Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Stavroula Christopoulou"'
Autor:
Eunice G Stefanou, Thomas Liehr, Stavroula Christopoulou, Lina Florentin, Francis Sachinidi, Alexandra Efthymiadou, Eleni Angelopoulou, Dionisios Chrysis, Voula Velissariou
Publikováno v:
Cytogenetic and Genome Research. 160:664-670
Trisomy 14 (T14) mosaicism is a rare chromosomal condition characterised by various clinical features, including developmental delay, growth impairment, and dysmorphism. Here, we report on a 12-year-old female referred for cytogenetic analysis due to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d61e7046b2d2d838fdb7d043252a1413
https://doi.org/10.1159/000511549
https://doi.org/10.1159/000511549
Autor:
Stavroula Christopoulou
Ο Γιώργος Σισιλιάνος (1920-2005) είναι ένας από τους σημαντικότερους εκπροσώπους του ελληνικού μουσικού μοντερνισμού. Η παρούσα διατριβή επ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d21ea4781a5822911a4e0b1a3f740471
https://doi.org/10.12681/eadd/33700
https://doi.org/10.12681/eadd/33700
Autor:
Stavros Sifakis, P. Kaminopetros, Stavroula Christopoulou, V. Velissariou, G. Christopoulou, A. Hatzaki, Jackie Donoghue, M. Karkaletsi, A. Hatzipouliou
Publikováno v:
Gynecologic and Obstetric Investigation. 68:255-261
Aim: The aim of this study is to assess the replacement of chromosomal analysis of chorionic villi (CV) direct preparation samples (DIR) by quantitative fluorescence PCR (QF-PCR) and to determine its advantages in routine prenatal diagnosis. Methods:
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f6a88a80e21f9dd0a3d21a5ed8e5f3ed
https://doi.org/10.1159/000240671
https://doi.org/10.1159/000240671
Publikováno v:
Personality and Individual Differences. 44:1138-1150
The number of studies using a modified Stroop task in the examination of health anxiety-related cognitive biases is limited, and their results are divergent. The use of research methods that preclude conscious processes is, however, essential. The pu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e09c02dc8bdb2484f39f86fd73215e65
https://doi.org/10.1016/j.paid.2007.11.007
https://doi.org/10.1016/j.paid.2007.11.007
Autor:
Jackie Donoghue, T. Konstantinidou, V. Velissariou, Stavroula Christopoulou, Stavros Sifakis, M. Karkaletsi, P. Kaminopetros
Publikováno v:
Prenatal Diagnosis. 28:1174-1176
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::337e8e67c38fa1d30433890da24e1410
https://doi.org/10.1002/pd.2134
https://doi.org/10.1002/pd.2134
Autor:
Thalia Antoniadi, Michael B. Petersen, Efstathia Katsarou, Jackie Donoghue, Katerina Bakou, Panagiotis Karatzis, Athina Hatzipouliou, Maria Grigoriadou, Jolanda Gyftodimou, Voula Velissariou, Stavroula Christopoulou
Publikováno v:
European journal of human genetics : EJHG. 10(11)
The clinical significance of trisomy 20 mosaicism detected prenatally remains uncertain due to the rarity of liveborn cases with inconsistent clinical findings, and lack of long-term follow-up and outcome. We describe a case of true trisomy 20 mosaic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::88a469361e10acaa4e7bef5c16133de5
https://pubmed.ncbi.nlm.nih.gov/12404100
https://pubmed.ncbi.nlm.nih.gov/12404100
Autor:
Philippos C. Patsalis, Katerina Bakou, Thalia Antoniadi, Voula Velissariou, Vassilis Athanassiou, Athina Hatzipouliou, Jackie Donoghue, P. Kaminopetros, Stavroula Christopoulou, Michael B. Petersen
Publikováno v:
Prenatal diagnosis. 21(6)
Two rare de novo structural aberrations of the Y chromosome were detected during routine prenatal diagnosis: a satellited non-fluorescent Y chromosome (Yqs), the first de novo Yqs to be reported in a fetus, and a terminal deletion of the Y chromosome
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::80a7fcba8b9ae51e5d8a03793fb45e03
https://pubmed.ncbi.nlm.nih.gov/11438955
https://pubmed.ncbi.nlm.nih.gov/11438955