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MAJOR PRINCIPLES OF EPILEPSY TREATMENT. ALGORITHM OF SELECTION OF ANTIEPILEPTIC DRUGS
Mukhin K.Y., Pylaeva O.A., Glukhova L.Y., Mironov M.B., Bobylova M.Y.
Genetic epilepsy caused by CDKL5 gene mutations as an example of epileptic encephalopathy and developmental encephalopathy: literature review and own observations
Mukhin K.Y., Pylaeva O.A., Bobylova M.Y., Chadaev V.A.
Clinical and genetic characteristics of patients with type 2 early infantile epileptic encephalopathy caused by CDKL5 gene mutations
Dadali E.L., Akimova I.A., Konovalov F.A., Shatalov P.A., Krasnenko A.Y., Strelnikov V.V., Ampleeva M.A.
Definition and classification of epilepsy. Classification of epileptic seizures 2016
Mukhin K.Y.
RUFINAMIDE (INOVELON) IN THE TREATMENT OF LENNOX–GASTAUT SYNDROME (A REVIEW OF LITERATURE AND CLINICAL CASE)
Mukhin K.Y., Pylaeva O.A.
Approaches to teaching children with epilepsy and/or past status epilepticus (within the prin- ciples of inclusive education)
Frolova V.M., Kozharskaya E.E.
RUFINAMIDE IN THE TREATMENT OF LENNOX–GASTAUT SYNDROME: REVIEW OF FOREIGN LITERATURE
Mukhin K.Y., Pylaeva O.A.
TYPICAL ABSENCES: RESULTS OF OWN INVESTIGATIONS
Mukhin K.Y., Mironov M.B.
Early infantile epileptic encephalopathy in the structure of microcephaly-capillary malformation syndrome: a clinical case
Maslov M.S., Sviridova A.M., Zalevskaya M.A.
Modern approaches in the treatment of Lennox–gastaut syndrome (a review of literature)
Мukhin К.Y., Pylaeva О.A.
Classification and definition of epilepsy. Position paper by the International League Against Epilepsy on Nosology and Definitions of Epilepsy Syndromes dated 2021
Mukhin K.Y., Pylaeva O.A., Kakaulina V.S., Bobylova M.Y.
Rufinamide (inovelon) in the treatment of Lennox–gastaut syndrome (a review of literature)
Мukhin К.Y., Pylaeva О.A.
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.
The case of development and epileptic encephalopathy with spike-wave activation in sleep in a boy with Smith–Magenis syndrome
Bobylova M.Y., Аbramov M.O., Pylaeva O.A., Мukhin K.Y., Petrukhin A.S.
Developmental encephalopathy and epilepsy associated with a heterozygous de novo mutation in the IRF2BPL gene: a case report
Lyukshina N.G., Sharkov A.A., Tolmacheva E.N.
Safety and tolerability of antiepileptic therapy: emphasis on the use of valproates (literature review)
Pylaeva O.A., Mukhin K.Y.
Efficacy and tolerability of brivaracetam in the treatment of epilepsy: literature review and own experience
Pylaeva O.A., Mukhin K.Y.
FOCAL EPILEPTIC MYOCLONUS IN KOZHEVNIKOV–RASMUSSEN SYNDROME
Kvaskova N.E., Mukhin K.Y.
EPILEPTIC ENCEPHALOPATHY WITH CONTINUOUS SPIKES-WAVES ACTIVITY DURING SLEEP
Belousova E.D.
Pontocerebellar hypoplasia caused by the TSEN54 mutation: clinical and electroencephalographic characteristics based on 3 cases
Bobylova M.Y., Abramov M.O., Mukhin K.Y.
Epilepsy with electrical status epilepticus during slow-wave sleep with a focus on electroencephalographic criteria
Mukhin K.Y., Glukhova L.Y., Makievskaya E.R.
PSEUDO-LENNOX SYNDROME: CLINICAL AND ELECTROENCEPHALOGRAPHIC CHARACTERISTICS
Mukhin K.Y.
ANOMALIES ON EEG IN PATIENTS WITH COGNITIVE EPILEPTIFORM DISINTEGRATION AND EPILEPTIC ENCEPHALOPATHIES, ASSOCIATED WITH С BENIGN EPILEPTIFORM PATTERNS OF CHILDHOOD
Mironov M.B.
EPILEPTIC SPASMS
Mukhin K.Y., Mironov M.B.
Pharmacoresistant epilepsy with electrical status epilepticus during slow-wave sleep: a clinical case
Maslov M.S.
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
Bobylova M.Y., Abramov M.O., Kovalskaya A.V., Alikhanov A.A., Mukhin K.Y.
A rare case of Cohen syndrome and early infantile epileptic encephalopathy (type 52) in two-year-old girl
Olshanskaya A.S., Dyuzhakova A.V., Shnayder N.A., Dmitrenko D.V.
EFFICACY AND TOLERABILITY OF LEVETIRACETAM (KEPPRA®) IN THE TREATMENT OF EPILEPSY: REVIEW OF LITERATURE
Mukhin K.Y., Pylaeva O.A.
FOCAL EPILEPTIC MYOCLONUS: DIFFERENTIAL DIAGNOSIS AND PROGNOSIS
Kvaskova N.E., Mukhin K.Y., Mironov M.B.
