Order results by:
| Issue | Title | |
| 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 | ||
| "... visual evoked potentials component P100 and optic nerve hypoplasia. Delay of latency and decrease ..." | ||
| 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 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 4, No 2 (2012) | EPILEPSY IN CHILDREN WITH MYTOCHONDRIAL DISEASES: DIAGNOSTICS AND TREATMENT FEATURES | Abstract similar documents |
| N. N. Zavadenko, A. A. Kholin | ||
| "... Mitochondrial diseases (MD) represent a large clinically heterogeneous group of disorders ..." | ||
| 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 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 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 10, No 2 (2018) | Hyperandrogenism as a side effect of anticonvulsants | Abstract similar documents |
| E. V. Tsallagova, V. O. Generalov, T. R. Sadykov | ||
| 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 9, No 1 (2017) | ILAE CLASSIFICATION OF THE EPILEPSIES: THE 2017 REVISION AND UPDATE | Abstract similar documents |
| G. N. Avakyan, D. V. Blinov, A. V. Lebedeva, S. G. Burd, G. G. Avakyan | ||
| "... syndrome. An etiologic diagnosis should be considered at each step along the diagnostic pathway ..." | ||
| 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 | ||
| 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 ..." | ||
| 1 - 30 of 30 Items | ||
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