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Therapeutic potential of ruxolitinib and ponatinib in patients with EPOR-rearranged Philadelphia chromosome-like acute lymphoblastic leukemia

Haematologica (Roma), 2021-10, Vol.106 (10), p.2763-2767

2021

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The cells are ambiguous, not the message

Blood, 2018-07, Vol.132 (3), p.239-240

Rohrlich, Pierre S.

2018

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Long‐term outcome evaluation of medium/high risk acute lymphoblastic leukaemia children treated with or without cranial radiotherapy in the EORTC 58832 randomized study

British journal of haematology, 2020-04, Vol.189 (2), p.351-362

2020

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Impaired Epstein-Barr virus–specific CD8+ T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family–positive B-cell targets

Blood, 2010-10, Vol.116 (17), p.3249-3257

2010

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Identifying Candidate Gene Drivers Associated with Relapse in Pediatric T-Cell Acute Lymphoblastic Leukemia Using a Gene Co-Expression Network Approach

Cancers, 2024-05, Vol.16 (9), p.1667

2024

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Malignancy and thrombotic microangiopathy or atypical haemolytic and uraemic syndrome?

British journal of haematology, 2014-09, Vol.166 (5), p.802-805

2014

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Different outcome of T cell acute lymphoblastic leukemia with translocation t(11;14) treated in two consecutive children leukemia group EORTC trials

Annals of hematology, 2016-01, Vol.95 (1), p.93-103

2016

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Loss of central and peripheral CD8+ T‐cell tolerance to HFE in mouse models of human familial hemochromatosis

European journal of immunology, 2012-04, Vol.42 (4), p.851-862

2012

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Successful mobilization and engraftment of PBSCs derived from donor cord blood cells after a previous allogeneic RIC single unrelated cord blood transplantation

Blood, 2011-07, Vol.118 (2), p.476-478

2011

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Direct Recognition by αβ Cytolytic T Cells of Hfe, a MHC Class Ib Molecule without Antigen-Presenting Function

Proceedings of the National Academy of Sciences - PNAS, 2005-09, Vol.102 (36), p.12855-12860

2005

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Ruxolitinib for Glucocorticoid-Refractory Acute Graft-versus-Host Disease

The New England journal of medicine, 2020-05, Vol.382 (19), p.1800-1810

2020

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Clinical picture and treatment of 2212 patients with common variable immunodeficiency

Journal of allergy and clinical immunology, 2014-07, Vol.134 (1), p.116-126.e11

2014

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Recurrent bacterial infections, but not fungal infections, characterise patients with ELANE‐related neutropenia: a French Severe Chronic Neutropenia Registry study

British journal of haematology, 2021-09, Vol.194 (5), p.908-920

2021

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Use of a lentiviral vector encoding a HCMV-Chimeric IE1-pp65 protein for epitope identification in HLA-Transgenic mice and for ex vivo stimulation and expansion of CD8 + cytotoxic T cells from human peripheral blood cells

Human immunology, 2004-05, Vol.65 (5), p.514-522

2004

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Total body irradiation + fludarabine compared to busulfan + fludarabine as “reduced-toxicity conditioning” for patients with acute myeloid leukemia treated with allogeneic hematopoietic cell transplantation in first complete remission: a study by the Acute Leukemia Working Party of the EBMT

Bone marrow transplantation (Basingstoke), 2021-02, Vol.56 (2), p.481-491

2021

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Transfusion requirements and complication rate in β‐thalassemia intermedia due to heterozygous β‐globin gene mutation and triplicated α‐globin genes

European journal of haematology, 2023-11, Vol.111 (5), p.742-747

2023

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Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): A multicentric French national observational cross‐sectional study based on the FranceCoag registry

Haemophilia : the official journal of the World Federation of Hemophilia, 2023-09, Vol.29 (5), p.1202-1218

2023

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Substance use disorder of equimolar oxygen-nitrous oxide mixture in French sickle-cell patients: results of the PHEDRE study

Orphanet journal of rare diseases, 2024-03, Vol.19 (1), p.124-124, Article 124

2024

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

Journal of allergy and clinical immunology, 2011-08, Vol.128 (2), p.382-389.e1

2011

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The French national registry of primary immunodeficiency diseases

