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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Russian Journal of Child Neurology</journal-id><journal-title-group><journal-title xml:lang="en">Russian Journal of Child Neurology</journal-title><trans-title-group xml:lang="ru"><trans-title>Русский журнал детской неврологии</trans-title></trans-title-group></journal-title-group><issn publication-format="print">2073-8803</issn><issn publication-format="electronic">2412-9178</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">497</article-id><article-id pub-id-type="doi">10.17650/2073-8803-2024-19-4-58-93</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>CONFERENCES, SYMPOSIA, MEETINGS</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>КОНФЕРЕНЦИИ, СИМПОЗИУМЫ, СОВЕЩАНИЯ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Scientific and practical conference “Absence epilepsy”</article-title><trans-title-group xml:lang="ru"><trans-title>Научно-практическая конференция «Абсансная эпилепсия»</trans-title></trans-title-group></title-group><pub-date date-type="pub" iso-8601-date="2024-12-15" publication-format="electronic"><day>15</day><month>12</month><year>2024</year></pub-date><volume>19</volume><issue>4</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>58</fpage><lpage>92</lpage><history><date date-type="received" iso-8601-date="2025-01-22"><day>22</day><month>01</month><year>2025</year></date><date date-type="accepted" iso-8601-date="2025-01-22"><day>22</day><month>01</month><year>2025</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2024, ABV-Press</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2024, АБВ-пресс</copyright-statement><copyright-year>2024</copyright-year><copyright-holder xml:lang="en">ABV-Press</copyright-holder><copyright-holder xml:lang="ru">АБВ-пресс</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://rjdn.abvpress.ru/jour/about/editorialPolicies</ali:license_ref></license></permissions><self-uri xlink:href="https://rjdn.abvpress.ru/jour/article/view/497">https://rjdn.abvpress.ru/jour/article/view/497</self-uri><abstract xml:lang="ru"><p>.</p></abstract><trans-abstract xml:lang="en"><p/></trans-abstract><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Avakyan G.N., Belousova E.D., Burd S.G. et al. Recommendations of the Expert Council of the Russian Antiepileptic League on the use of original and generic drugs for the treatment of epilepsy. Epilepsiya i paroksizmalnye sostoyaniya = Epilepsy and Paroxysmal Conditions 2011;3(1):17–9. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Авакян Г.Н., Белоусова Е.Д., Бурд С.Г. и др. Рекомендации экспертного совета Российской противоэпилептической лиги по применению оригинальных и воспроизведенных препаратов (дженериков) для лечения эпилепсии. Эпилепсия и пароксизмальные состояния 2011;3(1):17–9.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Gusyakov F.I., Belousov M.V., Morozova E.A., Gazizova D.G. Heterogenity of childhood absence epilepsies. Obozrenie psikhiatrii i meditsinskoi psikhologii im. V.M. Bekhtereva = V.M. Bekhterev Review of Psychiatry and Medical Psychology 2021;55(3):32–44. (In Russ.). DOI: 10.31363/2313-7053-2021-56-3-32-44</mixed-citation><mixed-citation xml:lang="ru">Гусяков Ф.И., Белоусова М.В., Морозова Е.А., Газизова Д.Г. Гетерогенность абсансных эпилепсий в детском возрасте. Обозрение психиатрии и медицинской психологии им. В.М. Бехтерева 2021;55(3):32–44. DOI: 10.31363/2313-7053-2021-56-3-32-44</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Ermolenko N.A., Rudakova I.G., Kalmykova G.V. et al. Assessment of the effectiveness and tolerability of therapy for patients with epilepsy: materials of the meeting of the Council of Experts of Neurologists-Epileptologists of the Central Federal District. Moscow, December 10, 2022. Klinicheskiy razbor v obshchey meditsine = Clinical Review in General Medicine 2023;4(6):13–9. (In Russ.). DOI: 10.47407/kr2023.4.5.00266</mixed-citation><mixed-citation xml:lang="ru">Ермоленко Н.А., Рудакова И.Г., Калмыкова Г.