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Issue | Title | |
Vol 9, No 2 (2017) | WEST SYNDROME REVISITED | Abstract similar documents |
T. G. Okhapkina, Z. K. Gorchanova, I. V. Shulyakova, E. S. Ilyina, E. S. Michurina, E. D. Belousova | ||
"... hypsarrhythmia, five versions of modified hypsarrhythmia are proposed: synchronized version, asymmetric version ..." | ||
Vol 10, No 2 (2018) | The spectrum and efficacy of antiepileptic drugs in patients with infantile spasms in Russia | Abstract similar documents |
T. G. Okhapkina, I. V. Shuljakova, E. S. Ilina, G. V. Kalmykova, M. V. Prytkina, E. D. Belousova | ||
"... ). As expected, the clinical effect (cessation of IS and suppression of hypsarrhythmia) of valproic acid ..." | ||
Vol 3, No 3 (2011) | PROGNOSTIC CRITERIA OF INFANTILE SPASMS | Abstract similar documents |
O. V. Gaponova, E. D. Belousova | ||
"... West's Syndrome prognosis is extremely complicate due to the large number of potential prognostic ..." | ||
Vol 12, No 1 (2020) | Interpretation of electroencephalography in infants | Abstract similar documents |
A. G. Koshchavtsev, S. V. Grechanyi | ||
"... -suppression», hypsarrhythmia», etc. Our own research was conducted using an Encephalan-EEGR-19/26 ..." | ||
Vol 3, No 4 (2011) | ОПТИМИЗАЦИЯ ДИАГНОСТИКИ И ЛЕЧЕНИЯ СИНДРОМА ВЕСТА В АРМЕНИИ | Abstract similar documents |
, | ||
Vol 7, No 1 (2015) | SEVERE EPILEPTIC ENCEPHALOPATHY OF EARLY CHILDHOOD DUE TO SCN2A MUTATION | Abstract similar documents |
I. S. Bachtin, E. D. Belousova, P. A. Shatalov, S. O. Ayvazyan | ||
"... антиэпилептической терапии. На межприступной ЭЭГ обнаруживалась модифицированная (синхронизированная) гипсаритмия ..." | ||
Vol 14, No 2 (2022) | Epilepsy syndromes: the 2022 ILAE definition and classification | Abstract similar documents |
D. V. Blinov | ||
"... Until recently, no classification of epileptic syndromes officially approved by the International ..." | ||
Vol 2, No 1 (2010) | BENIGN OCCIPITAL EPILEPSY OF CHILDHOOD: FACTORS AFFECTING THE PARTICULARS OF TREATMENT | Abstract similar documents |
I. O. Shederkina, V. A. Karlov | ||
"... syndrome (PS) and Gastaut syndrome (GS). This article reviews modern literature data on epidemiology ..." | ||
Vol 10, No 2 (2018) | Epilepsy in children with lymphoproliferative syndrome | Abstract similar documents |
I. O. Schederkina, O. A. Tiganova, I. E. Koltunov, N. V. Natrusova, K. L. Kondratchik | ||
Vol 7, No 1 (2015) | ALPERS-HUTTENLOCHER SYNDROME | Abstract similar documents |
T. T. Batysheva, V. M. Trepilets, L. Ya. Akhadova, G. S. Golosnaya | ||
"... Alpers-Huttenlocher syndrome is a rare mitochondrial disease connected with mutations ..." | ||
Vol 3, No 4 (2011) | KABUKI SYNDROME WITH EPILEPSY: CLINICAL CASE | Abstract similar documents |
N. Yu. Borovikova, K. S. Borovikov, K. Yu. Mukhin, M. B. Mironov | ||
"... Kabuki syndrome is rare genetic disorder. Patients with this syndrome are phenotypically similar ..." | ||
Vol 3, No 2 (2011) | Epileptic syndromes in children with cerebral palsy | Abstract similar documents |
T. T. Batysheva, A. N. Platonova, O. V. Bykova | ||
Vol 12, No 4 (2020) | Features of brain electrical activity in adult patients with POLG-related disorders | Abstract similar documents |
P. A. Fedin, E. P. Nuzhnyi, T. Yu. Noskova, Yu. A. Seliverstov, S. A. Klyushnikov, T. D. Krylova, P. G. Tsygankova, E. Yu. Zakharova, S. N. Illarioshkin | ||
"... were examined: 7 with SANDO (Sensory Ataxic Neuropathy, Dysarthria, Ophthalmoparesis) syndrome, and 1 ..." | ||
Vol 4, No 2 (2012) | EPILEPSY IN CHILDREN WITH MYTOCHONDRIAL DISEASES: DIAGNOSTICS AND TREATMENT FEATURES | Abstract similar documents |
N. N. Zavadenko, A. A. Kholin | ||
"... features of the MD, accompanying by epilepsy. Two case reports are presented of MELAS syndrome and Alpers ..." | ||
