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Clinical and biological features in PIEZO1 -hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients

Haematologica (Roma), 2019-08, Vol.104 (8), p.1554-1564

2019

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Prevalence and risk factors of the metabolic syndrome in adult survivors of childhood leukemia

Blood, 2011-04, Vol.117 (17), p.4442-4448

2011

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Pregnancy outcome in women with transfused beta-thalassemia in France

Annals of hematology, 2022-02, Vol.101 (2), p.289-296

2022

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Place de la thérapie génique dans les thalassémies

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2021-11, Vol.28 (4), p.S20

Thuret, Isabelle

2021

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Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the disease

Haematologica (Roma), 2011-11, Vol.96 (11), p.1712-1714

2011

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Overview of Sickle-cell disease management in the Pediatric Hematology and Oncology Center of Rabat (Morocco)

Journal of Taibah University Medical Sciences, 2023, Vol.18 (6), p.S23-S24

2023

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Complications and treatment of patients with β-thalassemia in France: results of the National Registry

Haematologica (Roma), 2010-05, Vol.95 (5), p.724-729

2010

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Peripheral blood cells chimerism after unrelated cord blood transplantation in children: kinetics, predictive factors and impact on post‐transplant outcome

British journal of haematology, 2014-08, Vol.166 (4), p.557-565

2014

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Les alternatives médicamenteuses à la TF : anciennes et nouvelles molécules

Transfusion clinique et biologique : journal de la Société française de transfusion sanguine, 2021-11, Vol.28 (4), p.S20

2021

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P1451: PUBERTAL DEVELOPMENT OF TRANSFUSION DEPENDENT THALASSEMIA PATIENTS AT THE ERA OF ORAL CHELATION WITH DEFERASIROX: RESULTS OF THE FRENCH NATIONAL REGISTRY NATHALY

HemaSphere, 2023-08, Vol.7 (S3), p.e77759aa-n/a

2023

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Post-transfusional iron overload in the haemoglobinopathies

Comptes rendus. Biologies, 2013-03, Vol.336 (3), p.164-172

Thuret, Isabelle

2013

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Persistence of natural killer cells with expansion of a hypofunctional CD56− CD16+ KIR+ NKG2C+ subset in a patient with atypical Janus kinase 3–deficient severe combined immunodeficiency

Journal of allergy and clinical immunology, 2013-04, Vol.131 (4), p.1230-1233.e2

2013

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Early versus Deferred Antiretroviral Multidrug Therapy in Infants Infected with HIV Type 1

Clinical infectious diseases, 2004-12, Vol.39 (11), p.1692-1698

2004

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Outcome in Children With Relapsed Acute Myeloid Leukemia After Initial Treatment With the French Leucémie Aiquë Myéloïde Enfant (LAME) 89/91 Protocol of the French Society of Pediatric Hematology and Immunology

Journal of clinical oncology, 2003-12, Vol.21 (23), p.4377-4385

2003

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Defective B-cell-negative selection and terminal differentiation in the ICF syndrome

Blood, 2004-04, Vol.103 (7), p.2683-2690

2004

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Mobilization and collection of CD34 + cells in patients with globin disorders: Providing the starting material to manufacturers of autologous gene therapies

Transfusion and apheresis science, 2024-06, Vol.63 (3), p.103926-103926, Article 103926

2024

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Hurdles to the Adoption of Gene Therapy as a Curative Option for Transfusion-Dependent Thalassemia

Stem cells translational medicine, 2022-04, Vol.11 (4), p.407-414

2022

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Betibeglogene Autotemcel Gene Therapy for Non–β0/β0 Genotype β-Thalassemia

The New England journal of medicine, 2022-02, Vol.386 (5), p.415-427

2022

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Impact of Addition of Maintenance Therapy to Intensive Induction and Consolidation Chemotherapy for Childhood Acute Myeloblastic Leukemia: Results of a Prospective Randomized Trial, LAME 89/91

Journal of clinical oncology, 2002-06, Vol.20 (12), p.2774-2782

2002

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A mutation in the Gardos channel is associated with hereditary xerocytosis

Blood, 2015-09, Vol.126 (11), p.1273-1280

2015

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Clinical and biological features in PIEZO1 -hereditary xerocytosis and Gardos channelopathy: a retrospective series of 126 patients

Prevalence and risk factors of the metabolic syndrome in adult survivors of childhood leukemia

A novel syndrome of congenital sideroblastic anemia, B-cell immunodeficiency, periodic fevers, and developmental delay (SIFD)

Pregnancy outcome in women with transfused beta-thalassemia in France

Place de la thérapie génique dans les thalassémies

Variants in genetic modifiers of β-thalassemia can help to predict the major or intermedia type of the disease

Overview of Sickle-cell disease management in the Pediatric Hematology and Oncology Center of Rabat (Morocco)

Complications and treatment of patients with β-thalassemia in France: results of the National Registry

Peripheral blood cells chimerism after unrelated cord blood transplantation in children: kinetics, predictive factors and impact on post‐transplant outcome

Evaluation of Outcomes and Quality of Care in Children with Sickle Cell Disease Diagnosed by Newborn Screening: A Real-World Nation-Wide Study in France

Les alternatives médicamenteuses à la TF : anciennes et nouvelles molécules

P1451: PUBERTAL DEVELOPMENT OF TRANSFUSION DEPENDENT THALASSEMIA PATIENTS AT THE ERA OF ORAL CHELATION WITH DEFERASIROX: RESULTS OF THE FRENCH NATIONAL REGISTRY NATHALY

Post-transfusional iron overload in the haemoglobinopathies

Persistence of natural killer cells with expansion of a hypofunctional CD56− CD16+ KIR+ NKG2C+ subset in a patient with atypical Janus kinase 3–deficient severe combined immunodeficiency

Early versus Deferred Antiretroviral Multidrug Therapy in Infants Infected with HIV Type 1

Outcome in Children With Relapsed Acute Myeloid Leukemia After Initial Treatment With the French Leucémie Aiquë Myéloïde Enfant (LAME) 89/91 Protocol of the French Society of Pediatric Hematology and Immunology

Defective B-cell-negative selection and terminal differentiation in the ICF syndrome

Mobilization and collection of CD34 + cells in patients with globin disorders: Providing the starting material to manufacturers of autologous gene therapies

Hurdles to the Adoption of Gene Therapy as a Curative Option for Transfusion-Dependent Thalassemia

Hematopoietic stem cell transplantation in thalassemia major and sickle cell disease: indications and management recommendations from an international expert panel

A Phase 3 Trial of Luspatercept in Patients with Transfusion-Dependent β-Thalassemia

Betibeglogene Autotemcel Gene Therapy for Non–β0/β0 Genotype β-Thalassemia

Impact of Addition of Maintenance Therapy to Intensive Induction and Consolidation Chemotherapy for Childhood Acute Myeloblastic Leukemia: Results of a Prospective Randomized Trial, LAME 89/91

Long-term event-free survival, chimerism and fertility outcomes in 234 patients with sickle-cell anemia younger than 30 years after myeloablative conditioning and matched-sibling transplantation in France

A mutation in the Gardos channel is associated with hereditary xerocytosis

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