В. и др. Оценка эффективности и переносимости терапии больных эпилепсией: материалы заседания Совета экспертов неврологов-эпилептологов Центрального федерального округа. Москва, 10 декабря 2022 г. Клинический разбор в общей медицине 2023;4(6):13–9. DOI: 10.47407/kr2023.4.5.00266</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Инструкция по применению лекарственного препарата для медицинского применения Сейзар. Instruction for use of the medicinal product Sazar. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Инструкция по применению лекарственного препарата для медицинского применения Сейзар. Instruction for use of the medicinal product Sazar. (In Russ.).</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">Karlov V.A. Absence seizure. Zhurnal nevrologii i psikhiatrii im. S.S. Korakova = S.S. Korsakov Journal of Neurology and Psychiatry 2005;105(3):55–60. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Карлов В.А. Абсанс. Журнал неврологии и психиатрии им. C.C. Корсакова 2005;105(3):55–60.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Karlov V.A. Epilepsy in children and adult women and men: a guide for doctors. Мoscow: Binom, 2019. 896 p. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Карлов В.А. Эпилепсия у детей и взрослых женщин и мужчин: руководство для врачей. М.: Бином, 2019. 896 c.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Karlov V.A., Ovnatanov B.S. Mediobasal epileptic foci and absence activity on the EEG. Zhurnal nevrologii i psikhiatrii im. S.S. Korakova = S.S. Korsakov Journal of Neurology and Psychiatry 1986;87(6):805–12. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Карлов В.А., Овнатанов Б.С. Медиобазальные эпилептические очаги и абсансная активность на ЭЭГ. Журнал невропатологии и психиатрии им. С.С. Корсакова 1986;87(6):805–12.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Клинические рекомендации. Эпилепсия и эпилептический статус у взрослых и детей. 2022. Доступно по: https://cr.minzdrav.gov.ru/recomend/741_1 Clinical recommendations. Epilepsy and status epilepticus in adults and children. 2022. Available at: https://cr.minzdrav.gov.ru/recomend/741_1. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Клинические рекомендации. Эпилепсия и эпилептический статус у взрослых и детей. 2022. Доступно по: https://cr.minzdrav.gov.ru/recomend/741_1</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Clinical recommendations. Epilepsy and status epilepticus in adults and children. 2023. Available at: https://npcpn.ru/doc/2021/krepilepsiya.pdf. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Клинические рекомендации. Эпилепсия и эпилептический статус у взрослых и детей. 2023. Доступно по: https://npcpn.ru/doc/2021/kr-epilepsiya.pdf</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Kulish E.A., Kotov A.S., Mukhina E.V. et al. Glucose transporter deficiency syndrome type 1: a case report. Russkiy zhurnal detskoy nevrologii = Russian Journal of Child Neurology 2019;14(2):23–8. (In Russ.). DOI: 10.17650/2073-8803-2019-14-2-23-28</mixed-citation><mixed-citation xml:lang="ru">Кулиш Е.А., Котов А.С., Мухина Е.В. и др. Синдром дефицита транспортера глюкозы I типа: клинический случай. Русский журнал детской неврологии 2019;14(2):23–8. DOI: 10.17650/2073-8803-2019-14-2-23-28</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Treatment of GLUT1 deficiency syndrome. Clinical recommendations of the Ministry of Health of Russia. Available at: https://diseases.medelement.com/disease/синдром-дефицитаglut1-кп-рф-2024/18123. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Лечение синдрома дефицита GLUT1. Клинические рекомендации Минздрава России. Доступно по: https://diseases.medelement.com/disease/синдром-дефицитаglut1-кп-рф-2024/18123.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Lukyanova E.G., Pyreva E.A., Sorvacheva T.N. et al. Ketogenic diet in the treatment of pharmacoresistent epilepsy. Domestic experience and perspectives. Rossiyskiy nevrologicheskiy zhurnal = Russian Neurological Journal 2021;26(5):52–60. (In Russ.). DOI: 10.30629/2658-7947-2021-26-5-52-60</mixed-citation><mixed-citation xml:lang="ru">Лукьянова Е.