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Chronic and acute anemia and extracranial internal carotid stenosis are risk factors for silent cerebral infarcts in sickle cell anemia

Blood, 2015-03, Vol.125 (10), p.1653-1661

2015

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Ovarian tissue cryopreservation for fertility preservation in 418 girls and adolescents up to 15 years of age facing highly gonadotoxic treatment. Twenty years of experience at a single center

Acta obstetricia et gynecologica Scandinavica, 2019-05, Vol.98 (5), p.630-637

2019

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Long-term treatment follow-up of children with sickle cell disease monitored with abnormal transcranial Doppler velocities

Blood, 2016-04, Vol.127 (14), p.1814-1822

2016

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ERCC6L2 Mutations Link a Distinct Bone-Marrow-Failure Syndrome to DNA Repair and Mitochondrial Function

American journal of human genetics, 2014-02, Vol.94 (2), p.246-256

2014

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Platelet and not erythrocyte microparticles are procoagulant in transfused thalassaemia major patients

British journal of haematology, 2015-11, Vol.171 (4), p.615-624

2015

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Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea

Blood advances, 2018-03, Vol.2 (6), p.626-637

2018

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Hemophagocytic lymphohistiocytosis with Munc13-4 mutation: a cause of recurrent fatal hydrops fetalis

Pediatrics (Evanston), 2011-07, Vol.128 (1), p.e251

2011

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Early lymphocyte reconstitution and viral infections in adolescents and adults transplanted for sickle cell disease

Bone marrow transplantation (Basingstoke), 2024-05, Vol.59 (5), p.708-710

2024

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Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia

Haematologica (Roma), 2011-06, Vol.96 (6), p.808-813

2011

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Lung function after matched‐related donor allogeneic hematopoietic stem cell transplantation in children with sickle cell disease

American journal of hematology, 2023-08, Vol.98 (8), p.E212-E215

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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Brain injury pathophysiology study by a multimodal approach in children with sickle cell anemia with no intra or extra cranial arteriopathy

Haematologica (Roma), 2022-04, Vol.107 (4), p.958-965

2022

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Thrombopoietin receptor agonists as an emergency treatment for severe newly diagnosed immune thrombocytopenia in children

Blood, 2021-01, Vol.137 (1), p.138-141

2021

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Mortality in children with sickle cell disease in mainland France from 2000 to 2015

Haematologica (Roma), 2020-09, Vol.105 (9), p.e440-e443

2020

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Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis

Blood, 2007-04, Vol.109 (8), p.3567-3569

2007

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A nonsense mutation in the DNA repair factor Hebo causes mild bone marrow failure and microcephaly

The Journal of experimental medicine, 2016-05, Vol.213 (6), p.1011-1028

2016

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Beta-thalassemias: molecular, epidemiological, diagnostical and clinical aspects

Annales de biologie clinique (Paris), 2014-11, Vol.72 (6), p.639-668

2014

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Chronic and acute anemia and extracranial internal carotid stenosis are risk factors for silent cerebral infarcts in sickle cell anemia

Ovarian tissue cryopreservation for fertility preservation in 418 girls and adolescents up to 15 years of age facing highly gonadotoxic treatment. Twenty years of experience at a single center

Long-term treatment follow-up of children with sickle cell disease monitored with abnormal transcranial Doppler velocities

ERCC6L2 Mutations Link a Distinct Bone-Marrow-Failure Syndrome to DNA Repair and Mitochondrial Function

Platelet and not erythrocyte microparticles are procoagulant in transfused thalassaemia major patients

Biological impact of α genes, β haplotypes, and G6PD activity in sickle cell anemia at baseline and with hydroxyurea

Hemophagocytic lymphohistiocytosis with Munc13-4 mutation: a cause of recurrent fatal hydrops fetalis

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

Paediatric multisystem inflammatory syndrome temporally associated with SARS-CoV-2 mimicking Kawasaki disease (Kawa-COVID-19): a multicentre cohort

Extensive multilineage analysis in patients with mixed chimerism after allogeneic transplantation for sickle cell disease: insight into hematopoiesis and engraftment thresholds for gene therapy

Early lymphocyte reconstitution and viral infections in adolescents and adults transplanted for sickle cell disease

Congenital macrothrombocytopenia with focal myelofibrosis due to mutations in human G6b-B is rescued in humanized mice

Ovarian tissue cryopreservation for fertility preservation before hematopoietic stem cell transplantation in patients with sickle cell disease: safety, ovarian function follow-up, and results of ovarian tissue transplantation

Pediatric Evans syndrome is associated with a high frequency of potentially damaging variants in immune genes

Missense SLC25A38 variations play an important role in autosomal recessive inherited sideroblastic anemia

Bone Marrow Failure in Fanconi Anemia Is Triggered by an Exacerbated p53/p21 DNA Damage Response that Impairs Hematopoietic Stem and Progenitor Cells

Lung function after matched‐related donor allogeneic hematopoietic stem cell transplantation in children with sickle cell disease

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

Delayed hemolytic transfusion reaction in children with sickle cell disease: first 5-year retrospective study in mainland France

Brain injury pathophysiology study by a multimodal approach in children with sickle cell anemia with no intra or extra cranial arteriopathy

Thrombopoietin receptor agonists as an emergency treatment for severe newly diagnosed immune thrombocytopenia in children

Mortality in children with sickle cell disease in mainland France from 2000 to 2015

Abcb7, the gene responsible for X-linked sideroblastic anemia with ataxia, is essential for hematopoiesis

A nonsense mutation in the DNA repair factor Hebo causes mild bone marrow failure and microcephaly

Beta-thalassemias: molecular, epidemiological, diagnostical and clinical aspects

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