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Evaluation of the applicability and effectiveness of a molecular strategy for identifying weak D and DEL phenotype among D- blood donors of mixed origin exhibiting high frequency of RHD*Ψ.
Dezan MR, Guardalini LGO, Pessoa E, Ribeiro IH, Oliveira VB, Luz F, Novac DR, Gallucci A, Bonifácio S, Gomes F, Levi JE, Pereira AC, Krieger JE, Mendrone-Junior A, Rocha V, Dinardo CL. Dezan MR, et al. Among authors: levi je. Transfusion. 2018 Feb;58(2):317-322. doi: 10.1111/trf.14425. Epub 2017 Nov 28. Transfusion. 2018. PMID: 29193119 Clinical Trial.
RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients.
Dezan MR, Ribeiro IH, Oliveira VB, Vieira JB, Gomes FC, Franco LAM, Varuzza L, Ribeiro R, Chinoca KZ, Levi JE, Krieger JE, Pereira AC, Gualandro SFM, Rocha VG, Mendrone-Junior A, Sabino EC, Dinardo CL. Dezan MR, et al. Among authors: levi je. Blood Cells Mol Dis. 2017 Jun;65:8-15. doi: 10.1016/j.bcmd.2017.03.014. Epub 2017 Mar 31. Blood Cells Mol Dis. 2017. PMID: 28388467
Validation of QF-PCR for prenatal diagnoses in a Brazilian population.
de Moraes RW, de Carvalho MHB, de Amorim-Filho AG, Francisco RPV, Romão RM, Levi JE, Zugaib M. de Moraes RW, et al. Among authors: levi je. Clinics (Sao Paulo). 2017 Jul;72(7):400-404. doi: 10.6061/clinics/2017(07)02. Clinics (Sao Paulo). 2017. PMID: 28792998 Free PMC article.
SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors.
Dezan MR, Costa-Neto A, Gomes CN, Ribeiro IH, Oliveira VB, Conrado MCAV, Oliveira TGM, Carvalho MLP, Aranha AF, Bosi SRA, Salles NA, Krieger JE, Pereira AC, Sabino EC, Rocha V, Mendrone-Junior A, Dinardo CL, Levi JE. Dezan MR, et al. Among authors: levi je. Blood Cells Mol Dis. 2019 Jul;77:23-28. doi: 10.1016/j.bcmd.2019.03.006. Epub 2019 Mar 25. Blood Cells Mol Dis. 2019. PMID: 30939337
185 results