Г., Пырьева Е.А., Сорвачева Т.Н. и др. Кетогенная диета в лечении детей с фармакорезистентной эпилепсией. Отечественный опыт и перспективы. Российский неврологический журнал 2021;26(5):52–60. DOI: 10.30629/2658-7947-2021-26-5-52-60</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Mukhin K.Yu., Mironov M.B., Pylaeva O.A. Myoclonic astatic epilepsy (Doose syndrome). Russkiy zhurnal detskoy nevrologii = Russian Journal of Child Neurology 2013;8(1):25–38. (In Russ.). DOI: 10.17650/2073-8803-2013-8-1-25-38</mixed-citation><mixed-citation xml:lang="ru">Мухин К.Ю., Миронов М.Б., Пылаева О.А. Эпилепсия с миоклонически-астатическими приступами (синдром Дозе). Русский журнал детской неврологии 2013;8(1):25–38. DOI: 10.17650/2073-8803-2013-8-1-25-38</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">Mukhin, L.Yu. Glukhova, M.Yu. Bobylova et al. 6th edn. Moscow: Russkiy Pechatniy Dvor, 2023. Pp. 146–323. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Мухин К.Ю., Петрухин А.С. Эпилептические синдромы. Клинико-электроэнцефалографическая диагностика и терапия. В кн.: Эпилептические синдромы. Диагностика и терапия. Под ред. К.Ю. Мухина, Л.Ю. Глуховой, М.Ю. Бобыловой и др. 6-е изд. М.: Русский печатный двор, 2023. С. 146–323.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">Mukhin K.Yu., Petrukhin A.S., Kalinina L.V. et al. Typical absence seizures: clinical systematization and therapy. Vestnik prakticheskoy nevrologii = Bulletin of Practical Neurology 1995;1(1):30–40. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Мухин К.Ю., Петрухин А.С., Калинина Л.В. и др. Типичные абсансы: клиническая систематизация и терапия. Вестник практической неврологии 1995;1(1):30–40.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">Mukhin K.Yu., Pylaeva O.A., Bobylova M.Yu., Freydkova N.V. Lamotrigine (Sazar) in the treatment of epilepsy: four years of experience in Svt. Luka’s Association of Medical institutions for the diagnosis, treatment, and rehabilitation of nervous system diseases and epilepsy. Russkiy zhurnal detskoy nevrologii = Russian Journal of Child Neurology 2022;17(3):8–36. (In Russ.). DOI: 10.17650/2073-8803-2022-17-3-8-36</mixed-citation><mixed-citation xml:lang="ru">Мухин К.Ю., Пылаева О.А., Бобылова М.Ю., Фрейдкова Н.В. Ламотриджин (Сейзар) в лечении эпилепсии: результаты 4-летнего применения препарата в Объединении медицинских учреждений по диагностике, лечению и реабилитации заболеваний нервной системы и эпилепсии им. Святителя Луки. Русский журнал детской неврологии 2022;17(3):8–36. DOI: 10.17650/2073-8803-2022-17-3-8-36</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">Katrenstyle: online magazine for pharmacists and medical professionals 2024;244. Available at: https://www.katrenstyle.ru/news/novye_dannye_o_bezopasnosti_populyarnykh_protivosudorozhnykh_preparatov. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Новые данные о безопасности популярных противосудорожных препаратов. Катренстиль: онлайн-журнал для фармацевтов и медицинских работников 2024;244. Доступно по: https://www.katrenstyle.ru/news/novye_dannye_o_bezopasnosti_populyarnykh_protivosudorozhnykh_preparatov.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">Pylaeva O.A., Mukhin K.Yu. Efficacy and tolerability of Seizar (lamotrigine) in the treatment of epilepsy (experience of Svt. Luka’s Institute of Child Neurology and Epilepsy). Russkiy zhurnal detskoy nevrologii = Russian Journal of Child Neurology 2020;15(2):17–41. (In Russ.). DOI: 10.17650/2073-8803-2020-15-2-17-41</mixed-citation><mixed-citation xml:lang="ru">Пылаева О.А., Мухин К.Ю. Эффективность и переносимость Сейзара (ламотриджин) в лечении эпилепсии (опыт Института детской неврологии и эпилепсии им. Свт. Луки). Русский журнал детской неврологии 2020;15(2):17–41. DOI: 10.17650/2073-8803-2020-15-2-17-41</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">Rudakova I.G. Treatment of epilepsy in a reciprocal mode and the quality of epilepsy control are current issues in clinical practice. Focus – lamotrigine. Vestnik epileptologii = Bulletin of Epileptology 2023;1:19–29. