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| Issue |
Title |
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| Vol 17, No 2 (2025) |
A novel X-linked immune-mediated actinopathy in a boy with anti-NMDA receptor encephalitis and variant in DOCK11 gene |
Abstract
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T. V. Kozhanova, S. S. Zhylina, T. I. Meshcheryakova, A. A. Abramov, M. M. Abidova, T. S. Kaminskaya, A. I. Krapivkin, N. N. Zavadenko |
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| Vol 17, No 2 (2025) |
Severe KCNT1-related developmental and epileptic encephalopathy |
Abstract
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A. G. Malov, L. Yu. Brokhin, A. V. Veselkova |
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| Vol 17, No 2 (2025) |
Neurological manifestations of hereditary chromosomal diseases |
Abstract
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L. B. Novikova, N. M. Faizullina, A. P. Akopyan, K. M. Ziultsle |
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| Vol 17, No 1 (2025) |
Migraine manifestations due to correction of secondary hyperhomocysteinaemia |
Abstract
PDF (Rus)
PDF (Eng)
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A. S. Bedenko |
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| Vol 16, No 4 (2024) |
Issues related to differential diagnosis of epilepsy and narcolepsy |
Abstract
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E. A. Kantimirova, D. V. Dmitrenko |
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| Vol 16, No 4 (2024) |
DEPDC5 mutations in familial epilepsy syndrome: genetic insights and therapeutic approaches |
Abstract
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M. K.C. Diallo, S. Mukesh, L. Kapil, R. Singla, D. Tar, S. N. Tammineedi, E. Singer, H. Chhayani, K. Arumaithurai, U. K. Patel, R. Arora |
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| Vol 16, No 4 (2024) |
Increased postictal creatine kinase in epilepsy patients |
Abstract
PDF (Rus)
PDF (Eng)
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L. V. Lipatova, I. V. Sakovsky |
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| Vol 16, No 2 (2024) |
Atypical course of severe myoclonic epilepsy of infancy (Dravet syndrome) |
Abstract
PDF (Rus)
PDF (Eng)
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B. A. Abusueva, M. D. Shanavazova, М. A. Askevova, V. S. Khalilov, M. Yu. Bobylova |
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| Vol 16, No 2 (2024) |
Transient epileptic amnesia versus transient global amnesia: aspects of differential diagnosis |
Abstract
PDF (Rus)
PDF (Eng)
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L. V. Lipatova, I. V. Sakovsky, M.-B. V. Gadaborshev |
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| Vol 16, No 2 (2024) |
A rare genetic Schuurs-Hoeijmakers syndrome (PACS1 syndrome) |
Abstract
PDF (Rus)
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T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, A. D. Mikhailova, A. I. Krapivkin, N. N. Zavadenko |
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| Vol 16, No 1 (2024) |
SEMA6B-related progressive myoclonus epilepsy in a patient with Klinefelter syndrome |
Abstract
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T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, L. M. Sushko, K. V. Osipova, A. M. Mazur, S. S. Fomenko, A. I. Krapivkin, N. N. Zavadenko |
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| Vol 15, No 4 (2023) |
The experience of applying vagus nerve stimulation in treatment of pharmacoresistant epilepsy |
Abstract
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A. A. Shatokhin, S. M. Karpov, E. V. Kushnareva, I. A. Peshkova, A. V. Shatokhin, I. A. Vyshlova |
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| Vol 15, No 4 (2023) |
Clinical features of developmental and epileptic encephalopathy caused by KCNQ2 gene mutation |
Abstract
PDF (Rus)
PDF (Eng)
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А. G. Malov, Т. P. Kalashnikova, N. А. Vdovina |
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| Vol 15, No 4 (2023) |
Epilepsy and MELAS syndrome: literature review and clinical observation |
Abstract
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А. М. Teplysheva, М. А. Glazova, R. N. Konovalov |
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| Vol 15, No 3 (2023) |
Stimulus-induced periodic discharges in response to low-frequency photostimulation in a female patient in recovery period after middle cerebral artery stroke |
Abstract
PDF (Rus)
PDF (Eng)
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D. S. Kanshina, I. V. Okuneva, M. A. Surma, O. Yu. Bronov, S. S. Nikitin |
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| Vol 15, No 3 (2023) |
Variable clinic-EEG trajectories in male patients with PCDH19 clustering epilepsy |
Abstract
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D. V. Dmitrenko, A. А. Sharkov, E. А. Domoratskaya, A. А. Usoltseva, I. V. Volkov, D. V. Pyankov |
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| Vol 15, No 3 (2023) |
SPTAN1-associated developmental and epileptic encephalopathy |
Abstract
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T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, E. G. Lukyanova, E. S. Bolshakova, S. O. Ayvazyan, K. V. Osipova, P. A. Vlasov, A. I. Krapivkin, N. N. Zavadenko |
