Stephane Moutereau

Université Paris Est
Creteil, France

Last Updated: 09/26/2026

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Found 37 publications

A Novel Plasma Heme Assay Reveals Disease Severity in Beta-Thalassemia and Sickle Cell Anemia.

A Novel Plasma Heme Assay Reveals Disease Severity in Beta-Thalassemia and Sickle Cell Anemia.

Journal: American journal of hematology

Published: November 18, 2025

Carbon monoxide treatment rescues leukofiltration and preserves storage quality of red blood cell concentrates from sickle cell trait donors.

Carbon monoxide treatment rescues leukofiltration and preserves storage quality of red blood cell concentrates from sickle cell trait donors.

Journal: Transfusion

Published: November 18, 2025

A Rare Case of Homozygous HbE With Coinherited Alpha-Thalassemia and Hb Constant Spring in a Neonate Reveals a Mild Hematologic Phenotype.

A Rare Case of Homozygous HbE With Coinherited Alpha-Thalassemia and Hb Constant Spring in a Neonate Reveals a Mild Hematologic Phenotype.

Journal: Journal of pediatric hematology/oncology

Published: October 22, 2025

Glucose-6-phosphate dehydrogenase variants: new WHO classification (2024)

Glucose-6-phosphate dehydrogenase variants: new WHO classification (2024)

Journal: Annales de biologie clinique

Published: May 12, 2025

Comprehensive analysis of sickle β+-thalassemia genotypes and their associated HbA levels in France.

Comprehensive analysis of sickle β+-thalassemia genotypes and their associated HbA levels in France.

Journal: Blood cells, molecules & diseases

Published: March 19, 2025

Biochemical screening of glucose-6-phosphate dehydrogenase deficiency in borderline cases: Complementary inputs of standardization enzymes and comparison with genetic status.

Biochemical screening of glucose-6-phosphate dehydrogenase deficiency in borderline cases: Complementary inputs of standardization enzymes and comparison with genetic status.

Journal: British journal of haematology

Published: September 29, 2024

Fetal Hemoglobin Decrease During Voxelotor Treatment.

Fetal Hemoglobin Decrease During Voxelotor Treatment.

Journal: European journal of haematology

Published: May 06, 2024

A replication study of novel fetal hemoglobin-associated genetic variants in sickle cell disease-only cohorts.

A replication study of novel fetal hemoglobin-associated genetic variants in sickle cell disease-only cohorts.

Journal: Human molecular genetics

Published: January 23, 2024

Study of the antigenic characteristics of red blood cells units and their sickle cell disease recipients and the G6PD activity of transfused red blood cells units.

Study of the antigenic characteristics of red blood cells units and their sickle cell disease recipients and the G6PD activity of transfused red blood cells units.

Journal: Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine

Published: September 02, 2023

Impact of voxelotor on hemoglobin electrophoretic and chromatographic profiles

Impact of voxelotor on hemoglobin electrophoretic and chromatographic profiles

Journal: Annales de biologie clinique

Published: July 21, 2023

Neonatal cyanosis with Hb St Mandé, a low O2 affinity hemoglobin variant affecting β-globin.

Neonatal cyanosis with Hb St Mandé, a low O2 affinity hemoglobin variant affecting β-globin.

Journal: Pediatric blood & cancer

Published: October 28, 2021

Erythrocytosis associated with IgA nephropathy.

Erythrocytosis associated with IgA nephropathy.

Journal: EBioMedicine

Published: June 25, 2021

Showing 1-12 of 37

Last Updated: 09/26/2026