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Рудакова И.Г. Лечение эпилепсии в режиме взаимозамен и качество контроля эпилепсии – актуальные вопросы клинической практики. Фокус – ламотриджин. Вестник эпилептологии 2023;1:19–29.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">Sazar. Register of Medicines of Russia. Available at: https://www.rlsnet.ru/drugs/seizar-36856. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Сейзар. Регистр лекарственных средств России. Доступно по: https://www.rlsnet.ru/drugs/seizar-36856.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">Sinkin M.V., Kvaskova N.E., Brutyan A.G. et al. Russian glossary of terms used in clinical electroencephalography. Nervnye bolezni = Nervous Diseases 2021;1:83–8. (In Russ.). DOI: 10.24412/2226- 0757-2021-12312</mixed-citation><mixed-citation xml:lang="ru">Синкин М.В., Кваскова Н.Е., Брутян А.Г. и др. Русскоязычный словарь терминов, используемых в клинической электроэнцефалографии. Нервные болезни 2021;1:83–8. DOI: 10.24412/2226- 0757-2021-12312</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">Usacheva E.L., Ayvazyan S.O., Sorvacheva T.N. et al. The use of a ketogenic diet in the treatment of drug-resistant epilepsies. Zhurnal nevrologii i psikhiatrii im. S.S. Korakova = S.S. Korsakov Journal of Neurology and Psychiatry 2004;7:29–34. (In Russ).</mixed-citation><mixed-citation xml:lang="ru">Усачева Е.Л., Айвазян С.О., Сорвачева Т.Н. и др. Применение кетогенной диеты в лечении фармакорезистентных эпилепсий. Журнал неврологии и психиатрии им. С.С. Корсакова 2004;7:29–34.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">Epilepsy. Atlas of electroclinical diagnostics and therapy. Vol. 1. Eds.: K.Yu. Mukhin, L.Yu. Glukhova, A.A. Kholin. Мoscow: Russkiy Pechatniy Dvor, 2023. 912 p. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Эпилепсия. Атлас электроклинической диагностики и терапии. T. 1. Под ред. К.Ю. Мухина, Л.Ю. Глуховой, А.А. Холина. М.: Русский Печатный Двор, 2023. 912 с.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">Epilepsy. Atlas of electroclinical diagnostics and therapy. Vol. 2. Eds.: K.Yu. Mukhin, L.Yu. Glukhova, A.A. Kholin. Мoscow: Russkiy Pechatniy Dvor, 2024. 884 p. (In Russ.).</mixed-citation><mixed-citation xml:lang="ru">Эпилепсия. Атлас электроклинической диагностики и терапии. Т. 2. Под ред. К.Ю. Мухина, Л.Ю. Глуховой, А.А. Холина. М.: Русский Печатный Двор, 2024. 884 с.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">Aldenkamp A.P., Baker G. A systematic review of the effects of lamotrigine on cognitive function and quality of life. Epilepsy Behav 2001;2(2):85–91. DOI: 10.1006/ebeh.2001.0168</mixed-citation><mixed-citation xml:lang="ru">Aldenkamp A.P., Baker G. A systematic review of the effects of lamotrigine on cognitive function and quality of life. Epilepsy Behav 2001;2(2):85–91. DOI: 10.1006/ebeh.2001.0168</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><mixed-citation>Bartolomei F., Genton P., Dravet Ch. et al. Comparative clinical and EEG study of Juvenile and childhood absence epilepsies. Epilepsia 1995;36(S3):S75–6.</mixed-citation></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">Ben-Zeev B., Watemberg N., Lerman P. et al. Sulthiame in childhood epilepsy. Pediatr Int 2004;46(5):521–4. DOI: 10.1111/j.1442-200x.2004.01954.x</mixed-citation><mixed-citation xml:lang="ru">Ben-Zeev B., Watemberg N., Lerman P. et al. Sulthiame in childhood epilepsy. Pediatr Int 2004;46(5):521–4. DOI: 10.1111/j.1442-200x.2004.01954.x</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><mixed-citation>Berg M., Welty T.E., Gidal B.E. Bioequivalence between generic and branded lamotrigine in people with epilepsy: the EQUIGEN randomized clinical trial. JAMA Neurol 2017;74(8):919–26. DOI: 10.1001/jamaneurol.2017.0497</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Brigo F., Igwe S.C. Ethosuximide, sodium valproate or lamotrigine for absence seizures in children and adolescents. Cochrane Database Syst Rev 2017;2(2):CD003032. DOI: 10.1002/14651858.CD003032.pub3</mixed-citation></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">Calmeil L.F. De 1’ pilepsie étudi e saus le rapport de son si ge et de son influence sur la production de ali nation mentale; th se pr sent e et soutenue la Facult de M decine de Paris. Paris, 1824. (In French).