Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

61 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
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: oliveira vb. Transfusion. 2018 Feb;58(2):317-322. doi: 10.1111/trf.14425. Epub 2017 Nov 28. Transfusion. 2018. PMID: 29193119 Clinical Trial.
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: oliveira tgm, oliveira vb. 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
Using droplet digital PCR to screen for rare blood donors: Proof of principle.
Dezan MR, Peron AC, Oliveira TGM, Oliveira VB, Gomes CN, Salles NA, Rocha V, Mendrone-Júnior A, Dinardo CL. Dezan MR, et al. Among authors: oliveira tgm, oliveira vb. Transfus Apher Sci. 2020 Dec;59(6):102882. doi: 10.1016/j.transci.2020.102882. Epub 2020 Jul 25. Transfus Apher Sci. 2020. PMID: 32741734
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: oliveira vb. 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
A novel mutation in RHAG causing Rhnull phenotype in Colombia.
Junca TG, Pinilla JJ, Sanjuanelo M, Lopez K, Dezan MR, Peron AC, Oliveira VB, Conrado MCAV, Rocha V, Mendrone-Júnior A, Dinardo CL. Junca TG, et al. Among authors: oliveira vb. Transfusion. 2021 Sep;61(9):E62-E64. doi: 10.1111/trf.16596. Epub 2021 Jul 26. Transfusion. 2021. PMID: 34309026 No abstract available.
61 results