Serge Pissard
University Paris Est
Creteil, France
Creteil, France
Last Updated: 09/26/2026
Save publications for later
Sign Up
Not sure about your diagnosis?
Check Your Symptoms
Found 59 publications
Expanding the PKLR mutation spectrum: discovery of two novel variants in two pediatric cases of pyruvate kinase deficiency.
Journal: Annals of hematology
Published: January 26, 2026
A Novel Plasma Heme Assay Reveals Disease Severity in Beta-Thalassemia and Sickle Cell Anemia.
Journal: American journal of hematology
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.
Journal: Journal of pediatric hematology/oncology
Published: October 22, 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
Marked microcytosis and increased transferrin saturation: Think about variants in SLC11A2 (DMT1).
Journal: Blood cells, molecules & diseases
Published: July 18, 2024
Prognostic significance of early acute splenic sequestration in children with severe sickle cell genotypes: A comprehensive longitudinal neonatal cohort study.
Journal: American journal of hematology
Published: July 12, 2024
Glucose-6-phosphate dehydrogenase deficiency detection using fluorocytometric assay: Evaluation after 1 year of clinical implementation.
Journal: Cytometry. Part B, Clinical cytometry
Published: May 03, 2024
High risk of progression for chronic major organ complications of sickle cell disease in adolescents and young adults: A long-term neonatal cohort study.
Journal: American journal of hematology
Published: February 19, 2024
Clinical events in a long-term prospective neonatal cohort of children with sickle cell disease: Evidence for a high disease burden without systematic preventive intensification with hydroxyurea.
Journal: American journal of hematology
Published: July 19, 2023
A high level of Hb F unmasks a new case of Hb Wanjiang (β (F3-F4) Ala87_Thr88delinsSer_Gln (HBB:c.255_264 delinsTTTTTCTCAG)) in a pregnant woman of African ancestry.
Journal: International journal of laboratory hematology
Published: March 10, 2023
Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families.
Journal: American journal of hematology
Published: June 08, 2022
Prenatal management of fetal anemia due to pyruvate kinase deficiency: A case report.
Journal: Transfusion
Published: April 06, 2022
Last Updated: 09/26/2026