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P-FSM and M-FSM Piezoelectric and Magnetic Fast Steering Mirrors

Proceedings of the 7th International Symposium of Space Optical Instruments and Applications, 2023, Vol.295, p.315-331

2023

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IKZF1 deletion is an independent prognostic marker in childhood B-cell precursor acute lymphoblastic leukemia, and distinguishes patients benefiting from pulses during maintenance therapy: results of the EORTC Children's Leukemia Group study 58951

Leukemia, 2015-11, Vol.29 (11), p.2154-2161

2015

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NOTCH1 and FBXW7 mutations have a favorable impact on early response to treatment, but not on outcome, in children with T-cell acute lymphoblastic leukemia (T-ALL) treated on EORTC trials 58881 and 58951

Leukemia, 2010-12, Vol.24 (12), p.2023-2031

2010

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The KMT2A recombinome of acute leukemias in 2023

Leukemia, 2023-05, Vol.37 (5), p.988-1005

2023

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PAX5 mutations occur frequently in adult B-cell progenitor acute lymphoblastic leukemia and PAX5 haploinsufficiency is associated with BCR-ABL1 and TCF3-PBX1 fusion genes: a GRAALL study

Leukemia, 2009-11, Vol.23 (11), p.1989-1998

2009

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Differential impact of drugs on the outcome of ETV6-RUNX1 positive childhood B-cell precursor acute lymphoblastic leukaemia: results of the EORTC CLG 58881 and 58951 trials

Leukemia, 2018-01, Vol.32 (1), p.244-248

2018

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CD3-CD4+ lymphoid variant of hypereosinophilic syndrome: nodal and extranodal histopathological and immunophenotypic features of a peripheral indolent clonal T-cell lymphoproliferative disorder

Haematologica (Roma), 2015-08, Vol.100 (8), p.1086

2015

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Clinical value of pre‐transplant minimal residual disease in childhood lymphoblastic leukaemia: the results of the French minimal residual disease‐guided protocol

British journal of haematology, 2014-05, Vol.165 (3), p.392-401

2014

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L’infection a SARS-CoV-2 pourrait-elle induire des rhumatismes inflammatoires chroniques ? Une enquête nationale française

Revue du rhumatisme (Ed. française : 1993), 2021-12, Vol.88, p.A45-A45

2021

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Subluxing arthropathy: an unusual manifestation of the antisynthetase syndrome

Annals of the rheumatic diseases, 2009-01, Vol.68 (1), p.152-153

2009

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Prognostic significance of FLT3 internal tandem repeat in patients with de novo acute myeloid leukemia treated with reinforced courses of chemotherapy

Leukemia, 2002-09, Vol.16 (9), p.1699-1704

2002

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Prognostic value of real-time quantitative PCR (RQ-PCR) in AML with t(8;21)

Leukemia, 2005-03, Vol.19 (3), p.367-372

2005

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Clinical value of pre‐transplant minimal residual disease in childhood lymphoblastic leukaemia: the results of the F rench minimal residual disease‐guided protocol

British journal of haematology, 2014-05, Vol.165 (3), p.392-401

2014

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Subluxing arthropathy : an unusual manifestation of the antisynthetase syndrome

Annals of the rheumatic diseases, 2009, Vol.68 (1), p.154-155

2009

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Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3)

Genes chromosomes & cancer, 2005-10, Vol.44 (2), p.154-160

2005

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Unlike AML1, CBFβ gene is not deregulated by point mutations in acute myeloid leukemia and in myelodysplastic syndromes

Blood, 2002-05, Vol.99 (10), p.3848-3850

2002

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Prognostic value of real-time quantitative PCR

Leukemia, 2005-03, Vol.19 (3), p.367

2005

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Osteomesopyknosis: Report of a new case with bone histology

Bone (New York, N.Y.), 1994, Vol.15 (1), p.81-83

1994

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TPA stimulation culture for improved detection of t(11;14)(q13;q32) in mantle cell lymphoma

Annales de génétique, 2002-07, Vol.45 (3), p.165-168

2002

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P-FSM and M-FSM Piezoelectric and Magnetic Fast Steering Mirrors

IKZF1 deletion is an independent prognostic marker in childhood B-cell precursor acute lymphoblastic leukemia, and distinguishes patients benefiting from pulses during maintenance therapy: results of the EORTC Children's Leukemia Group study 58951

NOTCH1 and FBXW7 mutations have a favorable impact on early response to treatment, but not on outcome, in children with T-cell acute lymphoblastic leukemia (T-ALL) treated on EORTC trials 58881 and 58951

The KMT2A recombinome of acute leukemias in 2023

CD200/BTLA deletions in pediatric precursor B-cell acute lymphoblastic leukemia treated according to the EORTC-CLG 58951 protocol

PAX5 mutations occur frequently in adult B-cell progenitor acute lymphoblastic leukemia and PAX5 haploinsufficiency is associated with BCR-ABL1 and TCF3-PBX1 fusion genes: a GRAALL study

Differential impact of drugs on the outcome of ETV6-RUNX1 positive childhood B-cell precursor acute lymphoblastic leukaemia: results of the EORTC CLG 58881 and 58951 trials

CD3-CD4+ lymphoid variant of hypereosinophilic syndrome: nodal and extranodal histopathological and immunophenotypic features of a peripheral indolent clonal T-cell lymphoproliferative disorder

Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951

Clinical value of pre‐transplant minimal residual disease in childhood lymphoblastic leukaemia: the results of the French minimal residual disease‐guided protocol

L’infection a SARS-CoV-2 pourrait-elle induire des rhumatismes inflammatoires chroniques ? Une enquête nationale française

Subluxing arthropathy: an unusual manifestation of the antisynthetase syndrome

Prognostic significance of FLT3 internal tandem repeat in patients with de novo acute myeloid leukemia treated with reinforced courses of chemotherapy

Prognostic value of real-time quantitative PCR (RQ-PCR) in AML with t(8;21)

Clinical value of pre‐transplant minimal residual disease in childhood lymphoblastic leukaemia: the results of the F rench minimal residual disease‐guided protocol

Subluxing arthropathy : an unusual manifestation of the antisynthetase syndrome

Familial occurrence of thymoma and autoimmune diseases with the constitutional translocation t(14;20)(q24.1;p12.3)

NOTCH1 and FBXW7 mutations have a favorable impact on early response to treatment, but not on outcome, in children with T-cell acute lymphoblastic leukemia (T-ALL) treated on EORTC trials 58881 and 58951 : Prognostic effects of NOTCH1 activing mutations in pediatrics T-ALL is treatment dependent

Unlike AML1, CBFβ gene is not deregulated by point mutations in acute myeloid leukemia and in myelodysplastic syndromes

Prognostic value of real-time quantitative PCR

Osteomesopyknosis: Report of a new case with bone histology

TPA stimulation culture for improved detection of t(11;14)(q13;q32) in mantle cell lymphoma

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