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You searched for: Author/Creator Dezan, Marcia Regina

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1. A blockage monoclonal antibody protocol as an alternative strategy to avoid anti‐CD38 interference in immunohematological testing. Issue 5 (18th February 2019)

2. A novel mutation in RHAG causing Rhnull phenotype in Colombia. Issue 9 (26th July 2021)

3. Effectiveness of strategies to screen for blood donors with RH variants in a mixed population. (April 2020)

4. 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. Issue 2 (28th November 2017)

5. High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak‐D phenotype. Issue 9 (26th June 2018)

6. Massive autoimmune hemolysis documented by monocyte monolayer assay in a multiply transfused patient using reticulocytes isolated by simple centrifugation in microhematocrit tubes. Issue 7 (6th August 2018)

7. Prevalence and laboratorial determinants of the clinical relevance of antibodies of undetermined specificity. Issue 6 (10th June 2019)

8. RHCE null allele causing D‐‐ phenotype in a Latin‐American blood donor. Issue 3 (13th February 2022)

9. Using droplet digital PCR to screen for rare blood donors: Proof of principle. (December 2020)

10. Variant genotypes associated with reduced expression of RhCE antigens among Brazilian blood donors. Issue 6 (9th March 2021)