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THE MITOCHONDRIAL DISEASE NARP SYNDROME IN THE PRACTICE OF A PEDIATRIC NEUROLOGIST
Shishkina E.V., Barkhatov M.V., Borisova E.V., Falalaleeva S.O., Shchekaleva N.A., Makarevskaya N.Y., Chubko M.A.
Moya-moya disease in a child with nephropatic cystinosis: a case report and literature review
Pivovarova A.M., Papizh S.V., Kаzakov D.O., Gorchkhanovа K.Z., Melnikov I.A.
Jacobsen syndrome. Literature review and a case report
Syrkina A.V., Chebanenko N.V., Zykov V.P., Mikhailova N.S.
LANDAU–KLEFFNER SYNDROME (ACQUIRED EPILEPTIC APHASIA) WITH A FOCUS ON ELECTROENCEPHALOGRAPHIC CRITERIA
Mukhin K.Y.
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.
West syndrome in patients with Kabuki syndrome (literature review and case report)
Zhitomirskaya M.L., Snegova E.V., Odintsova G.V.
SPASTIC FORM OF CEREBRAL PALSY, EPILEPSY WITH BENIGN EPILEPTIFORM DISCHARGE OF CHILDHOOD ON ELECTROENCEPHALOGRAM, AND IATROGENIC STEVENS–JOHNSON SYNDROME (CASE DESCRIPTION)
Kotov A.S., Borisova M.N., Panteleeva M.V., Shatalin A.V., Korobkina E.O.
HEMICONVULSION-HEMIPLEGIA-EPILEPSY SYNDROME (HHE SYNDROME) (A LECTURE)
Mukhin K.Y., Bobylova M.Y., Dolinina A.F., Pylaeva O.A.
The comorbidity of fetal alcohol syndrome and sleep apnea/hypopnea syndrome in a 7‑year-old girl (a clinical case)
Yakovleva K.D., Alekseeva O.V., Shnayder N.A., Sidorenko D.R., Dmitrenko D.V.
Mowat-Wilson syndrome: literature review and case series
Bobylova M.Y., Kakaulina V.S., Abramov M.O., Mukhin K.Y.
Definition and new approaches to understanding the pathogenesis of Drave syndrome in children
Ulyakov A.N., Bobylova M.Y., Lobanova V.S., Мukhin К.Y., Pylaeva O.A., Tishchenko I.S., Kazakov S.O.
Sleep disorder in Angelman syndrome: causes, mechanisms and methods of correction. Literature review
Psyanchin A.A., Bobylova M.Y., Yakupov T.Z.
EEG findings in patients with angelman syndrome. Notched slow waves and age-specific characteristics of the main EEG patterns
Kuzmich G.V., Bobylova M.Y., Mukhin K.Y., Pylaeva O.A., Glukhova L.Y., Bagdasaryan A.S., Zakharova A.Y.
Outcomes of West syndrome: literature review and own data
Prygunova T.M.
Rufinamide (inovelon) in the treatment of Lennox–gastaut syndrome (a review of literature)
Мukhin К.Y., Pylaeva О.A.
CURRENT APPROACHES TO THERAPY OF RETT’S SYNDROME (A REVIEW OF LITERATURE)
Borovikova N.Y., Bobylova M.Y.
ACUTE ATAXIA, TAKING PLACE AFTER ACUTE RESPIRATORY VIRAL INFECTION IN 2 Y. O. GIRL, AS A DEBUT NEUROLOGIC SIGN OF THE ANGELMAN SYNDROME
Voropanova E.B., Bobylova M.Y., Mironov M.B., Kulikov A.V.
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 rufinamide in the treatment of epilepsy (experience of the Svt. Luka’s Institute of Child Neurology and Epilepsy)
Mukhin K.Y., Pylaeva O.A., Bobylova M.Y., Freydkova N.V., Glukhova L.Y., Abramov M.O.
