Search Results - Voutoufianakis, S.

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  1. 1
    Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome

    Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome by Voutoufianakis, S, Psoni, S, Vorgia, P, Tsekoura, F, Kekou, K, Traeger-Synodinos, J, Kitsiou, S, Kanavakis, E, Fryssira, H

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  2. 2
    Vision-based absence seizure detection

    Vision-based absence seizure detection by Pediaditis, M., Tsiknakis, M., Koumakis, L., Karachaliou, M., Voutoufianakis, S., Vorgia, P.

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  3. 3
    Exploiting advanced video analysis technologies for a smart home monitoring platform for epileptic patients: Technological and legal preconditions

    Exploiting advanced video analysis technologies for a smart home monitoring platform for epileptic patients: Technological and legal preconditions by Pediaditis, M., Tsiknakis, M., Kritsotakis, V., Voutoufianakis, S., Góralczyk, M., Vorgia, P.

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  4. 4
    Tolosa-Hunt Syndrome: Clinical Manifestations in Children

    Tolosa-Hunt Syndrome: Clinical Manifestations in Children by Tsirigotaki, Maria, Ntoulios, George, Lioumpas, Michail, Voutoufianakis, Spyridon, Vorgia, Pelagia

    Published in Pediatric neurology
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  5. 5
    Evaluation of Oral Glucose Tolerance Test in Children With Epilepsy

    Evaluation of Oral Glucose Tolerance Test in Children With Epilepsy by Varlamis, Sotirios, Vavatsi, Norma, Pavlou, Evangelos, Kotsis, Vasileios, Spilioti, Martha, Kavga, Maria, Varlamis, George, Sotiriadou, Foteini, Agakidou, Eleni, Voutoufianakis, Spyridon, Evangeliou, Athanasios E.

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