Πλοήγηση ανά Συγγραφέα "Sotiriou, S."
-
Characterization of 23 small supernumerary marker chromosomes detected at pre-natal diagnosis: The value of fluorescence in situ hybridization
Manolakos, E.; Kefalas, K.; Neroutsou, R.; Lagou, M.; Kosyakova, N.; Ewers, E.; Ziegler, M.; Weise, A.; Tsoplou, P.; Rapti, S. M.; Papoulidis, I.; Anastasakis, E.; Garas, A.; Sotiriou, S.; Eleftheriades, M.; Peitsidis, P.; Malathrakis, D.; Thomaidis, L.; Kitsos, G.; Orru, S.; Liehr, T.; Petersen, M. B.; Kitsiou-Tzeli, S. (2010)Small supernumerary marker chromosomes (sSMCs) cannot be identified or characterized unambiguously by conventional cytogenetic banding techniques. Until recently, the large variety of marker chromosomes, as well as the ... -
A comparison in concentration of heat shock proteins (HSP) 70 and 90 on chorionic villi of human placenta in normal pregnancies and in missed miscarriages
Sotiriou, S.; Liatsos, K.; Ladopoulos, I.; Arvanitis, D. L. (2004)Purpose: To investigate the role of heat shock protein (HSP) on the chorionic villi of human placenta! cells and to compare the concentration of placental HSP70 & 90 in term deliveries and in missed miscarriages. Materials ... -
Deletion 2q31.2-q31.3 in a 4-Year-Old Girl With Microcephaly and Severe Mental Retardation
Manolakos, E.; Vetro, A.; Kefalas, K.; Thomaidis, L.; Aperis, G.; Sotiriou, S.; Kitsos, G.; Merkas, M.; Sifakis, S.; Papoulidis, I.; Liehr, T.; Zuffardi, O.; Petersen, M. B. (2011) -
Deletion of 4.4 Mb at 2q33.2q33.3 May Cause Growth Deficiency in a Patient with Mental Retardation, Facial Dysmorphic Features and Speech Delay
Papoulidis, I.; Paspaliaris, V.; Papageorgiou, E.; Siomou, E.; Dagklis, T.; Sotiriou, S.; Thomaidis, L.; Manolakos, E. (2015)A patient with a rare interstitial deletion of chromosomal band 2q33.2q33.3 is described. The clinical features resembled the 2q33.1 microdeletion syndrome (Glass syndrome), including mental retardation, facial dysmorphism, ... -
Detailed molecular and clinical investigation of a child with a partial deletion of chromosome 11 (Jacobsen syndrome)
Manolakos, E.; Orru, S.; Neroutsou, R.; Kefalas, K.; Louizou, E.; Papoulidis, I.; Thomaidis, L.; Peitsidis, P.; Sotiriou, S.; Kitsos, G.; Tsoplou, P.; Petersen, M. B.; Metaxotou, A. (2009)Background: Jacobsen syndrome (JBS) is a rare chromosomal disorder leading to multiple physical and mental impairment. This syndrome is caused by a partial deletion of chromosome 11, especially subband 11q24.1 has been ... -
Expression of 6 Common Antigenic Markers in Invasive Ductal Breast Carcinoma: Potential Clinical Implications
Lialiaris, T. S.; Kouskoukis, A.; Georgiou, G.; Tripsianis, G.; Fiska, A.; Giatromanolaki, A.; Chrisafi, S.; Sivridis, E.; Vamvakopoulou, D. N.; Soutopoulou, D. O.; Kiritsaka, A.; Athanassiou, E.; Lialios, G. A.; Sotiriou, S.; Sidiropoulos, A.; Vamvakopoulos, N. C. (2011)Expression of estrogen (ER) and progesterone receptors, c-erbB-2 oncogene, mutant p53 antioncogene (mp53), e-cadherin adhesion, and apoptotic caspase-8 antigens in tumor relative to matched normal tissue specimens from 102 ... -
Follicular Fluid Oocyte/Cumulus-Free DNA Concentrations as a Potential Biomolecular Marker of Embryo Quality and IVF Outcome
