Lista de obras -

A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency

artículo científico publicado en 2019

A cohort of French pediatric patients with primary immunodeficiencies: are patient preferences regarding replacement immunotherapy fulfilled in real-life conditions?

artículo científico publicado en 2017

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

artículo científico publicado en 2011

Acute lymphoblastic leukemia in the context of RASopathies

artículo científico publicado en 2016

Advanced stage nodular lymphocyte predominant Hodgkin lymphoma in children and adolescents: clinical characteristics and treatment outcome - a report from the SFCE & CCLG groups.

artículo científico publicado en 2017

Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey

artículo científico publicado en 2012

BRAF Mutation Correlates With High-Risk Langerhans Cell Histiocytosis and Increased Resistance to First-Line Therapy

artículo científico publicado en 2016

Benefits of rituximab as a second-line treatment for autoimmune haemolytic anaemia in children: a prospective French cohort study

artículo científico publicado en 2017

Brentuximab vedotin for paediatric relapsed or refractory Hodgkin's lymphoma and anaplastic large-cell lymphoma: a multicentre, open-label, phase 1/2 study

artículo científico publicado en 2018

Burden of Poor Health Conditions and Quality of Life in 656 Children with Primary Immunodeficiency

artículo científico publicado en 2017

Childhood Hodgkin's lymphoma, non-Hodgkin's lymphoma and factors related to the immune system: the Escale Study (SFCE).

artículo científico publicado en 2011

Childhood immune thrombocytopenia: A nationwide cohort study on condition management and outcomes

artículo científico publicado en 2016

Circulating cell-free BRAFV600E as a biomarker in children with Langerhans cell histiocytosis.

artículo científico publicado en 2017

Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome

artículo científico publicado en 2012

Cutaneous and Visceral Chronic Granulomatous Disease Triggered by a Rubella Virus Vaccine Strain in Children With Primary Immunodeficiencies.

artículo científico publicado en 2016

Donor-targeted serotherapy as a rescue therapy for steroid-resistant acute GVHD after HLA-mismatched kidney transplantation

artículo científico publicado en 2020

Early-onset hypogammaglobulinemia: A survey of 44 patients

artículo científico publicado en 2015

Evaluation of the efficiency of hydroxychloroquine in treating children with immune thrombocytopenia (ITP).

artículo científico publicado en 2017

Evans Syndrome in Children: Long-Term Outcome in a Prospective French National Observational Cohort

artículo científico publicado en 2015

Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIA

artículo científico publicado en 2020

Expression of PD-1/PD-L1 in children's classical Hodgkin lymphomas

scientific article published on 13 January 2019

Frequent and widespread vascular abnormalities in human signal transducer and activator of transcription 3 deficiency

artículo científico publicado en 2011

Functional classification of ATM variants in ataxia-telangiectasia patients

artículo científico publicado en 2019

Generalized Verrucosis Revealing a Life-Threatening and Unlabeled T-Cell Lymphopenia Associated With Autoimmune Hemolytic Anemia: A Case Report and Review of Literature

scientific article published on 19 September 2019

Immunopathological manifestations in Kabuki syndrome: a registry study of 177 individuals

artículo científico publicado en 2019

Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency

artículo científico publicado en 2017

Langerhans cell histiocytosis: therapeutic strategy and outcome in a 30-year nationwide cohort of 1478 patients under 18 years of age.

artículo científico publicado en 2016

Late effects after hematopoietic stem cell transplantation for β-thalassemia major: the French national experience.

artículo científico publicado en 2018

Long-term follow-up of children with risk organ-negative Langerhans cell histiocytosis after 2-chlorodeoxyadenosine treatment

scientific article published on 22 July 2020

Lung Involvement in Destombes-Rosai-Dorfman Disease: Clinical and Radiological Features and Response to the MEK Inhibitor Cobimetinib

scientific article published on 24 October 2019

Misdiagnosed CD19 deficiency leads to severe lung disease.

artículo científico publicado en 2014

Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype.

