Δημοσιεύσεις

Predictive value of the sFlt‑1/ PlGF ratio in women with suspected preeclampsia: An update (Review).

 Velegrakis, A., Kouvidi, E., Fragkiadaki, P., & Sifakis, S.

Int J Mol Med. 52(4), 89. 2023

 Chromosomal Abnormalities in Infertile Greek Men: A Single Institution’s Experience.

 Kouvidi E, Tsarouha H, Katsidi C, Zachaki S, Nitsos N, Samourgianidi S, Pantou A, Lazaros L, Kanavakis E, Mavrou A.

OBM Genetics 2023;7(1):178

 The impact of preimplantation genetic testing for aneuploidies (PGT-A) on clinical outcomes in high risk patients.

Pantou, A., Mitrakos, A., Kokkali, G., Petroutsou, K., Tounta, G., Lazaros, L., Dimopoulos, A., Sfakianoudis, K., Pantos, K., Koutsilieris, M., Mavrou, A., Kanavakis, E., & Tzetis, M.

 J Assist Reprod Genet. 39(6), 1341–1349. 2022

 A 46,XX Karyotype in Men with Infertility: Two New Cases and Review of the Literature.

 Kouvidi, E., Tsimela, H., Lazaros, L., Manola, K. N., Zachaki, S., Dobrescu, R., Sfakianoudis, K., Tsoni, T., Katsidi, C., Tsarouha, H., Kanavakis, E., & Mavrou, A. (2022).

J Hum Reprod Sci. 15(3),307–317. 2022

 Τelomerase inhibitors and activators in aging and cancer: A systematic review.

Fragkiadaki, P., Renieri, E., Kalliantasi, K., Kouvidi, E., Apalaki, E., Vakonaki, E., Mamoulakis, C., Spandidos, D. A., & Tsatsakis, A. (2022).

Mol med rep. 25(5),158. 2022

Novel sonic hedgehog gene variant in a patient with hyponatremia, microsomia, and midline defects; phenotype description in association with a variant of unknown significance [c.755_757del p.(Phe252del)] and an approach to salt-wasting in SHH-related adrenal disorders.

Retrocollis as the cardinal feature in a de novo ITRP1 variant.

Female Reproductive Ageing and Chromosomal Abnormalities in a Large Series of Women Undergoing IVF.

 Elisavet Kouvidi, Sophia Zachaki, Haralampia Tsarouha, Amelia Pantou, Kalliopi N Manola, Emmanuel Kanavakis, Ariadni Mavrou

Cytogenet Genome Res. 20;1-5, 2022.

Cytogenetic findings of ectopic endometriotic tissue in women with endometriosis and review of the literature.

Zachaki S., Kalomoiraki M., Kouvidi E., Promponas E., Syrkos S., Panopoulou B., Pantou A., Mavrou A., Kanavakis E., Manola KN.

Eur J Obstet Gynecol Reprod Biol. 264:212-218, 2021.

Determination of prenatal exposure to parabens and triclosan and estimation of maternal and fetal burden

Vasiliki Karzi, Manolis N. Tzatzarakis, Eleftheria Hatzidaki, Ioanna Katsikantami, Athanasios Alegakis, Elena Vakonaki, Alexandra Kalogeraki, Elisavet Kouvidi, Pelagia Xezonaki, Stavros Sifakis, Apostolos K. Rizos

Toxicol Rep. 8:808-815, 2021.

Detection of a novel unbalanced X;21 translocation in a girl with Turner syndrome phenotype

Kouvidi E., Zachaki S., Selenti N., Veltra D., Evmorfopoulou T., Tsoutsou E., Tzifa G., Sofocleous C., Gagos S., Mavrou A.

Gynecol Endocrinol. 37(4):377-381, 2021.

Pathways Involved in Premature Ovarian Failure: A Systematic Review of Experimental Studies.

Pargianas M, Salta S, Apostolopoulou K, Lazaros L, Kyrgiou M, Tinelli A, Malvasi A, Kalogiannidis I, Georgiou I, Kosmas IP

Curr Pharm Des. 2020;26(18):2087-2095

Coffin-Siris Syndrome 4-Related Spectrum in a Young Woman Caused by a Heterozygous SMARCA4 Deletion Detected by High-Resolution aCGH

Mitrakos A., Lazaros L., Pantou A., Mavrou A., Kanavakis E. Tzetis M.

Mol Syndromol (DOI:10.1159/000508563)

Low-level X Chromosome Mosaicism: A Common Finding in Women Undergoing IVF

Sophia Zachaki, Elisavet Kouvidi, Amelia Pantou, Haroula Tsarouha, Anastasios Mitrakos, Georgia Tounta, Ioanna Charalampous, Kalliopi N Manola, Emmanuel Kanavakis, Ariadni Mavrou

In Vivo 2020;34(3):1433-1437.

I-131 Postablation SPECT/CT Predicts Relapse of Papillary Thyroid Carcinoma more Accurately than Whole Body Scan.

 Malamitsi JV, Koutsikos JT, Giourgouli SI, Zachaki SF, Pipikos TA, Vlachou FJ, Prassopoulos VK

In Vivo. 2019;33(6):2255-2263

 Perinatal lipocalin-2 profile at the extremes of fetal growth.

