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The challenges that parents of children with epilepsy face: A qualitative study.
Epilepsy Behav. 2017 Jun;71(Pt A):94-103. doi: 10.1016/j.yebeh.2017.04.034. Epub 2017 May 28.
Epilepsy Behav. 2017.
PMID: 28564623
Teachers' knowledge about epilepsy in Greece: Information sources and attitudes towards children with epilepsy during school time.
Kampra M, Tzerakis NG, Losidis S, Katsarou E, Voudris K, Mastroyianni S, Mouskou S, Siatouni A, Gatzonis S.
Kampra M, et al. Among authors: mouskou s.
Epilepsy Behav. 2016 Jul;60:218-224. doi: 10.1016/j.yebeh.2016.04.004. Epub 2016 May 28.
Epilepsy Behav. 2016.
PMID: 27240308
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Α case of seronegative autoimmune encephalitis associated with human herpesvirus-7 (HHV-7).
Christou E, Mastrogianni S, Bourousis E, Bachou T, Tsikrikas T, Mouskou S, Voudris K, Delis D.
Christou E, et al. Among authors: mouskou s.
J Med Virol. 2022 Feb;94(2):795-798. doi: 10.1002/jmv.27411. Epub 2021 Oct 27.
J Med Virol. 2022.
PMID: 34676889
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Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy.
Mouskou S, Katerelos A, Doulgeraki A, Leka-Emiri S, Manolakos E, Papoulidis I, Ververi A, Vartzelis G, Korona A, Mastroyanni S, Voudris K.
Mouskou S, et al.
Mol Syndromol. 2021 Jun;12(3):194-199. doi: 10.1159/000514122. Epub 2021 Apr 19.
Mol Syndromol. 2021.
PMID: 34177437
Free PMC article.
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Long-term follow up of complete bladder exstrophy repair. A case report.
Mouskou S, Dionysis TT, Aivazoglou T, Kapouleas GP.
Mouskou S, et al.
Folia Med (Plovdiv). 2014 Jan-Mar;56(1):60-3. doi: 10.2478/folmed-2014-0010.
Folia Med (Plovdiv). 2014.
PMID: 24812925
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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: mouskou 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
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Growth Hormone Deficiency due to p.(Gln467Argfs*64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome.
Mouskou S, Leka-Emiri S, Korona A, Mastroyanni S, Manolakos E, Papoulidis I, Sekouris N, Katerelos A, Katsarou-Pectasides E, Voudris K.
Mouskou S, et al.
Mol Syndromol. 2022 Dec;13(5):425-432. doi: 10.1159/000522532. Epub 2022 Apr 8.
Mol Syndromol. 2022.
PMID: 36588753
Free PMC article.
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