Gwellaouen Bodivit
Creteil, 94000, France
Last Updated: 09/26/2026
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Found 14 publications
Preclinical evaluation of the preservation of red blood cell concentrates by hypoxic storage technology for transfusion in sickle cell disease.
Journal: Haematologica
Published: August 04, 2021
Ex Vivo Activation of Red Blood Cell Senescence by Plasma from Sickle-Cell Disease Patients: Correlation between Markers and Adhesion Consequences during Acute Disease Events.
Journal: Biomolecules
Published: May 18, 2021
Detection and follow-up of a soluble alpha-haemoglobin pool in the red cells of stored blood units.
Journal: Blood transfusion = Trasfusione del sangue
Published: September 25, 2020
Individual red blood cell fetal hemoglobin quantification allows to determine protective thresholds in sickle cell disease.
Journal: American journal of hematology
Published: January 07, 2020
Complement activation in sickle cell disease: Dependence on cell density, hemolysis and modulation by hydroxyurea therapy.
Journal: American journal of hematology
Published: December 06, 2019
Alloimmunization risk associated with amino acid 223 substitution in the RhD protein: analysis in the light of molecular modeling.
Journal: Transfusion
Published: July 24, 2017
Severe hemolysis after plasma transfusion in a neonate with necrotizing enterocolitis, Clostridium perfringens infection, and red blood cell T-polyagglutination.
Journal: Transfusion
Published: December 29, 2016
Neuraminidase enhances in vitro expansion of human erythroid progenitors.
Journal: European cytokine network
Published: August 02, 2016
In vitro characterization of patches of human mesenchymal stromal cells.
Journal: Tissue engineering. Part A
Published: July 23, 2014
Last Updated: 09/26/2026