Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

88 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
Alternative splicing expands the clinical spectrum of NDUFS6-related mitochondrial disorders.
Armirola-Ricaurte C, Zonnekein N, Koutsis G, Amor-Barris S, Pelayo-Negro AL, Atkinson D, Efthymiou S, Turchetti V, Dinopoulos A, Garcia A, Karakaya M, Moris G, Polat AI, Yiş U, Espinos C, Van de Vondel L, De Vriendt E, Karadima G, Wirth B, Hanna M, Houlden H, Berciano J, Jordanova A. Armirola-Ricaurte C, et al. Among authors: karadima g. Genet Med. 2024 Mar 6;26(6):101117. doi: 10.1016/j.gim.2024.101117. Online ahead of print. Genet Med. 2024. PMID: 38459834 Free article.
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 MJ, Danzi MC, Koniari C, Athanassopoulos K, Panas M, Stefanis L, Zuchner S, Brais B, Houlden H, Karadima G, Koutsis G. Kartanou C, et al. Among authors: karadima g. Clin Genet. 2024 Apr;105(4):446-452. doi: 10.1111/cge.14482. Epub 2024 Jan 14. Clin Genet. 2024. PMID: 38221848
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, Chroni E, Dinopoulos A, Panas M, Koutsis G, Karadima G. Kontogeorgiou Z, et al. Among authors: karadima g. J Peripher Nerv Syst. 2023 Dec;28(4):642-650. doi: 10.1111/jns.12598. Epub 2023 Oct 5. J Peripher Nerv Syst. 2023. PMID: 37747677
A Greek National Cross-Sectional Study on Myotonic Dystrophies.
Papadimas GK, Papadopoulos C, Kekou K, Kartanou C, Kladi A, Nitsa E, Sofocleous C, Tsanou E, Sarmas I, Kaninia S, Chroni E, Tsivgoulis G, Kimiskidis V, Arnaoutoglou M, Stefanis L, Panas M, Koutsis G, Karadima G, Traeger-Synodinos J. Papadimas GK, et al. Among authors: karadima g. Int J Mol Sci. 2022 Dec 7;23(24):15507. doi: 10.3390/ijms232415507. Int J Mol Sci. 2022. PMID: 36555146 Free PMC article.
Screening for the FMR1 premutation in Greek patients with late-onset movement disorders.
Kartanou C, Seferiadi M, Pomoni S, Potagas C, Sofocleous C, Traeger-Synodinos J, Stefanis L, Panas M, Koutsis G, Karadima G. Kartanou C, et al. Among authors: karadima g. Parkinsonism Relat Disord. 2023 Feb;107:105253. doi: 10.1016/j.parkreldis.2022.105253. Epub 2022 Dec 20. Parkinsonism Relat Disord. 2023. PMID: 36549234
Expanding the spectrum of C9ORF72-related neurodegenerative disorders in the Greek population.
Kartanou C, Kontogeorgiou Z, Rentzos M, Potagas C, Aristeidou S, Kapaki E, Paraskevas GP, Constantinides VC, Stefanis L, Papageorgiou SG, Houlden H, Panas M, Koutsis G, Karadima G. Kartanou C, et al. Among authors: karadima g. J Neurol Sci. 2022 Nov 15;442:120450. doi: 10.1016/j.jns.2022.120450. Epub 2022 Oct 5. J Neurol Sci. 2022. PMID: 36252286
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, Breza M, Kleopa KA, Christodoulou K, Oikonomou E, Anastasakis A, Angelidakis P, Sarmas I, Kargiotis O, Tzagournissakis M, Zaganas I, Foukarakis E, Sachpekidis V, Papathoma A, Panas M, Stefanis L, Dimopoulos MA, Karadima G. Koutsis G, et al. Among authors: karadima g. Neuromuscul Disord. 2021 Dec;31(12):1251-1258. doi: 10.1016/j.nmd.2021.09.008. Epub 2021 Sep 29. Neuromuscul Disord. 2021. PMID: 34740514
88 results