Kolexia
Thuret Isabelle
Pédiatrie
Hôpital La Timone Enfants
Marseille, France
128 Activités
0 Followers

Scientifique
Digital
Production scientifique
Activités par an
Expertise
Sujets de recherche
{{person.topmesh1.name}} Thalassémie Drépanocytose Bêta-Thalassémie Anémie Surcharge en fer Réaction transfusionnelle Accident vasculaire cérébral Maladie du greffon contre l'hôte Maladies vasculaires

Industries

Bluebird
5 collaboration(s)
Dernière en 2021
Vertex
4 collaboration(s)
Dernière en 2023
Novartis
3 collaboration(s)
Dernière en 2021
Pfizer
2 collaboration(s)
Dernière en 2023

Dernières activités

Talasemias en el niño
EMC. Pediatria   01 mars 2024
Pubertal development of transfusion-dependent thalassemia patients in the era of oral chelation with deferasirox: results from the French registry.
Haematologica   22 février 2024
Sustained Efficacy and Safety in Adult and Pediatric Patients with Transfusion-Dependent β-Thalassemia up to 9 Years Post Treatment with Betibeglogene Autotemcel (Beti-cel)
Abstracts from the 2024 Tandem Meetings of ASTCT and CIBMTR, February 21-24, 2024, San Antonio, Texas, USA   01 février 2024
Improvement in Iron Burden in Patients with Transfusion-Dependent β-Thalassemia (TDT) Treated with Betibeglogene Autotemcel (Beti-cel) Gene Therapy: Up to 9 Years of Follow-up
65th ASH Annual Meeting Abstracts   02 novembre 2023
Sustained Efficacy, Safety, and Improved Quality of Life in Adult and Pediatric Patients with Transfusion-Dependent β-Thalassemia up to 9 Years Post Treatment with Betibeglogene Autotemcel (Beti-cel)
65th ASH Annual Meeting Abstracts   02 novembre 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).
Bone marrow transplantation   04 août 2023
ESCORT-HU Extension: European Sickle Cell Disease Cohort - Hydroxyurea - Extension Study: ESCORT-HU Extension: European Sickle Cell Disease Cohort - Hydroxyurea - Extension
Essai Clinique (Addmedica)   14 juin 2023
A Study Evaluating the Efficacy and Safety of the LentiGlobin® BB305 Drug Product in Participants With Transfusion-Dependent β-Thalassemia, Who do Not Have a β0/β0 Genotype: A Phase 3 Single Arm Study Evaluating the Efficacy and Safety of Gene Therapy in Subjects With Transfusion-dependent β-Thalassemia, Who do Not Have a β0/β0 Genotype, by Transplantation of Autologous CD34+ Stem Cells Transduced Ex Vivo With a Lentiviral βA-T87Q-Globin Vector in Subjects ≤50 Years of Age
Essai Clinique (Bluebird)   22 mai 2023
β-Thalassemia in childhood: Current state of health in a high-income country.
British journal of haematology   06 janvier 2023
Overview of Sickle-cell disease management in the Pediatric Hematology and Oncology Center of Rabat (Morocco)
Middle East and North Africa Hematology Congress 2023 and 5th HEMNET forum   01 janvier 2023