Order results by:
| Issue | Title | |
| 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 15, No 4 (2023) | DEPDC5-related familial focal epilepsy | Abstract similar documents |
| T. V. Kozhanova, S. S. Zhilina, L. M. Sushko, E. G. Lukyanova, K. V. Osipova, A. I. Krapivkin, N. N. Zavadenko | ||
| "... in DEPDC5 gene were found in two probands and paired fathers with epilepsy. Focal cortical dysplasia ..." | ||
| Vol 9, No 4 (2017) | THE OPTIMIZED METHODS FOR DIAGNOSIS OF HEREDITARY FORMS OF EPILEPSY | Abstract similar documents |
| A. G. Malov | ||
| "... of epilepsy are reviewed. The optimal methods for laboratory confirmation of epilepsy are: in the case ..." | ||
| 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 | ||
| "... The idiopathic generalized epilepsies constitute roughly one-third of all epilepsies. Juvenile ..." | ||
| 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 | ||
| "... We present the clinical case of patient with epilepsy, developmental retardation and hearing loss ..." | ||
| Vol 7, No 2 (2015) | NEUROLOGICAL PAROXYSMAL DISORDERS IN CHILDREN WITH HYPOGLYCEMIA IN CONGENITAL HYPERINSULINISM: POLYMORPHISM OF CLINICAL IMPLICATIONS | Abstract similar documents |
| I. O. Shchederkina, M. A. Melikyan, A. N. Zavadenko, E. V. Kozlova, N. N. Zavadenko | ||
| "... lead to the development of epilepsy. Seizures in CHI do not always require a diagnosis of epilepsy ..." | ||
| Vol 15, No 4 (2023) | Clinical features of developmental and epileptic encephalopathy caused by KCNQ2 gene mutation | Abstract PDF (Eng) similar documents |
| А. G. Malov, Т. P. Kalashnikova, N. А. Vdovina | ||
| "... Epilepsy, developmental and epileptic encephalopathy (DEE) caused by mutation in the KCNQ2 gene ..." | ||
| Vol 11, No 4 (2019) | Early infantile epileptic encephalopathy type 16: the new clinical and genetic variant of TBC1D24 gene mutation | Abstract similar documents |
| A. A. Kholin, I. D. Fedonyuk, O. P. Dovelman, N. N. Zavadenko, T. V. Kozhanova, E. A. Kholina, G. Sh. Khondkarian, E. S. Il`ina | ||
| "... epileptic encephalopathy type 16 in a child with homozygous mutation in TBC1D24 gene. Material and methods ..." | ||
| Vol 11, No 1 (2019) | Mutation of the ALDH7A1 gene in a patient with pyridoxal phosphate-dependent neonatal epileptic encephalopathy: a clinical case | Abstract similar documents |
| T. V. Kozhanova, S. S. Zhilina, T. I. Mescheryakova, E. G. Lukyanova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko | ||
| "... The article presents a clinical case of severe infantile generalized idiopathic epilepsy ..." | ||
| Vol 16, No 3 (2024) | Drug-resistant epilepsy cases in chromosomal pathology | Abstract similar documents |
| L. B. Novikova, A. P. Akopyan, R. F. Latypova, N. M. Faizullina | ||
| "... Two cases of epilepsy in patients with a rare hereditary pathology associated with a chromosomal ..." | ||
| Vol 14, No 1 (2022) | Myoclonic epilepsy with ragged red fibers in childhood | Abstract similar documents |
| Z. G. Tadtaeva, A. N. Galustyan, М. Yu. Krivdina, V. V. Rusanovsky, E. A. Efet, A. Е. Krivoshein, N. A. Kuritsyna, О. A. Gromova | ||
| "... Myoclonic epilepsy with ragged red fibers (MERRF) is a maternally inherited disease characterized ..." | ||
| Vol 11, No 4 (2019) | Significance of exome sequencing for diagnosis of epilepsy in children | Abstract similar documents |