artículo científico publicado en 2011

Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome

artículo científico publicado en 2018

Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1).

artículo científico publicado en 2017

Neurological Involvement in Childhood Evans Syndrome

scientific article published on 22 January 2019

New insights into childhood autoimmune hemolytic anemia: a French national observational study of 265 children

artículo científico publicado en 2011

Outcome in children with relapsed acute myeloid leukemia after initial treatment with the French Leucemie Aique Myeloide Enfant (LAME) 89/91 protocol of the French Society of Pediatric Hematology and Immunology

scientific article published on 01 December 2003

Outcome of and prognostic factors for relapse in children and adolescents with mature B-cell lymphoma and leukemia treated in three consecutive prospective "Lymphomes Malins B" protocols. A Société Française des Cancers de l'Enfant study

artículo científico publicado en 2015

Outcome of relapse in children and adolescents with B-cell non-Hodgkin lymphoma and mature acute leukemia: A report from the French LMB study

scientific article published on 17 June 2019

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations

artículo científico publicado en 2018

Physical health conditions and quality of life in adults with primary immunodeficiency diagnosed during childhood: A French Reference Center for PIDs (CEREDIH) study

artículo científico publicado en 2016

Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemia

Reliable assessment of the incidence of childhood autoimmune hemolytic anemia

artículo científico publicado en 2017

Rituximab in the management of chronic immune thrombocytopenic purpura: what is its place?

artículo científico publicado en 2010

Rituximab therapy for childhood Evans syndrome

artículo científico publicado en 2007

Romiplostim in children with chronic immune thrombocytopenia (ITP): the French experience

artículo científico publicado en 2013

Second-line treatment trends and long-term outcomes of 392 children with chronic immune thrombocytopenic purpura: the French experience over the past 25 years

artículo científico publicado en 2020

The French paediatric cohort of Castleman disease: a retrospective report of 23 patients

scientific article published on 17 April 2020

Transient abnormal myelopoiesis (TAM) in a neonate without Down syndrome

scientific article published on 13 October 2014

Treatment with cyclosporin in auto-immune cytopenias in children: The experience from the French cohort OBS'CEREVANCE

artículo científico publicado en 2018

Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study

scientific article published on 12 September 2019

Lista de obras de

A 1-Year Prospective French Nationwide Study of Emergency Hospital Admissions in Children and Adults with Primary Immunodeficiency

A cohort of French pediatric patients with primary immunodeficiencies: are patient preferences regarding replacement immunotherapy fulfilled in real-life conditions?

A survey of 90 patients with autoimmune lymphoproliferative syndrome related to TNFRSF6 mutation

Acute lymphoblastic leukemia in the context of RASopathies

Advanced stage nodular lymphocyte predominant Hodgkin lymphoma in children and adolescents: clinical characteristics and treatment outcome - a report from the SFCE & CCLG groups.

Autosomal dominant STAT3 deficiency and hyper-IgE syndrome: molecular, cellular, and clinical features from a French national survey

BRAF Mutation Correlates With High-Risk Langerhans Cell Histiocytosis and Increased Resistance to First-Line Therapy

Benefits of rituximab as a second-line treatment for autoimmune haemolytic anaemia in children: a prospective French cohort study

Brentuximab vedotin for paediatric relapsed or refractory Hodgkin's lymphoma and anaplastic large-cell lymphoma: a multicentre, open-label, phase 1/2 study

Burden of Poor Health Conditions and Quality of Life in 656 Children with Primary Immunodeficiency

Childhood Hodgkin's lymphoma, non-Hodgkin's lymphoma and factors related to the immune system: the Escale Study (SFCE).

Childhood immune thrombocytopenia: A nationwide cohort study on condition management and outcomes

Circulating cell-free BRAFV600E as a biomarker in children with Langerhans cell histiocytosis.

Classification of and risk factors for hematologic complications in a French national cohort of 102 patients with Shwachman-Diamond syndrome

Cutaneous and Visceral Chronic Granulomatous Disease Triggered by a Rubella Virus Vaccine Strain in Children With Primary Immunodeficiencies.

