Manola KN - Search Results

1

A novel dic(1;10) in a patient with myelodysplastic syndrome.

Sambani C, La Starza R, Stavropoulou C, Manola KN, Harhalakis N, Mecucci C. Sambani C, et al. Among authors: manola kn. Cancer Genet Cytogenet. 2002 Feb;133(1):87-9. doi: 10.1016/s0165-4608(01)00571-4. Cancer Genet Cytogenet. 2002. PMID: 11890996

2

Leukemic recombinations involving heterochromatin in myeloproliferative disorders with t(1;9).

Sambani C, La Starza R, Pierini V, Vandenberghe P, Gonzales-Aguilera JJ, Rigana H, Koumbi D, Manola KN, Stavropoulou C, Georgakakos VN, Pagoni M, Wlodarska I, Mecucci C. Sambani C, et al. Among authors: manola kn. Cancer Genet Cytogenet. 2005 Oct 1;162(1):45-9. doi: 10.1016/j.cancergencyto.2005.02.021. Cancer Genet Cytogenet. 2005. PMID: 16157199

3

Switch in X-inactivation in a JAK2 V617F-negative case of polycythemia vera with two acquired X-autosome translocations.

Manola KN, Stavropoulou C, Georgakakos VN, Zoi K, Fisfis M, Evmorfiadis I, Zoi C, Pantelias GE, Stefanoudaki K, Sambani C. Manola KN, et al. Leuk Res. 2007 Jul;31(7):1009-14. doi: 10.1016/j.leukres.2006.11.014. Epub 2007 Jan 3. Leuk Res. 2007. PMID: 17204324

4

Translocation (X;12)(p11;p13) as a sole abnormality in biphenotypic acute leukemia.

Manola KN, Georgakakos VN, Marinakis T, Stavropoulou C, Paterakis G, Anagnostopoulos NI, Pantelias GE, Sambani C. Manola KN, et al. Cancer Genet Cytogenet. 2007 Mar;173(2):159-63. doi: 10.1016/j.cancergencyto.2006.10.012. Cancer Genet Cytogenet. 2007. PMID: 17321333

5

Leukemias associated with Turner syndrome: report of three cases and review of the literature.

Manola KN, Sambani C, Karakasis D, Kalliakosta G, Harhalakis N, Papaioannou M. Manola KN, et al. Leuk Res. 2008 Mar;32(3):481-6. doi: 10.1016/j.leukres.2007.06.004. Epub 2007 Jul 31. Leuk Res. 2008. PMID: 17669490 Review.

6

Disruption of the ETV6 gene as a consequence of a rare translocation (12;12)(p13;q13) in treatment-induced acute myeloid leukemia after breast cancer.

Manola KN, Georgakakos VN, Margaritis D, Stavropoulou C, Panos C, Kotsianidis I, Pantelias GE, Sambani C. Manola KN, et al. Cancer Genet Cytogenet. 2008 Jan 1;180(1):37-42. doi: 10.1016/j.cancergencyto.2007.09.004. Cancer Genet Cytogenet. 2008. PMID: 18068531

7

5'RARA submicroscopic deletion from new variant translocation involving chromosomes 15, 17, and 18, in a case of acute promyelocytic leukemia.

Stavropoulou C, Georgakakos VN, Manola KN, Pagoni M, Garofalaki M, Pantelias GE, Sambani C. Stavropoulou C, et al. Among authors: manola kn. Cancer Genet Cytogenet. 2008 Apr 1;182(1):50-5. doi: 10.1016/j.cancergencyto.2007.12.011. Cancer Genet Cytogenet. 2008. PMID: 18328952

8

Jumping translocations in hematological malignancies: a cytogenetic study of five cases.

Manola KN, Georgakakos VN, Stavropoulou C, Spyridonidis A, Angelopoulou MK, Vlachadami I, Katsigiannis A, Roussou P, Pantelias GE, Sambani C. Manola KN, et al. Cancer Genet Cytogenet. 2008 Dec;187(2):85-94. doi: 10.1016/j.cancergencyto.2008.07.010. Cancer Genet Cytogenet. 2008. PMID: 19027489

9

G2-checkpoint abrogation in irradiated lymphocytes: A new cytogenetic approach to assess individual radiosensitivity and predisposition to cancer.

Terzoudi GI, Hatzi VI, Barszczewska K, Manola KN, Stavropoulou C, Angelakis P, Pantelias GE. Terzoudi GI, et al. Among authors: manola kn. Int J Oncol. 2009 Nov;35(5):1223-30. doi: 10.3892/ijo_00000439. Int J Oncol. 2009. PMID: 19787278

10

Isochromosome der(17)(q10)t(15;17) in acute promyelocytic leukemia resulting in an additional copy of the RARA-PML fusion gene: report of 4 cases and review of the literature.

Manola KN, Karakosta M, Sambani C, Terzoudi G, Pagoni M, Gatsa E, Papaioannou M. Manola KN, et al. Acta Haematol. 2010;123(3):162-70. doi: 10.1159/000294959. Epub 2010 Mar 11. Acta Haematol. 2010. PMID: 20224268 Review.

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