22 results on '"Dezan, Marcia Regina"'
Search Results
2. Using droplet digital PCR to screen for rare blood donors: Proof of principle
3. Effectiveness of strategies to screen for blood donors with RH variants in a mixed population
4. SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors
5. 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
6. RHCE null allele causing D‐‐ phenotype in a Latin‐American blood donor
7. A novel mutation in RHAG causing Rhnull phenotype in Colombia
8. Variant genotypes associated with reduced expression of RhCE antigens among Brazilian blood donors
9. Prevalence and laboratorial determinants of the clinical relevance of antibodies of undetermined specificity
10. A blockage monoclonal antibody protocol as an alternative strategy to avoid anti‐CD38 interference in immunohematological testing
11. FCGR2B B2.4 Haplotype Predicts Increased Risk of Red Blood Cell Alloimmunization in Sickle Cell Disease Patients
12. Massive autoimmune hemolysis documented by monocyte monolayer assay in a multiply transfused patient using reticulocytes isolated by simple centrifugation in microhematocrit tubes
13. High frequency of variantRHDgenotypes among donors and patients of mixed origin with serologic weak‐D phenotype
14. A novel mutation in RHAG causing Rhnull phenotype in Colombia.
15. 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 ofRHD*Ψ
16. Sucesso no manejo da trombocitopenia aloimune neonatal na segunda gestação: relato de caso
17. Successful management of neonatal alloimmune thrombocytopenia in the second pregnancy: a case report
18. Sistema Vel: triagem molecular utilizando DNA obtido de pools de plasma de doadores de sangue
19. High frequency of variant RHD genotypes among donors and patients of mixed origin with serologic weak-D phenotype.
20. FCGR2BB2.4 Haplotype Predicts Increased Risk of Red Blood Cell Alloimmunization in Sickle Cell Disease Patients
21. A novel mutation in RHAG causing Rh null phenotype in Colombia.
22. Prevalence and laboratorial determinants of the clinical relevance of antibodies of undetermined specificity.
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