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  1. Article

    Open Access

    The KMT2A recombinome of acute leukemias in 2023

    Chromosomal rearrangements of the human KMT2A/MLL gene are associated with de novo as well as therapy-induced infant, pediatric, and adult acute leukemias. Here, we present the data obtained from 3401 acute leuke...

    C. Meyer, P. Larghero, B. Almeida Lopes, T. Burmeister, D. Gröger, R. Sutton in Leukemia (2023)

  2. Article

    Correction: Standardisation and consensus guidelines for minimal residual disease assessment in Philadelphia-positive acute lymphoblastic leukemia (Ph+ALL) by real-time quantitative reverse transcriptase PCR of e1a2 BCR-ABL1

    An amendment to this paper has been published and can be accessed via a link at the top of the paper.

    H. Pfeifer, G. Cazzaniga, V. H. J. van der Velden, J. M. Cayuela, B. Schäfer in Leukemia (2020)

  3. No Access

    Article

    Standardisation and consensus guidelines for minimal residual disease assessment in Philadelphia-positive acute lymphoblastic leukemia (Ph + ALL) by real-time quantitative reverse transcriptase PCR of e1a2 BCR-ABL1

    Minimal residual disease (MRD) is a powerful prognostic factor in acute lymphoblastic leukemia (ALL) and is used for patient stratification and treatment decisions, but its precise role in Philadelphia chromos...

    H. Pfeifer, G. Cazzaniga, V. H. J. van der Velden, J. M. Cayuela, B. Schäfer in Leukemia (2019)

  4. Article

    Open Access

    The MLL recombinome of acute leukemias in 2017

    Chromosomal rearrangements of the human MLL/KMT2A gene are associated with infant, pediatric, adult and therapy-induced acute leukemias. Here we present the data obtained from 2345 acute leukemia patients. Genomi...

    C Meyer, T Burmeister, D Gröger, G Tsaur, L Fechina, A Renneville, R Sutton in Leukemia (2018)

  5. No Access

    Article

    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

    C Piette, S Suciu, E Clappier, Y Bertrand, S Drunat, S Girard, K Yakouben in Leukemia (2018)

  6. Article

    Open Access

    Genomic and transcriptional landscape of P2RY8-CRLF2-positive childhood acute lymphoblastic leukemia

    Children with P2RY8-CRLF2-positive acute lymphoblastic leukemia have an increased relapse risk. Their mutational and transcriptional landscape, as well as the respective patterns at relapse remain largely elusive...

    C Vesely, C Frech, C Eckert, G Cario, A Mecklenbräuker, U zur Stadt, K Nebral in Leukemia (2017)

  7. No Access

    Article

    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

    The added value of IKZF1 gene deletion (IKZF1del) as a stratifying criterion in B-cell precursor acute lymphoblastic leukemia (BCP-ALL) is still debated. We performed a comprehensive analysis of the impact of IKZ...

    E Clappier, N Grardel, M Bakkus, J Rapion, B De Moerloose, P Kastner, A Caye in Leukemia (2015)

  8. No Access

    Article

    Refinement of IKZF1 status in pediatric Philadelphia-positive acute lymphoblastic leukemia

    T Lana, P de Lorenzo, S Bresolin, I Bronzini, M L den Boer, H Cavé, E Froňková in Leukemia (2015)

  9. No Access

    Article

    An intragenic ERG deletion is a marker of an oncogenic subtype of B-cell precursor acute lymphoblastic leukemia with a favorable outcome despite frequent IKZF1 deletions

    Oncogenic subtypes in childhood B-cell precursor acute lymphoblastic leukemia (BCP-ALL) are used for risk stratification. However, a significant number of BCP-ALL patients are still genetically unassigned. Usi...

