about
Molecular HPA genotyping by microarray in Brazilian blood donors.Successful management of neonatal alloimmune thrombocytopenia in the second pregnancy: a case report.RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients.-318C/T polymorphism of the CTLA-4 gene is an independent risk factor for RBC alloimmunization among sickle cell disease patients.Screening for the SMIM1*64_80 del Allele in blood donors in a population from Southern Brazil.Duffy null genotype or Fy(a-b-) phenotype are more accurate than self-declared race for diagnosing benign ethnic neutropenia in Brazilian population.Defining the clinical relevance of red blood cell autoantibodies by Monocyte Monolayer Assay.RHD allelic identification among D-Brazilian blood donors as a routine test using pools of DNA.Determination of Fetal RHD Genotype Including the RHD Pseudogene in Maternal Plasma.Prevalence of SMIM1 c.64_80del17 homozygotes in southeastern Brazil: the Vel-negative phenotypeA blockage monoclonal antibody protocol as an alternative strategy to avoid anti-CD38 interference in immunohematological testingDiversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies
P50
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P50
description
researcher ORCID ID = 0000-0002-3760-9843
@en
wetenschapper
@nl
name
Marcia Dezan
@ast
Marcia Dezan
@en
Marcia Dezan
@es
Marcia Dezan
@nl
type
label
Marcia Dezan
@ast
Marcia Dezan
@en
Marcia Dezan
@es
Marcia Dezan
@nl
prefLabel
Marcia Dezan
@ast
Marcia Dezan
@en
Marcia Dezan
@es
Marcia Dezan
@nl
P106
P21
P31
P496
0000-0002-3760-9843