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ATTENTION DEFICIT HYPERACTIVITY DISORDER. A CLINICAL LECTURE
Kotov A.S., Borisova M.N., Panteleeva M.V., Matyuk Y.V., Shatalin A.V.
TYPICAL ABSENCES: RESULTS OF OWN INVESTIGATIONS
Mukhin K.Y., Mironov M.B.
FOCAL EPILEPTIC MYOCLONUS IN KOZHEVNIKOV–RASMUSSEN SYNDROME
Kvaskova N.E., Mukhin K.Y.
INHIBITORY MOTOR SEIZURES: SEMIOLOGY AND THERAPY
Мukhin K.Y., Мironov M.B.
KOZHEVNIKOV–RASMUSSEN’S ENCEPHALITIS. A CASE REPORT
Kotov A.S., Rudakova I.G., Mukhin K.Y., Mironov M.B., Kvaskova N.E., Alihanov A.A.
SPECIFIC FEATURES OF ELECTROENCEPHALOGRAPHIC PAROXYSMAL ACTIVITY REGISTRATION IN OLD AGE GROUP PATIENTS
Gulyaev S.A., Arkhipenko I.V., Gulyaeva S.E., Ovchinnikova A.A., Ovchinnikov A.V.
DIFFERENTIAL DIAGNOSTICS OF PAROXYSMAL ACTIVITY ON EEG
Gulaev S.A.
CHILDREN’S GIFTEDNESS AND ASSOCIATED PROBLEMS. THE TWICE EXCEPTIONALITY PHENOMENON. GIFTEDNESS AND LEARNING PROBLEMS. GIFTEDNESS AND ATTENTION DEFICIT/ HYPERACTIVITY DISORDER (А REVIEW OF LITERATURE)
Pylaeva O.A.
Mowat-Wilson syndrome: literature review and case series
Bobylova M.Y., Kakaulina V.S., Abramov M.O., Mukhin K.Y.
JUVENILE MYOCLONIC EPILEPSY: A FOCUS ON THE EFFICACY OF THERAPY AND THE RATE OF RELAPSES ACCORDING TO LONG-TERM FOLLOW-UP DATA
Mukhin K.Y., Freidkova N.V., Glukhova L.Y., Pylaeva O.A., Mironov M.B., Kvaskova N.E.
CLINICAL AND ENCEPHALOGRAPHIC CHANGES AT LENNOX–GASTAUT SYNDROME
Mukhin K.Y.
Idiopathic toe-walking in childhood
Malmberg S.A.
KLEINE–LEVIN SYNDROME AFTER USE OF RECREATIONAL DRUGS
Semenova E.I., Tokareva Y.V., Belova Y.A., Kotov A.S., Eliseev Y.V.
JUVENILE MYOCLONIC EPILEPSY: FOCUS ON THE USE OF TOPIRAMATE (LITERATURE REVIEW AND OWN DATA)
Mukhin K.Y., Pylaeva O.A.
CHILDREN’S GIFTEDNESS AND ASSOCIATED PROBLEMS. THE TWICE EXCEPTIONALITY PHENOMENON. GIFTEDNESS AND LEARNING PROBLEMS. GIFTEDNESS AND ATTENTION DEFICIT/ HYPERACTIVITY DISORDER (А REVIEW OF LITERATURE). PART I
Pylaeva O.A.
EARLY ONSET BENIGN CHILDHOOD OCCIPITAL EPILEPSY (PANAYIOTOPOULOS SYNDROME). A CASE REPORT
Маtyuk Y.V., Kotov A.S., Borisova M.N., Panteleeva M.V., Shatalin A.V.
EPILEPSY CAUSED BY PCDH19 GENE MUTATION: A REVIEW OF LITERATURE AND THE AUTHORS’ OBSERVATIONS
Mukhin K.Y., Pylaeva O.A., Dolinina A.F., Moiseeva S., Verbitskaya Y.V., Petrukhin A.S., Kluger G., Holthausen H., Staudt M.
CLINICAL AND ELECTROENCEPHALOGRAPHIC CHARACTERISTICS OF IDIOPATHIC CHILDHOOD FOCAL EPILEPSY WITH CENTROTEMPORAL SPIKES
Mukhin K.Y.
ANALYSIS OF MAIN REASONS FOR MISTAKES IN DIAGNOSTICS OF EPILEPTIC SEIZURES AND EPILEPTIC SYNDROMES (CLINICAL PECULIARITIES OF EPILEPTIC SEIZURES)
Mironov M.B.
EPILEPSY IN 11 PATIENTS WITH TYPICAL RETT SYNDROME CAUSED BY MECP2 MUTATION: CLINICAL AND ELECTROENCEPHALOGRAPHIC CHARACTERISTICS, COURSE, THERAPY (RESULTS OF THE AUTHORS’ OBSERVATIONS)
Bobylova M.Y., Mukhin K.Y., Ivanova I.V., Nekrasova I.V., Pylaeva O.A., Borovikova N.Y., Il’ina E.S.
HEMICONVULSION-HEMIPLEGIA-EPILEPSY SYNDROME (HHE SYNDROME) (A LECTURE)
Mukhin K.Y., Bobylova M.Y., Dolinina A.F., Pylaeva O.A.
EPILEPTIC SPASMS
Mukhin K.Y., Mironov M.B.
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