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Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms.
Veltra D, Tilemis FN, Marinakis NM, Svingou M, Mitrakos A, Kosma K, Tsoutsou I, Makrythanasis P, Theodorou V, Katsalouli M, Vorgia P, Niotakis G, Vartzelis G, Dinopoulos A, Evangeliou A, Mouskou S, Korona A, Mastroyianni S, Papavasiliou A, Tzetis M, Pons R, Traeger-Synodinos J, Sofocleous C. Veltra D, et al. Among authors: mastroyianni s. Expert Rev Mol Diagn. 2023 Jan;23(1):85-103. doi: 10.1080/14737159.2023.2173578. Epub 2023 Feb 14. Expert Rev Mol Diagn. 2023. PMID: 36714946
Editorial: Cerebral Palsy: New Developments.
Papavasiliou A, Ben-Pazi H, Mastroyianni S, Ortibus E. Papavasiliou A, et al. Among authors: mastroyianni s. Front Neurol. 2021 Aug 11;12:738921. doi: 10.3389/fneur.2021.738921. eCollection 2021. Front Neurol. 2021. PMID: 34456856 Free PMC article. No abstract available.
HLA-DRB1 allele impact on pediatric multiple sclerosis in a Hellenic cohort.
Gontika M, Skarlis C, Artemiadis A, Pons R, Mastroyianni S, Vartzelis G, Theodorou V, Kilindireas K, Stefanis L, Dalakas M, Chrousos G, Anagnostouli M. Gontika M, et al. Among authors: mastroyianni s. Mult Scler J Exp Transl Clin. 2020 Feb 24;6(1):2055217320908046. doi: 10.1177/2055217320908046. eCollection 2020 Jan-Mar. Mult Scler J Exp Transl Clin. 2020. PMID: 32133149 Free PMC article.
Moderately and Late Preterm Infants: Short- and Long-Term Outcomes From a Registry-Based Cohort.
Smyrni N, Koutsaki M, Petra M, Nikaina E, Gontika M, Strataki H, Davora F, Bouza H, Damianos G, Skouteli H, Mastroyianni S, Dalivigka Z, Dinopoulos A, Tzaki M, Papavasiliou A. Smyrni N, et al. Among authors: mastroyianni s. Front Neurol. 2021 Feb 12;12:628066. doi: 10.3389/fneur.2021.628066. eCollection 2021. Front Neurol. 2021. PMID: 33643206 Free PMC article.
25 results