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Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients.
Mol Genet Metab Rep. 2020 Nov 30;25:100682. doi: 10.1016/j.ymgmr.2020.100682. eCollection 2020 Dec.
Mol Genet Metab Rep. 2020.
PMID: 33304817
Free PMC article.
Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes.
Zaganas I, Vorgia P, Spilioti M, Mathioudakis L, Raissaki M, Ilia S, Giorgi M, Skoula I, Chinitrakis G, Michaelidou K, Paraskevoulakos E, Grafakou O, Kariniotaki C, Psyllou T, Zafeiris S, Tzardi M, Briassoulis G, Dinopoulos A, Mitsias P, Evangeliou A.
Zaganas I, et al. Among authors: mathioudakis l.
Epilepsy Behav Rep. 2021 Aug 27;16:100477. doi: 10.1016/j.ebr.2021.100477. eCollection 2021.
Epilepsy Behav Rep. 2021.
PMID: 34568804
Free PMC article.
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High Hereditary Transthyretin-Related Amyloidosis Prevalence in Crete: Genetic Heterogeneity and Distinct Phenotypes.
Tzagournissakis M, Foukarakis E, Samonakis D, Tsilimbaris M, Michaelidou K, Mathioudakis L, Marinis A, Giannakoudakis E, Spanaki C, Skoula I, Erimaki S, Amoiridis G, Koutsis G, Koukouraki S, Stylianou K, Plaitakis A, Mitsias PD, Zaganas I.
Tzagournissakis M, et al. Among authors: mathioudakis l.
Neurol Genet. 2022 Sep 9;8(5):e200013. doi: 10.1212/NXG.0000000000200013. eCollection 2022 Oct.
Neurol Genet. 2022.
PMID: 36101541
Free PMC article.
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Localization of Human Glutamate Dehydrogenases Provides Insights into Their Metabolic Role and Their Involvement in Disease Processes.
Mathioudakis L, Bourbouli M, Daklada E, Kargatzi S, Michaelidou K, Zaganas I.
Mathioudakis L, et al.
Neurochem Res. 2019 Jan;44(1):170-187. doi: 10.1007/s11064-018-2575-y. Epub 2018 Jun 25.
Neurochem Res. 2019.
PMID: 29943084
Review.
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[No title available]
[No authors listed]
[No authors listed]
PMID: 35109002
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Study of Alzheimer's disease- and frontotemporal dementia-associated genes in the Cretan Aging Cohort.
Mathioudakis L, Dimovasili C, Bourbouli M, Latsoudis H, Kokosali E, Gouna G, Vogiatzi E, Basta M, Kapetanaki S, Panagiotakis S, Kanterakis A, Boumpas D, Lionis C, Plaitakis A, Simos P, Vgontzas A, Kafetzopoulos D, Zaganas I.
Mathioudakis L, et al.
Neurobiol Aging. 2023 Mar;123:111-128. doi: 10.1016/j.neurobiolaging.2022.07.002. Epub 2022 Jul 11.
Neurobiol Aging. 2023.
PMID: 36117051
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Genotyping and Plasma/Cerebrospinal Fluid Profiling of a Cohort of Frontotemporal Dementia-Amyotrophic Lateral Sclerosis Patients.
Bourbouli M, Paraskevas GP, Rentzos M, Mathioudakis L, Zouvelou V, Bougea A, Tychalas A, Kimiskidis VK, Constantinides V, Zafeiris S, Tzagournissakis M, Papadimas G, Karadima G, Koutsis G, Kroupis C, Kartanou C, Kapaki E, Zaganas I.
Bourbouli M, et al. Among authors: mathioudakis l.
Brain Sci. 2021 Sep 19;11(9):1239. doi: 10.3390/brainsci11091239.
Brain Sci. 2021.
PMID: 34573259
Free PMC article.
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Apolipoprotein E ɛ4 (APOE ɛ4) Allele is Associated with Long Sleep Duration Among Elderly with Cognitive Impairment.
Basta M, Zaganas I, Simos P, Koutentaki E, Dimovasili C, Mathioudakis L, Bourbouli M, Panagiotakis S, Kapetanaki S, Vgontzas A.
Basta M, et al. Among authors: mathioudakis l.
J Alzheimers Dis. 2021;79(2):763-771. doi: 10.3233/JAD-200958.
J Alzheimers Dis. 2021.
PMID: 33361595
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Cognitive Impairment and Dementia in Primary Care: Current Knowledge and Future Directions Based on Findings From a Large Cross-Sectional Study in Crete, Greece.
Bertsias A, Symvoulakis E, Tziraki C, Panagiotakis S, Mathioudakis L, Zaganas I, Basta M, Boumpas D, Simos P, Vgontzas A, Lionis C.
Bertsias A, et al. Among authors: mathioudakis l.
Front Med (Lausanne). 2020 Nov 23;7:592924. doi: 10.3389/fmed.2020.592924. eCollection 2020.
Front Med (Lausanne). 2020.
PMID: 33330553
Free PMC article.
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