Marios Kaliakatsos
London, ENG, United Kingdom
Last Updated: 09/26/2026
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Found 50 publications
Neurosurgical management of childhood-onset epilepsy in periventricular nodular heterotopia: A systematic review of effectiveness and outcomes.
Journal: Seizure
Published: May 25, 2026
Feasibility and optimization of a novel, cranially-mounted deep brain stimulation device for children with epilepsy - the CADET Pilot study.
Journal: Brain stimulation
Published: March 31, 2026
Peri-ictal magnetic resonance imaging findings in pediatric seizures: a scoping review on pearls and pitfalls from a heterogeneous population.
Journal: Translational pediatrics
Published: March 24, 2026
Which trial do we need? Treatment of severe measles.
Journal: Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases
Published: March 17, 2026
Diagnostic Yield of Comprehensive Reanalysis After Nondiagnostic Short-Read Genome Sequencing in Infants With Unexplained Epilepsy.
Journal: Neurology
Published: February 13, 2026
Identifying virulent avian paramyxovirus type-1: A paediatric case of progressive encephalitis diagnosed by clinical metagenomics with case series review.
Journal: IDCases
Published: October 23, 2025
Neuroimaging Findings and Treatment Update for Neuroinflammation, Autoinflammation, Splenomegaly, and Anemia, a Novel Autoinflammatory Disorder Caused by Bi-Allelic Variants in IRAK4.
Journal: AJNR. American journal of neuroradiology
Published: July 28, 2025
CSF IL-6 in children with neuroinflammatory conditions.
Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
Published: June 13, 2025
Late Onset Blinatumomab-Related Neurotoxicity in a Child With B-Cell Acute Lymphoblastic Leukemia.
Journal: Pediatric blood & cancer
Published: June 03, 2025
Molecular and clinical spectrum of epilepsy-dyskinesia syndromes: a cross-sectional study of 609 patients.
Journal: Brain : a journal of neurology
Published: March 15, 2025
Partial loss of FITM2 function causes hereditary spastic paraplegia.
Journal: medRxiv : the preprint server for health sciences
Published: February 20, 2025
Last Updated: 09/26/2026