Showing 1 - 11 results of 11 for search 'S. O. Ayvazyan', query time: 0.02s Refine Results
  1. 1
    COMORBIDITY IN HEMICONVULSION-HEMIPLEGIA-EPILEPSY SYNDROME IN CHILDREN

    COMORBIDITY IN HEMICONVULSION-HEMIPLEGIA-EPILEPSY SYNDROME IN CHILDREN by S. O. Ayvazyan

    Published 2018-05-01
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  2. 2
    FOCAL CORTICAL DYSPLASIA: ALGORITHM OF PREOPERATIVE EXAMINATION

    FOCAL CORTICAL DYSPLASIA: ALGORITHM OF PREOPERATIVE EXAMINATION by S. O. Ayvazyan

    Published 2016-09-01
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  3. 3
    MODERN TREATMENT OF DRUG-RESISTANT EPILEPSY, AVAILABLE IN RUSSIAN

    MODERN TREATMENT OF DRUG-RESISTANT EPILEPSY, AVAILABLE IN RUSSIAN by S. O. Ayvazyan, Yu. S. Shiryaev

    Published 2016-06-01
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  4. 4
    SEVERE EPILEPTIC ENCEPHALOPATHY OF EARLY CHILDHOOD DUE TO SCN2A MUTATION

    SEVERE EPILEPTIC ENCEPHALOPATHY OF EARLY CHILDHOOD DUE TO SCN2A MUTATION by I. S. Bachtin, E. D. Belousova, P. A. Shatalov, S. O. Ayvazyan

    Published 2016-05-01
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  5. 5
    EFFECT OF KETOGENIC DIET ON COGNITIVE AND MOTOR FUNCTIONS IN CHILDREN WITH DRUG-RESISTANT EPILEPSY

    EFFECT OF KETOGENIC DIET ON COGNITIVE AND MOTOR FUNCTIONS IN CHILDREN WITH DRUG-RESISTANT EPILEPSY by E. G. Lukyanova, S. O. Ayvazyan, K. V. Osipova, T. N. Sorvacheva, E. A. Pyreva

    Published 2016-06-01
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  6. 6
    Significance of exome sequencing for diagnosis of epilepsy in children

    Significance of exome sequencing for diagnosis of epilepsy in children by T. V. Kozhanova, S. S. Zhilina, T. I. Meshheryakova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko

    Published 2020-01-01
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  7. 7
    Mutation of the ALDH7A1 gene in a patient with pyridoxal phosphate-dependent neonatal epileptic encephalopathy: a clinical case

    Mutation of the ALDH7A1 gene in a patient with pyridoxal phosphate-dependent neonatal epileptic encephalopathy: a clinical case by T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Lukyanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko

    Published 2019-04-01
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  8. 8
    Helsmoortel-van der Aa syndrome syndrome in a patient with epilepsy, developmental delay, intellectual disability, and autism spectrum disorder

    Helsmoortel-van der Aa syndrome syndrome in a patient with epilepsy, developmental delay, intellectual disability, and autism spectrum disorder by T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Luk`yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko

    Published 2020-04-01
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  9. 9
    Clinical case of epilepsy, hearing loss and mental retardation syndrome associated with mutations in SPATA5 gene

    Clinical case of epilepsy, hearing loss and mental retardation syndrome associated with mutations in SPATA5 gene by T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, E. G. Luk’yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko, N. N. Zavadenko

    Published 2021-04-01
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  10. 10
    Epilepsy combined with Wolf-Hirschhorn syndrome: a literature review and description of clinical cases

    Epilepsy combined with Wolf-Hirschhorn syndrome: a literature review and description of clinical cases by M. B. Mironov, N. V. Chebanenko, S. O. Ayvazyan, S. A. Vladimirova, K. V. Osipova, S. G. Burd, Yu. V. Rubleva, T. M. Krasilshchikova, V. G. Bychenko

    Published 2019-03-01
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  11. 11
    <i>SPTAN1</i>-associated developmental and epileptic encephalopathy

    <i>SPTAN1</i>-associated developmental and epileptic encephalopathy by T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, E. G. Lukyanova, E. S. Bolshakova, S. O. Ayvazyan, K. V. Osipova, P. A. Vlasov, A. I. Krapivkin, N. N. Zavadenko

    Published 2023-09-01
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