    E Clappier, M-F Auclerc, J Rapion, M Bakkus, A Caye, A Khemiri, C Giroux in Leukemia (2014)

  10. No Access

    Article

    In hematopoietic cells with a germline mutation of CBL, loss of heterozygosity is not a signature of juvenile myelo-monocytic leukemia

    M Strullu, A Caye, B Cassinat, O Fenneteau, F Touzot, T Blauwblomme in Leukemia (2013)

  11. Article

    Open Access

    The MLL recombinome of acute leukemias in 2013

    Chromosomal rearrangements of the human MLL (mixed lineage leukemia) gene are associated with high-risk infant, pediatric, adult and therapy-induced acute leukemias. We used long-distance inverse-polymerase chain...

    C Meyer, J Hofmann, T Burmeister, D Gröger, T S Park, M Emerenciano in Leukemia (2013)

  12. No Access

    Article

    Flow cytometry and IG/TCR quantitative PCR for minimal residual disease quantitation in acute lymphoblastic leukemia: a French multicenter prospective study on behalf of the FRALLE, EORTC and GRAALL

    Minimal residual disease (MRD) quantification is widely used for therapeutic stratification in pediatric acute lymphoblastic leukemia (ALL). A robust, reproducible, sensitivity of at least 0.01% has been achie...

    R Garand, K Beldjord, H Cavé, C Fossat, I Arnoux, V Asnafi, Y Bertrand in Leukemia (2013)

  13. No Access

    Article

    The EuroChimerism concept for a standardized approach to chimerism analysis after allogeneic stem cell transplantation

    Hematopoietic stem cell transplantation is becoming an increasingly important approach to treatment of different malignant and non-malignant disorders. There is thus growing demand for diagnostic assays permit...

    T Lion, F Watzinger, S Preuner, H Kreyenberg, M Tilanus, R de Weger, J van Loon in Leukemia (2012)

  14. Article

    Open Access

    Identification of germline susceptibility loci in ETV6-RUNX1-rearranged childhood acute lymphoblastic leukemia

    Acute lymphoblastic leukemia (ALL) is a malignant disease of the white blood cells. The etiology of ALL is believed to be multifactorial and likely to involve an interplay of environmental and genetic variable...

    E Ellinghaus, M Stanulla, G Richter, D Ellinghaus, G te Kronnie, G Cario in Leukemia (2012)

  15. No Access

    Article

    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

    Risk-adjusted treatment stratification in T-cell acute lymphoblastic leukemias (T-ALLs) is currently based only on early response to chemotherapy. We investigated the prognostic implication of hyperactivation ...

    E Clappier, S Collette, N Grardel, S Girard, L Suarez, G Brunie, S Kaltenbach in Leukemia (2010)

  16. No Access

    Article

    A new recurrent translocation t(11;14)(q24;q32) involving IGH@ and miR-125b-1 in B-cell progenitor acute lymphoblastic leukemia

    E Chapiro, L J Russell, S Struski, H Cavé, I Radford-Weiss, V D Valle in Leukemia (2010)

  17. No Access

    Article

    Activating mutation in the TSLPR gene in B-cell precursor lymphoblastic leukemia

    E Chapiro, L Russell, E Lainey, S Kaltenbach, C Ragu, V Della-Valle, K Hanssens in Leukemia (2010)

  18. No Access

    Article

    Standardized MRD quantification in European ALL trials: Proceedings of the Second International Symposium on MRD assessment in Kiel, Germany, 18–20 September 2008

    Assessment of minimal residual disease (MRD) has acquired a prominent position in European treatment protocols for patients with acute lymphoblastic leukemia (ALL), on the basis of its high prognostic value fo...

    M Brüggemann, A Schrauder, T Raff, H Pfeifer, M Dworzak, O G Ottmann, V Asnafi in Leukemia (2010)

  19. No Access

    Article

    Wilms tumor 1 (WT1) gene mutations in pediatric T-cell malignancies

    A Renneville, S Kaltenbach, E Clappier, S Collette, J-B Micol, B Nelken in Leukemia (2010)

  20. No Access

    Article

    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

    Adult and child B-cell progenitor acute lymphoblastic leukemia (BCP-ALL) differ in terms of incidence and prognosis. These disparities are mainly due to the molecular abnormalities associated with these two cl...

    J Familiades, M Bousquet, M Lafage-Pochitaloff, M-C Béné, K Beldjord, J De Vos in Leukemia (2009)

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