Lessard M - Search Results

1

A new translocation t(9;11)(q34;p15) fuses NUP98 to a novel homeobox partner gene, PRRX2, in a therapy-related acute myeloid leukemia.

Gervais C, Mauvieux L, Perrusson N, Hélias C, Struski S, Leymarie V, Lioure B, Lessard M. Gervais C, et al. Among authors: lessard m. Leukemia. 2005 Jan;19(1):145-8. doi: 10.1038/sj.leu.2403565. Leukemia. 2005. PMID: 15496970 No abstract available.

2

Loss of the NPM1 gene in myeloid disorders with chromosome 5 rearrangements.

Berger R, Busson M, Baranger L, Hélias C, Lessard M, Dastugue N, Speleman F. Berger R, et al. Among authors: lessard m. Leukemia. 2006 Feb;20(2):319-21. doi: 10.1038/sj.leu.2404063. Leukemia. 2006. PMID: 16341035

3

Acute myeloid leukaemia with 8p11 (MYST3) rearrangement: an integrated cytologic, cytogenetic and molecular study by the groupe francophone de cytogénétique hématologique.

Gervais C, Murati A, Helias C, Struski S, Eischen A, Lippert E, Tigaud I, Penther D, Bastard C, Mugneret F, Poppe B, Speleman F, Talmant P, VanDen Akker J, Baranger L, Barin C, Luquet I, Nadal N, Nguyen-Khac F, Maarek O, Herens C, Sainty D, Flandrin G, Birnbaum D, Mozziconacci MJ, Lessard M; Groupe Francophone de Cytogénétique Hématologique. Gervais C, et al. Among authors: lessard m. Leukemia. 2008 Aug;22(8):1567-75. doi: 10.1038/leu.2008.128. Epub 2008 Jun 5. Leukemia. 2008. PMID: 18528428

4

Translocation t(5;14)(q35;q32) in three cases of childhood T cell acute lymphoblastic leukemia: a new recurring and cryptic abnormality.

Hélias C, Leymarie V, Entz-Werle N, Falkenrodt A, Eyer D, Costa JA, Cherif D, Lutz P, Lessard M. Hélias C, et al. Among authors: lessard m. Leukemia. 2002 Jan;16(1):7-12. doi: 10.1038/sj.leu.2402347. Leukemia. 2002. PMID: 11840257

5

High incidence of Hox11L2 expression in children with T-ALL.

Mauvieux L, Leymarie V, Helias C, Perrusson N, Falkenrodt A, Lioure B, Lutz P, Lessard M. Mauvieux L, et al. Among authors: lessard m. Leukemia. 2002 Dec;16(12):2417-22. doi: 10.1038/sj.leu.2402709. Leukemia. 2002. PMID: 12454747

6

ETV6 (TEL) gene amplification in a myelodysplastic syndrome with excess of blasts.

Mauvieux L, Helias C, Perrusson N, Lioure B, Sorel N, Brizard F, Lessard M. Mauvieux L, et al. Among authors: lessard m. Leukemia. 2004 Aug;18(8):1436-8. doi: 10.1038/sj.leu.2403403. Leukemia. 2004. PMID: 15175627 No abstract available.

7

Report of 34 patients with clonal chromosomal abnormalities in Philadelphia-negative cells during imatinib treatment of Philadelphia-positive chronic myeloid leukemia.

Terre C, Eclache V, Rousselot P, Imbert M, Charrin C, Gervais C, Mozziconacci MJ, Maarek O, Mossafa H, Auger N, Dastugue N, Talmant P, Van den Akker J, Leonard C, N'Guyen Khac F, Mugneret F, Viguié F, Lafage-Pochitaloff M, Bastie JN, Roux GL, Nicolini F, Maloisel F, Vey N, Laurent G, Recher C, Vigier M, Yacouben Y, Giraudier S, Vernant JP, Salles B, Roussi J, Castaigne S, Leymarie V, Flandrin G, Lessard M; France Intergroupe pour la Leucemie Myeloide Chronique. Terre C, et al. Among authors: lessard m. Leukemia. 2004 Aug;18(8):1340-6. doi: 10.1038/sj.leu.2403399. Leukemia. 2004. PMID: 15190256

8

Polycythemia vera transforming to acute myeloid leukemia and complex abnormalities including 9p homogeneously staining region with amplification of MLLT3, JMJD2C, JAK2, and SMARCA2.

Hélias C, Struski S, Gervais C, Leymarie V, Mauvieux L, Herbrecht R, Lessard M. Hélias C, et al. Among authors: lessard m. Cancer Genet Cytogenet. 2008 Jan 1;180(1):51-5. doi: 10.1016/j.cancergencyto.2007.09.010. Cancer Genet Cytogenet. 2008. PMID: 18068534

9

Cytogenetic studies of a series of 43 consecutive secondary myelodysplastic syndromes/acute myeloid leukemias: conventional cytogenetics, FISH, and multiplex FISH.

Shali W, Hélias C, Fohrer C, Struski S, Gervais C, Falkenrodt A, Leymarie V, Lioure B, Raby P, Herbrecht R, Lessard M. Shali W, et al. Among authors: lessard m. Cancer Genet Cytogenet. 2006 Jul 15;168(2):133-45. doi: 10.1016/j.cancergencyto.2006.02.006. Cancer Genet Cytogenet. 2006. PMID: 16843103

10

Clinical, cytogenetic and molecular characteristics of 14 T-ALL patients carrying the TCRbeta-HOXA rearrangement: a study of the Groupe Francophone de Cytogénétique Hématologique.

Cauwelier B, Cavé H, Gervais C, Lessard M, Barin C, Perot C, Van den Akker J, Mugneret F, Charrin C, Pagès MP, Grégoire MJ, Jonveaux P, Lafage-Pochitaloff M, Mozzicconacci MJ, Terré C, Luquet I, Cornillet-Lefebvre P, Laurence B, Plessis G, Lefebvre C, Leroux D, Antoine-Poirel H, Graux C, Mauvieux L, Heimann P, Chalas C, Clappier E, Verhasselt B, Benoit Y, Moerloose BD, Poppe B, Van Roy N, Keersmaecker KD, Cools J, Sigaux F, Soulier J, Hagemeijer A, Paepe AD, Dastugue N, Berger R, Speleman F. Cauwelier B, et al. Among authors: lessard m. Leukemia. 2007 Jan;21(1):121-8. doi: 10.1038/sj.leu.2404410. Epub 2006 Oct 12. Leukemia. 2007. PMID: 17039236

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