Search Results - "Dezan, Marcia"
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Diversity of RH and transfusion support in Brazilian sickle cell disease patients with unexplained Rh antibodies
Published in Transfusion (Philadelphia, Pa.) (01-10-2019)“…BACKGROUND Genetic diversity in the RH genes among sickle cell disease (SCD) patients is well described but not yet extensively explored in populations of…”
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Diversity of variant alleles encoding Kidd, Duffy, and Kell antigens in individuals with sickle cell disease using whole genome sequencing data from the NHLBI TOPMed Program
Published in Transfusion (Philadelphia, Pa.) (01-02-2021)“…Background Genetic variants in the SLC14A1, ACKR1, and KEL genes, which encode Kidd, Duffy, and Kell red blood cell antigens, respectively, may result in…”
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Prevalence of SMIM1 c.64_80del17 homozygotes in southeastern Brazil: the Vel‐negative phenotype
Published in Transfusion (Philadelphia, Pa.) (01-01-2019)Get full text
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Impact of HLA-G +3142C>G on the development of antibodies to blood group systems other than the Rh and Kell among sensitized patients with sickle cell disease
Published in Transfusion and apheresis science (01-10-2022)“…Patients' inflammatory history is an important factor underlying red blood cell (RBC) alloimmunization, which is a frequent transfusion complication among…”
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RHD and RHCE genotyping by next-generation sequencing is an effective strategy to identify molecular variants within sickle cell disease patients
Published in Blood cells, molecules, & diseases (01-06-2017)“…The complexity of Rh genetic variation among sickle cell disease (SCD) patients is high. Conventional molecular assays cannot identify all genetic variants…”
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Association between FY02N.01 and the severity of COVID-19: initial observations
Published in Hematology, Transfusion and Cell Therapy (01-04-2022)“…The pro-inflammatory immune response underlies severe cases of COVID-19. Antigens of the Duffy blood group systems are receptors for pro-inflammation…”
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Detection of alloimmunization in Glanzmann Thrombasthenia and Bernard-Soulier Syndrome: Data from a Brazilian Center
Published in Hematology, transfusion and cell therapy (01-07-2023)“…The Glanzmann Thrombasthenia (GT) and Bernard-Soulier Syndrome (BSS) are rare hereditary disorders of platelet function. Their treatment often requires…”
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High-throughput strategy for molecular identification of Vel- blood donors employing nucleic acids extracted from plasma pools used for viral nucleic acid test screening
Published in Transfusion (Philadelphia, Pa.) (01-06-2016)“…BACKGROUND Serologic methods to determine the Vel– phenotype require the use of rare human antisera and do not allow for many samples to be tested…”
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Defining the clinical relevance of red blood cell autoantibodies by Monocyte Monolayer Assay
Published in Journal of clinical laboratory analysis (01-02-2018)“…Background The Monocyte Monolayer Assay (MMA) is an in vitro simulation of red blood cell (RBC) alloantibody behavior. It has been classically applied to…”
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A blockage monoclonal antibody protocol as an alternative strategy to avoid anti‐CD38 interference in immunohematological testing
Published in Transfusion (Philadelphia, Pa.) (01-05-2019)“…BACKGROUND As CD38 is expressed on red blood cells (RBCs), the plasma of patients on daratumumab (DARA) reacts with the panel cells of pretransfusion tests,…”
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Transfusion of ABO non-identical platelets increases the severity of trauma patients at ICU admission
Published in Hematology, Transfusion and Cell Therapy (01-07-2021)“…BACKGROUNDTransfusion of ABO-compatible non-identical platelets (PTLs), fresh plasma (FP) and red blood cells (RBCs) has been associated with increased…”
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Successful management of neonatal alloimmune thrombocytopenia in the second pregnancy: a case report
Published in Einstein (São Paulo, Brazil) (01-01-2014)“…Neonatal alloimmune thrombocytopenia is a serious disease, in which the mother produces antibodies against fetal platelet antigens inherited from the father;…”
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A novel mutation in RHAG causing Rh null phenotype in Colombia
Published in Transfusion (Philadelphia, Pa.) (01-09-2021)Get full text
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FcγR2B B2 .4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patients
Published in Transfusion (Philadelphia, Pa.) (01-07-2020)“…BACKGROUND Red blood cell (RBC) alloimmunization is an important transfusion complication which is prevalent among sickle cell disease (SCD) patients…”
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A novel mutation in RHAG causing Rhnull phenotype in Colombia
Published in Transfusion (Philadelphia, Pa.) (01-09-2021)Get full text
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RHCE null allele causing D‐‐ phenotype in a Latin‐American blood donor
Published in Transfusion (Philadelphia, Pa.) (01-03-2022)Get full text
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FcγR2B B2.4 haplotype predicts increased risk of red blood cell alloimmunization in sickle cell disease patients
Published in Transfusion (Philadelphia, Pa.) (01-07-2020)“…BACKGROUND Red blood cell (RBC) alloimmunization is an important transfusion complication which is prevalent among sickle cell disease (SCD) patients…”
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Variant genotypes associated with reduced expression of RhCE antigens among Brazilian blood donors
Published in Transfusion (Philadelphia, Pa.) (01-06-2021)“…Background The genetic diversity of the RHCE gene locus has been explored in diverse populations of different racial backgrounds. Data referring to the…”
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Using droplet digital PCR to screen for rare blood donors: Proof of principle
Published in Transfusion and apheresis science (01-12-2020)“…Digital droplet PCR (ddPCR) is a very sensitive high throughput genotyping methodology. To date, the use of ddPCR in immunohematology is restricted to fetal…”
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