Order results by:
| Issue | Title | |
| Vol 16, No 2 (2024) | Atypical course of severe myoclonic epilepsy of infancy (Dravet syndrome) | Abstract PDF (Eng) similar documents |
| B. A. Abusueva, M. D. Shanavazova, М. A. Askevova, V. S. Khalilov, M. Yu. Bobylova | ||
| "... A clinical observation of a patient with Dravet syndrome caused by SCN1A gene mutation ..." | ||
| 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 | ||
| "... with Dravet syndrome, the risk of SUDEP is 40 times higher than that in children with common epilepsy ..." | ||
| Vol 12, No 1S (2020) | Genetic epilepsy with febrile seizures plus (GEFS+) | Abstract similar documents |
| A. A. Sharkov | ||
| "... , disorders in the SCN1B, SCN1A, GABRG2, GABRD, SCN9A, STX1B, HCN1 genes, etc.) and copy number variations ..." | ||
| 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 15, No 2 (2023) | Third generation antiepileptic drugs: mechanism of action, pharmacokinetics, interaction and use in childhood | Abstract similar documents |
| Z. G. Tadtaeva, A. N. Galustyan, O. A. Gromova, I. S. Sardaryan | ||
| "... seizures, as well as in specific epileptic syndromes (Lennox–Gastaut syndrome, Dravet syndrome ..." | ||
| 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 | ||
| "... SCN2A mutations are traditionally described in benign infantile seizures. We are describing rather ..." | ||
| 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 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 | ||
| "... . Цель: оценить динамику проявления эпилептического синдрома и когнитивно-поведенческих особенностей у ..." | ||
| Vol 10, No 4 (2018) | Epileptic manifestations, cognitive impairment and autism spectrum disorders in patients with agenesis of the corpus callosum: the results of neuropsychological testing | Abstract similar documents |
| O. A. Milovanova, O. A. Коmissarovа, T. Yu. Tarakanova, S. V. Bugry, G. G. Avakyan | ||
| "... syndrome (n=3), microdeletion of the 3X long shoulder (n=1), and Miller-Dieker syndrome (n=1). Group II ..." | ||
| 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 16, No 2 (2024) | Transient epileptic amnesia versus transient global amnesia: aspects of differential diagnosis | Abstract PDF (Eng) similar documents |
| L. V. Lipatova, I. V. Sakovsky, M.-B. V. Gadaborshev | ||
| "... approaches. TGA is a clinical syndrome characterized by sudden anterograde amnesia of the event lasting up ..." | ||
| 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) | 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 14, No 4 (2022) | Cognitive impairment in temporal lobe epilepsy | Abstract similar documents |
| A. M. Teplyshova, E. V. Shalimanova | ||
| "... Когнитивные нарушения (КН) являются распространенной коморбидной патологией у пациентов с ..." | ||
| 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 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 | ||
| "... препаратами, влиянию ПЭП на когнитивные функции и качество жизни пациентов с эпилепсией, ассоциированной с ОГМ ..." | ||
| Vol 5, No 2 (2013) | EXPERIENCE WITH THE DRUG MEMANTINE IN PATIENTS WITH FOCAL EPILEPSY AND COGNITIVE IMPAIRMENT | Abstract similar documents |
| Yu. V. Solomatin, V. V. Kurbatova, I. E. Serdyuk, Yu. I. Logvinov, M. M. Shamokhova, S. G. Burd, A. V. Lebedeva | ||
| "... Когнитивные нарушения различной степени выраженности выявляются у пациентов с фокальной эпилепсией ..." | ||
| 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 | ||
| "... астения, ухудшение когнитивных функций, умеренные нарушения сна по сравнению с контрольной группой ..." | ||
| Vol 16, No 4 (2024) | DEPDC5 mutations in familial epilepsy syndrome: genetic insights and therapeutic approaches | Abstract PDF (Eng) similar documents |
| 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 | ||
| "... epilepsy syndrome is a group of epilepsy disorders caused by mutations in DEPDC5 gene, which is a part ..." | ||
| 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 16, No 1 (2024) | Cognitive impairment in patients with juvenile myoclonic epilepsy | Abstract PDF (Eng) similar documents |
| K. D. Lysova, I. K. Kuznetsov, A. I. Paramonova, A. A. Usoltseva, E. A. Kantimirova, N. A. Shnayder, D. V. Dmitrenko | ||
| "... Актуальность. Когнитивные нарушения являются одними из основных коморбидных состояний при ..." | ||