| T. V. Kozhanova, S. S. Zhilina, T. I. Meshheryakova, K. V. Osipova, S. O. Ayvazyan, A. G. Prityko | ||
| "... Introduction. Epilepsy is a neurological disorder characterized by periodic seizure attacks ..." | ||
| 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 | ||
| "... patient with MELAS syndrome with identified A3243G mutation and epilepsy. The disease course developed ..." | ||
| Vol 15, No 3 (2023) | Variable clinic-EEG trajectories in male patients with PCDH19 clustering epilepsy | Abstract PDF (Eng) similar documents |
| D. V. Dmitrenko, A. А. Sharkov, E. А. Domoratskaya, A. А. Usoltseva, I. V. Volkov, D. V. Pyankov | ||
| "... early diagnosis and long-term management of patients with epilepsy and PCDH19 mutations. ..." | ||
| Vol 14, No 3 (2022) | Whole-exome sequencing of patients with juvenile myoclonic epilepsy | Abstract similar documents |
| E. E. Timechko, O. S. Shilkina, N. V. Oreshkova, V. O. Kobanenko, E. A. Osipova, N. A. Shnayder, D. V. Dmitrenko | ||
| "... Background. Juvenile myoclonic epilepsy (JME) is the most common type of idiopathic generalized ..." | ||
| 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 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 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 | ||
| "... development, specific facial dysmorphia, impaired behavior, and a detected mutation in the ADNP gene. When ..." | ||
| 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 | ||
| "... It is well known that sudden unexpected death in epilepsy (SUDEP) is one of the most significant ..." | ||
| 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 11, No 4 (2019) | RLAE | Abstract similar documents |
| Russian League Against Epilepsy | ||
| "... Epilepsy. Message from V.A. Karlov ..." | ||
| Vol 11, No 2 (2019) | Early infantile epileptic encephalopathy type 4: clinical, neurophysiological and therapeutic aspects | Abstract similar documents |
| A. A. Kholin, N. N. Zavadenko, L. M. Kolpakchi, I. D. Fedonyuk, A. S. Papikyan, А. N. Zavadenko, E. S. Ilina | ||
| "... encephalopathy type 4 (EIEE4) caused by a STXBP1 gene mutation. Material and methods. During 2016-2019, we ..." | ||
| 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 | ||
| "... Introduction. Epilepsy is a common feature of mitochondrial disorders, including those associated ..." | ||
| Vol 4, No 3 (2012) | KT-PERFUSION DYNAMICS OF A BRAIN AT PATIENTS WITH SYMPTOMATIC EPILEPSY AT TREATMENT WITH PREGABALIN | Abstract similar documents |
| A. S. Shershever, M. A. Zhuravlyov, S. A. Lavrova, E. V. Sorokov, E. A. Grebenev | ||
| "... ) at the age from 17 till 35 years (middle age 27±8,18 years) with various forms of symptomatic epilepsy during ..." | ||
| Vol 14, No 2 (2022) | Epilepsy syndromes: the 2022 ILAE definition and classification | Abstract similar documents |
| D. V. Blinov | ||
| "... League Against Epilepsy (ILAE) was available. In 2022, owing to many year-persistent efforts made ..." | ||
| Vol 4, No 1 (2012) | CLINICAL-EPIDEMIOLOGICAL EPILEPSY CHARACTERISTICS IN TRANSBAIKALIA | Abstract similar documents |
| Yu. A. Kritskaya, N. A. Shnayder, Yu. A. Shirshov | ||
| "... The epidemiological study of epilepsy in the Transbaikal region, using the homestead bypass ..." | ||
| Vol 14, No 1 (2022) | Autoimmune epilepsy | Abstract similar documents |