Vol 12, No 1S (2020) | What’s hidden behind Lennox-Gastaut syndrome? | Abstract similar documents |
E. D. Belousova | ||
"... A number of epileptologists often diagnose Lennox-Gastaut syndrome, while others almost never do ..." | ||
Vol 10, No 1 (2018) | COMORBIDITY IN HEMICONVULSION-HEMIPLEGIA-EPILEPSY SYNDROME IN CHILDREN | Abstract similar documents |
S. O. Ayvazyan | ||
"... Hemiconvulsion-hemiplegia-epilepsy (HHE) syndrome is a rare consequence of focal status ..." | ||
Vol 5, No 2 (2013) | FEJERMAN SYNDROME (BENIGN NONEPILEPTIC MYOCLONUS OF INFANCY) | Abstract similar documents |
M. B. Mironov, V. Iu. Nogovitsyn, M. O. Abramov, E. A. Dobrovskaya, N. E. Kvaskova, K. Yu. Mukhin | ||
"... Abstract: Fejerman syndrome (benign nonepileptic myoclonus of infancy) is a rare nonepileptic ..." | ||
Vol 15, No 4 (2023) | Epilepsy and MELAS syndrome: literature review and clinical observation | Abstract similar documents |
А. М. Teplysheva, М. А. Glazova, R. N. Konovalov | ||
"... MELAS syndrome (mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes) belongs ..." | ||
Vol 14, No 2 (2022) | Clinical case of distal arthrogryposis in combination with epilepsy due to an unbalanced translocation | Abstract similar documents |
T. V. Kozhanova, S. S. Zhilina, T. I. Meshсheryakova, N. P. Prokopyeva, A. G. Prityko, N. N. Zavadenko | ||
"... with Freeman–Sheldon syndrome had no mutations in genes associated with distal arthrogryposis. Chromosomal ..." | ||
Vol 10, No 2 (2018) | Hyperandrogenism as a side effect of anticonvulsants | Abstract similar documents |
E. V. Tsallagova, V. O. Generalov, T. R. Sadykov | ||
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 similar documents |
T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Luk`yanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko | ||
"... for patients with Helsmoortel-van der Aa syndrome (OMIM: # 615873). Mutations in the ADNP gene are the genetic ..." | ||
Vol 12, No 1 (2020) | Childhood autism associated with neurological manifestations and corpus callosum hypoplasia: literature review and clinical cases | Abstract similar documents |
O. A. Komissarova, O. A. Milovanova, G. G. Avakyan, S. V. Bugriy | ||
"... Aim. To consolidate literature data and to demonstrate rare hereditary neurogenetic syndromes ..." | ||
Vol 8, No 3 (2016) | FREQUENCY OF CLINICAL PHENOTYPES OF JUVENILE MYOCLONIC EPILEPSY: PILOT STUDY IN SIBERIAN FEDERAL DISTRICT | Abstract similar documents |
N. A. Shnayder, O. S. Shilkina, K. V. Petrov, A. V. Duyzhakova, N. A. Marueva | ||
Vol 8, No 4 (2016) | EPILEPSY MANIFESTATIONS IN PATIENTS WITH MALFORMATIONS OF THE CORPUS CALLOSUM | Abstract similar documents |
O. A. Milovanova, E. R. Moyzykevich, G. G. Avakian, Y. Yu. Tarakanova | ||
"... of the example of two disembriogenetic syndromes (Aicardi syndrome and Pierre-Robin syndrome). These hereditary ..." | ||
Vol 11, No 3 (2019) | Epilepsy in de Vivo syndrome: a literature review and a clinical case | Abstract similar documents |
M. B. Mironov, N. I. Andreeva, D. S. Fomchenkova, N. V. Chebanenko, Yu. V. Rubleva, T. M. Krasilshchikova, S. G. Burd | ||
"... GLUT 1 transporter deficiency syndrome (De Vivo syndrome, GLUT 1 deficiency syndrome, De Vivo ..." | ||
Vol 12, No 1 (2020) | Epilepsy in Sturge-Weber syndrome: a literature review and description of a clinical case | Abstract similar documents |
N. I. Shova, V. A. Mikhailov, S. A. Korovina, D. V. Alekseeva | ||
"... The Struge-Weber syndrome is the third most common neurodermal disease after neurofibromatosis ..." | ||
Vol 10, No 4 (2018) | Epilepsy combined with Wolf-Hirschhorn syndrome: a literature review and description of clinical cases | Abstract similar documents |
M. B. Mironov, N. V. Chebanenko, S. O. Ayvazyan, S. A. Vladimirova, K. V. Osipova, S. G. Burd, Yu. V. Rubleva, T. M. Krasilshchikova, V. G. Bychenko | ||
