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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: spilioti m. 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.
Strabismus and nystagmus in a 4-year-old boy.
Raissaki M, Spilioti M, Kalaidopoulou P, Iliaki O, Mavrokosta M, Nikolaidis N, Evangeliou A. Raissaki M, et al. Among authors: spilioti m. Pediatr Ann. 2008 Sep;37(9):590-3. doi: 10.3928/00904481-20080901-03. Pediatr Ann. 2008. PMID: 18795568 No abstract available.
Ketogenic diet in a patient with Angelman syndrome.
Evangeliou A, Doulioglou V, Haidopoulou K, Aptouramani M, Spilioti M, Varlamis G. Evangeliou A, et al. Among authors: spilioti m. Pediatr Int. 2010 Oct;52(5):831-4. doi: 10.1111/j.1442-200X.2010.03118.x. Pediatr Int. 2010. PMID: 20880305 No abstract available.
Evidence for treatable inborn errors of metabolism in a cohort of 187 Greek patients with autism spectrum disorder (ASD).
Spilioti M, Evangeliou AE, Tramma D, Theodoridou Z, Metaxas S, Michailidi E, Bonti E, Frysira H, Haidopoulou A, Asprangathou D, Tsalkidis AJ, Kardaras P, Wevers RA, Jakobs C, Gibson KM. Spilioti M, et al. Front Hum Neurosci. 2013 Dec 24;7:858. doi: 10.3389/fnhum.2013.00858. eCollection 2013. Front Hum Neurosci. 2013. PMID: 24399946 Free PMC article.
56 results