Δημήτριος Ζαφειρίου

Πρωτεύουσες καρτέλες

Ο κατάλογος των δημοσιεύσεων είναι ενδεικτικός και μπορεί να μην περιλαμβάνει το σύνολο των δημοσιεύσεων.

2018
Biegstraaten, M., Cox T. M., Belmatoug N., Berger M. G., Collin-Histed T., S Dahl V., et al. (2018).  Management goals for type 1 Gaucher disease: An expert consensus document from the European working group on Gaucher disease.. Blood Cells Mol Dis. 68, 203-208.
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.
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.
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), 
2017
Kimiskidis, V. K., Papaliagkas V., Papagiannopoulos S., Zafeiriou D., Kazis D., Tsatsali-Foroglou E., et al. (2017).  Investigation of the motor system in two siblings with Canavan's disease: a combined transcranial magnetic stimulation (TMS) - diffusion tensor imaging (DTI) study.. Metab Brain Dis. 32(2), 307-310.
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.
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.
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.
2016
Vargiami, E., Dimitriadou M., Economou M., Christoforidis A., & Zafeiriou D. I. (2016).  Long-term response in biochemical markers of bone turnover during enzyme replacement therapy in a case-series of patients with Gaucher disease type I from Northern Greece.. Hippokratia. 20(2), 153-159.
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.
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.
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.
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.
Vargiami, E., Papathanasiou E., Batzios S., Kyriazi M., Dimitriou E., Anastasiou A., et al. (2016).  Neuroradiological, neurophysiological and molecular findings in infantile Krabbe disease: two case reports.. Balkan J Med Genet. 19(1), 85-90.
2015
Zafeiriou, D. I., & Vargiami E. (2015).  High-fidelity over the somatosensory cortex revisited: back to basics.. Clin Neurophysiol. 126(2), 223-4.
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.
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.
Zafeiriou, D. I. (2015).  Paroxysmal tonic upward gaze of childhood "plus": an oculomotor channelopathy?. Eur J Paediatr Neurol. 19(3), 278-9.
Sarafidis, K., Piretzi K., Agakidou E., Kohlhase J., & Zafeiriou D. (2015).  Stüve-Wiedemann syndrome in a neonate.. Pediatr Int. 57(2), 302-4.
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.
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.
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.
2014
Trakadis, Y. J., Alfares A., Bodamer O. A., Buyukavci M., Christodoulou J., Connor P., et al. (2014).  Update on transcobalamin deficiency: clinical presentation, treatment and outcome.. J Inherit Metab Dis. 37(3), 461-73.
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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