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» Authors » Zoi Kontogeorgiou

Zoi Kontogeorgiou

Explore the profile of Zoi Kontogeorgiou including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 12
Citations 31
Followers 0
Related Specialties
Neurology
Genetics
Radiology
Top 10 Co-Authors
Georgia Karadima
Georgios Koutsis
Chrisoula Kartanou
Marios Panas
Leonidas Stefanis
Michail Rentzos
Marianthi Breza
Henry Houlden
Evangelos Anagnostou
Constantin Potagas
Published In
J Peripher Nerv Syst
Clin Genet
J Neurol Sci
Nitric Oxide
Data Brief
Affiliations
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Recent Articles
1.
Screening for SCA27B, CANVAS and other repeat expansion disorders in Greek patients with late-onset cerebellar ataxia suggests a need to update current diagnostic algorithms
Koutsis G, Kartanou C, Kontogeorgiou Z, Koniari C, Mitrousias A, Pellerin D, et al.
J Neurol Sci . 2024 Nov; 467:123309. PMID: 39571249
Objective: Late-onset cerebellar ataxia (LOCA) is a slowly progressive cerebellar disorder with symptom onset ≥30years of age. Intronic tandem repeat expansions (TREs) in RFC1 and FGF14 have recently emerged as...
2.
The FGF14 GAA repeat expansion in Greek patients with late-onset cerebellar ataxia and an overview of the SCA27B phenotype across populations
Kartanou C, Mitrousias A, Pellerin D, Kontogeorgiou Z, Iruzubieta P, Dicaire M, et al.
Clin Genet . 2024 Jan; 105(4):446-452. PMID: 38221848
A pathogenic GAA repeat expansion in the first intron of the fibroblast growth factor 14 gene (FGF14) has been recently identified as the cause of spinocerebellar ataxia 27B (SCA27B). We...
3.
Mutational screening of Greek patients with axonal Charcot-Marie-Tooth disease using targeted next-generation sequencing: Clinical and molecular spectrum delineation
Kontogeorgiou Z, Kartanou C, Rentzos M, Kokotis P, Anagnostou E, Zambelis T, et al.
J Peripher Nerv Syst . 2023 Sep; 28(4):642-650. PMID: 37747677
Background And Aims: Axonal forms of Charcot-Marie-Tooth disease (CMT) are classified as CMT2, distal hereditary motor neuropathy (dHMN) or hereditary sensory neuropathy (HSN) and can be caused by mutations in...
4.
Transthyretin (Pro24Ser) variant amyloidosis: A case report of the first patient in Greece
Panagiotopoulos I, Papatheodorou E, Anastasakis A, Kastritis E, Gourzi P, Kontogeorgiou Z, et al.
Hell J Nucl Med . 2023 Aug; 26(2):145-149. PMID: 37610765
Objective: Transthyretin cardiac amyloidosis (ATTR-CA) is a rare and potentially fatal disease caused by the accumulation of insoluble transthyretin (TTR) amyloid fibrils in the heart. The symptoms of ATTR-CA are...
5.
Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population
Kartanou C, Kontogeorgiou Z, Rentzos M, Potagas C, Aristeidou S, Kapaki E, et al.
J Neurol Sci . 2022 Oct; 442:120450. PMID: 36252286
The C9ORF72 hexanucleotide repeat expansion is an established cause of amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) and has also been associated with Huntington disease (HD)-like syndromes and rarely...
6.
Variant transthyretin amyloidosis (ATTRv) polyneuropathy in Greece: a broad overview with a focus on non-endemic unexplored regions of the country
Koutsis G, Kastritis E, Kontogeorgiou Z, Kartanou C, Kokotis P, Rentzos M, et al.
Neuromuscul Disord . 2021 Nov; 31(12):1251-1258. PMID: 34740514
Comprehensive data on variant transthyretin amyloidosis polyneuropathy (ATTRv-PN) in Greece are lacking. We presently provide an overview of ATTRv-PN in Greece, focusing on unexplored non-endemic regions of the country. In...
7.
HINT1-related neuropathy in Greek patients with Charcot-Marie-Tooth disease
Kontogeorgiou Z, Voudommatis C, Kartanou C, Pandis D, Breza M, Zambelis T, et al.
J Peripher Nerv Syst . 2021 Oct; 26(4):444-448. PMID: 34694653
Autosomal recessive axonal neuropathy with neuromyotonia (ARAN-NM) is a rare hereditary neuropathy within the Charcot-Marie-Tooth disease (CMT) spectrum, linked to mutations in the histidine triad nucleotide-binding protein 1 (HINT1) gene....
8.
Structural and functional brain changes in X-linked Charcot-Marie-Tooth disease: insights from a multimodal neuroimaging study
Karavasilis E, Christidi F, Pantou E, Angelopoulou G, Kasselimis D, Breza M, et al.
Neuroradiology . 2021 Sep; 64(3):543-552. PMID: 34498107
Purpose: Brain involvement in X-linked Charcot-Marie-Tooth disease (CMTX) has been previously reported. We studied the brain structural and functional integrity using a multimodal neuroimaging approach in patients with no current...
9.
Biallelic RFC1 pentanucleotide repeat expansions in Greek patients with late-onset ataxia
Kontogeorgiou Z, Kartanou C, Tsirligkani C, Anagnostou E, Rentzos M, Stefanis L, et al.
Clin Genet . 2021 Mar; 100(1):90-94. PMID: 33745133
Cerebellar ataxia, neuropathy and vestibular areflexia syndrome (CANVAS) has been recently linked to biallelic expansions of a pentanucleotide repeat in the replication factor C subunit 1 (RFC1) gene. Herein, we...
10.
Mutational screening of the SH3TC2 gene in Greek patients with suspected demyelinating recessive Charcot-Marie-Tooth disease reveals a varied and unusual phenotypic spectrum
Kontogeorgiou Z, Nikolaou K, Kartanou C, Breza M, Panas M, Karadima G, et al.
J Peripher Nerv Syst . 2019 Jan; 24(1):125-130. PMID: 30653784
Charcot-Marie-Tooth disease type 4 C (CMT4C) is an autosomal recessive form of demyelinating peripheral neuropathy caused by mutations in SH3TC2, characterized by early onset, spine deformities, and cranial nerve involvement....