Preudhomme C - Search Results

1

Prognostic impact of RUNX1 mutations and deletions in pediatric acute myeloid leukemia: results from the French ELAM02 study group.

Lew-Derivry L, Marceau-Renaut A, Fenwarth L, Cuccuini W, Ballerini P, Ferreboeuf M, Guilmatre A, Petit A, Gandemer V, Rialland F, Schneider P, Michel G, Bertrand Y, Baruchel A, Preudhomme C, Leverger G, Lapillonne H. Lew-Derivry L, et al. Among authors: preudhomme c. Leukemia. 2023 Aug;37(8):1723-1726. doi: 10.1038/s41375-023-01931-y. Epub 2023 Jun 16. Leukemia. 2023. PMID: 37328541 Free PMC article. No abstract available.

2

Mutations of the p53 gene in B-cell lymphoblastic acute leukemia: a report on 60 cases.

Fenaux P, Jonveaux P, Quiquandon I, Preudhomme C, Lai JL, Vanrumbeke M, Loucheux-Lefebvre MH, Bauters F, Berger R, Kerckaert JP. Fenaux P, et al. Among authors: preudhomme c. Leukemia. 1992 Jan;6(1):42-6. Leukemia. 1992. PMID: 1736012

3

Myelodysplastic syndromes and acute myeloid leukemia with 17p deletion. An entity characterized by specific dysgranulopoïesis and a high incidence of P53 mutations.

Lai JL, Preudhomme C, Zandecki M, Flactif M, Vanrumbeke M, Lepelley P, Wattel E, Fenaux P. Lai JL, et al. Among authors: preudhomme c. Leukemia. 1995 Mar;9(3):370-81. Leukemia. 1995. PMID: 7885035

4

Detection of serum anti p53 antibodies and their correlation with p53 mutations in myelodysplastic syndromes and acute myeloid leukemia.

Preudhomme C, Lubin R, Lepelley P, Vanrumbeke M, Fenaux P. Preudhomme C, et al. Leukemia. 1994 Sep;8(9):1589-91. Leukemia. 1994. PMID: 8090036

5

Absence of rearrangement of the neurofibromatosis 1 (NF1) gene in myelodysplastic syndromes and acute myeloid leukemia.

Quesnel B, Preudhomme C, Vanrumbeke M, Vachee A, Lai JL, Fenaux P. Quesnel B, et al. Among authors: preudhomme c. Leukemia. 1994 May;8(5):878-80. Leukemia. 1994. PMID: 8182944

6

Detection of BCR-ABL transcripts in chronic myeloid leukemia (CML) using an in situ RT-PCR assay.

Preudhomme C, Chams-Eddine L, Roumier C, Duflos-Grardel N, Denis C, Cosson A, Fenaux P. Preudhomme C, et al. Leukemia. 1999 May;13(5):818-23. doi: 10.1038/sj.leu.2401393. Leukemia. 1999. PMID: 10374889

7

Amplification of AML1 gene is present in childhood acute lymphoblastic leukemia but not in adult, and is not associated with AML1 gene mutation.

Penther D, Preudhomme C, Talmant P, Roumier C, Godon A, Méchinaud F, Milpied N, Bataille R, Avet-Loiseau H. Penther D, et al. Among authors: preudhomme c. Leukemia. 2002 Jun;16(6):1131-4. doi: 10.1038/sj.leu.2402479. Leukemia. 2002. PMID: 12040444

8

Prognostic significance of FLT3 internal tandem repeat in patients with de novo acute myeloid leukemia treated with reinforced courses of chemotherapy.

Boissel N, Cayuela JM, Preudhomme C, Thomas X, Grardel N, Fund X, Tigaud I, Raffoux E, Rousselot P, Sigaux F, Degos L, Castaigne S, Fenaux P, Dombret H. Boissel N, et al. Among authors: preudhomme c. Leukemia. 2002 Sep;16(9):1699-704. doi: 10.1038/sj.leu.2402622. Leukemia. 2002. PMID: 12200684 Clinical Trial.

9

Cooperation of activating Ras/rtk signal transduction pathway mutations and inactivating myeloid differentiation gene mutations in M0 AML: a study of 45 patients.

Roumier C, Lejeune-Dumoulin S, Renneville A, Goethgeluck AS, Philippe N, Fenaux P, Preudhomme C. Roumier C, et al. Among authors: preudhomme c. Leukemia. 2006 Mar;20(3):433-6. doi: 10.1038/sj.leu.2404097. Leukemia. 2006. PMID: 16424869

10

High WT1 expression after induction therapy predicts high risk of relapse and death in pediatric acute myeloid leukemia.

Lapillonne H, Renneville A, Auvrignon A, Flamant C, Blaise A, Perot C, Lai JL, Ballerini P, Mazingue F, Fasola S, Dehée A, Bellman F, Adam M, Labopin M, Douay L, Leverger G, Preudhomme C, Landman-Parker J. Lapillonne H, et al. Among authors: preudhomme c. J Clin Oncol. 2006 Apr 1;24(10):1507-15. doi: 10.1200/JCO.2005.03.5303. J Clin Oncol. 2006. PMID: 16575000

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