Dimopoulou, M.; Anifandis, G.; Messini, C. I.; Dafopoulos, K.; Kouris, S.; Sotiriou, S.; Satra, M.; Vamvakopoulos, N.; Messinis, I. E. (2014)The present prospective study examined the follicular fluid oocyte/cumulus-free DNA concentrations (ff o/c-free DNA) during ovarian stimulation and the possible association between ff o/c-free DNA and embryological results ... -
The impact of cigarette smoking and alcohol consumption on sperm parameters and sperm DNA fragmentation (SDF) measured by Halosperm(A (R))
Anifandis, G.; Bounartzi, T.; Messini, C. I.; Dafopoulos, K.; Sotiriou, S.; Messinis, I. E. (2014)Both cigarette smoking and alcohol consumption are somehow implicated in sperm function, but the impact of these two lifestyle factors on sperm parameters remains controversial. The present study is focused on the impact ... -
Interstitial deletion at 11q14.2-11q22.1 may cause severe learning difficulties, mental retardation and mild heart defects in 13-year old male
Papoulidis, I.; Paspaliaris, V.; Siomou, E.; Orru, S.; Murru, R.; Sifakis, S.; Nikolaidis, P.; Garas, A.; Sotiriou, S.; Thomaidis, L.; Manolakos, E. (2015)Interstitial deletions of the long arm of chromosome 11 are rare, and they could be assumed as non-recurrent chromosomal rearrangements due to high variability of the size and the breakpoints of the deleted region. The ... -
Molecular and Cellular Mechanisms of Sperm-Oocyte Interactions Opinions Relative to in Vitro Fertilization (IVF)
Anifandis, G.; Messini, C.; Dafopoulos, K.; Sotiriou, S.; Messinis, I. (2014)One of the biggest prerequisites for pregnancy is the fertilization step, where a human haploid spermatozoon interacts and penetrates one haploid oocyte in order to produce the diploid zygote. Although fertilization is ... -
Prenatal detection of an inverted duplication deletion in the long arm of chromosome 1 in a fetus with increased nuchal translucency. Molecular cytogenetic analysis and review of the literature
Manolakos, E.; Sifakis, S.; Sotiriou, S.; Peitsidis, P.; Eleftheriades, M.; Mersinias, V.; Liehr, T.; Thomaidis, L.; Kitsos, G.; Papoulidis, I.; Petersen, M. B.; Orru, S. (2012) -
Sequence-based genotyping HPV L1 DNA and RNA transcripts in clinical specimens
Satra, M.; Vamvakopoulou, D. N.; Sioutopoulou, D. O.; Kollia, P.; Kiritsaka, A.; Sotiriou, S.; Antonakopoulos, G.; Alexandris, E.; Costantoulakis, P.; Vamvakopoulos, N. C. (2009)We developed a direct sequence-based genotyping method to detect single and multiple HPV L1 DNA and RNA types in genital and dermatological specimens. Our method couples PCR amplification of a highly conserved HPV L1 segment ... -
Sonographic antenatal diagnosis of congenital dacryocystoceles
Sotiriou, S.; Manolakos, E.; Peitsidis, P.; Garas, A. (2012)Congenital dacryocystoceles are a relatively rare variant of nasolacrimal duct obstruction, accounting for only 0.1% of infants with congenital nasolacrimal duct obstruction. We report a new case of bilateral congenital ... -
Sperm DNA fragmentation measured by Halosperm does not impact on embryo quality and ongoing pregnancy rates in IVF/ICSI treatments
Anifandis, G.; Bounartzi, T.; Messini, C. I.; Dafopoulos, K.; Markandona, R.; Sotiriou, S.; Tzavella, A.; Messinis, I. E. (2015)Sperm DNA fragmentation (SDF) has been proposed to be one of the main markers regarding male infertility. A prospective study was performed to assess primarily whether sperm DNA damage has any impact on embryological data ...