RETT SYNDROME: DIFFICULTIES OF DIAGNOSTICS (CLINICAL AND PSYCHOPATHOLOGICAL ASPECTS)
Malinina E.V., Zabozlaeva I.V.
KLEINE–LEVIN SYNDROME AFTER USE OF RECREATIONAL DRUGS
Semenova E.I., Tokareva Y.V., Belova Y.A., Kotov A.S., Eliseev Y.V.
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.
Selective serotonin reuptake inhibitors in pediatric neurology: a safety issue (systematic review)
Shnayder N.A., Makarov E.A., Kidyaeva A.V., Grechkina V.V., Petrova M.M., Nasyrova R.F.
Epileptic encephalopathy caused by 1p36 deletion: literature review and case series
Bobylova M.Y., Konurina O.V., Borovikova N.A., Chadaev V.A.
Difficulties of differential diagnostics of Guillain–Barré syndrome in children. The discussion of two clinical cases
Kotov A.S., Mukhina E.V., Shatalin A.V., Panteleeva M.V., Bunak M.S.
Glucose transporter deficiency syndrome type 1: a case report
Kulish E.A., Kotov A.S., Mukhina E.V., Kotalevskaya Y.Y., Svetlichnaya D.V., Panteleeva M.V.
Schimmelpenning–Feuerstein–Mims syndrome (a case report)
Ol’shanskaya A.S., Dyuzhakova A.V., Shnayder N.A., Dmitrenko D.V., Guzey T.N.
RESISTANT EPILEPSY FORMS, ASSOCIATED WITH FEVER-PROVOKED (FEBRILE) EPILEPTIC SEIZURES (DRAVET SYNDROME, DESC, HHE) (A LECTURE)
Bobylova M.Y.
EPILEPTIC SPASMS
Mukhin K.Y., Mironov M.B.
Clinical and electroencephalographic characteristics of neurodegeneration with brain iron accumulation type 5 in children on the example of 5 cases
Perunova N.Y., Bobylova M.Y., Prygunova T.M.
Gillespiе syndrome, caused by previously undescribed mutation in the gene ITPR1
Sharkova I.V., Akimova I.A., Khlebnikova O.V., Dadali E.L.
COMPARATIVE ANALYSIS OF THERAPY OUTCOMES IN PATIENTS WITH WEST SYNDROME RECEIVING TETRAСOSACTIDЕ AND OTHER ANTIEPILEPTIC DRUGS
Farnosova M.E., Gamirova R.G.
ELECTROENCEPHALOGRAPHIC CHANGES WITH DRAVET SYNDROME
Mukhin K.Y., Pylaeva O.A., Mironov M.B., Dolinina A.F., Morozov D.V., Nikitina M.A.
Epilepsy and congenital cerebral palsy: Parallels between the location of genome anomalies and clinical manifestations
Sokolov P.L., Chebanenko N.V., Fedotova Y.A., Mednaya D.M.
Pericallosal lipoma in an infant with fetal alcohol syndrome: a case report
Golosnaya G.S., Novikov M.Y., Knyazeva N.Y., Volodina D.Y., Skobeltsyn A.A., Perepelov V.A., Ogurtsov A.V., Larionova T.A., Ledyaykina L.V., Seleznev K.A.
Febrile infection-related epilepsy syndrome: long-term consequences (own observations)
Drobitova A.V., Karas A.Y., Maslova N.V., Mukhin K.Y.
Attention deficit hyperactivity disorder: new in understanding and treatment approaches
Morozova E.A., Madyakina A.A.
ELECTROENCEPHALOGRAPHIC CHANGES AND PROGNOSIS FOR THE DEVELOPMENT OF EPILEPSY IN PATIENTS WITH POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME (PRES): LITERATURE REVIEW
Bobylova M.Y., Zakharova A.Y., Khomyakova S.P.
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.
MYOCLONIC ASTATIC EPILEPSY (DOOSE SYNDROME)
Mukhin K.Y., Mironov M.B., Pylaeva O.A.
