Pelagia Vorgia

Irakleion, ESYE43, Greece

Last Updated: 09/26/2026

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Found 18 publications

"Tuberous sclerosis in Greece: A national cohort study on clinical features and rare manifestations".

"Tuberous sclerosis in Greece: A national cohort study on clinical features and rare manifestations".

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: March 29, 2025

A programmed decline in ribosome levels governs human early neurodevelopment.

A programmed decline in ribosome levels governs human early neurodevelopment.

Journal: Nature cell biology
Published: May 01, 2024

SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations.

SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations.

Journal: International journal of molecular sciences
Published: April 03, 2024

Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms.

Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms.

Journal: Expert review of molecular diagnostics
Published: January 30, 2023

Correction to: Pediatric tumefactive multiple sclerosis case (with baló‑like lesions), diagnostic and treatment challenges.

Correction to: Pediatric tumefactive multiple sclerosis case (with baló‑like lesions), diagnostic and treatment challenges.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: November 17, 2022

Frontal lobe epilepsy and mild malformation with oligodendroglial hyperplasia: Further observations on electroclinical and imaging phenotypes, and surgical perspectives.

Frontal lobe epilepsy and mild malformation with oligodendroglial hyperplasia: Further observations on electroclinical and imaging phenotypes, and surgical perspectives.

Journal: Epileptic disorders : international epilepsy journal with videotape
Published: October 07, 2022

Pediatric tumefactive multiple sclerosis case (with baló-like lesions), diagnostic and treatment challenges.

Pediatric tumefactive multiple sclerosis case (with baló-like lesions), diagnostic and treatment challenges.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
Published: July 08, 2022

Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes.

Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes.

Journal: Epilepsy & behavior reports
Published: April 27, 2021

Case Report: Intracranial Hypertension Secondary to Guillain-Barre Syndrome.

Case Report: Intracranial Hypertension Secondary to Guillain-Barre Syndrome.

Journal: Frontiers in pediatrics
Published: September 21, 2020

Evaluation of Genotypes and Epidemiology of Spinal Muscular Atrophy in Greece: A Nationwide Study Spanning 24 Years.

Evaluation of Genotypes and Epidemiology of Spinal Muscular Atrophy in Greece: A Nationwide Study Spanning 24 Years.

Journal: Journal of neuromuscular diseases
Published: May 18, 2020

Focal epileptic seizures anticipation based on patterns of heart rate variability parameters.

Focal epileptic seizures anticipation based on patterns of heart rate variability parameters.

Journal: Computer methods and programs in biomedicine
Published: December 19, 2018

Tolosa-Hunt Syndrome: Clinical Manifestations in Children.

Tolosa-Hunt Syndrome: Clinical Manifestations in Children.

Journal: Pediatric neurology
Published: June 30, 2018
Showing 1-12 of 18

Last Updated: 09/26/2026