Marina V. Conrado - Publications

Clinical application of a modified platelet desialylation test for mechanistic characterization of platelet transfusion refractoriness.

Journal: Transfusion

Published: December 17, 2025

Functional validation of a modified platelet desialylation test for immune and hereditary thrombocytopenias.

Journal: Transfusion medicine (Oxford, England)

Published: November 20, 2025

Determination of IgG1 and IgG3 subclasses of red blood cell antibodies: An important tool for predicting harmfulness.

Journal: Vox sanguinis

Published: August 27, 2025

Application of Monocyte Monolayer Assay technique to predict hyperhemolysis in patients with sickle cell disease.

Journal: Hematology, transfusion and cell therapy

Published: December 30, 2022

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.

Journal: Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Published: January 06, 2022

RHCE null allele causing D-- phenotype in a Latin-American blood donor.

Journal: Transfusion

Published: October 04, 2021

A novel mutation in RHAG causing Rhnull phenotype in Colombia.

Journal: Transfusion

Published: March 09, 2021

Association between FY*02N.01 and the severity of COVID-19: initial observations.

Journal: Hematology, transfusion and cell therapy

Published: February 26, 2021

Variant genotypes associated with reduced expression of RhCE antigens among Brazilian blood donors.

Journal: Transfusion

Published: July 28, 2020

Weak D types 38 and 11: determination of frequencies in a Brazilian population and validation of an easy molecular assay for detection.

Journal: Immunohematology

Published: July 16, 2020

Transfusion of ABO non-identical platelets increases the severity of trauma patients at ICU admission.

Journal: Hematology, transfusion and cell therapy

Published: April 16, 2020

SMIM1 intron 2 gene variations leading to variability in Vel antigen expression among Brazilian blood donors.

Journal: Blood cells, molecules & diseases

Published: February 11, 2019