Georgia Karadima

Athens, ESYE31, Greece

Last Updated: 09/26/2026

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Found 65 publications

Beyond motor impairment: investigating cognitive aspects of hereditary spastic paraplegia in a Greek case series.

Beyond motor impairment: investigating cognitive aspects of hereditary spastic paraplegia in a Greek case series.

Journal: Neurocase

Published: March 03, 2026

Correction to: SCA27B: a treatable ataxia-from falls to independence.

Correction to: SCA27B: a treatable ataxia-from falls to independence.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: February 09, 2026

Unraveling the genetic landscape of ALS in Greece: identification of known and novel causative variants in a 353-patient cohort.

Unraveling the genetic landscape of ALS in Greece: identification of known and novel causative variants in a 353-patient cohort.

Journal: Amyotrophic lateral sclerosis & frontotemporal degeneration

Published: November 06, 2025

In Vivo Mapping of Catecholaminergic Loss and Iron Deposition in Huntington's Disease.

In Vivo Mapping of Catecholaminergic Loss and Iron Deposition in Huntington's Disease.

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 31, 2025

B cell tolerance checkpoint function in multiple sclerosis and transient CD52 depletion.

B cell tolerance checkpoint function in multiple sclerosis and transient CD52 depletion.

Journal: Journal of neuroimmunology

Published: October 28, 2025

Niemann Pick Type C Presenting as Familial Late-Onset Richardson Syndrome. A Case Series of Four Siblings.

Niemann Pick Type C Presenting as Familial Late-Onset Richardson Syndrome. A Case Series of Four Siblings.

Journal: Movement disorders clinical practice

Published: October 17, 2025

SCA27B: a treatable ataxia-from falls to independence.

SCA27B: a treatable ataxia-from falls to independence.

Journal: Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology

Published: October 07, 2025

Cranial Nerve Involvement With Diplopia as Presenting Feature of CMT1H Caused by Recurring FBLN5 Variant.

Cranial Nerve Involvement With Diplopia as Presenting Feature of CMT1H Caused by Recurring FBLN5 Variant.

Journal: Journal of the peripheral nervous system : JPNS

Published: September 30, 2025

Huntington's Disease-like Syndrome as a Rare Presentation of CACNA1A-Related Disorder.

Huntington's Disease-like Syndrome as a Rare Presentation of CACNA1A-Related Disorder.

Journal: Movement disorders clinical practice

Published: September 15, 2025

The Genetic Landscape of Hereditary Spastic Paraplegia in Greece.

The Genetic Landscape of Hereditary Spastic Paraplegia in Greece.

Journal: Clinical genetics

Published: September 11, 2025

Genetic and clinical characterization of SPG10: a case series of novel pathogenic variants and phenotypic diversity.

Genetic and clinical characterization of SPG10: a case series of novel pathogenic variants and phenotypic diversity.

Journal: Annals of medicine and surgery (2012)

Published: April 15, 2025

Partial loss of FITM2 function causes hereditary spastic paraplegia.

Partial loss of FITM2 function causes hereditary spastic paraplegia.

Journal: medRxiv : the preprint server for health sciences

Published: February 20, 2025

Showing 1-12 of 65

Last Updated: 09/26/2026