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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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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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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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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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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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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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Alloimmunization and hyperhemolysis in sickle cell disease

Hematology, 2023-12, Vol.2023 (1), p.653

2023

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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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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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Iron-responsive degradation of iron-regulatory protein 1 does not require the Fe-S cluster

The EMBO journal, 2006-02, Vol.25 (3), p.544-553

2006

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Sexual health of French adolescents with sickle cell disease

The European journal of contraception & reproductive health care, 2020-07, Vol.25 (4), p.293-298

2020

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In vivo treatment with CPT-11 leads to differentiation of neuroblastoma xenografts and topoisomerase I alterations

Cancer research (Chicago, Ill.), 2004-05, Vol.64 (9), p.3223-3229

2004

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G6PD deficiency and absence of α-thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia

European journal of haematology, 2016-04, Vol.96 (4), p.404-408

2016

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Spontaneous abrogation of the G₂DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients

The Journal of clinical investigation, 2011-01, Vol.121 (1), p.184-194

2011

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In vivo sequencing of camptothecin-induced topoisomerase I cleavage sites in human colon carcinoma cells

Nucleic acids research, 1997-10, Vol.25 (20), p.4111

1997

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Thalassemia alpha

La revue du praticien, 2014-10, Vol.64 (8), p.1138

Pondarré, Corinne

2014

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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

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

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

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

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

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)

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

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

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

Alloimmunization and hyperhemolysis in sickle cell disease

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

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

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

Iron-responsive degradation of iron-regulatory protein 1 does not require the Fe-S cluster

Sexual health of French adolescents with sickle cell disease

In vivo treatment with CPT-11 leads to differentiation of neuroblastoma xenografts and topoisomerase I alterations

G6PD deficiency and absence of α-thalassemia increase the risk for cerebral vasculopathy in children with sickle cell anemia

Spontaneous abrogation of the G₂DNA damage checkpoint has clinical benefits but promotes leukemogenesis in Fanconi anemia patients

In vivo sequencing of camptothecin-induced topoisomerase I cleavage sites in human colon carcinoma cells

Thalassemia alpha

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