Vilmer E - Search Results

1

Quantification of TEL-AML1 transcript for minimal residual disease assessment in childhood acute lymphoblastic leukaemia.

Drunat S, Olivi M, Brunie G, Grandchamp B, Vilmer E, Bièche I, Cavé H. Drunat S, et al. Among authors: vilmer e. Br J Haematol. 2001 Aug;114(2):281-9. doi: 10.1046/j.1365-2141.2001.02922.x. Br J Haematol. 2001. PMID: 11529845 Free article.

2

Deletion mapping indicates that MTS1 is the target of frequent deletions at chromosome 9p21 in paediatric acute lymphoblastic leukaemias.

Guidal-Giroux C, Gérard B, Cavé H, Duval M, Rohrlich P, Elion J, Vilmer E, Grandchamp B. Guidal-Giroux C, et al. Among authors: vilmer e. Br J Haematol. 1996 Feb;92(2):410-9. doi: 10.1046/j.1365-2141.1996.d01-1497.x. Br J Haematol. 1996. PMID: 8603008

3

The 12;21 translocation involving TEL and deletion of the other TEL allele: two frequently associated alterations found in childhood acute lymphoblastic leukemia.

Raynaud S, Cave H, Baens M, Bastard C, Cacheux V, Grosgeorge J, Guidal-Giroux C, Guo C, Vilmer E, Marynen P, Grandchamp B. Raynaud S, et al. Among authors: vilmer e. Blood. 1996 Apr 1;87(7):2891-9. Blood. 1996. PMID: 8639909 Free article.

4

[Study of residual disease in acute lymphoblastic leukemia in children].

Vilmer E, Cave H, Granchamp B. Vilmer E, et al. Arch Pediatr. 1996;3 Suppl 1:204s-205s. doi: 10.1016/0929-693x(96)86042-8. Arch Pediatr. 1996. PMID: 8796017 Clinical Trial. French. No abstract available.

5

Analysis of ETV6 and ETV6-AML1 proteins in acute lymphoblastic leukaemia.

Agape P, Gerard B, Cave H, Devaux I, Vilmer E, Lecomte MC, Grandchamp B. Agape P, et al. Among authors: vilmer e. Br J Haematol. 1997 Jul;98(1):234-9. doi: 10.1046/j.1365-2141.1997.1973014.x. Br J Haematol. 1997. PMID: 9233592 Free article.

6

ETV6 is the target of chromosome 12p deletions in t(12;21) childhood acute lymphocytic leukemia.

Cavé H, Cacheux V, Raynaud S, Brunie G, Bakkus M, Cochaux P, Preudhomme C, Laï JL, Vilmer E, Grandchamp B. Cavé H, et al. Among authors: vilmer e. Leukemia. 1997 Sep;11(9):1459-64. doi: 10.1038/sj.leu.2400798. Leukemia. 1997. PMID: 9305598

7

Clinical significance of minimal residual disease in childhood acute lymphoblastic leukemia. European Organization for Research and Treatment of Cancer--Childhood Leukemia Cooperative Group.

Cavé H, van der Werff ten Bosch J, Suciu S, Guidal C, Waterkeyn C, Otten J, Bakkus M, Thielemans K, Grandchamp B, Vilmer E. Cavé H, et al. Among authors: vilmer e. N Engl J Med. 1998 Aug 27;339(9):591-8. doi: 10.1056/NEJM199808273390904. N Engl J Med. 1998. PMID: 9718378 Free article.

8

CDKN2A, CDKN2B, and MTAP gene dosage permits precise characterization of mono- and bi-allelic 9p21 deletions in childhood acute lymphoblastic leukemia.

Bertin R, Acquaviva C, Mirebeau D, Guidal-Giroux C, Vilmer E, Cavé H. Bertin R, et al. Among authors: vilmer e. Genes Chromosomes Cancer. 2003 May;37(1):44-57. doi: 10.1002/gcc.10188. Genes Chromosomes Cancer. 2003. PMID: 12661005

9

Clinical significance of HOX11L2 expression linked to t(5;14)(q35;q32), of HOX11 expression, and of SIL-TAL fusion in childhood T-cell malignancies: results of EORTC studies 58881 and 58951.

Cavé H, Suciu S, Preudhomme C, Poppe B, Robert A, Uyttebroeck A, Malet M, Boutard P, Benoit Y, Mauvieux L, Lutz P, Méchinaud F, Grardel N, Mazingue F, Dupont M, Margueritte G, Pages MP, Bertrand Y, Plouvier E, Brunie G, Bastard C, Plantaz D, Vande Velde I, Hagemeijer A, Speleman F, Lessard M, Otten J, Vilmer E, Dastugue N; EORTC-CLG. Cavé H, et al. Among authors: vilmer e. Blood. 2004 Jan 15;103(2):442-50. doi: 10.1182/blood-2003-05-1495. Epub 2003 Sep 22. Blood. 2004. PMID: 14504110 Free article.

10

Loss of heterozygosity in the chromosomal region 12p12-13 is very common in childhood acute lymphoblastic leukemia and permits the precise localization of a tumor-suppressor gene distinct from p27KIP1.

Cavé H, Gérard B, Martin E, Guidal C, Devaux I, Weissenbach J, Elion J, Vilmer E, Grandchamp B. Cavé H, et al. Among authors: vilmer e. Blood. 1995 Nov 15;86(10):3869-75. Blood. 1995. PMID: 7579355 Free article.

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