FOCAL MOTOR SEIZURES WITH TYPICAL AUTOMATISMS (FOCAL AUTOMOTOR SEIZURES)

by M. B. Mironov, M. O. Abramov, K. Yu. Mukhin
Published 2015-04-01

EATING EPILEPSY

by I. G. Rudakova, K. Yu. Mukhin, M. B. Mironov, M. O. Abramov
Published 2015-04-01

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

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

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

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

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

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

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

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

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