Order results by:
| Issue | Title | |
| 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 | ||
| 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 16, No 4 (2024) | Phantoms and phantom limbs: history of describing the phenomenon | Abstract similar documents |
| D. I. Korabelnikov, E. V. Tkachenko, M. O. Magomedaliev | ||
| Vol 16, No 4 (2024) | Epilepsy and sleep: current diagnostic and treatment approaches | Abstract similar documents |
| N. I. Shova, A. K. Bolshakova, V. A. Mikhailov | ||
| "... ”, “obstructive sleep apnea syndrome”, “restless legs syndrome”, “depression”, “anxiety”, “non-psychotic mental ..." | ||
| 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 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 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 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 | ||
| "... for patients with Helsmoortel-van der Aa syndrome (OMIM: # 615873). Mutations in the ADNP gene are the genetic ..." | ||
| 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 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 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 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 16, No 1 (2024) | SEMA6B-related progressive myoclonus epilepsy in a patient with Klinefelter syndrome | Abstract similar documents |
| 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 | ||
| 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 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 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 | ||
| "... development, developmental microanomalies, pyramidal atactic syndrome and hand joint hypermobility ..." | ||
| 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 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 | ||
| "... использованием опросника Ахенбаха. Результаты. В 84% случаев эпилептический синдром регрессировал полностью в ..." | ||
| Vol 13, No 2 (2021) | Pharmacological predictors of heart rate and conductivity disorders in juvenile myoclonic epilepsy | Abstract similar documents |
| N. A. Shnayder, M. M. Petrova, K. V. Petrov, R. F. Nasyrova | ||
| "... death syndrome due to several potential mechanisms: genetic, clinical, neuroanatomical, pharmacological ..." | ||
| 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 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 16, No 4 (2024) | Role of neuropeptide Y in development of valproate-induced eating behaviour disorder | Abstract PDF (Eng) similar documents |
| N. A. Shnayder, V. V. Grechkina, M. Ya. Kissin, D. V. Dmitrenko, R. F. Nasyrova | ||
| "... -induced metabolic syndrome (MetS). About 20% of patients receiving VPA have weight gain, which is also ..." | ||
| 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 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 | ||
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