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 Manolakos, Emmanouil  [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.
Eleftheriades, M., Tsapakis E., Sotiriadis A., Manolakos E., Hassiakos D., & Botsis D. (2012).  Detection of congenital heart defects throughout pregnancy; impact of first trimester ultrasound screening for cardiac abnormalities.. J Matern Fetal Neonatal Med. 25(12), 2546-50.
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.
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.
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.

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