Eirini Papathanasiou A, Malamitsi-Puchner A, Gavrili S, Zachaki S, Georgantzi S, Marmarinos A, Christou C, Voulgaris K, Gourgiotis D, Briana DD.

J Matern Fetal Neonatal Med. 2019 Sep 8:1-7

 Paraoxonase 1 (PON1) Q192R and L55M Polymorphisms as Potential Predisposition Factors for Chronic Lymphocytic Leukemia.

Ioannidou A, Zachaki S, Daraki A, Margariti IM, Pantelia D, Diamantopoulou P, Sambani C, Roussou P, Manola KN.

Anticancer Res. 2019;39(6):2861-2869.

Identification of a Novel Intragenic Deletion of the PHKD1 Gene in a Patient with Autosomal Recessive Polycystic Kidney Disease.

Leandros Lazaros, Danai Palaiologou, Amelia Pantou, Chaido Koumanzeli, Ιoannis Κapetanakis, Εmmanouel Κanavakis

Int J Pediatr 2019; 7(10): 10291-297. DOI: 10.22038/ijp.2019.42674.3576

Successful Implantation and Live Birth Following Autologous Platelet-rich Plasma Treatment for a Patient with Recurrent Implantation Failure and Chronic Endometritis.

Sfakianoudis K., Simopoulou M., Nitsos N. Lazaros L., Rapani A., Pantou A., Koutsilieris M., Nikas Y., Pantos K.

In Vivo 2019;33:515-521

A novel de novo paracentric inversion [inv(20)(q13.1q13.3)] accompanied by a 11q14.3-q21  microdeletion in a pediatric patient with an intellectual disability

Zachaki S., Kouvidi E., Mitrakos A., Lazaros L., Pantou A., Mavrou A., Tzetis M., Manola KN.

Balkan J Med Genet 21:63-67, 2018

Cohesin RAD21  Gene Promoter Methylation in Patients with Chronic Lymphocytic Leukemia

Ioannidou A, Zachaki S, Karakosta M, Daraki A, Roussou P, Manola KN.

Cytogenet Genome Res 2018;154:126–131

Early Identification of Women at Risk of Gestation Diabetes Mellitus

Danay Mavreli and Ariadni Mavrou

Res Rep Med Sci 2017, 1:1

A Rare Familial Paracentric Inversion in the Long Arm of Chromosome 8: Case Report and Review of the Literature.

Kouvidi E, Tsarouha H, Zachaki S, Mitrakos A, Sfakianoudis K, Kanavakis E., Mavrou A.

J Genet Disor Genet Rep 2017, 6:2. doi: 10.4172/2327-5790.1000152

Retrotransposon expression and incorporation of cloned human and mouse retroelements in human spermatozoa.

Lazaros L, Kitsou C, Kostoulas C, Bellou S, Hatzi E, Ladias P, Stefos T, Markoula S, Galani V, Vartholomatos G, Tzavaras T, Georgiou I.

Fertil Steril. 2017 Mar;107(3):821-830.

Association of GSTP1 inactivating polymorphism with acute myeloid leukemia and its specific chromosomal abnormalities.

Daraki A, Zachaki S, Rosmaraki F, Kalomoiraki M, Aleporou-Marinou V, Sambani C, Kollia P, Manola KN.

Leuk Lymphoma. 2017 Mar 2:1-3.

GSTP1 and CYP2B6 Genetic Polymorphisms and the Risk of Bronchopulmonary Dysplasia in Preterm Neonates.

Zachaki S, Daraki A, Polycarpou E, Stavropoulou C, Manola KN, Gavrili S.

Am J Perinatol. 2017 Jan 12.

Σύνδρομο αναστροφής φύλου (46,ΧΧ άρρεν) σε άνδρα με υπογονιμότητα.

Ε. Κουβίδη, Σ. Ζαχάκη, Λ. Λάζαρος, Κ. Μανωλά, R. Dobrescu, Χ. Τσιμέλα, Ε. Καρανδρέα, Ε. Καναβάκης, Α. Μαύρου

Αρχεία Ελληνικής Ιατρικής 39, Τεύχος 6, Νοέμβριος-Δεκέμβριος 2022, 853-856.

Χαμηλό ποσοστό μωσαϊκισμού του χρωμοσώματος του φύλου Χ. Ένα συχνό εύρημα σε γυναίκες με υπογονιμότητα.

Ε. Κουβίδη, Σ. Ζαχάκη, Χ. Τσαρουχά, Α. Πάντου, Ε. Καναβάκης, Α. Μαύρου

Αρχεία Ελληνικής Ιατρικής 35, Τεύχος 6, Νοέμβριος-Δεκέμβριος 2018, 802-806.

Καρυότυπος 47,ΧΥΥ σε ασθενή με Διαταραχές Αυτιστικού Φάσματος.

Κουβίδη Ε., Ζαχάκη Σ., Μητράκος Α., Τσαρουχά Χ., Πάντου Α., Καναβάκης Ε., Μαύρου Α.

Παιδιατρική 80, Τεύχος 3, Σεπτέμβριος–Δεκέμβριος 2017, 228 – 232.