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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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Modalités transfusionnelles spécifiques des syndromes thalassémiques

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

Pondarre, Corinne

2021

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AKT activity orchestrates marginal zone B cell development in mice and humans

Cell reports (Cambridge), 2023-04, Vol.42 (4), p.112378-112378, Article 112378

2023

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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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High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients

Transfusion (Philadelphia, Pa.), 2018-06, Vol.58 (6), p.1527-1535

2018

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Deferasirox-induced renal impairment in children: an increasing concern for pediatricians

Pediatric nephrology (Berlin, West), 2012-11, Vol.27 (11), p.2115-2122

2012

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Allogeneic/Matched Related Transplantation for β-Thalassemia and Sickle Cell Anemia

Advances in experimental medicine and biology, 2017, Vol.1013, p.89-122

2017

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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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Newly Diagnosed Immune Thrombocytopenic Purpura in Childhood: Successful Implementation of a Limited Intervention Strategy in the Setting of Pediatric Emergency Care

The Journal of pediatrics, 2015-02, Vol.166 (2), p.480-482

2015

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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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Identification of Clinical and Laboratory Parameters Associated with the Development of Acute Chest Syndrome during Vaso-Occlusive Episodes in Children with Sickle Cell Disease: A Preliminary Step before Assessing Specific and Early Treatment Strategies

Journal of clinical medicine, 2019-11, Vol.8 (11), p.1839

2019

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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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Short-Term Femoral Catheter Insertion: A Promising Alternative to Consistently Allow Long-Term Erythrocytapheresis Therapy in Children with Sickle Cell Anemia

The Journal of pediatrics, 2013-02, Vol.162 (2), p.423-426

2013

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The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score

European journal of haematology, 2012-01, Vol.88 (1), p.61-67

2012

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Design of the DREPAGREFFE trial: A prospective controlled multicenter study evaluating the benefit of genoidentical hematopoietic stem cell transplantation over chronic transfusion in sickle cell anemia children detected to be at risk of stroke by transcranial Doppler (NCT 01340404)

Contemporary clinical trials, 2017-11, Vol.62, p.91-104

2017

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Characterization of mitochondrial ferritin‐deficient mice

American journal of hematology, 2010-12, Vol.85 (12), p.958-960

2010

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The mitochondrial ATP-binding cassette transporter Abcb7 is essential in mice and participates in cytosolic iron–sulfur cluster biogenesis

Human molecular genetics, 2006-03, Vol.15 (6), p.953-964

2006

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Neonatal Alloimmune Thrombocytopenia With Amegakaryocytosis, B Lymphopenia, and Villitis

Pediatrics (Evanston), 2018-04, Vol.141 (Suppl 5), p.S506

2018

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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

Modalités transfusionnelles spécifiques des syndromes thalassémiques

AKT activity orchestrates marginal zone B cell development in mice and humans

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

High immunogenicity of red blood cell antigens restricted to the population of African descent in a cohort of sickle cell disease patients

Deferasirox-induced renal impairment in children: an increasing concern for pediatricians

Allogeneic/Matched Related Transplantation for β-Thalassemia and Sickle Cell Anemia

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

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

Newly Diagnosed Immune Thrombocytopenic Purpura in Childhood: Successful Implementation of a Limited Intervention Strategy in the Setting of Pediatric Emergency Care

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

Identification of Clinical and Laboratory Parameters Associated with the Development of Acute Chest Syndrome during Vaso-Occlusive Episodes in Children with Sickle Cell Disease: A Preliminary Step before Assessing Specific and Early Treatment Strategies

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

Short-Term Femoral Catheter Insertion: A Promising Alternative to Consistently Allow Long-Term Erythrocytapheresis Therapy in Children with Sickle Cell Anemia

The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score

Design of the DREPAGREFFE trial: A prospective controlled multicenter study evaluating the benefit of genoidentical hematopoietic stem cell transplantation over chronic transfusion in sickle cell anemia children detected to be at risk of stroke by transcranial Doppler (NCT 01340404)

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

Characterization of mitochondrial ferritin‐deficient mice

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

The mitochondrial ATP-binding cassette transporter Abcb7 is essential in mice and participates in cytosolic iron–sulfur cluster biogenesis

Neonatal Alloimmune Thrombocytopenia With Amegakaryocytosis, B Lymphopenia, and Villitis

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

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