</mixed-citation><mixed-citation xml:lang="ru">Calmeil L.F. De 1’ pilepsie étudi e saus le rapport de son si ge et de son influence sur la production de ali nation mentale; th se pr sent e et soutenue la Facult de M decine de Paris. Paris, 1824. (In French).</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">Carter E.G., Armour E.A., Pagano L.M., Reddy S.B. Epilepsy with myoclonic absences: a case series highlighting clinical heterogeneity and surgical management. Epileptic Disord 2022;24(3):541–7. DOI: 10.1684/epd.2022.1420</mixed-citation><mixed-citation xml:lang="ru">Carter E.G., Armour E.A., Pagano L.M., Reddy S.B. Epilepsy with myoclonic absences: a case series highlighting clinical heterogeneity and surgical management. Epileptic Disord 2022;24(3):541–7. DOI: 10.1684/epd.2022.1420</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">Cerulli Irelli E., Cocchi E., Morano A. et al. Women with Epilepsy Treatment Options and Research (WETOR) Study Group. Levetiracetam vs lamotrigine as first-line antiseizure medication in female patients with idiopathic generalized epilepsy. JAMA Neurol 2023;80(11):1174–81. DOI: 10.1001/jamaneurol.2023.3400</mixed-citation><mixed-citation xml:lang="ru">Cerulli Irelli E., Cocchi E., Morano A. et al. Women with Epilepsy Treatment Options and Research (WETOR) Study Group. Levetiracetam vs lamotrigine as first-line antiseizure medication in female patients with idiopathic generalized epilepsy. JAMA Neurol 2023;80(11):1174–81. DOI: 10.1001/jamaneurol.2023.3400</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><mixed-citation>Kuo C.C. A common anticonvulsant binding site for phenytoin, carbamazepine, and lamotrigine in neuronal Na+ channels. Mol Pharmacol 1998;54:712–21.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Cnaan A., Shinnar S., Arya R. et al. Childhood Absence Epilepsy Study Group. Second monotherapy in childhood absence epilepsy. Neurology 2017;88(2):182–90. DOI: 10.1212/WNL.0000000000003480</mixed-citation></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">Conrad E.C., Chugh N., Ganguly T.M. et al. Using generalized polyspike train to predict drug-resistant idiopathic generalized epilepsy. J Clin Neurophysiol 2022;39(6):459–65. DOI: 10.1097/WNP.0000000000000803</mixed-citation><mixed-citation xml:lang="ru">Conrad E.C., Chugh N., Ganguly T.M. et al. Using generalized polyspike train to predict drug-resistant idiopathic generalized epilepsy. J Clin Neurophysiol 2022;39(6):459–65. DOI: 10.1097/WNP.0000000000000803</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">Coppola G., Licciardi F., Sciscio N. et al. Lamotrigine as first-line drug in childhood absence epilepsy: a clinical and neurophysiological study. Brain Dev 2004;26(1):26–9. DOI: 10.1016/s0387-7604(03)00090-1</mixed-citation><mixed-citation xml:lang="ru">Coppola G., Licciardi F., Sciscio N. et al. Lamotrigine as first-line drug in childhood absence epilepsy: a clinical and neurophysiological study. Brain Dev 2004;26(1):26–9. DOI: 10.1016/s0387-7604(03)00090-1</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">Coppola G., Veggiotti P., Cusmai R. et al. The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an Italian multicentric experience. Epilepsy Res 2002;48(3):221–7. DOI: 10.1016/s0920-1211(01)00315-1</mixed-citation><mixed-citation xml:lang="ru">Coppola G., Veggiotti P., Cusmai R. et al. The ketogenic diet in children, adolescents and young adults with refractory epilepsy: an Italian multicentric experience. Epilepsy Res 2002;48(3):221–7. DOI: 10.1016/s0920-1211(01)00315-1</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">Crunelli V., Leresch N., Cope D.W. GABA-A receptor function in typical absence seizures. In: Jasper’s basic mechanisms of the epilepsies. Eds.: J.L. Noebels, M. Avoli, M.A. Rogawski. 