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| Vol 15, No 1 (2023) |
Opsoclonus-myoclonus-ataxia syndrome as a complication of pembrolizumab treatment in an adult patient (a case report and literature review) |
Abstract
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K. A. Rumiantseva, A. Yu. Polushin, N. Kh. Abduloeva, Ya. B. Skiba, V. M. Moiseenko |
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| Vol 15, No 1 (2023) |
After-discharge activity as a basis to change intraoperative mapping protocol for functionally significant brain areas |
Abstract
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M. G. Podgurskaya, D. S. Kanshina, A. V. Dimertsev, M. V. Alexandrov, S. S. Nikitin |
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| Vol 14, No 4 (2022) |
Clinical case of a patient with focal cortical dysplasia IIa adjacent to the speech center: diagnostic and therapeutic algorithms |
Abstract
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N. V. Muzhikina, N. Yu. Koroleva, V. R. Kasumov, P. V. Pushnoy, A. D. Korotkov, I. A. Kotomin, M. V. Kireev |
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| Vol 14, No 2 (2022) |
Clinical case of distal arthrogryposis in combination with epilepsy due to an unbalanced translocation |
Abstract
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T. V. Kozhanova, S. S. Zhilina, T. I. Meshсheryakova, N. P. Prokopyeva, A. G. Prityko, N. N. Zavadenko |
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| Vol 14, No 1 (2022) |
Epilepsy in Norrie disease |
Abstract
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V. A. Aysina, О. V. Kozhevnikova, О. V. Osipova, A. V. Lashkova |
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| Vol 14, No 1 (2022) |
Myoclonic epilepsy with ragged red fibers in childhood |
Abstract
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Z. G. Tadtaeva, A. N. Galustyan, М. Yu. Krivdina, V. V. Rusanovsky, E. A. Efet, A. Е. Krivoshein, N. A. Kuritsyna, О. A. Gromova |
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| Vol 14, No 1 (2022) |
The effect of benign epileptiform discharges of childhood on cognitive function, behavior and speech |
Abstract
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E. A. Morozova, M. V. Belousova, D. V. Morozov, M. A. Utkuzova |
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| Vol 13, No 4 (2021) |
Experience of using EpiTapp application in structural focal epilepsy |
Abstract
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E. A. Narodova, N. A. Shnayder, V. E. Karnaukhov, V. V. Narodova |
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| Vol 13, No 3 (2021) |
Applying the International Classification of Functioning, Disability and Health in establishing a rehabilitation diagnosis for patients with juvenile myoclonic epilepsy |
Abstract
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K. V. Petrov, E. Yu. Mozheyko, N. A. Shnayder, M. M. Petrova, E. A. Narodova |
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| Vol 13, No 3 (2021) |
Reiterating the role of corpus callosum in generalization of interictal and ictal epileptiform discharges: a case report with post-callosotomy intracranial electroencephalography in Lennox–Gastaut syndrome |
Abstract
PDF (Eng)
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S. Gopinath, A. Pillai, A. G. Diwan, J. V. Pattisapu, K. Radhakrishnan |
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| Vol 13, No 1 (2021) |
Problems of diagnosing focal cortical dysplasia |
Abstract
PDF (Rus)
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K. D. Yakovleva, E. A. Kantemirova, D. V. Dmitrenko |
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| Vol 13, No 1 (2021) |
Clinical case of epilepsy, hearing loss and mental retardation syndrome associated with mutations in SPATA5 gene |
Abstract
PDF (Rus)
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T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, E. G. Luk’yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko, N. N. Zavadenko |
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| Vol 12, No 3 (2020) |
Clinical cases of cerebral venous thrombosis at the onset of paroxysmal conditions |
Abstract
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I. N. Stepanov, N. Yu. Ryazantseva |
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| Vol 12, No 3 (2020) |
New-Onset Refractory Status Epilepticus (NORSE): literature review and clinical case description |
Abstract
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S. G. Burd, M. B. Mironov, E. R. Moizykevich, Yu. V. Rubleva, M. A. Bogomazova, А. V. Yurchenko, T. M. Krasilshchikova, A. Yu. Suvorov, A. V. Lebedeva, R. T. Tairova |
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| Vol 12, No 1 (2020) |
Childhood autism associated with neurological manifestations and corpus callosum hypoplasia: literature review and clinical cases |
Abstract
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O. A. Komissarova, O. A. Milovanova, G. G. Avakyan, S. V. Bugriy |
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| Vol 12, No 1 (2020) |
Helsmoortel-van der Aa syndrome syndrome in a patient with epilepsy, developmental delay, intellectual disability, and autism spectrum disorder |
Abstract
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T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Luk`yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko |
