Showing 1 - 14 results of 14 for search 'M.O. Abramov', query time: 0.07s Refine Results
  1. 1
    Pontocerebellar hypoplasia caused by the <i>TSEN54</i> mutation: clinical and electroencephalographic characteristics based on 3 cases

    Pontocerebellar hypoplasia caused by the <i>TSEN54</i> mutation: clinical and electroencephalographic characteristics based on 3 cases by M. Yu. Bobylova, M. O. Abramov, K. Yu. Mukhin

    Published 2024-07-01
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  2. 2
    FOCAL MOTOR SEIZURES WITH TYPICAL AUTOMATISMS (FOCAL AUTOMOTOR SEIZURES)

    FOCAL MOTOR SEIZURES WITH TYPICAL AUTOMATISMS (FOCAL AUTOMOTOR SEIZURES) by M. B. Mironov, M. O. Abramov, K. Yu. Mukhin

    Published 2015-04-01
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  3. 3
    Mowat-Wilson syndrome: literature review and case series

    Mowat-Wilson syndrome: literature review and case series by M. Yu. Bobylova, V. S. Kakaulina, M. O. Abramov, K. Yu. Mukhin

    Published 2021-11-01
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  4. 4
    EATING EPILEPSY

    EATING EPILEPSY by I. G. Rudakova, K. Yu. Mukhin, M. B. Mironov, M. O. Abramov

    Published 2015-04-01
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  5. 5
    DEFINITION AND ANALYSIS OF MOTION ACTIVITY AFTER-STROKE PATIENT FROM THE VIDEO STREAM

    DEFINITION AND ANALYSIS OF MOTION ACTIVITY AFTER-STROKE PATIENT FROM THE VIDEO STREAM by M. Yu. Katayev, N. G. Katayeva, S. G. Katayev, M. O. Abramov, V. A. Chistyakova

    Published 2014-10-01
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  6. 6
    A case of inversion of chromosome 4 and an unbalanced transloca- tion between the short arm of chromosome 4 and long arm of chromosome 18 in a girl: evolution of clinical and electroencephalographic manifestations

    A case of inversion of chromosome 4 and an unbalanced transloca- tion between the short arm of chromosome 4 and long arm of chromosome 18 in a girl: evolution of clinical and elect... by M. Yu. Bobylova, M. O. Abramov, A. V. Kovalskaya, A. A. Alikhanov, K. Yu. Mukhin

    Published 2021-02-01
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  7. 7
    VIDEO-EEG-MONITORING IN DIAGNOSIS OF MYOCLONIC ABSENCES

    VIDEO-EEG-MONITORING IN DIAGNOSIS OF MYOCLONIC ABSENCES by M. B. Mironov, K. Yu. Mukhin, M. O. Abramov, M. Yu. Bobylova, T. M. Krasilschikova, A. S. Petrukhin

    Published 2016-06-01
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  8. 8
    Motor and sensory alalia: diagnostic difficulties

    Motor and sensory alalia: diagnostic difficulties by M. Yu. Bobylova, A. A. Kapustina, T. A. Braudo, M. O. Abramov, N. I. Klepikov, E. V. Panfilova

    Published 2018-01-01
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  9. 9
    Efficacy and tolerability of rufinamide in the treatment of epilepsy (experience of the Svt. Luka’s Institute of Child Neurology and Epilepsy)

    Efficacy and tolerability of rufinamide in the treatment of epilepsy (experience of the Svt. Luka’s Institute of Child Neurology and Epilepsy) by K. Yu. Mukhin, O. A. Pylaeva, M. Yu. Bobylova, N. V. Freydkova, L. Yu. Glukhova, M. O. Abramov

    Published 2018-11-01
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  10. 10
    FEJERMAN SYNDROME (BENIGN NONEPILEPTIC MYOCLONUS OF INFANCY)

    FEJERMAN SYNDROME (BENIGN NONEPILEPTIC MYOCLONUS OF INFANCY) by M. B. Mironov, V. Iu. Nogovitsyn, M. O. Abramov, E. A. Dobrovskaya, N. E. Kvaskova, K. Yu. Mukhin

    Published 2016-05-01
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  11. 11
    EPILEPSY ASSOCIATED WITH EPILEPTIC EYELID MYOCLONIA WITH OR WITHOUT ABSENCES

    EPILEPSY ASSOCIATED WITH EPILEPTIC EYELID MYOCLONIA WITH OR WITHOUT ABSENCES by M. B. Mironov, M. Yu. Bobylova, M. O. Abramov, T. M. Krasilshchikova, A. N. Zavadenko, I. O. Shchederkina, А. S. Petrukhin

    Published 2016-12-01
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  12. 12
    Artificial intelligence applied for the diagnosis of absence epilepsy with simultaneously tested patient’s consciousness level in ictal event

    Artificial intelligence applied for the diagnosis of absence epilepsy with simultaneously tested patient’s consciousness level in ictal event by M. B. Mironov, M. O. Abramov, V. V. Kondratenko, I. R. Vafin, S. Yu. Smirnov, S. E. Vaganov, A. A. Ivanov

    Published 2024-04-01
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  13. 13
    A CLINICAL CASE OF SYNGAP1 GENE MUTATION IN A GIRL WITH EPILEPSY, MENTAL RETARDATION, AUTISM, AND MOTOR DISORDERS

    A CLINICAL CASE OF SYNGAP1 GENE MUTATION IN A GIRL WITH EPILEPSY, MENTAL RETARDATION, AUTISM, AND MOTOR DISORDERS by M. Yu. Bobylova, M. B. Mironov, M. O. Abramov, A. V. Kulikov, M. V. Kazakova, L. Yu. Glukhova, E. I. Barletova, K. Yu. Mukhin

    Published 2015-11-01
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  14. 14
    A clinical case of SYNGAP1, с2214_2217delTGAG de novo gene mutations in a girl with epilepsy, mental retardation, autism, and movement disorders

    A clinical case of SYNGAP1, с2214_2217delTGAG de novo gene mutations in a girl with epilepsy, mental retardation, autism, and movement disorders by M.Yu Bobylova, M.B. Mironov, A.V. Kulikov, M.V Kazakova, M.A. Bogacheva, Yu.A. Tankevich, L.Yu. Glukhova, E.I Barletova, M.O. Abramov, K.Yu. Mukhin, G.E. Rudenskaya

    Published 2014-06-01
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