| О. S. Shilkina, E. A. Kantimirova, A. A. Usoltseva, Т. I. Prusova, D. V. Dmitrenko | ||
| "... Investigation of autoimmune epilepsy (AIE) has been attracting increasingly more attention due ..." | ||
| Vol 1, No 1 (2009) | MIGRAINE AND EPILEPSY | Abstract similar documents |
| Yu. E. Azimova, G. R. Tabeeva | ||
| "... Migraine and epilepsy are comorbid neurological diseases that have common clinical ..." | ||
| Vol 15, No 2 (2023) | Epilepsy in literature | Abstract similar documents |
| А. Yu. Ulitin, А. V. Vasilenko, A. V. Ivanenko, S. S. Kolosov, I. А. Sokolov, S. А. Turanov, G. А. Ulitin, А. А. Vinogradova | ||
| "... understanding and began to consider epilepsy not only as a severe, chronic, and widespread brain disease ..." | ||
| Vol 16, No 2 (2024) | Stigmatization of epilepsy | Abstract similar documents |
| А. Yu. Ulitin, А. V. Vasilenko, S. G. Ismailov, S. N. Chudievich, S. Kh. Soltanov, А. Z. Gagiev, М. А. Kholodova, А. S. Golikova, М. А. Likhachev, М. А. Bulaeva, G. А. Ulitin | ||
| "... Epilepsy belongs to one of the most ancient diseases. From the days of yore, patients suffering ..." | ||
| Vol 6, No 2 (2014) | STUDY OF THE INCIDENCE AND PREVALENCE OF EPILEPSY IN MINSK | Abstract similar documents |
| T. V. Dokukina, T. S. Golubeva, I. V. Matveichuk, M. V. Mahrov, V. M. Loseva, E. V. Krupenkina, S. A. Marchuk | ||
| "... and prevalence of epilepsy in the gender-age population groups in Minsk. Materials and Methods: A retrospective ..." | ||
| Vol 15, No 3 (2023) | SPTAN1-associated developmental and epileptic encephalopathy | Abstract similar documents |
| 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 | ||
| "... The article presents the clinical cases of 6 patients with epilepsy, psychomotor and speech ..." | ||
| Vol 3, No 1 (2011) | Topiramate as an anti-epileptic medication | Abstract similar documents |
| S. G. Burd | ||
| "... of focal and generalized epilepsy, as well as a host of epileptic syndromes. Topamax can be a first-choice ..." | ||
| Vol 13, No 2 (2021) | Early infantile epileptic encephalopathy type 54: clinical and neurophysiological aspects | Abstract similar documents |
| D. V. I, V. A. Aysina | ||
| "... ) type 54 due to mutated HNRNPU gene presumably suffering from genetic generalized epilepsy and impaired ..." | ||
| Vol 13, No 3 (2021) | Mozart effect in patients with epilepsy | Abstract similar documents |
| Ya. B. Skiba, M. M. Odinak, A. Yu. Polushin, M. Yu. Prokudin, M. V. Selikhova, S. N. Bardakov, M. Yu. Ratanov, V. I. Pustovoyt | ||
| "... with epilepsy. Material and methods. A search for scientific publications has been performed in PubMed, Scopus ..." | ||
| Vol 14, No 1 (2022) | Epilepsy in Norrie disease | Abstract similar documents |
| V. A. Aysina, О. V. Kozhevnikova, О. V. Osipova, A. V. Lashkova | ||
| "... of refractory epilepsy relevant to the disease are considered. Epilepsy rarely accompanies Norrie disease ..." | ||
| Vol 15, No 1 (2023) | Epilepsy – a disease of geniuses? | Abstract similar documents |
| A. Yu. Ulitin, A. V. Vasilenko, I. A. Sokolov, M. A. Bulaeva, S. S. Kolosov, S. A. Turanov, G. A. Ulitin, A. A. Vinogradova | ||
| "... For a long time, people suffering from epilepsy have been feared, suspected, and misunderstood ..." | ||
| Vol 3, No 4 (2011) | DEREALIZATION DISORDERS IN EPILEPSY | Abstract similar documents |
