La Starza R - Search Results

1

Different mechanisms lead to a karyotypically identical t(20;21) in myelodysplastic syndrome and in acute myelocytic leukemia.

Matteucci C, La Starza R, Crescenzi B, Romoli S, Santoro A, Magrin S, Lauria F, Coco FL, Martelli MF, Mecucci C. Matteucci C, et al. Among authors: la starza r. Cancer Genet Cytogenet. 2003 Jan 1;140(1):13-7. doi: 10.1016/s0165-4608(02)00622-2. Cancer Genet Cytogenet. 2003. PMID: 12550752

2

TEL gene is involved in myelodysplastic syndromes with either the typical t(5;12)(q33;p13) translocation or its variant t(10;12)(q24;p13).

Wlodarska I, Mecucci C, Marynen P, Guo C, Franckx D, La Starza R, Aventin A, Bosly A, Martelli MF, Cassiman JJ, et al. Wlodarska I, et al. Among authors: la starza r. Blood. 1995 May 15;85(10):2848-52. Blood. 1995. PMID: 7742547 Free article.

3

3q aberration and monosomy 7 in ANLL presenting with high platelet count and diabetes insipidus.

La Starza R, Falzetti D, Fania C, Tabilio A, Martelli MF, Mecucci C. La Starza R, et al. Haematologica. 1994 Jul-Aug;79(4):356-9. Haematologica. 1994. PMID: 7806090

4

Cytogenetic and FISH investigations on tetrasomy 8 in ANLL.

La Starza R, Crescenzi B, Matteucci C, Martelli MF, Mecucci C. La Starza R, et al. Cancer Genet Cytogenet. 1995 Feb;79(2):182-5. doi: 10.1016/0165-4608(94)00120-z. Cancer Genet Cytogenet. 1995. PMID: 7889517

5

T-lymphoid/myeloid biphenotypic leukemia morphologically resembling malignant histiocytosis. Immunological, cytogenetic and molecular studies.

La Starza R, Falini B, Amici A, Falzetti D, Tabilio A, Fagioli M, Martelli MF, Mecucci C. La Starza R, et al. Haematologica. 1993 May-Jun;78(3):187-91. Haematologica. 1993. PMID: 8375751 No abstract available.

6

14q+ chromosome marker in a T-cell-rich B-cell lymphoma.

La Starza R, Aventin A, Falzetti D, Stul M, Martelli MF, Falini B, Mecucci C. La Starza R, et al. J Pathol. 1996 Feb;178(2):227-31. doi: 10.1002/(SICI)1096-9896(199602)178:2<227::AID-PATH437>3.0.CO;2-9. J Pathol. 1996. PMID: 8683394

7

Successful use of the same slide for consecutive fluorescence in situ hybridization experiments.

Dierlamm J, Wlodarska I, Michaux L, La Starza R, Zeller W, Mecucci C, Van den Berghe H. Dierlamm J, et al. Among authors: la starza r. Genes Chromosomes Cancer. 1996 Aug;16(4):261-4. doi: 10.1002/(SICI)1098-2264(199608)16:4<261::AID-GCC6>3.0.CO;2-W. Genes Chromosomes Cancer. 1996. PMID: 8875240

8

The ETV6, CDKN1B and D12S178 loci are involved in a segment commonly deleted in various 12p aberration in different hematological malignancies.

Wlodarska I, Marynen P, La Starza R, Mecucci C, Van den Berghe H. Wlodarska I, et al. Among authors: la starza r. Cytogenet Cell Genet. 1996;72(2-3):229-35. doi: 10.1159/000134197. Cytogenet Cell Genet. 1996. PMID: 8978784

9

Molecular delineation of 13q deletion boundaries in 20 patients with myeloid malignancies.

La Starza R, Wlodarska I, Aventin A, Falzetti D, Crescenzi B, Martelli MF, Van den Berghe H, Mecucci C. La Starza R, et al. Blood. 1998 Jan 1;91(1):231-7. Blood. 1998. PMID: 9414289 Free article.

10

Fluorescence in situ hybridization characterization of new translocations involving TEL (ETV6) in a wide spectrum of hematologic malignancies.

Wlodarska I, La Starza R, Baens M, Dierlamm J, Uyttebroeck A, Selleslag D, Francine A, Mecucci C, Hagemeijer A, Van den Berghe H, Marynen P. Wlodarska I, et al. Among authors: la starza r. Blood. 1998 Feb 15;91(4):1399-406. Blood. 1998. PMID: 9454771 Free article.

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