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
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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
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Improved outcome of children transplanted for high-risk leukemia by using a new strategy of cyclosporine-based GVHD prophylaxis
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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
Piette, C, Suciu, S, Clappier, E, Bertrand, Y, Drunat, S, Girard, S, Yakouben, K, Plat, G, Dastugue, N, Mazingue, F, Grardel, N, van Roy, N, Uyttebroeck, A, Costa, V, Minckes, O, Sirvent, N, Simon, P, Lutz, P, Ferster, A, Pluchart, C, Poirée, M, Freycon, C, Dresse, M-F, Millot, F, Chantrain, C, van der Werff ten Bosch, J, Norga, K, Gilotay, C, Rohrlich, P-S, Benoit, Y, Cavé, H
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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
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JAK2V617F-positive polycythemia vera and Philadelphia chromosome-positive chronic myeloid leukemia: one patient with two distinct myeloproliferative disorders
Cambier, N, Renneville, A, Cazaentre, T, Soenen, V, Cossement, C, Giraudier, S, Grardel, N, Laï, J-L, Rose, C, Preudhomme, C
Published in Leukemia (01.07.2008)
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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
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Detection of BCR-ABL transcripts in chronic myeloid leukemia (CML) using a 'real time' quantitative RT-PCR assay
PREUDHOMME, C, REVILLION, F, MERLAT, A, HORNEZ, L, ROUMIER, C, DUFLOS-GRARDEL, N, JOUET, J. P, COSSON, A, PEYRAT, J. P, FENAUX, P
Published in Leukemia (01.06.1999)
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Successful treatment of imatinib-resistant acute megakaryoblastic leukemia with e6a2 BCR ABL: use of dasatinib and reduced-conditioning stem-cell transplantation
Corm, S, Renneville, A, Rad-Quesnel, E, Grardel, N, Preudhomme, C, Quesnel, B
Published in Leukemia (01.11.2007)
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Hypereosinophilia with abnormal T cells, trisomy 7 and elevated TARC serum level
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Published in Haematologica (Roma) (01.07.2003)
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The KMT2A recombinome of acute leukemias in 2023
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High incidence of biallelic point mutations in the Runt domain of the AML1/PEBP2αB gene in Mo acute myeloid leukemia and in myeloid malignancies with acquired trisomy 21
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Detection of BCR-ABL transcripts in chronic myeloid leukemia (CML) using an in situ RT-PCR assay
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Improved outcome of children transplanted for high-risk leukemia by using a new strategy of cyclosporine-based GVHD prophylaxis
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Développement et validation du « fip-score » : un outil utile pour cibler la recherche de syndrome hyperéosinophilies clonaux associés à FIP1L1::PDGFRA
Stammler, R., Vallée, A., Rohmer, J., Couteau-Chardon, A., Duployez, N., Grardel, N., Kahn, J.E., Lefevre, G., Groh, M.
Published in La revue de medecine interne (01.12.2023)
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CD200/BTLA deletions in pediatric precursor B-cell acute lymphoblastic leukemia treated according to the EORTC-CLG 58951 protocol
Ghazavi, Farzaneh, Clappier, Emmanuelle, Lammens, Tim, Suciu, Stefan, Caye, Aurélie, Zegrari, Samira, Bakkus, Marleen, Grardel, Nathalie, Benoit, Yves, Bertrand, Yves, Minckes, Odile, Costa, Vitor, Ferster, Alina, Mazingue, Françoise, Plat, Geneviève, Plouvier, Emmanuel, Poirée, Marilyne, Uyttebroeck, Anne, van der Werff-Ten Bosch, Jutte, Yakouben, Karima, Helsmoortel, Hetty, Meul, Magali, Van Roy, Nadine, Philippé, Jan, Speleman, Frank, Cavé, Hélène, Van Vlierberghe, Pieter, De Moerloose, Barbara
Published in Haematologica (Roma) (01.10.2015)
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Identification de nouvelles anomalies clonales par séquençage haut débit dans les syndromes hyperéosinophiliques inexpliqués
Couteau-Chardon, A., Groh, M., Grardel, N., Lefèvre, G., Renneville, A., Preudhomme, C., Kahn, J.E.
Published in La revue de medecine interne (01.12.2018)
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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
Cavé, Hélène, Suciu, Stefan, Preudhomme, Claude, Poppe, Bruce, Robert, Alain, Uyttebroeck, Anne, Malet, Michèle, Boutard, Patrick, Benoit, Yves, Mauvieux, Laurent, Lutz, Patrick, Méchinaud, Françoise, Grardel, Nathalie, Mazingue, Françoise, Dupont, Madeleine, Margueritte, Geneviève, Pages, Marie-Pierre, Bertrand, Yves, Plouvier, Emmanuel, Brunie, Ghislaine, Bastard, Christian, Plantaz, Dominique, Velde, Isabel Vande, Hagemeijer, Anne, Speleman, Frank, Lessard, Michel, Otten, Jacques, Vilmer, Etienne, Dastugue, Nicole
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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
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Published in Haematologica (Roma) (01.08.2015)
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