Sandra Manceau
Paris, 75015, France
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 24 publications
Base editing of β0-thalassemia mutations as a therapeutic strategy for severe β-hemoglobinopathies.
Journal: Science translational medicine
Published: November 26, 2025
Protein S Enhances the Phagocytosis of Phosphatidylserine-Exposing Erythrocytes: Implications in Sickle Cell Disease.
Journal: American journal of hematology
Published: April 04, 2025
MMS22L is a novel key actor of normal and pathological erythropoiesis.
Journal: HemaSphere
Published: November 04, 2024
Maternal and perinatal outcomes of sickle cell disease in pregnancy: A nationwide study in France.
Journal: British journal of haematology
Published: September 30, 2024
Severe inflammation and lineage skewing are associated with poor engraftment of engineered hematopoietic stem cells in patients with sickle cell disease.
Journal: Nature communications
Published: August 14, 2024
Clearance of pathogenic erythrocytes is maintained despite spleen dysfunction in children with sickle cell disease.
Journal: American journal of hematology
Published: July 03, 2024
Erythropoietin downregulates red blood cell clearance, increasing transfusion efficacy in severely anemic recipients.
Journal: American journal of hematology
Published: August 09, 2023
Safety of coronavirus disease 2019 vaccines in 213 adult patients with sickle cell disease.
Journal: British journal of haematology
Published: July 13, 2022
Erythrocytic vacuoles that accumulate a fluorescent dye predict spleen size and function in sickle cell disease.
Journal: American journal of hematology
Published: May 11, 2022
Last Updated: 09/26/2026