Manola KN - Search Results

1

Cohesin RAD21 Gene Promoter Methylation in Patients with Chronic Lymphocytic Leukemia.

Ioannidou A, Zachaki S, Karakosta M, Daraki A, Roussou P, Manola KN. Ioannidou A, et al. Among authors: manola kn. Cytogenet Genome Res. 2018;154(3):126-131. doi: 10.1159/000487868. Epub 2018 Mar 24. Cytogenet Genome Res. 2018. PMID: 29587287

2

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

3

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.

4

Translocation (6;13)(p21;q14.1) as a rare nonrandom cytogenetic abnormality in chronic lymphocytic leukemia.

Karakosta M, Voulgarelis M, Vlachadami I, Manola KN. Karakosta M, et al. Among authors: manola kn. Cancer Genet Cytogenet. 2010 Apr 1;198(1):66-70. doi: 10.1016/j.cancergencyto.2009.12.009. Cancer Genet Cytogenet. 2010. PMID: 20303017

5

Deletion of 5q as a rare abnormality in chronic lymphocytic leukemia.

Karakosta M, Tsakiridou A, Korantzis I, Manola KN. Karakosta M, et al. Among authors: manola kn. Cancer Genet Cytogenet. 2010 Jul 15;200(2):175-9. doi: 10.1016/j.cancergencyto.2010.04.002. Cancer Genet Cytogenet. 2010. PMID: 20620603

6

Association of A(313)G glutathione S-transferase P1 germline polymorphism with susceptibility to de novo myelodysplastic syndrome.

Zachaki S, Stavropoulou C, Kalomoiraki M, Koromila T, Daraki A, Manola KN, Mavrou A, Kanavakis E, Pantelias GE, Sambani C. Zachaki S, et al. Among authors: manola kn. Leuk Lymphoma. 2013 Aug;54(8):1756-61. doi: 10.3109/10428194.2012.762647. Epub 2013 Jan 28. Leuk Lymphoma. 2013. PMID: 23278642

7

Cytogenetic abnormalities and monosomal karyotypes in children and adolescents with acute myeloid leukemia: correlations with clinical characteristics and outcome.

Manola KN, Panitsas F, Polychronopoulou S, Daraki A, Karakosta M, Stavropoulou C, Avgerinou G, Hatzipantelis E, Pantelias G, Sambani C, Pagoni M. Manola KN, et al. Cancer Genet. 2013 Mar;206(3):63-72. doi: 10.1016/j.cancergen.2013.01.001. Epub 2013 Feb 12. Cancer Genet. 2013. PMID: 23411131

8

Translocation t(5;18)(q35;q21) as a rare nonrandom abnormality in acute myeloid leukemia.

Daraki A, Bourantas LK, Manola KN. Daraki A, et al. Among authors: manola kn. Cytogenet Genome Res. 2013;139(4):289-94. doi: 10.1159/000348786. Epub 2013 Mar 23. Cytogenet Genome Res. 2013. PMID: 23548668

9

High frequency of NAD(P)H:quinone oxidoreductase 1 (NQO1) C(609)T germline polymorphism in MDS/AML with trisomy 8.

Zachaki S, Stavropoulou C, Koromila T, Manola KN, Kalomoiraki M, Daraki A, Koumbi D, Athanasiadou A, Kanavakis E, Kollia P, Sambani C. Zachaki S, et al. Among authors: manola kn. Leuk Res. 2013 Jul;37(7):742-6. doi: 10.1016/j.leukres.2013.04.015. Epub 2013 May 1. Leuk Res. 2013. PMID: 23643325

10

UGT1A1*28 polymorphism in chronic lymphocytic leukemia: the first investigation of the polymorphism in disease susceptibility and its specific cytogenetic abnormalities.

Karakosta M, Kalotychou V, Kostakis A, Pantelias G, Rombos I, Kouraklis G, Manola KN. Karakosta M, et al. Among authors: manola kn. Acta Haematol. 2014;132(1):59-67. doi: 10.1159/000355714. Epub 2014 Jan 23. Acta Haematol. 2014. PMID: 24458221

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