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Publications

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

Export 7 results:
Author Title [ Type(Desc)] Year
Filters: Author is Ververi, Athina  [Clear All Filters]
Journal Article
Moutafi, M., Gkiourtzis N., Ververi A., Kavga M., Morichovitou A., Papadopoulou-Legbelou K., et al. (2023).  Beckwith-Wiedemann syndrome with multiple hepatic and cutaneous hemangiomas in a female patient of Albanian origin: Diagnostic and therapeutic considerations.. Am J Med Genet A.
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.
Hitoglou, M., Ververi A., Antoniadis A., & Zafeiriou D. I. (2010).  Childhood autism and auditory system abnormalities.. Pediatr Neurol. 42(5), 309-14.
Ververi, A., Vargiami E., Papadopoulou V., Tryfonas D., & Zafeiriou D. I. (2012).  Clinical and laboratory data in a sample of Greek children with autism spectrum disorders.. J Autism Dev Disord. 42(7), 1470-6.
Printza, N., Ververi A., Bandouraki M., Vargiami E., Gidaris D., & Papachristou F. (2012).  Life-threatening hyponatremia and acute renal failure due to iatrogenic neonatal bladder rupture.. Urol Int. 88(2), 238-40.
Vargiami, E., Ververi A., Al-Mutawa H., Gioula G., Gerou S., Rouvalis F., et al. (2016).  Multiple Coronary Artery Microfistulas in a Girl with Kleefstra Syndrome.. Case Rep Genet. 2016, 3056053.
Vargiami, E., Ververi A., Kyriazi M., Papathanasiou E., Gioula G., Gerou S., et al. (2014).  Severe clinical presentation in monozygotic twins with 10p15.3 microdeletion syndrome.. Am J Med Genet A. 164A(3), 764-8.

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