Quesnel B - Search Results

1

High occurrence of JAK2 V617 mutation in refractory anemia with ringed sideroblasts associated with marked thrombocytosis.

Renneville A, Quesnel B, Charpentier A, Terriou L, Crinquette A, Laï JL, Cossement C, Lionne-Huyghe P, Rose C, Bauters F, Preudhomme C. Renneville A, et al. Among authors: quesnel b. Leukemia. 2006 Nov;20(11):2067-70. doi: 10.1038/sj.leu.2404405. Epub 2006 Sep 21. Leukemia. 2006. PMID: 16990759 No abstract available.

2

A case of refractory anemia with 17p- syndrome following azathioprine treatment for heart transplantation.

Depil S, Lepelley P, Soenen V, Preudhomme C, Lai JL, Broly F, Quesnel B. Depil S, et al. Among authors: quesnel b. Leukemia. 2004 Apr;18(4):878. doi: 10.1038/sj.leu.2403305. Leukemia. 2004. PMID: 14961032 No abstract available.

3

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: quesnel b. Leukemia. 2001 Jul;15(7):1054-9. doi: 10.1038/sj.leu.2402153. Leukemia. 2001. PMID: 11455973

4

Successful treatment of imatinib-resistant acute megakaryoblastic leukemia with e6a2 BCR/ABL: use of dasatinib and reduced-conditioning stem-cell transplantation.

Corm S, Renneville A, Rad-Quesnel E, Grardel N, Preudhomme C, Quesnel B. Corm S, et al. Among authors: quesnel b. Leukemia. 2007 Nov;21(11):2376-7. doi: 10.1038/sj.leu.2404792. Epub 2007 Jun 7. Leukemia. 2007. PMID: 17554376 No abstract available.

5

p16ink4a gene and hematological malignancies.

Quesnel B, Preudhomme C, Fenaux P. Quesnel B, et al. Leuk Lymphoma. 1996 Jun;22(1-2):11-24. doi: 10.3109/10428199609051724. Leuk Lymphoma. 1996. PMID: 8724524 Review.

6

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

7

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: quesnel b. Leukemia. 2005 May;19(5):792-8. doi: 10.1038/sj.leu.2403722. Leukemia. 2005. PMID: 15772698

8

Copy-number analysis identified new prognostic marker in acute myeloid leukemia.

Nibourel O, Guihard S, Roumier C, Pottier N, Terre C, Paquet A, Peyrouze P, Geffroy S, Quentin S, Alberdi A, Abdelali RB, Renneville A, Demay C, Celli-Lebras K, Barbry P, Quesnel B, Castaigne S, Dombret H, Soulier J, Preudhomme C, Cheok MH. Nibourel O, et al. Among authors: quesnel b. Leukemia. 2017 Mar;31(3):555-564. doi: 10.1038/leu.2016.265. Epub 2016 Sep 30. Leukemia. 2017. PMID: 27686867

9

Rare occurrence of mutations of the FLR exon of the neurofibromatosis 1 (NF1) gene in myelodysplastic syndromes (MDS) and acute myeloid leukemia (AML).

Preudhomme C, Vachee A, Quesnel B, Wattel E, Cosson A, Fenaux P. Preudhomme C, et al. Among authors: quesnel b. Leukemia. 1993 Jul;7(7):1071. Leukemia. 1993. PMID: 8321023 No abstract available.

10

BCR-ABL mutants spread resistance to non-mutated cells through a paracrine mechanism.

Liu J, Joha S, Idziorek T, Corm S, Hetuin D, Philippe N, Preudhomme C, Quesnel B. Liu J, et al. Among authors: quesnel b. Leukemia. 2008 Apr;22(4):791-9. doi: 10.1038/leu.2008.3. Epub 2008 Jan 24. Leukemia. 2008. PMID: 18216868

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