4th edn. Bethesda: National Center for Biotechnology Information, 2012.</mixed-citation><mixed-citation xml:lang="ru">Crunelli V., Leresch N., Cope D.W. GABA-A receptor function in typical absence seizures. In: Jasper’s basic mechanisms of the epilepsies. Eds.: J.L. Noebels, M. Avoli, M.A. Rogawski. 4th edn. Bethesda: National Center for Biotechnology Information, 2012.</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><mixed-citation>Crunelli V., Leresche N. Childhood absence epilepsy: genes, channels, neurons and networks. Nat Rev Neurosci 2002;3(5):371–82. DOI: 10.1038/nrn811</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>Temkin O. The Falling sickness. John Hopkins University Press, 1994.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Dlugos D., Shinnar S., Cnaan A. et al. Childhood Absence Epilepsy Study Team. Pretreatment EEG in childhood absence epilepsy: associations with attention and treatment outcome. Neurology 2013;81(2):150–6. DOI: 10.1212/WNL.0b013e31829a3373</mixed-citation></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">Doose H. Myoclonic astatic epilepsy of early childhood. In: Epileptic syndromes in infancy, childhood and adolescence. Eds.: J. Roger, M. Bureau, Ch. Dravet et al. London, 1992. Pp. 103–114.</mixed-citation><mixed-citation xml:lang="ru">Doose H. Myoclonic astatic epilepsy of early childhood. In: Epileptic syndromes in infancy, childhood and adolescence. Eds.: J. Roger, M. Bureau, Ch. Dravet et al. London, 1992. Pp. 103–114.</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><mixed-citation>Duchowny M., Pellock J.M., Graf W.D. et al. A placebo-controlled trial of lamotrigine add-on therapy for partial seizures in children. Neurology 1999;53(8):1724–31. DOI: 10.1212/wnl.53.8.1724</mixed-citation></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">Dusanter C., Houot M., Mere M. et al. Cognitive effect of antiseizure medications in medial temporal lobe epilepsy. Eur J Neurol 2023;30(12):3692–702. DOI: 10.1111/ene.16050</mixed-citation><mixed-citation xml:lang="ru">Dusanter C., Houot M., Mere M. et al. Cognitive effect of antiseizure medications in medial temporal lobe epilepsy. Eur J Neurol 2023;30(12):3692–702. DOI: 10.1111/ene.16050</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><mixed-citation>Ferner R.E., Panayiotopoulos C.P. “Phantom” typical absences, absence status and experiential phenomena. Seizure 1993;2:253–6. DOI: 10.1016/s1059-1311(05)80135-9</mixed-citation></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">Fisher R.S., Cross J.H., D’Souza C. et al. Instruction manual for the ILAE 2017 operational classification of seizure types. Epilepsia 2017;58(4):531–42. DOI: 10.1111/epi.13671</mixed-citation><mixed-citation xml:lang="ru">Fisher R.S., Cross J.H., D’Souza C. et al. Instruction manual for the ILAE 2017 operational classification of seizure types. Epilepsia 2017;58(4):531–42. DOI: 10.1111/epi.13671</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">Fonseca Wald E.L.A., Klinkenberg S., Voncken T.P.C. et al. Cognitive development in absence epilepsy during long-term followup. Child Neuropsychol 2019;25(8):1003–21. DOI: 10.1080/09297049.2019.1614156</mixed-citation><mixed-citation xml:lang="ru">Fonseca Wald E.L.A., Klinkenberg S., Voncken T.P.C. et al. Cognitive development in absence epilepsy during long-term followup. Child Neuropsychol 2019;25(8):1003–21. DOI: 10.1080/09297049.2019.1614156</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><mixed-citation>Frank L.M., Enlow T., Holmes G.L. et al. Lamictal (lamotrigine) monotherapy for typical absence seizures in children. Epilepsia 1999;40(7):973–9. DOI: 10.1111/j.1528-1157.1999.tb00805.x</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Garnett W.R., St Louis E.K., Henry T.R., Bramley T. Transitional polytherapy: tricks of the trade for monotherapy to monotherapy AED conversions. Curr Neuropharmacol 2009;7(2):83–95. DOI: 10.2174/157015909788848884</mixed-citation></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">Gibbs F.A., Davis H., Lennox W.G. The