemocentro Regional de Governador Valadares, Fundação Hemominas, Governador Valadares, MG, Brazil., Machado CDS; Universidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil., Velloso-Rodrigues C; Universidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil., Gerheim PSAS; Universidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil., Mendonça LM; Universidade Federal de Juiz de Fora, Juiz de Fora, MG, Brazil.
Publikováno v:
Einstein (Sao Paulo, Brazil) [Einstein (Sao Paulo)] 2019 Sep 09; Vol. 17 (4), pp. eAO4742. Date of Electronic Publication: 2019 Sep 09.