Sifakis S, Eleftheriades M, Kappou D, Murru R, Konstantinidou A, Orru S, Ziegler M, Liehr T, Manolakos E, Papoulidis I. Proximal Partial Trisomy 1q Confirmed By Comparative Genomic Hybridization Array: Prenatal Diagnosis, Molecular Cytogenetic Analysis, And Fetal Pathology. Journal of Perinatal Medicine. 2013;41:1184.

Gourvas V, Soulitzis N, Konstantinidou A, Dalpa E, Koukoura O, Koutroulakis D, Spandidos DA, Sifakis S. ANXA5 expression downregulation in pregnancies complicated by preeclampsia. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE. 2013;32:S83-S83.

Kappou D, Androutsopoulos V, Papantoniou N, Konstantinidou A, Koutroulakis D, Spandidos DA, Sifakis S. The expression of angiopoietins (Ang-1 & Ang-2) and their receptor TIE-1 in placentas from pregnancies complicated with preeclampsia. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE. 2013;32:S83-S83.

Manolakos E, Papoulidis I, Daskalakis G, Psara N, Sevastopoulou E, Konstantinidou A, Sifakis S. Prenatal Diagnosis Of 4q35-qter Characterized By Comparative Genomic Hybridization Array In Two Fetuses. Journal of Perinatal Medicine. 2013;41:1355.

Kappou D, Androutsopoulos V, Papantoniou N, Konstantinidou A, Koutroulakis D, Spandidos DA, Sifakis S. Placental expression of PlGF and sFlt-1 in pregnancies complicated with preeclampsia with or without fetal growth restriction. INTERNATIONAL JOURNAL OF MOLECULAR MEDICINE. 2013;32:S83-S83.

Pagida MA, Konstantinidou AE, Malidelis YI, Ganou V, Tsekoura E, Patsouris E, Panayotacopoulou MT. The human neurosecretory neurones under perinatal hypoxia: a quantitative immunohistochemical study of the supraoptic nucleus in autopsy material. Journal of neuroendocrinology. 2013;25(12):1255-1263.

Konstantinidou AE, Souka A, Sofocleous C, Paraskevakou H. Osteogenesis imperfecta type II: postmortem histological diagnosis on curettage material. OA Case Reports. 2013;2(7):67.

Mammas CS, Geropoulos S, Saatsakis G, Konstantinidou A, Lemonidou C, Patsouris E. Telepathology as a method to optimize quality in organ transplantation: a feasibility and reliability study of the virtual benching of liver graft. ICIMTH. 2013:276-278.

Eleftheriades M, Iavazzo C, Manolakos E, Hassiakos D, Botsis D, Petersen M, Konstantinidou A. Recurrent short rib polydactyly syndrome. Journal of Obstetrics and Gynaecology. 2013;33(1):14-16.

Manolakos E, Kefalas K, Vetro A, Oikonomidou E, Daskalakis G, Psara N, Siomou E, Papageorgiou E, Sevastopoulou E, Konstantinidou A. Prenatal diagnosis of two de novo 4q35-qter deletions characterized by array-CGH. Molecular cytogenetics. 2013;6(1):47.

Sismani C, Donoghue J, Alexandrou A, Karkaletsi M, Christopoulou S, Konstantinidou AE, Livanos P, Patsalis PC, Velissariou V. A prenatally ascertained, maternally inherited 14.8 Mb duplication of chromosomal bands Xq13. 2–q21. 31 associated with multiple congenital abnormalities in a male fetus. Gene. 2013;530(1):138-142.

Eleftheriades M, Grigoriadis C, Sotiriadis A, Botsis D, Konstantinidou A, Souka AP. Intracranial translucency and spinal cord defects: early prenatal diagnosis of diastematomyelia. Journal of Ultrasound in Medicine. 2013;32(9):1676-1677.

Pagida MA, Konstantinidou AE, Tsekoura E, Mangoura D, Patsouris E, Panayotacopoulou MT. Vulnerability of the mesencephalic dopaminergic neurons of the human neonate to prolonged perinatal hypoxia: an immunohistochemical study of tyrosine hydroxylase expression in autopsy material. Journal of Neuropathology & Experimental Neurology. 2013;72(4):337-350.

Konstantinidou AE, Tasoulas J, Kallipolitis G, Gasparatos S, Velissariou V, Paraskevakou H. Mandibulofacial dysostosis (Treacher‐Collins syndrome) in the fetus: Novel association with pectus carinatum in a molecularly confirmed case and review of the fetal phenotype. Birth Defects Research Part A: Clinical and Molecular Teratology. 2013;97(12):774-780.

Pagida MA, Konstantinidou AE, Tsekoura E, Patsouris E, Panayotacopoulou MT. Immunohistochemical demonstration of urocortin 1 in Edinger–Westphal nucleus of the human neonate: Colocalization with tyrosine hydroxylase under acute perinatal hypoxia. Neuroscience letters. 2013;554:47-52.

Gkegkes ID, Aroni K, Agrogiannis G, Patsouris ES, Konstantinidou AE. Expression of caspase-14 and keratin-19 in the human epidermis and appendages during fetal skin development. Archives of dermatological research. 2013;305(5):379-387.

Hoffer JL, Fryssira H, Konstantinidou AE, Ropers HH, Tzschach A. Novel WDR35 mutations in patients with cranioectodermal dysplasia (Sensenbrenner syndrome). Clinical genetics. 2013;83(1):92-95.