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 Zafeiriou, Dimitrios  [Clear All Filters]
Journal Article
Tsoutsou, E., Tzetis M., Giannikou K., Braoudaki M., Mitrakos A., Amenta S., et al. (2017).  Application of high-resolution array comparative genomic hybridization in children with unknown syndromic microcephaly.. Pediatr Res. 82(2), 253-260.
Stabouli, S., Vargiami E., Maliachova O., Printza N., Dotis J., Kyriazi M., et al. (2018).  Arterial Stiffness in a Toddler with Neurofibromatosis Type 1 and Refractory Hypertension.. Case Rep Pediatr. 2018, 5957987.
Gkampeta, A., Fidani L., Clarimón J., Kalinderi K., Katopodi T., Zafeiriou D., et al. (2014).  Association of brain-derived neurotrophic factor (BDNF) and elongator protein complex 4 (ELP4) polymorphisms with benign epilepsy with centrotemporal spikes in a Greek population.. Epilepsy Res. 108(10), 1734-9.
Velikos, K., Soubasi V., Michalettou I., Sarafidis K., Nakas C., Papadopoulou V., et al. (2015).  Bayley-III scales at 12 months of corrected age in preterm infants: Patterns of developmental performance and correlations to environmental and biological influences.. Res Dev Disabil. 45-46, 110-9.
Gkampeta, A., Fidani L., Zafeiriou D., & Pavlou E. (2015).  Benign epilepsy with centrotemporal spikes: Relationship between type of seizures and response to medication in a Greek population.. J Neurosci Rural Pract. 6(4), 545-8.
Ververi, A., Vargiami E., Papadopoulou V., Tryfonas D., & Zafeiriou D. (2015).  Brainstem Auditory Evoked Potentials in Boys with Autism: Still Searching for the Hidden Truth.. Iran J Child Neurol. 9(2), 21-8.
Tarailo-Graovac, M., Shyr C., Ross C. J., Horvath G. A., Salvarinova R., Ye X. C., et al. (2016).  Exome Sequencing and the Management of Neurometabolic Disorders.. N Engl J Med. 374(23), 2246-55.
Karagiozoglou-Lampoudi, T., Daskalou E., Vargiami E., & Zafeiriou D. (2012).  Identification of feeding risk factors for impaired nutrition status in paediatric patients with cerebral palsy.. Acta Paediatr. 101(6), 649-54.
Héron, B., Mikaeloff Y., Froissart R., Caridade G., Maire I., Caillaud C., et al. (2011).  Incidence and natural history of mucopolysaccharidosis type III in France and comparison with United Kingdom and Greece.. Am J Med Genet A. 155A(1), 58-68.
Beslow, L. A., Dowling M. M., Hassanein S. M. A., Lynch J. K., Zafeiriou D., Sun L. R., et al. (2018).  Mortality After Pediatric Arterial Ischemic Stroke.. Pediatrics. 141(5), 
Chatziioannidis, I., Kyriakidou M., Exadaktylou S., Antoniou E., Zafeiriou D., & Nikolaidis N. (2018).  Neurological outcome at 6 and 12 months corrected age in hospitalised late preterm infants -a prospective study.. Eur J Paediatr Neurol. 22(4), 602-609.
Triantafyllou, P., Katzos G., Rousso I., & Zafeiriou D. (2015).  Neurophysiologic evaluation of infants with congenital hypothyroidism before and after treatment.. Acta Neurol Belg. 115(2), 129-36.
Printza, N., Roilides E., Kotsiou M., Zafeiriou D., Hatzidimitriou V., & Papachristou F. (2011).  Pandemic influenza A (H1N1) 2009-associated hemolytic uremic syndrome.. Pediatr Nephrol. 26(1), 143-4.
Panagopoulou, P., Athanasiadis D., Αnastasiou Α., Zafeiriou D., & Papakonstantinou Ε. (2023).  Pediatric Optic Pathway Gliomas: A Report From Northern Greece.. J Pediatr Hematol Oncol. 45(8), 445-451.
Ilia, T. Soultana, Dragoumi P., Papanikolopoulou S., Goulis D. G., Pavlou E., & Zafeiriou D. (2022).  Is the prevalence of thyroid disease higher in children receiving antiepileptic medication? A systematic review and meta-analysis.. Seizure. 94, 117-125.
Papadopoulou, A., Dinopoulos A., Koutsodontis G., Pons R., Vorgia P., Koute V., et al. (2018).  Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome.. Eur J Paediatr Neurol. 22(3), 419-426.
Stabouli, S., Gidaris D., Printza N., Dotis J., Papadimitriou E., Chrysaidou K., et al. (2019).  Sleep disorders and executive function in children and adolescents with chronic kidney disease.. Sleep Med. 55, 33-39.
Mavridou, I., Dimitriou E., Vanier M. T., Vilageliu L., Grinberg D., Latour P., et al. (2017).  The Spectrum of Niemann-Pick Type C Disease in Greece.. JIMD Rep. 36, 41-48.
Perrault, I., Hanein S., Gerard X., Delphin N., Fares-Taie L., Gerber S., et al. (2010).  Spectrum of SPATA7 mutations in Leber congenital amaurosis and delineation of the associated phenotype.. Hum Mutat. 31(3), E1241-50.
Sarafidis, K., Piretzi K., Agakidou E., Kohlhase J., & Zafeiriou D. (2015).  Stüve-Wiedemann syndrome in a neonate.. Pediatr Int. 57(2), 302-4.
Teli, A., Economou M., Rudolf J., Tzovaras F., Gourtsa V., Kondou A., et al. (2012).  Subclinical central nervous system involvement and thrombophilic status in young thalassemia intermedia patients of Greek origin.. Blood Coagul Fibrinolysis. 23(3), 195-202.
Gavriilaki, E., Tsiftsoglou S. A., Touloumenidou T., Farmaki E., Panagopoulou P., Michailidou E., et al. (2022).  Targeted Genotyping of MIS-C Patients Reveals a Potential Alternative Pathway Mediated Complement Dysregulation during COVID-19 Infection.. Curr Issues Mol Biol. 44(7), 2811-2824.

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