"... in 5 patients with epilepsy combined with Wolf-Hirschhorn syndrome (WHS). According to our data ..." | ||
Vol 8, No 4 (2016) | EPILEPSY SYNDROMES WITH CONTINIUOS SPIKE AND WAVE ACTIVITY DURING SLEEP | Abstract similar documents |
O. A. Shidlovskaya, E. D. Belousova | ||
"... Syndromes with continuous spikes and waves during sleep (CSWS) are being actively studied now ..." | ||
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) similar documents |
S. Gopinath, A. Pillai, A. G. Diwan, J. V. Pattisapu, K. Radhakrishnan | ||
"... Lennox–Gastaut syndrome (LGS) is an epileptic encephalopathy characterized by delayed mental ..." | ||
Vol 13, No 3 (2021) | Mental development of children from paired mothers with epilepsy: assessing remote teratogenic effects and predictors of developmental disorders | Abstract PDF (Eng) similar documents |
N. F. Mikhailova, A. S. Krasko, G. V. Odintsova, I. V. Larina, V. A. Mikhailov | ||
Vol 14, No 1 (2022) | Idiopathic and symptomatic forms of genetic epilepsy | Abstract similar documents |
A. G. Malov | ||
"... epilepsies (e.g., Dravet syndrome) as well as symptomatic epilepsies due to other genetically ..." | ||
Vol 11, No 1 (2019) | Surgical treatment of drug resistant epilepsy in Sturge-Weber syndrome: review of the literature and clinical case presentation | Abstract similar documents |
G. S. Ibatova, S. K. Akshulakov, S. M. Malyshev, R. G. Khachatryan, T. M. Alekseeva, A. S. Shershever, W. A. Khachatryan | ||
"... The paper addresses the relatively rare inherited neurodermal disorder – Sturge-Weber syndrome ..." | ||
Vol 6, No 1 (2014) | OCCIPITAL EPILEPSY IN CHILDREN: DIAGNOSTIC FEATURES AND TACTICS | Abstract similar documents |
I. O. Shchederkina | ||
"... % – Panayiotopoulosao syndrome, 4% – Gastaut type ). Particular difficulty is the abundance of autonomous symptoms ..." | ||
Vol 7, No 4 (2015) | EPILEPSY AND NON-EPILEPTIC PAROXYSMS AT CHILDREN OF THE MOGILEV AREA (on materials of work of children's neurologic branch of establishment of public health services «Mogilev regional children's hospital» during 2008-2012) | Abstract similar documents |
S. N. Prusakov, I. L. Malashko, T. S. Kaskova, M. G. Orlova | ||
Vol 14, No 3 (2022) | Diagnostics and age-related evolution of Lennox–Gastaut syndrome. Management in diverse patient age periods | Abstract similar documents |
E. D. Belousova, S. G. Burd, N. A. Ermolenko, K. Yu. Mukhin | ||
"... Lennox–Gastaut syndrome is an epileptic encephalopathy with onset in childhood. The classical ..." | ||
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 similar documents |
K. A. Rumiantseva, A. Yu. Polushin, N. Kh. Abduloeva, Ya. B. Skiba, V. M. Moiseenko | ||
"... Background. Opsoclonus-myoclonus-ataxia syndrome (OMAS) in adults is an extremely rare condition ..." | ||
Vol 13, No 1 (2021) | Clinical case of epilepsy, hearing loss and mental retardation syndrome associated with mutations in SPATA5 gene | Abstract similar documents |
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 | ||
"... with epilepsy, hearing loss and mental retardation syndrome (MIM 616577). Paired parents were carriers of one ..." | ||
Vol 6, No 2 (2014) | PECULIARITIES OF AMINO ACID METABOLISM IN SERUM AND CEREBROSPINAL FLUID OF PATIENTS WITH CHRONIC VIRAL ENCEPHALITIS WITH CONVULSIVE SYNDROME | Abstract similar documents |
N. F. Philippovich, N. V. Staheyko | ||
"... patients with epileptic syndrome in chronic viral neurological infection. The dependence ..." | ||
Vol 6, No 1 (2014) | CLINICAL AND EEG CHARACTERISTICS OF THE EARLY ONSET BENIGN CHILDHOOD OCCIPITAL EPILEPSY (PANAYOTOPOULOS SYNDROME) | Abstract similar documents |
M. R. Kremenchugskaya, L. M. Kuzenkova, O. V. Globa, A. A. Buksh | ||
