Lai JL - Search Results

1

Prognostic significance of p16INK4a immunocytochemistry in adult ALL with standard risk karyotype.

Soenen V, Lepelley P, Gyan E, Preudhomme C, Lai JL, Bauters F, Fenaux P, Quesnel B. Soenen V, et al. Among authors: lai jl. Leukemia. 2001 Jul;15(7):1054-9. doi: 10.1038/sj.leu.2402153. Leukemia. 2001. PMID: 11455973

2

Prognostic value of real-time quantitative PCR (RQ-PCR) in AML with t(8;21).

Leroy H, de Botton S, Grardel-Duflos N, Darre S, Leleu X, Roumier C, Morschhauser F, Lai JL, Bauters F, Fenaux P, Preudhomme C. Leroy H, et al. Among authors: lai jl. Leukemia. 2005 Mar;19(3):367-72. doi: 10.1038/sj.leu.2403627. Leukemia. 2005. PMID: 15674426 Clinical Trial.

3

Molecular characterization of the idiopathic hypereosinophilic syndrome (HES) in 35 French patients with normal conventional cytogenetics.

Roche-Lestienne C, Lepers S, Soenen-Cornu V, Kahn JE, Laï JL, Hachulla E, Drupt F, Demarty AL, Roumier AS, Gardembas M, Dib M, Philippe N, Cambier N, Barete S, Libersa C, Bletry O, Hatron PY, Quesnel B, Rose C, Maloum K, Blanchet O, Fenaux P, Prin L, Preudhomme C. Roche-Lestienne C, et al. Among authors: lai jl. Leukemia. 2005 May;19(5):792-8. doi: 10.1038/sj.leu.2403722. Leukemia. 2005. PMID: 15772698

4

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: lai jl. Leukemia. 1992 Jan;6(1):42-6. Leukemia. 1992. PMID: 1736012

5

de novo myelodysplastic syndromes in adults aged 50 or less. A report on 37 cases.

Fenaux P, Preudhomme C, Hélène Estienne M, Morel P, Laï JL, Gardin C, Jouet JP, Bauters F. Fenaux P, et al. Among authors: lai jl. Leuk Res. 1990;14(11-12):1053-9. doi: 10.1016/0145-2126(90)90119-t. Leuk Res. 1990. PMID: 2280603

6

Expression of the multidrug resistance P-glycoprotein and its relationship to hematological characteristics and response to treatment in myelodysplastic syndromes.

Lepelley P, Soenen V, Preudhomme C, Lai JL, Cosson A, Fenaux P. Lepelley P, et al. Among authors: lai jl. Leukemia. 1994 Jun;8(6):998-1004. Leukemia. 1994. PMID: 7516032

7

p16 gene homozygous deletions in acute lymphoblastic leukemia.

Quesnel B, Preudhomme C, Philippe N, Vanrumbeke M, Dervite I, Lai JL, Bauters F, Wattel E, Fenaux P. Quesnel B, et al. Among authors: lai jl. Blood. 1995 Feb 1;85(3):657-63. Blood. 1995. PMID: 7833469 Free article.

8

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. Leukemia. 1995 Mar;9(3):370-81. Leukemia. 1995. PMID: 7885035

9

Inv(16) may be one of the only 'favorable' factors in acute myeloid leukemia: a report on 19 cases with prolonged follow-up.

Plantier I, Lai JL, Wattel E, Bauters F, Fenaux P. Plantier I, et al. Among authors: lai jl. Leuk Res. 1994 Dec;18(12):885-8. doi: 10.1016/0145-2126(94)90098-1. Leuk Res. 1994. PMID: 7996869 Clinical Trial.

10

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: lai jl. Leukemia. 1994 May;8(5):878-80. Leukemia. 1994. PMID: 8182944

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