Κατάλογος ενδεικτικών δημοσιεύσεων του τμήματος Ιατρικής ΑΠΘ σε διεθνή επιστημονικά περιοδικά κατά τα τελευταία 5 έτη.
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Author Title [ Type] Year Filters: Author is Papoulidis, Ioannis [Clear All Filters]
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.
(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.
(2015). A fetus with ring chromosome 21 characterized by aCGH shows no clinical findings after birth..
Prenat Diagn. 30(6), 586-8.
(2010). A Girl with 10 Mb Distal Xp Deletion Arising from Maternal Pericentric Inversion: Clinical Data and Molecular Characterization..
Curr Genomics. 19(3), 240-246.
(2018). Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome Associated With a Novel Mutation of Gene..
Front Pediatr. 7, 20.
(2019). Invasive Prenatal Diagnostic Testing for Aneuploidies in Singleton Pregnancies: A Comparative Review of Major Guidelines..
Medicina (Kaunas). 58(10),
(2022). The multiple faces of Danon disease..
Hellenic J Cardiol.
(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.
(2020). A New Gene Mutation c.3445G>A (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress Syndrome..
Medicina (Kaunas). 55(7),
(2019). Non-invasive prenatal screening versus prenatal diagnosis by array comparative genomic hybridization: a comparative retrospective study..
Prenat Diagn. 37(6), 583-592.
(2017). A novel desmoplakin mutation associated with left dominant arrhythmogenic cardiomyopathy and cutaneous phenotype..
Hellenic J Cardiol.
(2020). 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.
(2015). 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.
(2011).