electroencephalogram in epilepsy and in conditions of impaired consciousness. Arch Neurol Psych 1935;34(6):1135–48. DOI: 10.1001/archneurpsyc.1935.02250240002001</mixed-citation><mixed-citation xml:lang="ru">Gibbs F.A., Davis H., Lennox W.G. The electroencephalogram in epilepsy and in conditions of impaired consciousness. Arch Neurol Psych 1935;34(6):1135–48. DOI: 10.1001/archneurpsyc.1935.02250240002001</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><mixed-citation>Glauser T.A., Holland K., O’Brien V.P. et al. Childhood Absence Epilepsy Study Group. Pharmacogenetics of antiepileptic drug efficacy in childhood absence epilepsy. Ann Neurol 2017;81(3):444–53. DOI: 10.1002/ana.24886</mixed-citation></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">Glauser T.A., Cnaan A., Shinnar S. et al. Childhood Absence Epilepsy Study Team. Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy: initial monotherapy outcomes at 12 months. Epilepsia 2013;54(1):141–55. DOI: 10.1111/epi.12028</mixed-citation><mixed-citation xml:lang="ru">Glauser T.A., Cnaan A., Shinnar S. et al. Childhood Absence Epilepsy Study Team. Ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy: initial monotherapy outcomes at 12 months. Epilepsia 2013;54(1):141–55. DOI: 10.1111/epi.12028</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><mixed-citation>Gossman W., Albuja A.C., Murphy P.B. Absence Seizure. StatPearls Publishing, 2019.</mixed-citation></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">Grunze H., Greene R.W., Moller H.J. et al. Lamotrigine may limit pathological excitation in the hippocampus by modulating a transient potassium outward current. Brain Res 1998;791:330–4. DOI: 10.1016/s0006-8993(98)00180-2</mixed-citation><mixed-citation xml:lang="ru">Grunze H., Greene R.W., Moller H.J. et al. Lamotrigine may limit pathological excitation in the hippocampus by modulating a transient potassium outward current. Brain Res 1998;791:330–4. DOI: 10.1016/s0006-8993(98)00180-2</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">Grunze H., Von Wegerer J., Greene R.W., Walden J. Modulation of calcium and potassium currents by lamotrigine. Neuropsychobiology 1998;38:131–8. DOI: 10.1159/000026528</mixed-citation><mixed-citation xml:lang="ru">Grunze H., Von Wegerer J., Greene R.W., Walden J. Modulation of calcium and potassium currents by lamotrigine. Neuropsychobiology 1998;38:131–8. DOI: 10.1159/000026528</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">Guerrini R., Mari F., Auvin S., Dravet C. Myoclonic epilepsies in infancy and early childhood. In: Epileptic Syndromes in infancy, childhood and adolescence. Eds.: M. Bureau, P. Genton, A.V. Delgado-Escueta et al. 6th edn. Paris: John Libbey Eurotext Ltd., 2019. Pp.173–188.</mixed-citation><mixed-citation xml:lang="ru">Guerrini R., Mari F., Auvin S., Dravet C. Myoclonic epilepsies in infancy and early childhood. In: Epileptic Syndromes in infancy, childhood and adolescence. Eds.: M. Bureau, P. Genton, A.V. Delgado-Escueta et al. 6th edn. Paris: John Libbey Eurotext Ltd., 2019. Pp.173–188.</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">Guilhoto L.M. Absence epilepsy: continuum of clinical presentation and epigenetics? Seizure 2017;44:53–7. DOI: 10.1016/j.seizure.2016.11.031</mixed-citation><mixed-citation xml:lang="ru">Guilhoto L.M. Absence epilepsy: continuum of clinical presentation and epigenetics? Seizure 2017;44:53–7. DOI: 10.1016/j.seizure.2016.11.031</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><mixed-citation>Han M.J., Kim S.J. Effects of antiepileptic drugs on language abilities in benign epilepsy of childhood with centrotemporal spikes. J Clin Neurol 2018;14(4):523–9. DOI: 10.3988/jcn.2018.14.4.523</mixed-citation></ref><ref id="B59"><label>59.