Search Results - "Bouriche, Lakhdar"

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  1. 1
    Detection of dysplasia in peripheral blood: Proposal of an algorithm to detect myelodysplastic syndromes and chronic myelomonocytic leukemias on a high‐speed technical platform using the Sysmex XN™ analyser

    Detection of dysplasia in peripheral blood: Proposal of an algorithm to detect myelodysplastic syndromes and chronic myelomonocytic leukemias on a high‐speed technical platform using the Sysmex XN™ analyser by Bouriche, Lakhdar, Fuster, Léa, Laurent, Hugo, Soler, Christophe, Benhabib, Sofiane

    “…Introduction Chronic Myelomonocytic Leukemia (CMML) and Myelodysplastic Syndromes (MDS) are increasingly represented in the general population. We propose a…”
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  2. 2
    Detection of Minimal Residual Disease in B Cell Acute Lymphoblastic Leukemia Using an Eight‐Color Tube with Dried Antibody Reagents

    Detection of Minimal Residual Disease in B Cell Acute Lymphoblastic Leukemia Using an Eight‐Color Tube with Dried Antibody Reagents by Bouriche, Lakhdar, Bernot, Denis, Nivaggioni, Vanessa, Arnoux, Isabelle, Loosveld, Marie

    Published in Cytometry. Part B, Clinical cytometry (01-03-2019)
    “…Background Flow cytometry is a powerful tool for the detection of minimal residual disease (MRD) of B cell precursor acute lymphoblastic leukemia (BCP‐ALL)…”
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  3. 3
    Lineage switch from B acute lymphoblastic leukemia to acute monocytic leukemia with persistent t(4;11)(q21;q23) and cytogenetic evolution under CD19-targeted therapy

    Lineage switch from B acute lymphoblastic leukemia to acute monocytic leukemia with persistent t(4;11)(q21;q23) and cytogenetic evolution under CD19-targeted therapy by Balducci, Estelle, Nivaggioni, Vanessa, Boudjarane, John, Bouriche, Lakhdar, Rahal, Ilhem, Bernot, Denis, Alazard, Emilie, Duployez, Nicolas, Grardel, Nathalie, Arnoux, Isabelle, Lafage-Pochitaloff, Marina, Michel, Gérard, Nadel, Bertrand, Loosveld, Marie

    Published in Annals of hematology (01-09-2017)
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  4. 4
    Use of Sysmex XN‐10 red blood cell parameters for screening of hereditary red blood cell diseases and iron deficiency anaemia

    Use of Sysmex XN‐10 red blood cell parameters for screening of hereditary red blood cell diseases and iron deficiency anaemia by Nivaggioni, Vanessa, Bouriche, Lakhdar, Coito, Sylvie, Le Floch, Anne‐Sophie, Ibrahim‐Kosta, Manal, Leonnet, Caroline, Arnoux, Isabelle, Loosveld, Marie

    “…Introduction In daily practice in haematology laboratories, red blood cell (RBC) abnormalities are frequent and their management is a real challenge. The aim…”
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  5. 5
    Lineage switch from B acute lymphoblastic leukemia to acute monocytic leukemia with persistent t(4;11)(q21;q23) and cytogenetic evolution under CD19-targeted therapy

    Lineage switch from B acute lymphoblastic leukemia to acute monocytic leukemia with persistent t(4;11)(q21;q23) and cytogenetic evolution under CD19-targeted therapy by Balducci, Estelle, Nivaggioni, Vanessa, Boudjarane, John, Bouriche, Lakhdar, Rahal, Ilhem, Bernot, Denis, Alazard, Emilie, Duployez, Nicolas, Grardel, Nathalie, Arnoux, Isabelle, Lafage-Pochitaloff, Marina, Michel, Gérard, Nadel, Bertrand, Loosveld, Marie

    Published in Annals of hematology (01-09-2017)
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