Raynaud S - Search Results

1

Congenital leukemia cutis preceding monoblastic leukemia by 3 months.

Monpoux F, Lacour JP, Hatchuel Y, Hofman P, Raynaud S, Sudaka I, Ortonne JP, Mariani R. Monpoux F, et al. Among authors: raynaud s. Pediatr Dermatol. 1996 Nov-Dec;13(6):472-6. doi: 10.1111/j.1525-1470.1996.tb00727.x. Pediatr Dermatol. 1996. PMID: 8987056

2

[Assessment of an immature platelet fraction (IFP%) in the diagnosis of thrombocytopenia].

Cannavo I, Ferrero-Vacher C, Sudaka I, Aquaronne D, Berthier F, Raynaud S. Cannavo I, et al. Among authors: raynaud s. Ann Biol Clin (Paris). 2010 Jul-Aug;68(4):415-20. doi: 10.1684/abc.2010.0449. Ann Biol Clin (Paris). 2010. PMID: 20650736 Free article. French.

3

Inversion (14)(q11q32) in a case of acute myeloid leukemia expressing lymphoid-associated antigens.

Raynaud SD, Brunet B, Ayraud N, Monpoux F, Philip P, Bayle J. Raynaud SD, et al. Cancer Genet Cytogenet. 1993 Nov;71(1):100-1. doi: 10.1016/0165-4608(93)90209-5. Cancer Genet Cytogenet. 1993. PMID: 8275446 No abstract available.

4

Fusion of TEL, the ETS-variant gene 6 (ETV6), to the receptor-associated kinase JAK2 as a result of t(9;12) in a lymphoid and t(9;15;12) in a myeloid leukemia.

Peeters P, Raynaud SD, Cools J, Wlodarska I, Grosgeorge J, Philip P, Monpoux F, Van Rompaey L, Baens M, Van den Berghe H, Marynen P. Peeters P, et al. Among authors: raynaud sd. Blood. 1997 Oct 1;90(7):2535-40. Blood. 1997. PMID: 9326218 Free article.

5

Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a recurring chromosomal abnormality involving the TEL gene (ETV6) in myelodysplastic syndromes.

Raynaud SD, Baens M, Grosgeorge J, Rodgers K, Reid CD, Dainton M, Dyer M, Fuzibet JG, Gratecos N, Taillan B, Ayraud N, Marynen P. Raynaud SD, et al. Blood. 1996 Jul 15;88(2):682-9. Blood. 1996. PMID: 8695816 Free article.

6

Rearrangement of proximal 11q13 band in a CMML in acute transformation.

Courseaux A, Grosgeorge J, Garnier G, Larsson C, Ayraud N, Gaudray P, Raynaud SD. Courseaux A, et al. Among authors: raynaud sd. Leukemia. 1995 Aug;9(8):1313-7. Leukemia. 1995. PMID: 7643618

7

Recurrent cytogenetic abnormalities observed in complete remission of acute myeloid leukemia do not necessarily mark preleukemic cells.

Raynaud SD, Brunet B, Chischportich M, Bayle J, Gratecos N, Pesce A, Dujardin P, Flandrin G, Ayraud N. Raynaud SD, et al. Leukemia. 1994 Feb;8(2):245-9. Leukemia. 1994. PMID: 8309249

8

Cytogenetic abnormalities associated with the t(12;21): a collaborative study of 169 children with t(12;21)-positive acute lymphoblastic leukemia.

Raynaud SD, Dastugue N, Zoccola D, Shurtleff SA, Mathew S, Raimondi SC. Raynaud SD, et al. Leukemia. 1999 Sep;13(9):1325-30. doi: 10.1038/sj.leu.2401506. Leukemia. 1999. PMID: 10482981 Clinical Trial.

9

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. Blood. 1996 Apr 1;87(7):2891-9. Blood. 1996. PMID: 8639909 Free article.

10

Clonal selection in therapy-related myelodysplastic syndromes and acute myeloid leukemia under azacitidine treatment.

Calleja A, Yun S, Moreilhon C, Karsenti JM, Gastaud L, Mannone L, Komrokji R, Al Ali N, Dadone-Montaudie B, Robert G, Auberger P, Raynaud S, Sallman DA, Cluzeau T. Calleja A, et al. Among authors: raynaud s. Eur J Haematol. 2020 May;104(5):488-498. doi: 10.1111/ejh.13390. Epub 2020 Mar 9. Eur J Haematol. 2020. PMID: 31990086

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