| Vol 8, No 3 (2016) | IMPACT OF ANTIEPILEPTIC DRUGS ON COGNITIVE FUNCTIONS: FOCUS ON PERAMPANEL | Abstract similar documents |
| E. D. Belousova | ||
| "... Когнитивные нарушения при эпилепсии широко распространены и являются мультифакторными, они ..." | ||
| Vol 16, No 1 (2024) | Cognitive impairment in childhood-onset epilepsy | Abstract PDF (Eng) similar documents |
| A. I. Paramonova, K. D. Lysova, E. E. Timechko, G. V. Senchenko, M. R. Sapronova, D. V. Dmitrenko | ||
| "... интеллекта ребенка. Широко исследуются когнитивные дисфункции, возникающие при идиопатических ..." | ||
| 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 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 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 | ||
| "... West syndrome is an epileptic syndrome, characterized by a triad of symptoms: infantile spasms ..." | ||
| 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 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 | ||
| "... когнитивных функций или появлении/ухудшении психоневрологической симптоматики РПЭЛ рекомендует использовать ..." | ||
| Vol 16, No 2 (2024) | A rare genetic Schuurs-Hoeijmakers syndrome (PACS1 syndrome) | Abstract similar documents |
| T. V. Kozhanova, S. S. Zhilina, T. I. Meshcheryakova, A. D. Mikhailova, A. I. Krapivkin, N. N. Zavadenko | ||
| "... PACS1 neurodevelopmental disorder (Schuurs-Hoeijmakers syndrome; MIM #615009) is a rare autosomal ..." | ||
| Vol 3, No 4 (2011) | SOME FEATURES OF PSYCHOLOGICAL FUNCTIONING IN CHILDREN WHILE BENIGN EPILEPTIFORM DISCHARGES OF CHILDHOOD ARE BEING FORMED | Abstract similar documents |
| D. E. Zaitsev, N. A. Titov, E. S. Mironova | ||
| "... фокальной эпилепсии и имели ту или иную степень когнитивного дефицита. Всем пациентам проводилось ..." | ||
| Vol 9, No 1 (2017) | CHILDHOOD ABSENCE EPILEPSY: SPECIFIC FEATURES OF THE DISEASE COURSE AND OUTCOMES | Abstract similar documents |
| I. O. Schederkina, A. A. Shadrova, N. N. Zavadenko, I. E. Koltunov | ||
| "... -электроэнцефалографические характеристики. Данные о когнитивных нарушениях у детей с ДАЭ до настоящего времени противоречивы ..." | ||
| 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 14, No 1 (2022) | The effect of benign epileptiform discharges of childhood on cognitive function, behavior and speech | Abstract similar documents |
| E. A. Morozova, M. V. Belousova, D. V. Morozov, M. A. Utkuzova | ||
| "... , касающиеся доброкачественных эпилептиформных паттернов детства (ДЭПД) и их влияния на когнитивное и речевое ..." | ||
| Vol 8, No 1 (2016) | EFFECT OF KETOGENIC DIET ON COGNITIVE AND MOTOR FUNCTIONS IN CHILDREN WITH DRUG-RESISTANT EPILEPSY | Abstract similar documents |
| E. G. Lukyanova, S. O. Ayvazyan, K. V. Osipova, T. N. Sorvacheva, E. A. Pyreva | ||
| "... возрасте, вызывая так называемую эпилептическую энцефалопатию, приводящую к регрессу когнитивных и ..." | ||
| Vol 8, No 1 (2016) | EEG AND EVENT-RELATED POTENTIAL (P300) IN ELDERLY PATIENTS WITH APHASIA AND EPILEPSY AFTER STROKE | Abstract similar documents |
| V. V. Gnezditskiy, O. S. Korepina, V. A. Karlov, E. E. Koshyrnikova, A. V. Chatskaya | ||
| "... Цель работы — проанализировать паттерны ЭЭГ и когнитивные вызванные потенциалы (Р300) у больных с ..." | ||
| 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 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 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 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 2 (2020) | Results of the Expert Forum on the application of perampanel in routine clinical practice | Abstract similar documents |
| article Editorial | ||
| Vol 12, No 4 (2020) | Results of the expert forum on the use of perampanel in adolescents with epilepsy in everyday clinical practice | Abstract similar documents |
| article Editorial | ||
| 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 10, No 1 (2018) | EPILEPTIC ENCEPHALOPATHIES WITH ELECTRICAL STATUS EPILEPTICUS OF SLOW-WAVE SLEEP (ESES): DIAGNOSIS AND PHARMACOTHERAPY | Abstract similar documents |
| A. A. Kholin | ||
| "... epileptiform discharges of childhood (BEDC). Epilepsy with ESES (or Penelope Syndrome) is a form of age ..." | ||
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