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Pelagia Vorgia
Pelagia Vorgia
HELLENIC MEDITERRANEAN UNIVERSITY
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Cited by
Cited by
Year
Absence seizure epilepsy detection using linear and nonlinear EEG analysis methods
V Sakkalis, G Giannakakis, C Farmaki, A Mousas, M Pediaditis, P Vorgia, ...
2013 35th Annual International Conference of the IEEE Engineering in …, 2013
392013
A Short Proximal Promoter and the Distal Hepatic Control Region-1 (HCR-1) contribute to the Liver Specificity of the Human Apolipoprotein C-II Gene: Hepatic Enhancement by Hcr …
P Vorgia, VI Zannis, D Kardassis
Journal of Biological Chemistry 273 (7), 4188-4196, 1998
311998
Focal epileptic seizures anticipation based on patterns of heart rate variability parameters
G Giannakakis, M Tsiknakis, P Vorgia
Computer methods and programs in biomedicine 178, 123-133, 2019
292019
Tolosa-Hunt syndrome: clinical manifestations in children
M Tsirigotaki, G Ntoulios, M Lioumpas, S Voutoufianakis, P Vorgia
Pediatric Neurology 99, 60-63, 2019
272019
The impact of mode of delivery and gestational age on cord blood hematopoietic stem/progenitor cells
H Dimitriou, C Perdikogianni, E Stiakaki, P Vorgia, E Hatzidaki, ...
Annals of hematology 85, 381-385, 2006
242006
An approach to absence epileptic seizures detection using approximate entropy
G Giannakakis, V Sakkalis, M Pediaditis, C Farmaki, P Vorgia, ...
2013 35th Annual International Conference of the IEEE Engineering in …, 2013
182013
Vision-based human motion analysis in epilepsy-methods and challenges
M Pediaditis, M Tsiknakis, P Vorgia, D Kafetzopoulos, V Danilatou, ...
Proceedings of the 10th IEEE International Conference on Information …, 2010
172010
In vitro proliferative and differentiating characteristics of CD133+ and CD34+ cord blood cells in the presence of thrombopoietin (TPO) or erythropoietin (EPO): Potential …
H Dimitriou, P Vorgia, E Stiakaki, D Mavroudis, EA Markaki, ...
Leukemia research 27 (12), 1143-1151, 2003
162003
Pica and the elephant's ear
H Mihailidou, E Galanakis, P Paspalaki, P Borgia, E Mantzouranis
Journal of child neurology 17 (11), 855-856, 2002
152002
Vision-based absence seizure detection
M Pediaditis, M Tsiknakis, L Koumakis, M Karachaliou, S Voutoufianakis, ...
2012 Annual International Conference of the IEEE Engineering in Medicine and …, 2012
142012
Decision support system for classification of epilepsies in childhood
V Kostas, MS Vorgia, Lagia
Decision support system for classification of epilepsies in childhood 17 ((5 …, 2002
14*2002
Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome
A Papadopoulou, A Dinopoulos, G Koutsodontis, R Pons, P Vorgia, ...
European Journal of Paediatric Neurology 22 (3), 419-426, 2018
122018
A8344G tRNALys mutation associated with recurrent brain stem stroke-like episodes
I Zaganas, H Latsoudis, E Papadaki, P Vorgia, M Spilioti, A Plaitakis
Journal of neurology 256 (2), 271-273, 2009
102009
Evaluation of genotypes and epidemiology of spinal muscular atrophy in Greece: a nationwide study spanning 24 years
K Kekou, M Svingou, C Sofocleous, N Mourtzi, E Nitsa, G Konstantinidis, ...
Journal of neuromuscular diseases 7 (3), 247-256, 2020
92020
Model-free vision-based facial motion analysis in epilepsy
M Pediaditis, M Tsiknakis, V Bologna, P Vorgia
2011 10th International Workshop on Biomedical Engineering, 1-4, 2011
92011
Case report: intracranial hypertension secondary to Guillain-Barre syndrome
C Doxaki, E Papadopoulou, I Maniadaki, NG Tsakalis, K Palikaras, ...
Frontiers in Pediatrics 8, 608695, 2021
62021
A dynamic trinucleotide repeat (TNR) expansion in the DMD gene
K Kekou, C Sofocleous, G Papadimas, D Petichakis, M Svingou, RM Pons, ...
Molecular and cellular probes 30 (4), 254-260, 2016
62016
Exploiting advanced video analysis technologies for a smart home monitoring platform for epileptic patients: Technological and legal preconditions
M Pediaditis, M Tsiknakis, V Kritsotakis, M Góralczyk, S Voutoufianakis, ...
2012 International Conference on Telecommunications and Multimedia (TEMU …, 2012
62012
Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome
S Voutoufianakis, S Psoni, P Vorgia, F Tsekoura, K Kekou, ...
European Journal of Paediatric Neurology 11 (4), 235-239, 2007
62007
Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes
I Zaganas, P Vorgia, M Spilioti, L Mathioudakis, M Raissaki, S Ilia, ...
Epilepsy & Behavior Reports 16, 100477, 2021
52021
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