Georgios Niotakis
Irakleion, ESYE43, Greece
Last Updated: 09/26/2026
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Found 10 publications
"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.
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.
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.
Journal: Expert review of molecular diagnostics
Published: January 30, 2023
Abnormal gait and hypoglycorrhachia in a toddler with seizures.
Journal: Pediatric investigation
Published: November 07, 2021
Miller Fisher Syndrome Triggered by Infections: A Review of the Literature and a Case Report.
Journal: Journal of child neurology
Published: August 27, 2021
Miller Fisher Syndrome Triggered by Infections: A Review of the Literature and a Case Report.
Journal: Journal of child neurology
Published: February 11, 2021
Aldolase A deficiency: Report of new cases and literature review.
Journal: Molecular genetics and metabolism reports
Published: December 22, 2020
Clinical and Functional Characterization of the Recurrent TUBA1A p.(Arg2His) Mutation.
Journal: Brain sciences
Published: May 30, 2018
Chorea revealing systemic lupus erythematosus in a 13-year old boy: A case report and short review of the literature.
Journal: International reviews of immunology
Published: March 30, 2018
Showing 1-10 of 10
Last Updated: 09/26/2026