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Rural primary care in Greece: working under limited resources.
Oikonomidou E, Anastasiou F, Dervas D, Patri F, Karaklidis D, Moustakas P, Andreadou N, Mantzanas E, Merkouris B. Oikonomidou E, et al. Int J Qual Health Care. 2010 Aug;22(4):333-7. doi: 10.1093/intqhc/mzq032. Epub 2010 Jun 25. Int J Qual Health Care. 2010. PMID: 20581119
Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases.
Papoulidis I, Sotiriadis A, Siomou E, Papageorgiou E, Eleftheriades M, Papadopoulos V, Oikonomidou E, Orru S, Manolakos E, Athanasiadis A. Papoulidis I, et al. Among authors: oikonomidou e. Prenat Diagn. 2015 Dec;35(13):1269-77. doi: 10.1002/pd.4685. Epub 2015 Oct 26. Prenat Diagn. 2015. PMID: 26289927
Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH.
Manolakos E, Kefalas K, Vetro A, Oikonomidou E, Daskalakis G, Psara N, Siomou E, Papageorgiou E, Sevastopoulou E, Konstantinidou A, Vrachnis N, Thomaidis L, Zuffardi O, Papoulidis I. Manolakos E, et al. Among authors: oikonomidou e. Mol Cytogenet. 2013 Oct 31;6(1):47. doi: 10.1186/1755-8166-6-47. Mol Cytogenet. 2013. PMID: 24176130 Free PMC article.
Expanded Prader-Willi Syndrome due to an Unbalanced de novo Translocation t(14;15): Report and Review of the Literature.
Xefteris A, Sekerli E, Arampatzi A, Charisiou S, Oikonomidou E, Efstathiou G, Peroulis N, Malamidou A, Tsoulou-Panidou E, Agakidou E, Sarafidis K, Psarakis A, Kataras T, Daskalakis G. Xefteris A, et al. Among authors: oikonomidou e. Cytogenet Genome Res. 2019;159(3):109-118. doi: 10.1159/000504159. Epub 2019 Dec 10. Cytogenet Genome Res. 2019. PMID: 31816617 Review.
16 results