Stella Mouskou
Athens, ESYE31, Greece
Last Updated: 09/26/2026
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Found 9 publications
Myasthenia Gravis as a Manifestation of Aicardi-Goutières Syndrome Due to a SAMHD1 Variant Successfully Treated With Baricitinib.
Journal: Cureus
Published: September 02, 2025
"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
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
Α case of seronegative autoimmune encephalitis associated with human herpesvirus-7 (HHV-7).
Journal: Journal of medical virology
Published: March 29, 2021
Growth Hormone Deficiency due to p.(Gln467Argfs*64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome.
Journal: Molecular syndromology
Published: February 23, 2021
The challenges that parents of children with epilepsy face: A qualitative study.
Journal: Epilepsy & behavior : E&B
Published: October 06, 2016
Teachers' knowledge about epilepsy in Greece: Information sources and attitudes towards children with epilepsy during school time.
Journal: Epilepsy & behavior : E&B
Published: January 27, 2016
Long-term follow up of complete bladder exstrophy repair. A case report.
Journal: Folia medica
Published: May 13, 2014
Showing 1-9 of 9
Last Updated: 09/26/2026