Clinical immunology (Orlando, Fla.), 2010-05, Vol.135 (2), p.264-272

Anon

2010

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Loss of central and peripheral CD8 super(+) T-cell tolerance to HFE in mouse models of human familial hemochromatosis

European journal of immunology, 2012-04, Vol.42 (4), p.851-862

2012

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Loss of central and peripheral CD 8 + T ‐cell tolerance to HFE in mouse models of human familial hemochromatosis

European journal of immunology, 2012-04, Vol.42 (4), p.851-862

2012

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Direct recognition by alpha beta cytolytic T cells of Hfe, a MHC class Ib molecule without antigen-presenting function

Proceedings of the National Academy of Sciences - PNAS, 2005-09, Vol.102 (36), p.12855-12860

2005

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From The Cover: Direct recognition by alphabeta cytolytic T cells of Hfe, a MHC class Ib molecule without antigen-presenting function

Proceedings of the National Academy of Sciences - PNAS, 2005-09, Vol.102 (36), p.12855

2005

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Therapeutic potential of ruxolitinib and ponatinib in patients with EPOR-rearranged Philadelphia chromosome-like acute lymphoblastic leukemia

The cells are ambiguous, not the message

Long‐term outcome evaluation of medium/high risk acute lymphoblastic leukaemia children treated with or without cranial radiotherapy in the EORTC 58832 randomized study

Impaired Epstein-Barr virus–specific CD8+ T-cell function in X-linked lymphoproliferative disease is restricted to SLAM family–positive B-cell targets

Identifying Candidate Gene Drivers Associated with Relapse in Pediatric T-Cell Acute Lymphoblastic Leukemia Using a Gene Co-Expression Network Approach

Malignancy and thrombotic microangiopathy or atypical haemolytic and uraemic syndrome?

Different outcome of T cell acute lymphoblastic leukemia with translocation t(11;14) treated in two consecutive children leukemia group EORTC trials

Loss of central and peripheral CD8+ T‐cell tolerance to HFE in mouse models of human familial hemochromatosis

Successful mobilization and engraftment of PBSCs derived from donor cord blood cells after a previous allogeneic RIC single unrelated cord blood transplantation

Direct Recognition by αβ Cytolytic T Cells of Hfe, a MHC Class Ib Molecule without Antigen-Presenting Function

Ruxolitinib for Glucocorticoid-Refractory Acute Graft-versus-Host Disease

Heterozygous STAT1 gain-of-function mutations underlie an unexpectedly broad clinical phenotype

Clinical picture and treatment of 2212 patients with common variable immunodeficiency

Recurrent bacterial infections, but not fungal infections, characterise patients with ELANE‐related neutropenia: a French Severe Chronic Neutropenia Registry study

Use of a lentiviral vector encoding a HCMV-Chimeric IE1-pp65 protein for epitope identification in HLA-Transgenic mice and for ex vivo stimulation and expansion of CD8 + cytotoxic T cells from human peripheral blood cells

Total body irradiation + fludarabine compared to busulfan + fludarabine as “reduced-toxicity conditioning” for patients with acute myeloid leukemia treated with allogeneic hematopoietic cell transplantation in first complete remission: a study by the Acute Leukemia Working Party of the EBMT

Transfusion requirements and complication rate in β‐thalassemia intermedia due to heterozygous β‐globin gene mutation and triplicated α‐globin genes

Determinants of adherence and consequences of the transition from adolescence to adulthood among young people with severe haemophilia (TRANSHEMO): A multicentric French national observational cross‐sectional study based on the FranceCoag registry

Substance use disorder of equimolar oxygen-nitrous oxide mixture in French sickle-cell patients: results of the PHEDRE study

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

The French national registry of primary immunodeficiency diseases

Loss of central and peripheral CD8 super(+) T-cell tolerance to HFE in mouse models of human familial hemochromatosis

Loss of central and peripheral CD 8 + T ‐cell tolerance to HFE in mouse models of human familial hemochromatosis

Direct recognition by alpha beta cytolytic T cells of Hfe, a MHC class Ib molecule without antigen-presenting function

From The Cover: Direct recognition by alphabeta cytolytic T cells of Hfe, a MHC class Ib molecule without antigen-presenting function

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