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 I  [Clear All Filters]
Journal Article
Papageorgiou, V., Vargiami E., Kontopoulos E., Kardaras P., Economou M., Athanassiou-Mataxa M., et al. (2015).  Association between iron deficiency and febrile seizures.. Eur J Paediatr Neurol. 19(5), 591-6.
Zafeiriou, D. I. (2016).  The brainstem in late preterm birth: Born small-for-gestational-age is the "tip of the iceberg".. Clin Neurophysiol. 127(9), 3178-3179.
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.
Dragoumi, P., Tzetzi O., Vargiami E., Pavlou E., Krikonis K., Kontopoulos E., et al. (2013).  Clinical course and seizure outcome of idiopathic childhood epilepsy: determinants of early and long-term prognosis.. BMC Neurol. 13, 206.
Kozeis, N., Panos G. D., Zafeiriou D. I., de Gottrau P., & Gatzioufas Z. (2015).  Comparative Study of Refractive Errors, Strabismus, Microsaccades, and Visual Perception Between Preterm and Full-Term Children With Infantile Cerebral Palsy.. J Child Neurol. 30(8), 972-5.
Batzios, S. P., & Zafeiriou D. I. (2012).  Developing treatment options for metachromatic leukodystrophy.. Mol Genet Metab. 105(1), 56-63.
Zafeiriou, D. I., Pavlidou E. L., & Vargiami E. (2011).  Diverse clinical and genetic aspects of craniofrontonasal syndrome.. Pediatr Neurol. 44(2), 83-7.
Triantafyllou, P., Vargiami E., Vagianou I., Badouraki M., Julier C., & Zafeiriou D. I. (2014).  Early-onset diabetes mellitus and neurodevelopmental retardation: the first Greek case of Wolcott-Rallison syndrome.. J Pediatr Endocrinol Metab. 27(9-10), 967-70.
Triantafyllou, P., Christoforidis A., Vargiami E., & Zafeiriou D. I. (2014).  Growth hormone replacement therapy in Costello syndrome.. Growth Horm IGF Res. 24(6), 271-5.
Zafeiriou, D. I., & Vargiami E. (2015).  High-fidelity over the somatosensory cortex revisited: back to basics.. Clin Neurophysiol. 126(2), 223-4.
Zafeiriou, D. I., Vargiami E., Hatzidimitriou V., & Kyriazi M. (2013).  Incontinentia pigmenti: a skin, brain, and eye matter.. J Pediatr. 163(5), 1520.
Steenweg, M. E., Salomons G. S., Yapici Z., Uziel G., Scalais E., Zafeiriou D. I., et al. (2009).  L-2-Hydroxyglutaric aciduria: pattern of MR imaging abnormalities in 56 patients.. Radiology. 251(3), 856-65.
Vargiami, E., Sapountzi E., Samakovitis D., Batzios S., Kyriazi M., Anastasiou A., et al. (2014).  Moyamoya syndrome and neurofibromatosis type 1.. Ital J Pediatr. 40, 59.
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.
Triantafyllou, P., Economou M., Vlachaki E., Aggelaki M., Athanassiou-Mataxa M., Michelakaki E., et al. (2014).  Multiple endocrine disorders associated with adrenomyeloneuropathy and a novel mutation of the ABCD1 gene.. Pediatr Neurol. 50(6), 622-4.
Vargiami, E., Printza N., Papadimiditriou E., Batzios S., Kyriazi M., Papachristou F., et al. (2016).  Nephrocalcinosis and Renal Failure in Lesch-Nyhan Syndrome: Report of Two Familial Cases and Review of the Literature.. Urology. 97, 194-196.
Zafeiriou, D. I., & Vargiami E. (2012).  Noninvasive ultra high-frequency (1kHz) oscillations' recording: high-fidelity over somatosensory cortex.. Clin Neurophysiol. 123(12), 2323-4.
Steenweg, M. E., Jakobs C., Errami A., van Dooren S. J. M., Bartolomé M. T. Adeva, Aerssens P., et al. (2010).  An overview of L-2-hydroxyglutarate dehydrogenase gene (L2HGDH) variants: a genotype-phenotype study.. Hum Mutat. 31(4), 380-90.
Vardarinos, A., Zafeiriou D. I., Vargiami E., Pratsidou-Gertsi P., Kontopoulos E., Kanakoudi-Tsakalidou F., et al. (2009).  Parental reports of health-related quality of life in greek children with neurofibromatosis type 1.. J Pediatr. 155(3), 453; author reply 454.
Zafeiriou, D. I. (2015).  Paroxysmal tonic upward gaze of childhood "plus": an oculomotor channelopathy?. Eur J Paediatr Neurol. 19(3), 278-9.
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.
Teflioudi, E. P., Zafeiriou D. I., Vargiami E., Kontopoulos E., & Tsikoulas I. (2011).  Somatosensory evoked potentials in children with bilateral spastic cerebral palsy.. Pediatr Neurol. 44(3), 177-82.
Kupferman, J. C., Zafeiriou D. I., Lande M. B., Kirkham F. J., & Pavlakis S. G. (2017).  Stroke and Hypertension in Children and Adolescents.. J Child Neurol. 32(4), 408-417.
Willemsen, M. A., Verbeek M. M., Kamsteeg E-J., van Andel J. F. de Rijk-, Aeby A., Blau N., et al. (2010).  Tyrosine hydroxylase deficiency: a treatable disorder of brain catecholamine biosynthesis.. Brain. 133(Pt 6), 1810-22.

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