Vilmer E - Search Results

1

Beta-globin gene cluster haplotype and alpha-thalassemia do not correlate with the acute clinical manifestations of sickle cell disease in children.

de Montalembert M, Maier-Redelsperger M, Girot R, Belloy M, Vilmer E, Ducrocq R, Guidal C, Elion J. de Montalembert M, et al. Among authors: vilmer e. Blood. 1993 Oct 15;82(8):2595-6. Blood. 1993. PMID: 8400306 Free article. No abstract available.

2

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.

3

Hydroxyurea corrects the dysregulated L-selectin expression and increased H(2)O(2) production of polymorphonuclear neutrophils from patients with sickle cell anemia.

Benkerrou M, Delarche C, Brahimi L, Fay M, Vilmer E, Elion J, Gougerot-Pocidalo MA, Elbim C. Benkerrou M, et al. Among authors: vilmer e. Blood. 2002 Apr 1;99(7):2297-303. doi: 10.1182/blood.v99.7.2297. Blood. 2002. PMID: 11895759 Free article.

4

[Neonatal screening for sickle cell anemia: evaluation of a five-year experience in an area of northern Paris].

Ducrocq R, Benkerrou M, Brahimi L, Belloy M, Briard ML, Vilmer E, Elion J. Ducrocq R, et al. Among authors: vilmer e. Arch Pediatr. 2001 May;8(5):474-80. doi: 10.1016/s0929-693x(00)00248-7. Arch Pediatr. 2001. PMID: 11396106 French.

5

HLA-mismatched cord blood transplantation: immunological studies.

Vilmer E, Quelvennec E, Plouvier E, Denamur E, Rohrlich P, Elion J, Sterkers G. Vilmer E, et al. Blood Cells. 1994;20(2-3):235-41. Blood Cells. 1994. PMID: 7538336

6

A low rate of loss of heterozygosity is found at many different loci in childhood B-lineage acute lymphocytic leukemia.

Cavé H, Guidal C, Elion J, Vilmer E, Grandchamp B. Cavé H, et al. Among authors: vilmer e. Leukemia. 1996 Sep;10(9):1486-91. Leukemia. 1996. PMID: 8751467

7

Erythroid hypoplasia due to chronic infection with parvovirus B19.

Belloy M, Morinet F, Blondin G, Courouce AM, Peyrol Y, Vilmer E. Belloy M, et al. Among authors: vilmer e. N Engl J Med. 1990 Mar 1;322(9):633-4. doi: 10.1056/NEJM199003013220916. N Engl J Med. 1990. PMID: 2154693 No abstract available.

8

A competitive PCR-based method using TCRD, TCRG and IGH rearrangements for rapid detection of patients with high levels of minimal residual disease in acute lymphoblastic leukemia.

Guidal C, Vilmer E, Grandchamp B, Cavé H. Guidal C, et al. Among authors: vilmer e. Leukemia. 2002 Apr;16(4):762-4. doi: 10.1038/sj.leu.2402396. Leukemia. 2002. PMID: 11960365 No abstract available.

9

Delineation of a 6 cM commonly deleted region in childhood acute lymphoblastic leukemia on the 6q chromosomal arm.

Gérard B, Cavé H, Guidal C, Dastugue N, Vilmer E, Grandchamp B. Gérard B, et al. Among authors: vilmer e. Leukemia. 1997 Feb;11(2):228-32. doi: 10.1038/sj.leu.2400566. Leukemia. 1997. PMID: 9009085

10

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.

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