Eyes wide open—an atypical presentation of Miller Fisher syndrome (MFS): case report von Korona Anastasia, Maritsi Despoina, Markante Aikaterini, Stamati Andromachi, Mouskou Stella, Vartzelis George

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Ruptured intracranial dermoid cyst in a child. Cause of atypical neurological symptoms von Mouskou, Stella, Stamati, Adiana, Sfakianos, George, Malama, Astero, Gavra, Maria, Vartzelis, George, Korona, Anastasia, Mastrogianni, Sotiria, Voudris, Kostas

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Α case of seronegative autoimmune encephalitis associated with human herpesvirus‐7 (HHV‐7) von Christou, Evangelos, Mastrogianni, Sotiria, Bourousis, Evangelos, Bachou, Theodora, Tsikrikas, Theodoros, Mouskou, Stella, Voudris, Konstantinos, Delis, Dimitrios

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Growth Hormone Deficiency due to p.(Gln467Argfs64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome von Mouskou, Stella, Leka-Emiri, Sofia, Korona, Anastasia, Mastroyanni, Sotiria, Manolakos, Emmanouil, Papoulidis, Ioannis, Sekouris, Nick, Katerelos, Adamantios, Katsarou-Pectasides, Efstathia, Voudris, Konstantinos

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The challenges that parents of children with epilepsy face: A qualitative study von Kampra, Matina, Tzerakis, Nikolaos, Lund Holm Thomsen, Louise, Katsarou, Efstathia, Voudris, Konstantinos, D. Mastroyianni, Sotiria, Mouskou, Stella, Drossou, Kyriaki S, Siatouni, Anna, Gatzonis, Stylianos

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Teachers' knowledge about epilepsy in Greece: Information sources and attitudes towards children with epilepsy during school time von Kampra, Matina, Tzerakis, Nikolaos G, Losidis, Sotiris, Katsarou, Efstathia, Voudris, Konstantinos, Mastroyianni, Sotiria, Mouskou, Stella, Siatouni, Anna, Gatzonis, Stylianos

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Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy von Mouskou, Stella, Katerelos, Adamantios, Doulgeraki, Artemis, Leka-Emiri, Sofia, Manolakos, Emmanouil, Papoulidis, Ioannis, Ververi, Athina, Vartzelis, Georgios, Korona, Anastasia, Mastroyanni, Sotiria, Voudris, Konstantinos

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Pharmacoresistant epilepsy associated with mutations in the KCNB1 and RELN genes. A case report von Katerelos, Adamantios, Zagkos, Nikolaos, Alexopoulou, Dimitra, Mouskou, Stella, Korona, Anastasia, Manolakos, Emmanouil

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Long Term Follow Up of Complete Bladder Exstrophy Repair. A Case Report von Mouskou, Stella, Dionysis, Theodoros T., Aivazoglou, Theodoros, Kapouleas, George P.

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Growth Hormone Deficiency due to p.(Gln467Argfs64) Mutation in the ARID1B Gene in a Girl with Coffin-Siris Syndrome von Mouskou, Stella, Leka-Emiri, Sofia, Korona, Anastasia, Mastroyanni, Sotiria, Manolakos, Emmanouil, Papoulidis, Ioannis, Sekouris, Nick, Katerelos, Adamantios, Katsarou-Pectasides, Efstathia, Voudris, Konstantinos

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Novel Hemizygous Missense Variant of Spermine Synthase (SMS) Gene Causes Snyder-Robinson Syndrome in a Four-Year-Old Boy von Mouskou, Stella, Katerelos, Adamantios, Doulgeraki, Artemis, Leka-Emiri, Sofia, Manolakos, Emmanouil, Papoulidis, Ioannis, Ververi, Athina, Vartzelis, Georgios, Korona, Anastasia, Mastroyanni, Sotiria, Voudris, Konstantinos

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