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| Vol 12, No 1 (2020) |
Epilepsy in Sturge-Weber syndrome: a literature review and description of a clinical case |
Abstract
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N. I. Shova, V. A. Mikhailov, S. A. Korovina, D. V. Alekseeva |
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| Vol 11, No 4 (2019) |
Vagus Nerve Stimulator implantation in a pregnant woman with drug resistant epilepsy |
Abstract
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M. N. Klochkov, S. A. Katyshev, A. V. Vtorov, M. M. Bondareva, T. A. Skoromets, A. G. Naryshkin, A. A. Feygina |
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| Vol 11, No 2 (2019) |
Early infantile epileptic encephalopathy type 4: clinical, neurophysiological and therapeutic aspects |
Abstract
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A. A. Kholin, N. N. Zavadenko, L. M. Kolpakchi, I. D. Fedonyuk, A. S. Papikyan, А. N. Zavadenko, E. S. Ilina |
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| Vol 11, No 2 (2019) |
Use of autologous mesenchymal stem cells in the combined treatment of symptomatic epilepsy |
Abstract
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F. P. Khlebokazov, T. V. Dokukina, N. Yu. Paramonova, S. I. Gotto, I. I. Khvostova, N. N. Misyuk, A. I. Martynenko, Е. L. Slobina, I. V. Shamruk |
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| Vol 11, No 2 (2019) |
Evolution of genetically determined generalized epilepsies |
Abstract
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E. A. Morozova, F. I. Gusyakov |
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| Vol 11, No 1 (2019) |
Surgical treatment of drug resistant epilepsy in Sturge-Weber syndrome: review of the literature and clinical case presentation |
Abstract
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G. S. Ibatova, S. K. Akshulakov, S. M. Malyshev, R. G. Khachatryan, T. M. Alekseeva, A. S. Shershever, W. A. Khachatryan |
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| Vol 11, No 1 (2019) |
Efficacy of levetiracetam monotherapy in epilepsy associated with benign epileptiform discharges of childhood |
Abstract
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N. A. Borovkova, A. G. Malov |
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| Vol 11, No 1 (2019) |
Mutation of the ALDH7A1 gene in a patient with pyridoxal phosphate-dependent neonatal epileptic encephalopathy: a clinical case |
Abstract
PDF (Rus)
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T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Lukyanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko |
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| Vol 9, No 3 (2017) |
EPILEPSY WITH GELASTIC SEIZURES AND HYPOTHALAMIC HAMARTOMA: A RARE CLINICAL CASE |
Abstract
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V. A. Mikhailov, A. K. Druzhinin, N. A. Shova, E. A. Korsakova |
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| Vol 7, No 2 (2015) |
NEUROLOGICAL PAROXYSMAL DISORDERS IN CHILDREN WITH HYPOGLYCEMIA IN CONGENITAL HYPERINSULINISM: POLYMORPHISM OF CLINICAL IMPLICATIONS |
Abstract
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I. O. Shchederkina, M. A. Melikyan, A. N. Zavadenko, E. V. Kozlova, N. N. Zavadenko |
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| Vol 7, No 1 (2015) |
SEVERE EPILEPTIC ENCEPHALOPATHY OF EARLY CHILDHOOD DUE TO SCN2A MUTATION |
Abstract
PDF (Rus)
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I. S. Bachtin, E. D. Belousova, P. A. Shatalov, S. O. Ayvazyan |
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| Vol 7, No 1 (2015) |
TICS IN CHILDREN. CLINICAL RESULT OF THE TREATMENT TIC DISORDERS BY LEVETIRACETAM |
Abstract
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Ju. V. Borodina, N. V. Jur’eva, N. N. Maslova |
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| Vol 7, No 1 (2015) |
ALPERS-HUTTENLOCHER SYNDROME |
Abstract
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T. T. Batysheva, V. M. Trepilets, L. Ya. Akhadova, G. S. Golosnaya |
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| Vol 7, No 2 (2015) |
CLINICAL CASE OF PREGNANT PATIENT WITH TEMPORAL EPILEPSY AND MYOCLONIC EPILEPTIC SEIZURES |
Abstract
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V. O. Generalov, T. R. Sadykov, N. I. Klimenchenko, A. M. Yugay, Yu. V. Kazakova, E. V. Tsalagova, O. V. Shetikova |
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| Vol 5, No 4 (2013) |
ICTAL EEG IN A PATIENT WITH ROLANDIC EPILEPSY. CASE STUDY |
Abstract
PDF (Rus)
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I. V. Volkov, E. M. Stasyshina, O. K. Volkova |
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| Vol 5, No 2 (2013) |
FEJERMAN SYNDROME (BENIGN NONEPILEPTIC MYOCLONUS OF INFANCY) |
Abstract
PDF (Rus)
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M. B. Mironov, V. Iu. Nogovitsyn, M. O. Abramov, E. A. Dobrovskaya, N. E. Kvaskova, K. Yu. Mukhin |
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| Vol 6, No 2 (2014) |
ATYPICAL EVOLUTION OF BENIGN CHILDHOOD EPILEPSY WITH CENTRAL TEMPORAL SPIKES AS A MANIFESTATION OF EPILEPTIC ENCEPHALOPATHY |
Abstract
PDF (Rus)
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D. A. Kot, L. V. Shalkevich |
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