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Gain-of-function variant in GLUD2 glutamate dehydrogenase modifies Parkinson's disease onset.
Plaitakis A, Latsoudis H, Kanavouras K, Ritz B, Bronstein JM, Skoula I, Mastorodemos V, Papapetropoulos S, Borompokas N, Zaganas I, Xiromerisiou G, Hadjigeorgiou GM, Spanaki C. Plaitakis A, et al. Among authors: latsoudis h. Eur J Hum Genet. 2010 Mar;18(3):336-41. doi: 10.1038/ejhg.2009.179. Epub 2009 Oct 14. Eur J Hum Genet. 2010. PMID: 19826450 Free PMC article.
Genetic cause of heterogeneous inherited myopathies in a cohort of Greek patients.
Zaganas I, Mastorodemos V, Spilioti M, Mathioudakis L, Latsoudis H, Michaelidou K, Kotzamani D, Notas K, Dimitrakopoulos K, Skoula I, Ioannidis S, Klothaki E, Erimaki S, Stavropoulos G, Vassilikos V, Amoiridis G, Efthimiadis G, Evangeliou A, Mitsias P. Zaganas I, et al. Among authors: latsoudis h. 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.
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. Among authors: latsoudis h. Neurobiol Aging. 2023 Mar;123:111-128. doi: 10.1016/j.neurobiolaging.2022.07.002. Epub 2022 Jul 11. Neurobiol Aging. 2023. PMID: 36117051
Novel mutation of the PRNP gene of a clinical CJD case.
Kotta K, Paspaltsis I, Bostantjopoulou S, Latsoudis H, Plaitakis A, Kazis D, Collinge J, Sklaviadis T. Kotta K, et al. Among authors: latsoudis h. BMC Infect Dis. 2006 Nov 27;6:169. doi: 10.1186/1471-2334-6-169. BMC Infect Dis. 2006. PMID: 17129366 Free PMC article.
24 results