"... occipital epilepsy of childhood with early debut – Panayiotopoulos syndrome, and the results of own research ..." | ||
Vol 13, No 4 (2021) | Short-term and long-term changes in seizure frequency and neurocognitive status in pediatric patients after surgery for mixed neuronal-glial brain tumors | Abstract similar documents |
L. A. Gorlova, O. O. Shmeleva, E. V. Fedorov, A. V. Kim, Yu. V. Dinikina, W. A. Khachatryan, K. A. Samochernykh | ||
Vol 13, No 3 (2021) | Treatment of epilepsy associated with primary and metastatic brain tumors | Abstract similar documents |
A V. Lebedeva, S. G. Burd, P. N. Vlasov, N. A. Ermolenko, I. A. Zhidkova, S. K. Zyryanov, I. Yu. Kovaleva, D. R. Naskhletashvili, N. Yu. Perunova, I. G. Rudakova, R. K. Shikhkerimov, M. A. Yamin | ||
Vol 15, No 1 (2023) | Clinical features of epilepsy course during COVID-19 | Abstract similar documents |
V. A. Mikhailov, N. A. Sivakova, Z. K. Idrisova, N. I. Shova | ||
Vol 12, No 4 (2020) | Heart rate and conductivity disorders in juvenile myoclonic epilepsy: genetic predictors | Abstract similar documents |
N. A. Shnayder, M. M. Petrova, K. V. Petrov, D. V. Dmitrenko, R. F. Nasyrova | ||
"... ) regarding cerebrocardial syndrome, primarily heart rhythm and conduction disorders in epilepsy and sudden ..." | ||
Vol 10, No 3 (2018) | Sudden unexpected death in genetic epileptic encephalopathies: a role of neurocardiac genes | Abstract similar documents |
E. D. Belousova, M. A. Shkolnikova | ||
"... encephalopathies (EE), partly because those syndromes are associated with mutations in the “neurocardiac” genes ..." | ||
Vol 10, No 4 (2018) | Functional hemispherotomy in the treatment of drug-resistant epilepsy: a clinical case | Abstract similar documents |
A. A. Sufianov, R. T. Deniel, S. Zh. Stefanov, G. Z. Sufianova, A. S. Orlov, S. V. Churkin, S. I. Kostarev, S. V. Mirkhaydarov | ||
"... . In this article; we present an example of successful surgical treatment of Dyke-Davidoff-Masson syndrome. Here ..." | ||
Vol 5, No 3 (2013) | CLINICAL AND ELECTROENCEPHALOGRAPHIC SEMIOLOGY OF MYOCLONIC-ATONIC SEIZURES | Abstract similar documents |
M. B. Mironov, K. Yu. Mukhin, T. M. Krasilschikova, A. F. Dolinina, A. S. Petrukhin | ||
"... .2% of the patients. Lennox-Gastaut syndrome was revealed in 23.6% of cases. Onset of epilepsy with MAS varied widely ..." | ||
Vol 8, No 2 (2016) | CLINICAL AND GENETIC HETEROGENITY OF JUVENILE MYOCLONIC EPILEPSY | Abstract similar documents |
N. A. Shnayder, O. S. Shilkina, K. V. Petrov, I. A. Chernykh, A. V. Diuzhakova | ||
"... myoclonic epilepsy (Janz syndrome) is characterized by myoclonic jerks on awakening, generalized tonic ..." | ||
Vol 1, No 1 (2009) | VISUAL EVOKED POTENTIALS OF SICK INFANTS WITH EPILEPSY | Abstract similar documents |
V. P. Zykov, I. M. Mosin, D. L. Safronov, E. B. Izumova, I. L. Stepanishev, O. A. Voronenko | ||
Vol 15, No 3 (2023) | Algorithm for the provision of comprehensive psychotherapeutic support to women experiencing neuropsychiatric symptoms during rehabilitation following the treatment of malignant neoplasms of the reproductive system | Abstract similar documents |
D. V. Blinov, A. G. Solopova, E. E. Achkasov, E. S. Akarachkova, O. V. Kotova, S. A. Akavova, V. N. Galkin, G. K. Bykovshchenko, L. N. Sandzhieva, D. I. Korabelnikov, T. A. Blbulyan, D. A. Petrenko, A. Yu. Vlasina | ||
"... serious consequences. Chronic pain syndrome, distress, anxiety and depression, decreased self-esteem ..." | ||
Vol 11, No 3 (2019) | Recommendations of the Russian League Against Epilepsy (RLAE) on the use of magnetic resonance imaging in the diagnosis of epilepsy | Abstract similar documents |
G. N. Avakyan, D. V. Blinov, A. A. Alikhanov, E. M. Perepelova, V. A. Perepelov, S. G. Burd, A. V. Lebedeva, G. G. Avakyan | ||
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