THE DIAGNOSIS AND TREATMENT OF PANDAS SYNDROME: A CASE REPORT
Kharitonov V.I., Vinnik Y.M., Selyukov G.I.
The modern approaches to the diagnostics and treatment of Lennox–Gastaut syndrome (literature review)
Mukhin K.Y., Pylaeva O.A.
Neuropsychological mechanisms underlying reading and writing disorders in primary school children
Sableva A.S.
Mental disorders in children with intractable epilepsy as a manifestation of forced normalization of the electroencephalogram (Landolt syndrome)
Gagara D.A., Evtushenko S.K.
EFFICACY OF RUFINAMIDE IN THE TREATMENT OF DRUG-RESISTANT FOCAL EPILEPSIES IN PAEDIATRIC PRACTICE
Shchederkina I.O., Orlova K.A., Koltunov I.E., Dorofeeva M.Y.
FOCAL EPILEPTIC MYOCLONUS IN KOZHEVNIKOV–RASMUSSEN SYNDROME
Kvaskova N.E., Mukhin K.Y.
RUFINAMIDE IN THE TREATMENT OF LENNOX–GASTAUT SYNDROME: REVIEW OF FOREIGN LITERATURE
Mukhin K.Y., Pylaeva O.A.
THE DIAGNOSIS AND TREATMENT OF JEAVONS SYNDROME
Kulagin V.N., Mikhailichenko N.V.
Efficacy and tolerability of rufinamide in the treatment of Lennox–Gastaut syndrome (experience of the Svt. Luka’s Association of Medical Institutions)
Mukhin K.Y., Pylaeva O.A., Bobylova M.Y., Glukhova L.Y., Freydkova N.V.
Kleefstra syndrome and epilepsy
Gamirova R.G., Lyukshina N.G., Gamirova R.R., Farnosova M.E.
West syndrome: long-term outcomes depending on etiology and treatment (literature review)
Prygunova T.M.
PHELAN–MCDERMID SYNDROM (del 22q13 AND r(22)): LITERATURE REVIEW AND 2 CASE REPORTS
Bobylova M.Y., Nikitina M.A., Mukhin K.Y., Kulikov A.V.
PSEUDO-LENNOX SYNDROME: CLINICAL AND ELECTROENCEPHALOGRAPHIC CHARACTERISTICS
Mukhin K.Y.
CLINICAL AND ENCEPHALOGRAPHIC CHANGES AT LENNOX–GASTAUT SYNDROME
Mukhin K.Y.
Early infantile epileptic encephalopathy in the structure of microcephaly-capillary malformation syndrome: a clinical case
Maslov M.S., Sviridova A.M., Zalevskaya M.A.
On the question of the features of pain syndrome in oncopediatric practice
Suetina O.A., Kravchenko N.E.
Continuous spike-and-wave activity during slow-wave sleep in patients with rett syndrome
Kulikova S.L., Kozyreva I.V., Likhachev S.A., Bobylova M.Y.
Modern neurogenetic representations of MELAS syndrome. Clinical cases (the lecture)
Shatalin A.V., Mukhina E.V., Kotov A.S., Amirkhanyan M.G.
Modern approaches in the treatment of Lennox–gastaut syndrome (a review of literature)
Мukhin К.Y., Pylaeva О.A.
POSSIBILITIES FOR ANTIEPILEPTIC DRUGS USE IN THE TREATMENT OF TIC HYPERKINESIS AND TOURETTE SYNDROME IN CHILDREN
Zykov V.P., Kashirina E.A., Naugol’nykh Y.V.
RUFINAMIDE (INOVELON) IN THE TREATMENT OF LENNOX–GASTAUT SYNDROME (A REVIEW OF LITERATURE AND CLINICAL CASE)
Mukhin K.Y., Pylaeva O.A.
THE INCIDENCE OF JUVENILE MYOCLONIC EPILEPSY AND ANALYSIS OF ITS THERAPY ACCORDING TO THE DATA OF THE “EPICENTER” (VOLGOGRAD)
Belyaev O.V., Volkova E.A.
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