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Vol 16, No 1-2 (2021)
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.
PDF
(Rus)
Vol 20, No 1 (2025)
Early infantile epileptic encephalopathy in the structure of microcephaly-capillary malformation syndrome: a clinical case
Maslov M.S., Sviridova A.M., Zalevskaya M.A.
PDF
(Rus)
Vol 17, No 2 (2022)
Epileptic encephalopathy caused by 1p36 deletion: literature review and case series
Bobylova M.Y., Konurina O.V., Borovikova N.A., Chadaev V.A.
PDF
(Rus)
Vol 16, No 1-2 (2021)
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.
PDF
(Rus)
Vol 19, No 2 (2024)
Pontocerebellar hypoplasia caused by the TSEN54 mutation: clinical and electroencephalographic characteristics based on 3 cases
Bobylova M.Y., Abramov M.O., Mukhin K.Y.
PDF
(Rus)
Vol 18, No 2-3 (2023)
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.
PDF
(Rus)
Vol 14, No 2 (2019)
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.
PDF
(Rus)
Vol 19, No 4 (2024)
Cerebral palsy: current status of the problem (review of literature)
Kolesnikova E.V., Vyshlova I.A., Karpov S.M., Soboleva O.A.
PDF
(Rus)
Vol 12, No 1 (2017)
Epilepsy with electrical status epilepticus during slow-wave sleep with a focus on electroencephalographic criteria
Mukhin K.Y., Glukhova L.Y., Makievskaya E.R.
PDF
(Rus)
Vol 19, No 4 (2024)
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.
PDF
(Rus)
Vol 16, No 3 (2021)
Experience with the use of a ketogenic diet with type 1 glucose transporter deficiency (De Vivo disease)
Lyukshina N.G.
PDF
(Rus)
Vol 11, No 4 (2016)
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.
PDF
(Rus)
Vol 19, No 3 (2024)
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.
PDF
(Rus)
Vol 11, No 3 (2016)
LANDAU–KLEFFNER SYNDROME (ACQUIRED EPILEPTIC APHASIA) WITH A FOCUS ON ELECTROENCEPHALOGRAPHIC CRITERIA
Mukhin K.Y.
PDF
(Rus)
Vol 11, No 1 (2016)
PSEUDO-LENNOX SYNDROME: CLINICAL AND ELECTROENCEPHALOGRAPHIC CHARACTERISTICS
Mukhin K.Y.
PDF
(Rus)
Vol 19, No 1 (2024)
Wernicke encephalopathy in combination with acute polyneuropathy under the guise of a demyelinating disease in a teenager with an eating disorder
Ovchinnikova E.O., Kotov A.S., Panteleeva M.V., Mukhina E.V.
PDF
(Rus)
Vol 15, No 3-4 (2020)
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.
PDF
(Rus)
Vol 10, No 3 (2015)
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.
PDF
(Rus)
Vol 19, No 1 (2024)
Pharmacoresistant epilepsy with electrical status epilepticus during slow-wave sleep: a clinical case
Maslov M.S.
PDF
(Rus)
Vol 14, No 3 (2019)
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.
PDF
(Rus)
Vol 7, No 1 (2012)
EPILEPTIC ENCEPHALOPATHY WITH CONTINUOUS SPIKES-WAVES ACTIVITY DURING SLEEP
Belousova E.D.
PDF
(Rus)
Vol 20, No 2 (2025)
Phenobarbital in HECW2-associated epileptic encephalopathy: unexpected clinical efficacy
Batyrov M.A., Per Н., Mamytova E.M., Nurbekova U.A.
PDF
(Rus)
Vol 19, No 1 (2024)
Efficacy and tolerability of sulthiame in the treatment of epilepsy: a literature review
Mukhin K.Y., Pylaeva O.A., Мarkin А.V.
PDF
(Rus)
Vol 14, No 2 (2019)
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.
PDF
(Rus)
Vol 7, No 1 (2012)
ANOMALIES ON EEG IN PATIENTS WITH COGNITIVE EPILEPTIFORM DISINTEGRATION AND EPILEPTIC ENCEPHALOPATHIES, ASSOCIATED WITH С BENIGN EPILEPTIFORM PATTERNS OF CHILDHOOD
Mironov M.B.
PDF
(Rus)
1 - 25 of 25 Items

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