Manola K - Search Results

1

Acute promyelocytic leukemia: an experience on 95 greek patients treated in the all-trans-retinoic Acid era.

Pagoni M, Garofalaki M, Panitsas F, Manola K, Psarra K, Economopoulos P, Vourtsi A, Antoniades M, Gkirkas K, Tzouvara E, Katis F, Prokopiou C, Tziotziou I, Balta A, Lemissiou E, Tsirigotis P, Repoussis P, Harhalakis N. Pagoni M, et al. Among authors: manola k. Mediterr J Hematol Infect Dis. 2011;3(1):e2011053. doi: 10.4084/MJHID.2011.053. Epub 2011 Nov 28. Mediterr J Hematol Infect Dis. 2011. PMID: 22220250 Free PMC article.

2

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. Cancer Genet Cytogenet. 2008 Apr 1;182(1):50-5. doi: 10.1016/j.cancergencyto.2007.12.011. Cancer Genet Cytogenet. 2008. PMID: 18328952

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

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

5

Specific abnormalities versus number of abnormalities and cytogenetic scoring systems for outcome prediction after allogeneic hematopoietic SCT for myelodysplastic syndromes.

Kelaidi C, Tzannou I, Baltadakis I, Batsis I, Mallouri D, Spyridonidis A, Gigantes S, Tsirigotis P, Apostolidis I, Athanasiadou A, Manola K, Anagnostopoulos A, Harhalakis N, Sakellari I, Karakasis D. Kelaidi C, et al. Among authors: manola k. Bone Marrow Transplant. 2014 Aug;49(8):1022-8. doi: 10.1038/bmt.2014.87. Epub 2014 May 5. Bone Marrow Transplant. 2014. PMID: 24797183

6

ASXL1 mutations in AML are associated with specific clinical and cytogenetic characteristics.

Kakosaiou K, Panitsas F, Daraki A, Pagoni M, Apostolou P, Ioannidou A, Vlachadami I, Marinakis T, Giatra C, Vasilatou D, Sambani C, Pappa V, Manola KN. Kakosaiou K, et al. Among authors: manola kn. Leuk Lymphoma. 2018 Oct;59(10):2439-2446. doi: 10.1080/10428194.2018.1433298. Epub 2018 Feb 7. Leuk Lymphoma. 2018. PMID: 29411666

7

Identification of two novel mutations in human acute myeloid leukemia cases.

O'Brien G, Zyla J, Manola KN, Pagoni MN, Polanska J, Badie C. O'Brien G, et al. Among authors: manola kn. Leuk Lymphoma. 2021 Feb;62(2):454-461. doi: 10.1080/10428194.2020.1832664. Epub 2020 Oct 14. Leuk Lymphoma. 2021. PMID: 33161783 Free article.

8

Epigenetic signature of ionizing radiation in therapy-related AML patients.

O'Brien G, Cecotka A, Manola KN, Pagoni MN, Polanska J, Badie C. O'Brien G, et al. Among authors: manola kn. Heliyon. 2023 Dec 2;10(1):e23244. doi: 10.1016/j.heliyon.2023.e23244. eCollection 2024 Jan 15. Heliyon. 2023. PMID: 38163095 Free PMC article.

9

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. Cancer Genet Cytogenet. 2005 Oct 1;162(1):45-9. doi: 10.1016/j.cancergencyto.2005.02.021. Cancer Genet Cytogenet. 2005. PMID: 16157199

10

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

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