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| Issue | Title | |
| 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 17, No 2 (2025) | Severe KCNT1-related developmental and epileptic encephalopathy | Abstract similar documents |
| A. G. Malov, L. Yu. Brokhin, A. V. Veselkova | ||
| "... Developmental and epileptic encephalopathy (DEE) caused by a mutation in the KCNT1 gene (KCNT1-DEE ..." | ||
| 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 | ||
| "... rare case of epileptic encephalopathy associated with incertion of ctg/ctGg in SCN2A. The female child ..." | ||
| Vol 9, No 2 (2017) | EFFICACY AND SAFETY OF LEVETIRACETAM IN CHILDREN WITH ELECTRICAL STATUS EPILEPTICUS DURING SLOW-WAVE SLEEP (ESES) | Abstract similar documents |
| A. A. Kholin, N. N. Zavadenko, I. D. Fedonyuk, E. S. Il`ina | ||
| "... ”) is a form of age-dependent epileptic encephalopathies with the phenomenon of continuous spike-waves during ..." | ||
| Vol 8, No 1 (2016) | NEURODEVELOPMENTAL DISORDERS IN CHILDREN WITH EPILEPSY | Abstract similar documents |
| N. N. Zavadenko | ||
| "... and regression of acquired skills are typical for epileptic encephalopathies. On the other hand ..." | ||
| Vol 4, No 2 (2012) | MULTIFOCAL EPILEPSY – VIEW OF MODERN NEUROPHYSIOLOGIST | Abstract similar documents |
| V. O. Generalov, G. N. Avakyan, T. R. Sadykov, Yu. V. Kazakova | ||
| "... are epileptic encephalopathies, genetic canalopathies and consequences of perinatal brain lesions. Formation ..." | ||
| 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 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 | ||
| 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 | ||
| "... anamnesis, children with epileptic encephalopathy need genetic examination using the Next Generation ..." | ||
| Vol 10, No 3 (2018) | Etiologies of neonatal seizures in infants of different gestational age | Abstract similar documents |
| A. N. Zavadenko, M. I. Medvedev, M. G. Degtyareva, S. O. Rogatkin, N. N. Zavadenko | ||
| 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 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 | ||
| "... and epileptic encephalopathy 5 (ОMIM: 613477). The clinical history, electroencephalographic and magnetic ..." | ||
| Vol 9, No 4 (2017) | NEURODEVELOPMENTAL DISORDERS IN CHILDREN WITH EPILEPSY: INTELLECTUAL DISABILITY AND AUTISM SPECTRUM DISORDERS | Abstract similar documents |
| N. N. Zavadenko | ||
| Vol 8, No 1 (2016) | EPILEPTIC ENCEPHALOPTHIES WITH ELECTRICAL STATUS EPILEPTICUS SLOW SLEEP (ESES) | Abstract similar documents |
| A. A. Kholin | ||
| "... epileptiform activity on the EEG is a serious problem. Quite often the EEG patterns in epileptic ..." | ||
| 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 | ||
| "... factors of mortality in epileptic patients. There is an increased risk of SUDEP in genetic epileptic ..." | ||
| Vol 13, No 2 (2021) | Early infantile epileptic encephalopathy type 54: clinical and neurophysiological aspects | Abstract similar documents |
| D. V. I, V. A. Aysina | ||
| "... A clinical case of a boy aged 20 months old with early infantile epileptic encephalopathy (EIEE ..." | ||
| 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 | ||
| "... -dependent epileptic encephalopathies with continuous spike-wave activity during slow wave sleep. This group ..." | ||
| 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 | ||
| "... with epileptic encephalopathy (NGS), we detected a nucleotide heterozygous variant of the ALDH7A1 gene ..." | ||
| 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 | ||
| "... be asymptomatic or become manifested by diverse psychoneurological symptoms accounted for by developed epileptic ..." | ||
| 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 | ||
| "... ) in patients with epileptic encephalopathy, ASD, and characteristic phenotype, it is advisable to take ..." | ||
| 1 - 20 of 20 Items | ||
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