Publications by Year: 2012

2012
Panayotacopoulou MT, Ganou V, Pagida MA, Malidelis YI, Kontostavlaki DP, Tsekoura E, Patsouris E, Konstantinidou AE. 4. Expression of Tyrosine Hydroxylase in Magnocellular Neurosecretory Neurons of the Human Neonate under Hypoxic Conditions: A Potential Neuropathological Marker for Hypoxic-ischemic Encephalopathy. Pediatric & Developmental Pathology. 2012;15(5):418.
Konstantinidou A, Katsimbali A, Dalkaraki N. 32. The trio of cleft lip/palate, poly/syndactyly and genital abnormalities as associated with rare genetic syndromes: 3 cases of fetal autopsy. Pediatric & Developmental Pathology. 2012;15(5):426.
Sifakis S, Anagnostopoulou K, Plastira K, Vrachnis N, Konstantinidou A, Sklavounou E. Rare case of XX/XY mosaicism and trisomy 13 in early prenatal diagnosis. Birth Defects Research Part A: Clinical and Molecular Teratology. 2012;94(4):245-248.
Konstantinidou A. Skeletal dysplasias of the human fetus: postmortem diagnosis. INTECH Open Access Publisher; 2012.
Kitsiou‐Tzeli S, Konstantinidou A, Sofocleous C, Kosma K, Syrmou A, Giannikou K, Sifakis S, Makrythanasis P, Tzetis M. Familial Pelizaeus–Merzbacher disease caused by a 320.6‐kb Xq22. 2 duplication and the pathological findings of a male fetus. Birth Defects Research Part A: Clinical and Molecular Teratology. 2012;94(6):494-498.
Christopoulou G, Tzetis M, Konstantinidou AE, Tsezou A, Kanavakis E, Kitsiou-Tzeli S, Velissariou V. Clinical and molecular description of a fetus in prenatal diagnosis with a rare de novo ring 10 and deletions of 12.59 Mb in 10p15. 3–p14 and 4.22 Mb in 10q26. 3. European journal of medical genetics. 2012;55(1):75-79.
Gourvas V, Dalpa E, Konstantinidou A, Vrachnis N, Spandidos DA, Sifakis S. Angiogenic factors in placentas from pregnancies complicated by fetal growth restriction (review). Mol Med Rep. 2012;6(1):23-27.