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Ξενόγλωσσες δημοσιεύσεις

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.

Δημοσιεύσεις σε ελληνικά περιοδικά

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.