-318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients (2017)
- Authors:
- USP affiliated authors: GUALANDRO, SANDRA FATIMA MENOSI - FM ; KRIEGER, JOSE EDUARDO - FM ; ROCHA, VANDERSON GERALDO - FM ; SABINO, ESTER CERDEIRA - FM
- Unidade: FM
- DOI: 10.1111/iji.12334
- Subjects: POLIMORFISMO; ANEMIA FALCIFORME; TRANSFUSÃO DE SANGUE; ANTICORPOS
- Agências de fomento:
- Language: Inglês
- Imprenta:
- Source:
- Título do periódico: International journal of immunogenetics
- ISSN: 1744-3121
- Volume/Número/Paginação/Ano: v. 44, n. 5, p. 219-224, 2017
- Este periódico é de assinatura
- Este artigo NÃO é de acesso aberto
- Cor do Acesso Aberto: closed
-
ABNT
OLIVEIRA, V. B. et al. -318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients. International journal of immunogenetics, v. 44, n. 5, p. 219-224, 2017Tradução . . Disponível em: https://doi.org/10.1111/iji.12334. Acesso em: 21 maio 2024. -
APA
Oliveira, V. B., Dezan, M. R., Gomes, F. C. A., Gualandro, S. F. M., Krieger, J. E., Pereira, A. C., et al. (2017). -318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients. International journal of immunogenetics, 44( 5), 219-224. doi:10.1111/iji.12334 -
NLM
Oliveira VB, Dezan MR, Gomes FCA, Gualandro SFM, Krieger JE, Pereira AC, Marsiglia JD, Levi JE, Rocha VG, Mendrone Junior A, Sabino EC, Dinardo CL. -318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients [Internet]. International journal of immunogenetics. 2017 ; 44( 5): 219-224.[citado 2024 maio 21 ] Available from: https://doi.org/10.1111/iji.12334 -
Vancouver
Oliveira VB, Dezan MR, Gomes FCA, Gualandro SFM, Krieger JE, Pereira AC, Marsiglia JD, Levi JE, Rocha VG, Mendrone Junior A, Sabino EC, Dinardo CL. -318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients [Internet]. International journal of immunogenetics. 2017 ; 44( 5): 219-224.[citado 2024 maio 21 ] Available from: https://doi.org/10.1111/iji.12334 - RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients
- Effectiveness of strategies to screen for blood donors with RH variants in a mixed population
- Prevalence and laboratorial determinants of the clinical relevance of antibodies of undetermined specificity
- SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors
- High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype
- 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
- Massive autoimmune hemolysis documented by monocyte monolayer assay in a multiply transfused patient using reticulocytes isolated by simple centrifugation in microhematocrit tubes
- Is Severity Score Associated With Indication for Hematopoietic Stem Cell Transplantation in Individuals With Sickle Cell Anemia?
- Identification and Characterization of Hematopoietic Stem Cell Transplant Candidates in a Sickle Cell Disease Cohort
- Risk factors for deferral due to low hematocrit and iron depletion among prospective blood donors in a Brazilian center
Informações sobre o DOI: 10.1111/iji.12334 (Fonte: oaDOI API)
How to cite
A citação é gerada automaticamente e pode não estar totalmente de acordo com as normas
