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Pelagia Vorgia

Observed names: P. Vorgia, Vorgia Pelagia, Vorgia, Pelagia
Observed institutions: University of Crete, Hellenic Mediterranean University, FORTH Institute of Molecular Biology and Biotechnology, University Hospital of Heraklion, Technical University of Crete, Foundation for Research and Technology Hellas
ORCID: 0000-0002-7061-146X
Observed ORCID: 0000-0002-7061-146X
OpenAlex ID: A5002706965
Focal epileptic seizures anticipation based on patterns of heart rate variability parameters
2019 · Giorgos Giannakakis, Manolis Tsiknakis, et al. · Computer Methods and Programs in Biomedicine · 42
Tolosa-Hunt Syndrome: Clinical Manifestations in Children
2019 · Maria Tsirigotaki, George Ntoulios, et al. · Pediatric Neurology · 29
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
1998 · Pelagia Vorgia, Vassilis I. Zannis, et al. · Journal of Biological Chemistry · 27
Absence seizure epilepsy detection using linear and nonlinear eeg analysis methods
2013 · Vangelis Sakkalis, Giorgos Giannakakis, et al. · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · 26
A programmed decline in ribosome levels governs human early neurodevelopment
2025 · Chunyang Ni, Yudong Wei, et al. · Nature Cell Biology · 25
Evaluation of Genotypes and Epidemiology of Spinal Muscular Atrophy in Greece: A Nationwide Study Spanning 24 Years
2020 · Kyriaki Kekou, Maria Svingou, et al. · Journal of Neuromuscular Diseases · 22
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The impact of mode of delivery and gestational age on cord blood hematopoietic stem/progenitor cells
2006 · Helen Dimitriou, Chryssoula Perdikogianni, et al. · Annals of Hematology · 22
An approach to absence epileptic seizures detection using Approximate Entropy
2013 · Giorgos Giannakakis, Vangelis Sakkalis, et al. · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · 18
Vision-based absence seizure detection
2012 · M. Pediaditis, M. Tsiknakis, et al. · Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC) · 18
Case Report: Intracranial Hypertension Secondary to Guillain-Barre Syndrome
2021 · Christina Doxaki, Eleftheria Papadopoulou, et al. · Frontiers in Pediatrics · 15
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Vision-based human motion analysis in epilepsy - Methods and challenges
2010 · M. Pediaditis, M. Tsiknakis, et al. · IEEE International Conference on Information Technology and Applications in Biomedicine · 15
Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome
2018 · Anna Papadopoulou, Argyrios Dinopoulos, et al. · European Journal of Paediatric Neurology · 13
Semi-Supervised anomaly detection for the prediction and detection of pediatric focal epileptic seizures on fused EEG and ECG data
2024 · Apostolos Karasmanoglou, Giorgos Giannakakis, et al. · Biomedical Signal Processing and Control · 12
A dynamic trinucleotide repeat (TNR) expansion in the DMD gene
2016 · Kyriaki Kekou, Christalena Sofocleous, et al. · Molecular and Cellular Probes · 12
Frontal lobe epilepsy and mild malformation with oligodendroglial hyperplasia: Further observations on electroclinical and imaging phenotypes, and surgical perspectives
2023 · Kyriakos Garganis, Kostakis Gkiatis, et al. · Epileptic Disorders · 10
A8344G tRNALys mutation associated with recurrent brain stem stroke-like episodes
2009 · I. Zaganas, H. Latsoudis, et al. · Journal of Neurology · 10
In vitro proliferative and differentiating characteristics of CD133+ and CD34+ cord blood cells in the presence of thrombopoietin (TPO) or erythropoietin (EPO)
2003 · Helen Dimitriou, Pelagia Vorgia, et al. · Leukemia Research · 10
Model-free vision-based facial motion analysis in epilepsy
2011 · M. Pediaditis, M. Tsiknakis, et al. · International Workshop on Biomedical Engineering (IWBE) · 9
SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations
2024 · Danai Veltra, Virginia Theodorou, et al. · International Journal of Molecular Sciences · 7
Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes
2021 · Ioannis Zaganas, Pelagia Vorgia, et al. · Epilepsy & Behavior Reports · 7
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Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome
2007 · S. Voutoufianakis, S. Psoni, et al. · European Journal of Paediatric Neurology · 7
Pediatric tumefactive multiple sclerosis case (with baló-like lesions), diagnostic and treatment challenges
2022 · Christina Kamari, Emmanouil Galanakis, et al. · Neurological Sciences · 6
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Automatic Absence Seizure Detection Evaluating Matching Pursuit Features of EEG Signals
2019 · Katerina Giannakaki, Giorgos Giannakakis, et al. · IEEE International Conference on Bioinformatics and Bioengineering (BIBE) · 6
Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms
2023 · Danai Veltra, Faidon-Nikolaos Tilemis, et al. · Expert Review of Molecular Diagnostics · 5
Exploiting advanced video analysis technologies for a smart home monitoring platform for epileptic patients: Technological and legal preconditions
2012 · M. Pediaditis, M. Tsiknakis, et al. · International Conference on Telecommunications and Multimedia (TEMU) · 5
Works count: 38
Citation count: 395
H-index: 12
I10-index: 17
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