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The Hellenic type of nondeletional hereditary persistence of fetal hemoglobin results from a novel mutation (g.-109G>T) in the HBG2 gene promoter.
Chassanidis C, Kalamaras A, Phylactides M, Pourfarzad F, Likousi S, Maroulis V, Papadakis MN, Vamvakopoulos NK, Aleporou-Marinou V, Patrinos GP, Kollia P. Chassanidis C, et al. Among authors: kollia p. Ann Hematol. 2009 Jun;88(6):549-55. doi: 10.1007/s00277-008-0643-0. Epub 2008 Dec 3. Ann Hematol. 2009. PMID: 19050890 Free PMC article.
Impact of renin-angiotensin-aldosterone system polymorphisms on myocardial perfusion: Correlations with myocardial single photon emission computed tomography-derived parameters.
Angelidis G, Samara M, Papathanassiou M, Satra M, Valotassiou V, Tsougos I, Psimadas D, Tzavara C, Alexiou S, Koutsikos J, Demakopoulos N, Giamouzis G, Triposkiadis F, Skoularigis J, Kollia P, Georgoulias P. Angelidis G, et al. Among authors: kollia p. J Nucl Cardiol. 2019 Aug;26(4):1298-1308. doi: 10.1007/s12350-017-1181-8. Epub 2018 Jan 17. J Nucl Cardiol. 2019. PMID: 29344922
Thumb duplication: molecular analysis of different clinical types.
Kyriazis Z, Kollia P, Grivea I, Varitimidis SE, Constantoulakis P, Dailiana ZH. Kyriazis Z, et al. Among authors: kollia p. Eur J Orthop Surg Traumatol. 2019 Feb;29(2):421-426. doi: 10.1007/s00590-018-2343-3. Epub 2018 Nov 29. Eur J Orthop Surg Traumatol. 2019. PMID: 30498907
Tumor Protein 53 Gene Mutations Without 17p13 Deletion Have No Significant Clinical Implications in Chronic Lymphocytic Leukemia. Detection of a New Mutation.
Diamantopoulos PT, Samara S, Kollia P, Giannakopoulou N, Sofotasiou M, Kalala F, Kodandreopoulou E, Zervakis P, Vassilakopoulos T, Siakantaris M, Mantzourani M, Angelopoulou M, Kyrtshonis MC, Korkolopoulou P, Patsouris E, Viniou NA. Diamantopoulos PT, et al. Among authors: kollia p. Anticancer Res. 2017 May;37(5):2387-2391. doi: 10.21873/anticanres.11577. Anticancer Res. 2017. PMID: 28476805
112 results