Sarah Szepetowski

Marseille, 13385, France

Last Updated: 09/26/2026

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Found 11 publications

Transition from Pediatric to Adult Care in Patients with Transfusion-Dependent Beta-Thalassemia in France: A National Study Concerning a Rare Disease.

Transition from Pediatric to Adult Care in Patients with Transfusion-Dependent Beta-Thalassemia in France: A National Study Concerning a Rare Disease.

Journal: Journal of clinical medicine

Published: January 22, 2026

Splenectomy in β-thalassemia patients: Practices and risks in a nationwide study.

Splenectomy in β-thalassemia patients: Practices and risks in a nationwide study.

Journal: HemaSphere

Published: November 26, 2025

A new unstable haemoglobin, Hb Alger, causes a transfusion-dependent anaemia in early childhood.

A new unstable haemoglobin, Hb Alger, causes a transfusion-dependent anaemia in early childhood.

Journal: British journal of haematology

Published: April 25, 2025

Pubertal development of transfusion-dependent thalassemia patients in the era of oral chelation with deferasirox: results from the French registry.

Pubertal development of transfusion-dependent thalassemia patients in the era of oral chelation with deferasirox: results from the French registry.

Journal: Haematologica

Published: September 20, 2023

Recent results of hematopoietic stem cell transplantation for thalassemia with busulfan-based conditioning regimen in France: improved thalassemia free survival despite frequent mixed chimerism. A retrospective study from the Francophone Society of Stem Cell Transplantation and Cellular Therapy (SFGM-TC).

Recent results of hematopoietic stem cell transplantation for thalassemia with busulfan-based conditioning regimen in France: improved thalassemia free survival despite frequent mixed chimerism. A retrospective study from the Francophone Society of Stem Cell Transplantation and Cellular Therapy (SFGM-TC).

Journal: Bone marrow transplantation

Published: March 26, 2023

Homozygosity for the hyperunstable hemoglobin variant Hb Agrinio (HBA2:c.89T>C) leads to severe antenatal anemia: Eight new cases in three families.

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

Monoclonal antibodies for the treatment of COVID-19 in a patient with high-risk acute leukaemia.

Monoclonal antibodies for the treatment of COVID-19 in a patient with high-risk acute leukaemia.

Journal: British journal of haematology

Published: August 02, 2021

Symptom Screening in Pediatrics Tool in children and adolescents with high-risk malignancies: a pilot study.

Symptom Screening in Pediatrics Tool in children and adolescents with high-risk malignancies: a pilot study.

Journal: BMJ supportive & palliative care

Published: October 20, 2020

First step toward high-intensity end-of-life care definition in pediatric oncology: Response to bereaved parents' views on end-of-life care for children with cancer: Quality marker implications.

First step toward high-intensity end-of-life care definition in pediatric oncology: Response to bereaved parents' views on end-of-life care for children with cancer: Quality marker implications.

Journal: Cancer

Published: July 24, 2020

Long-term management of leukocyte adhesion deficiency type III without hematopoietic stem cell transplantation.

Long-term management of leukocyte adhesion deficiency type III without hematopoietic stem cell transplantation.

Journal: Haematologica

Published: February 24, 2018

NISCH syndrome, a rare cause of neonatal cholestasis: A case report

NISCH syndrome, a rare cause of neonatal cholestasis: A case report

Journal: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie

Published: November 09, 2016

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Last Updated: 09/26/2026