FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patients (2020)
- Authors:
- USP affiliated authors: COVAS, DIMAS TADEU - FMRP ; HADDAD, SIMONE KASHIMA - FMRP ; KRIEGER, JOSE EDUARDO - FM ; GUALANDRO, SANDRA FATIMA MENOSI - FM ; ROCHA, VANDERSON GERALDO - FM
- Unidades: FMRP; FM
- DOI: 10.1111/trf.15832
- Subjects: AUTOIMUNIDADE; DOENÇAS AUTOIMUNES; GENÓTIPOS; PACIENTES
- Language: Inglês
- Imprenta:
- Source:
- Título: Transfusion
- ISSN: 0041-1132
- Volume/Número/Paginação/Ano: v. 60, n. 7, p. 1573-1578, 2020
- Este periódico é de acesso aberto
- Este artigo NÃO é de acesso aberto
-
ABNT
COSTA NETO, Abel et al. FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patients. Transfusion, v. 60, n. 7, p. 1573-1578, 2020Tradução . . Disponível em: https://doi.org/10.1111/trf.15832. Acesso em: 20 jan. 2026. -
APA
Costa Neto, A., Santos, F., Ribeiro, I., Oliveira, V., Dezan, M., Kashima, S., et al. (2020). FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patients. Transfusion, 60( 7), 1573-1578. doi:10.1111/trf.15832 -
NLM
Costa Neto A, Santos F, Ribeiro I, Oliveira V, Dezan M, Kashima S, Covas DT, Krieger JE, Gualandro SFM, Rocha VG. FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patients [Internet]. Transfusion. 2020 ; 60( 7): 1573-1578.[citado 2026 jan. 20 ] Available from: https://doi.org/10.1111/trf.15832 -
Vancouver
Costa Neto A, Santos F, Ribeiro I, Oliveira V, Dezan M, Kashima S, Covas DT, Krieger JE, Gualandro SFM, Rocha VG. FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patients [Internet]. Transfusion. 2020 ; 60( 7): 1573-1578.[citado 2026 jan. 20 ] Available from: https://doi.org/10.1111/trf.15832 - Impact of HLA-G+3142C>G on the development of antibodies to blood group systems other than the Rh and Kell among sensitized patients with sickle cell disease
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- -318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients
- Short form health survey (SF-36) differs between genotypic groups of patients with suspected hereditary hemochromatosis
- Quality of life scores differs between genotypic groups of patients with suspected hereditary hemochromatosis
- Evaluation of the applicability and effectiveness of a molecular strategy for identifying weakD and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD*
- Hemoglobinuria paroxistica noturna: a proposito de 11 casos
- Coronary flow velocity reserve is preserved in patients with sickle cell diasease and left ventricular hypertrophy
- Atypical 'beta POT.S' haplotypes are generated by diverse genetic mechanisms
Informações sobre o DOI: 10.1111/trf.15832 (Fonte: oaDOI API)
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