Δημοσιεύσεις

Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.

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Συντάκτης Τίτλος [ Τύπος(Desc)] Έτος
Φίλτρα: Συντάκτης is Papoulidis, Ioannis  [Clear All Filters]
Journal Article
Kontodiou, M., Daskalakis G., Vetro A., Paspaliaris V., Papaioannou G., Dagklis T., et al. (2015).  Complex Rearrangement Involving Three Chromosomes, Four Breakpoints and a 2.7-Mb Deletion in the 18q Segment Observed in a Girl with Mild Learning Difficulties.. Cytogenet Genome Res. 147(2-3), 118-23.
Papoulidis, I., Paspaliaris V., Papageorgiou E., Siomou E., Dagklis T., Sotiriou S., et al. (2015).  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.. Cytogenet Genome Res. 145(1), 19-24.
Papoulidis, I., Manolakos E., Siomou E., Kefalas K., Thomaidis L., Liehr T., et al. (2010).  A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth.. Prenat Diagn. 30(6), 586-8.
Papoulidis, I., Vetro A., Paspaliaris V., Ziegler M., Kreskowski K., Daskalakis G., et al. (2018).  A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization.. Curr Genomics. 19(3), 240-246.
Agakidis, C., Agakidou E., Sarafidis K., Papoulidis I., Xinias I., & Farmaki E. (2019).  Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome Associated With a Novel Mutation of Gene.. Front Pediatr. 7, 20.
Giovannopoulou, E., Tsakiridis I., Mamopoulos A., Kalogiannidis I., Papoulidis I., Athanasiadis A., et al. (2022).  Invasive Prenatal Diagnostic Testing for Aneuploidies in Singleton Pregnancies: A Comparative Review of Major Guidelines.. Medicina (Kaunas). 58(10), 
Ntelios, D., Parcharidou D., Zegkos T., Paraskevaidis S., Manolakos E., Papoulidis I., et al. (2020).  The multiple faces of Danon disease.. Hellenic J Cardiol.
Zecevic, N., Arsenijevic V., Manolakos E., Papoulidis I., Theocharis G., Sartsidis A., et al. (2020).  New Compound Heterozygous Splice Site Mutations of the Skeletal Muscle Ryanodine Receptor () Gene Manifest Fetal Akinesia: A Linkage with Congenital Myopathies.. Mol Syndromol. 11(2), 104-109.
Mitsiakos, G., Tsakalidis C., Karagianni P., Gialamprinou D., Chatziioannidis I., Papoulidis I., et al. (2019).  A New Gene Mutation c.3445G>A (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress Syndrome.. Medicina (Kaunas). 55(7), 
Sotiriadis, A., Papoulidis I., Siomou E., Papageorgiou E., Eleftheriades M., Papadopoulos V., et al. (2017).  Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study.. Prenat Diagn. 37(6), 583-592.
Efthimiadis, G., Zegkos T., Meditskou S., Karamitsos T., Manolakos E., Papoulidis I., et al. (2020).  A novel desmoplakin mutation associated with left dominant arrhythmogenic cardiomyopathy and cutaneous phenotype.. Hellenic J Cardiol.
Papoulidis, I., Sotiriadis A., Siomou E., Papageorgiou E., Eleftheriades M., Papadopoulos V., et al. (2015).  Routine use of array comparative genomic hybridization (aCGH) as standard approach for prenatal diagnosis of chromosomal abnormalities. Clinical experience of 1763 prenatal cases.. Prenat Diagn. 35(13), 1269-77.
Bouchlariotou, S., Tsikouras P., Dimitraki M., Athanasiadis A., Papoulidis I., Maroulis G., et al. (2011).  Turner's syndrome and pregnancy: has the 45,X/47,XXX mosaicism a different prognosis? Own clinical experience and literature review.. J Matern Fetal Neonatal Med. 24(5), 668-72.

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