Donor-targeted serotherapy as a rescue therapy for steroid-resistant acute GVHD after HLA-mismatched kidney transplantation

Early-onset hypogammaglobulinemia: A survey of 44 patients

Evaluation of the efficiency of hydroxychloroquine in treating children with immune thrombocytopenia (ITP).

Evans Syndrome in Children: Long-Term Outcome in a Prospective French National Observational Cohort

Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIA

Expression of PD-1/PD-L1 in children's classical Hodgkin lymphomas

Frequent and widespread vascular abnormalities in human signal transducer and activator of transcription 3 deficiency

Functional classification of ATM variants in ataxia-telangiectasia patients

Generalized Verrucosis Revealing a Life-Threatening and Unlabeled T-Cell Lymphopenia Associated With Autoimmune Hemolytic Anemia: A Case Report and Review of Literature

Immunopathological manifestations in Kabuki syndrome: a registry study of 177 individuals

Inherited GINS1 deficiency underlies growth retardation along with neutropenia and NK cell deficiency

Langerhans cell histiocytosis: therapeutic strategy and outcome in a 30-year nationwide cohort of 1478 patients under 18 years of age.

Late effects after hematopoietic stem cell transplantation for β-thalassemia major: the French national experience.

Long-term follow-up of children with risk organ-negative Langerhans cell histiocytosis after 2-chlorodeoxyadenosine treatment

Lung Involvement in Destombes-Rosai-Dorfman Disease: Clinical and Radiological Features and Response to the MEK Inhibitor Cobimetinib

Misdiagnosed CD19 deficiency leads to severe lung disease.

Morbidity and mortality from ataxia-telangiectasia are associated with ATM genotype.

Mutations in the SRP54 gene cause severe congenital neutropenia as well as Shwachman-Diamond-like syndrome

Mutations in the adaptor-binding domain and associated linker region of p110δ cause Activated PI3K-δ Syndrome 1 (APDS1).

Neurological Involvement in Childhood Evans Syndrome

New insights into childhood autoimmune hemolytic anemia: a French national observational study of 265 children

Outcome in children with relapsed acute myeloid leukemia after initial treatment with the French Leucemie Aique Myeloide Enfant (LAME) 89/91 protocol of the French Society of Pediatric Hematology and Immunology

Outcome of and prognostic factors for relapse in children and adolescents with mature B-cell lymphoma and leukemia treated in three consecutive prospective "Lymphomes Malins B" protocols. A Société Française des Cancers de l'Enfant study

Outcome of relapse in children and adolescents with B-cell non-Hodgkin lymphoma and mature acute leukemia: A report from the French LMB study

Pediatric-onset Evans syndrome: Heterogeneous presentation and high frequency of monogenic disorders including LRBA and CTLA4 mutations

Physical health conditions and quality of life in adults with primary immunodeficiency diagnosed during childhood: A French Reference Center for PIDs (CEREDIH) study

Protective effect of IgM against colonization of the respiratory tract by nontypeable Haemophilus influenzae in patients with hypogammaglobulinemia

Reliable assessment of the incidence of childhood autoimmune hemolytic anemia

Rituximab in the management of chronic immune thrombocytopenic purpura: what is its place?

Rituximab therapy for childhood Evans syndrome

Romiplostim in children with chronic immune thrombocytopenia (ITP): the French experience

Second-line treatment trends and long-term outcomes of 392 children with chronic immune thrombocytopenic purpura: the French experience over the past 25 years

The French paediatric cohort of Castleman disease: a retrospective report of 23 patients

Transient abnormal myelopoiesis (TAM) in a neonate without Down syndrome

Treatment with cyclosporin in auto-immune cytopenias in children: The experience from the French cohort OBS'CEREVANCE

Vemurafenib for Refractory Multisystem Langerhans Cell Histiocytosis in Children: An International Observational Study