Search Results - "Bardet, V"

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    Flow cytometric detection of dyserythropoiesis: a sensitive and powerful diagnostic tool for myelodysplastic syndromes by Mathis, S, Chapuis, N, Debord, C, Rouquette, A, Radford-Weiss, I, Park, S, Dreyfus, F, Lacombe, C, Béné, M C, Kosmider, O, Fontenay, M, Bardet, V

    Published in Leukemia (01-10-2013)
    “…Several groups have published flow cytometry scores useful for the diagnosis or prognosis of myelodysplastic syndromes (MDS), mainly based on the detection of…”
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    Journal Article
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    Perspectives on inhibiting mTOR as a future treatment strategy for hematological malignancies by Chapuis, N, Tamburini, J, Green, A S, Willems, L, Bardet, V, Park, S, Lacombe, C, Mayeux, P, Bouscary, D

    Published in Leukemia (01-10-2010)
    “…Mammalian target of rapamycin (mTOR) is a protein kinase implicated in the regulation of various cellular processes, including those required for tumor…”
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    PI-103, a dual inhibitor of Class IA phosphatidylinositide 3-kinase and mTOR, has antileukemic activity in AML by Park, S, Chapuis, N, Bardet, V, Tamburini, J, Gallay, N, Willems, L, Knight, Z A, Shokat, K M, Azar, N, Viguié, F, Ifrah, N, Dreyfus, F, Mayeux, P, Lacombe, C, Bouscary, D

    Published in Leukemia (01-09-2008)
    “…The phosphatidylinositol 3-kinase (PI3K)/Akt and mammalian target of rapamycin complex 1 (mTORC1) signaling pathways are frequently activated in acute…”
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    Role of the PI3K/AKT and mTOR signaling pathways in acute myeloid leukemia by PARK, Sophie, CHAPUIS, Nicolas, TAMBURINI, Jérôme, BARDET, Valérie, CORNILLET-LEFEBVRE, Pascale, WILLEMS, Lise, GREEN, Alexa, MAYEUX, Patrick, LACOMBE, Catherine, BOUSCARY, Didier

    Published in Haematologica (Roma) (01-05-2010)
    “…The PI3K/AKT and mTOR signaling pathways are activated in acute myeloid leukemia, including in the more immature leukemic populations. Constitutive PI3K…”
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    Schistocytes in disseminated intravascular coagulation by Lesesve, J.-F., Martin, M., Banasiak, C., André-Kerneïs, E., Bardet, V., Lusina, D., Kharbach, A., Geneviève, F., Lecompte, T.

    “…Summary Introduction The presence of schistocytes on the peripheral blood film during disseminated intravascular coagulation (DIC) remains controversial…”
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    Diagnostic and therapeutic considerations on inherited platelet disorders in neonates and children by Schlegel, N, Bardet, V, Kenet, G, Muntean, W, Zieger, B, Nowak-Göttl, U

    Published in Klinische Padiatrie (01-05-2010)
    “…Inherited disorders of platelets constitute a group of rare diseases that give rise to bleeding syndromes of variety severity, with more severe cases being…”
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    The MYH9 syndrome: report of a new case with a new mutation of the MYH9 gene by Schleinitz, N, Favier, R, Mazodier, K, Difeo, A, Ebbo, M, Veit, V, Berda-Haddad, Y, Bernit, E, Heudier, P, Kaplanski, G, Camoin, L, Bardet, V, Harle, J-R

    Published in La revue de medecine interne (01-10-2006)
    “…Familial macrothrombocytopenias are a group of rare autosomal dominant platelet disorders including many syndromes in particular the May-Hegglin anomaly. They…”
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    Mapping of chromosome 20 for loss of heterozygosity in childhood ALL reveals a 1000-kb deletion in one patient by COUQUE, N, CHAMBON-PAUTAS, C, CAVE, H, BARDET, V, DUVAL, M, VILMER, E, GRANDCHAMP, B

    Published in Leukemia (01-12-1999)
    “…The long arm of chromosome 20 displays recurrent loss of heterozygosity (LOH) for microsatellite markers in blast cells from children with acute lymphoblastic…”
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    Le syndrome MYH9 : à propos d'une nouvelle observation et de la mise en évidence d'une nouvelle mutation du gène MYH9 by Schleinitz, N., Favier, R., Mazodier, K., Difeo, A., Ebbo, M., Veit, V., Berda-Haddad, Y., Bernit, E., Heudier, P., Kaplanski, G., Camoin, L., Bardet, V., Harle, J.-R.

    Published in La revue de medecine interne (01-10-2006)
    “…Le groupe des thrombopénies constitutionnelles avec macroplaquettes associées à des inclusions leucocytaires comprend plusieurs syndromes dont le syndrome de…”
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