Efficacy and tolerability of sulthiame in the treatment of epilepsy: a literature review
Mukhin K.Y., Pylaeva O.A., Мarkin А.V.
Difficulties of diagnostics of epilepsy due to molybdenum cofactor deficiency: a case report
Malov A.G., Karakulova Y.V., Severino M., Kravtsov Y.I.
FEBRILE INFECTION-RELATED EPILEPSY SYNDROME (FIRES) IN SCHOOLCHILDREN: LITERATURE REVIEW AND OWN OBSERVATIONS
Kulikova S.L., Likhachev S.A., Belaya S.A., Svinkovskaya T.V., Kashyna A.R.
CURRENT APPROACHES TO THERAPY OF RETT’S SYNDROME (A REVIEW OF LITERATURE)
Borovikova N.Y., Bobylova M.Y.
THE DIAGNOSIS AND TREATMENT OF JEAVONS SYNDROME
Kulagin V.N., Mikhailichenko N.V.
Comorbidity of cerebral palsy and epilepsy with autism in children
Abusueva B.A., Askevova M.A., Shanavazova M.D., Nasrutdinova B.M., Bobylova M.Y., Gadzhieva A.S.
The effectiveness of therapy correction in children with paroxysmal disorders of consciousness based on the results of video electroencephalographic monitoring
Guzeva V.I., Guzeva O.V., Guzeva V.V., Okhrim I.V., Eremkina Y.A., Orel V.V.
Heart rate variability during epileptic seizures as a factor in the development of sudden unexpected death in epilepsy (literature review)
Monakhova A.V., Yakshina A.Y., Belousova E.D.
LANDAU–KLEFFNER SYNDROME (ACQUIRED EPILEPTIC APHASIA) WITH A FOCUS ON ELECTROENCEPHALOGRAPHIC CRITERIA
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.
MYOCLONUS IN CHILDREN: DEFINITIONS AND CLASSIFICATIONS, DIFFERENTIAL DIAGNOSIS, APPROACHES TO THERAPY (A LECTURE)
Bobylova M.Y., Nekrasova I.V., Ilyina Y.S., Kvaskova N.V.
Phenobarbital in HECW2-associated epileptic encephalopathy: unexpected clinical efficacy
Batyrov M.A., Per Н., Mamytova E.M., Nurbekova U.A.
Lamotrigine (Sazar) in the treatment of epilepsy: four years of experience in Svt. Luka's Association of Medical institutions for the Diagnosis, Treatment, and Rehabilitation of Nervous System Diseases and Epilepsy
Mukhin K.Y., Pylaeva O.A., Bobylova M.Y., Freydkova N.V.
Management of patients with single and rare epileptic seizures
Kotov A.S.
Efficiency of vagus nerve stimulation in epilepsy (literature review and case report)
Pylaeva O.A., Chadaev V.A., Bobylova M.Y., Mukhin K.Y.
HEREDITARY DISEASES AND SYNDROMES ACCOMPANIED BY FEBRILE CONVULSIONS: CLINICAL AND GENETIC CHARACTERISTICS AND DIAGNOSTIC PROCEDURES
Dadali E.L., Sharkov A.A., Sharkova I.V., Kanivets I.V., Konovalov F.A., Akimova I.A.
A CLINICAL CASE OF SYNGAP1 GENE MUTATION IN A GIRL WITH EPILEPSY, MENTAL RETARDATION, AUTISM, AND MOTOR DISORDERS
Bobylova M.Y., Mironov M.B., Abramov M.O., Kulikov A.V., Kazakova M.V., Glukhova L.Y., Barletova E.I., Mukhin K.Y.
THE CLINICAL, ELECTROENCEPHALOGRAPHIC, AND NEUROIMAGING CHARACTERISTICS OF PATIENTS WITH EPILEPTIC EYELID MYOCLONIA
Mironov M.B., Mukhin K.Y.
Epileptic encephalopathy caused by 1p36 deletion: literature review and case series
Bobylova M.Y., Konurina O.V., Borovikova N.A., Chadaev V.A.
Kleefstra syndrome and epilepsy
Gamirova R.G., Lyukshina N.G., Gamirova R.R., Farnosova M.E.
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.
VALPARIN XR IN THE TREATMENT OF EPILEPSY (А REVIEW OF LITERATURE AND A DESCRIPTION OF CLINICAL CASES)
Freidkova N.V., Pylaeva O.A., Mukhin K.Y.
DYSTONIA IN CHILDREN (A LECTURE)
Bobylova M.Y., Kakaulina V.S., Ilyina E.S., Nekrasova I.V., Pechatnikova N.L., Mikhailova S.V., Mironov M.B., Mukhin K.Y.
Dynamics of management of monogenic epilepsies, developmental and epileptic encephalopathies in routine clinical practice
Rakhmanina О.A., Volkov I.V., Tomenko Т.R., Shestakova O.I., Volkova О.К.
Modern neurogenetic representations of MELAS syndrome. Clinical cases (the lecture)
Shatalin A.V., Mukhina E.V., Kotov A.S., Amirkhanyan M.G.
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.
1 - 57 of 57 Items

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