| P. N. Vlasov, A. V. Chervyakov, G. R. Drozzhina, M. V. Antonyuk, N. V. Orekhova, V. V. Gnezditsky, T. Yu. Noskova, P. A. Fedin | ||
| "... disorders (DD) in epilepsy. Materials and Methods: the total study group was 152 persons (mean age 25,17±9 ..." | ||
| Vol 8, No 2 (2016) | TREATMENT OF EPILEPSY IN TUBEROUS SCLEROSIS | Abstract similar documents |
| E. D. Belousova, M. Y. Dorofeeva, T. G. Ohapkina | ||
| "... Epilepsy is the most frequent neurological sign of tuberous sclerosis complex (TSC) and it ..." | ||
| Vol 11, No 1 (2019) | Pathogenesis of drug resistant epilepsy | Abstract similar documents |
| S. M. Malyshev, T. M. Alekseeva, W. A. Khachatryan, M. M. Galagudza | ||
| "... Pharmacotherapy is the first-line treatment modality for epilepsy. However, in 20-40% of patients ..." | ||
| Vol 11, No 1 (2019) | Resolved epilepsy: an updated insight | Abstract similar documents |
| S. A. Gromov, N. A. Sivakova | ||
| "... Classification of epilepsy is of great importance at the stages of rehabilitation when the disease ..." | ||
| Vol 12, No 1S (2020) | EEG in genetic generalized epilepsies | Abstract similar documents |
| V. Yu. Nogovitsyn, A. A. Sharkov | ||
| "... Genetic, or idiopathic, generalized epilepsies (GGEs or IGEs) includes childhood absence epilepsy ..." | ||
| Vol 12, No 1S (2020) | Juvenile Myoclonic Epilepsy. Update | Abstract similar documents |
| I. V. Volkov, O. K. Volkova | ||
| "... Juvenile myoclonic epilepsy (JME) is a common disease. However, some aspects of etiology ..." | ||
| Vol 12, No 4 (2020) | “Suicidal passport” for epilepsy | Abstract similar documents |
| N. I. Shova, V. А. Mikhailov, G. V. Odintsova | ||
| "... to psychiatric comorbidity and suicidal behaviour in people with epilepsy. It is particularly important to find ..." | ||
| 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 | ||
| "... There are considerable variations in the reported incidence of early and late epilepsy in children ..." | ||
| Vol 10, No 2 (2018) | Is there a universal drug for epilepsy? | Abstract similar documents |
| S. G. Burd, A. V. Lebedeva, Yu. V. Rubleva, M. B. Mironov, T. M. Krasilshikova | ||
| "... The article reviews the use of antiepileptic drugs in various forms of epilepsy. We present ..." | ||
| Vol 8, No 4 (2016) | EPILEPSY IN CHILDREN WITH STROKE | Abstract similar documents |
| A. E. Khalilova, Yo. N. Madjidova | ||
| "... – to identify the characteristics of symptomatic epilepsy, occurred against the backdrop of stroke in children ..." | ||
| Vol 4, No 1 (2012) | ROLE OF TOPIRAMATE IN TREATMENT OF EPILEPSY | Abstract similar documents |
| S. G. Burd | ||
| "... of epilepsy. Pharmacokinetic and pharmacodynamiccharacteristics of the medicine are presented in the article ..." | ||
| Vol 9, No 3 (2017) | DIAGNOSIS OF OCCIPITAL LOBE EPILEPSY | Abstract similar documents |
| M. A. Lutskiy, M. V. Uvarova, V. P. Savinykh, V. A. Bykova | ||
| "... -encephalography (EEG) monitoring in diagnosis of occipital lobe epilepsy. Materials and methods. The study ..." | ||
| Vol 8, No 1 (2016) | EPILEPSY IN INBORN ERRORS OF METABOLISM | Abstract similar documents |
| E. D. Belousova | ||
| "... Epilepsy is a frequent and sometimes leading symptom in inborn errors of metabolism, especially ..." | ||
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