</label><citation-alternatives><mixed-citation xml:lang="en">Hansen C.C., Ljung H., Brodtkorb E., Reimers A. Mechanisms underlying aggressive behavior induced by antiepileptic drugs: focus on topiramate, levetiracetam, and perampanel. Behav Neurol 2018;2018:2064027. DOI: 10.1155/2018/2064027</mixed-citation><mixed-citation xml:lang="ru">Hansen C.C., Ljung H., Brodtkorb E., Reimers A. Mechanisms underlying aggressive behavior induced by antiepileptic drugs: focus on topiramate, levetiracetam, and perampanel. Behav Neurol 2018;2018:2064027. DOI: 10.1155/2018/2064027</mixed-citation></citation-alternatives></ref><ref id="B60"><label>60.</label><citation-alternatives><mixed-citation xml:lang="en">Holmes G.L., Fisher R. Childhood absence epilepsy. 2013. Available at: https://www.epilepsy.com/what-is-epilepsy/syndromes/childhood-absence-epilepsy.</mixed-citation><mixed-citation xml:lang="ru">Holmes G.L., Fisher R. Childhood absence epilepsy. 2013. Available at: https://www.epilepsy.com/what-is-epilepsy/syndromes/childhood-absence-epilepsy.</mixed-citation></citation-alternatives></ref><ref id="B61"><label>61.</label><citation-alternatives><mixed-citation xml:lang="en">Holmes G.L., Frank L.M., Sheth R.D. et al. Lamotrigine monotherapy for newly diagnosed typical absence seizures in children. Epilepsy Res 2008;82(2–3):124–32. DOI: 10.1016/j.eplepsyres.2008.07.016</mixed-citation><mixed-citation xml:lang="ru">Holmes G.L., Frank L.M., Sheth R.D. et al. Lamotrigine monotherapy for newly diagnosed typical absence seizures in children. Epilepsy Res 2008;82(2–3):124–32. DOI: 10.1016/j.eplepsyres.2008.07.016</mixed-citation></citation-alternatives></ref><ref id="B62"><label>62.</label><citation-alternatives><mixed-citation xml:lang="en">Holtkamp M., Theodore W.H. Generic antiepileptic drugs-safe or harmful in patients with epilepsy? Epilepsia 2018;59(7):1273–81. DOI: 10.1111/epi.14439</mixed-citation><mixed-citation xml:lang="ru">Holtkamp M., Theodore W.H. Generic antiepileptic drugs-safe or harmful in patients with epilepsy? Epilepsia 2018;59(7):1273–81. DOI: 10.1111/epi.14439</mixed-citation></citation-alternatives></ref><ref id="B63"><label>63.</label><citation-alternatives><mixed-citation xml:lang="en">Hwang H., Kim H., Kim S.H. et al. Long-term effectiveness of ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy. Brain Dev 2012;34(5):344–8. DOI: 10.1016/j.braindev.2011.08.007</mixed-citation><mixed-citation xml:lang="ru">Hwang H., Kim H., Kim S.H. et al. Long-term effectiveness of ethosuximide, valproic acid, and lamotrigine in childhood absence epilepsy. Brain Dev 2012;34(5):344–8. DOI: 10.1016/j.braindev.2011.08.007</mixed-citation></citation-alternatives></ref><ref id="B64"><label>64.</label><citation-alternatives><mixed-citation xml:lang="en">IJff D.M., van Veenendaal T.M., Debeij-van Hall M.H. et al. The cognitive profile of ethosuximide in children. Paediatr Drugs 2016;18(5):379–85. DOI: 10.1007/s40272-016-0187-z</mixed-citation><mixed-citation xml:lang="ru">IJff D.M., van Veenendaal T.M., Debeij-van Hall M.H. et al. The cognitive profile of ethosuximide in children. Paediatr Drugs 2016;18(5):379–85. DOI: 10.1007/s40272-016-0187-z</mixed-citation></citation-alternatives></ref><ref id="B65"><label>65.</label><citation-alternatives><mixed-citation xml:lang="en">Information on the risks of Valproate use in girls (of any age) and women of childbearing potential (Epilim, Depakote, Convulex, Episenta, Epival, Kentlim, Orlept, Sodium Valproate, Syonell, Valpal, Belvo &amp; Dyzantil). Medicines and Healthcare Products Regulatory Agency. 2020. Available at: https://assets.publishing.service.gov.uk/ government/uploads/system/uploads/attachment_data/file/950802/107995_Valproate_HCP_Booklet_DR15_v07_DS_07-01-2021.pdf.</mixed-citation><mixed-citation xml:lang="ru">Information on the risks of Valproate use in girls (of any age) and women of childbearing potential (Epilim, Depakote, Convulex, Episenta, Epival, Kentlim, Orlept, Sodium Valproate, Syonell, Valpal, Belvo &amp; Dyzantil). Medicines and Healthcare Products Regulatory Agency. 2020. Available at: https://assets.publishing.service.gov.uk/government/uploads/system/uploads/attachment_data/file/950802/107995_Valproate_HCP_Booklet_DR15_v07_DS_07-01-2021.pdf.</mixed-citation></citation-alternatives></ref><ref id="B66"><label>66.</label><citation-alternatives><mixed-citation xml:lang="en">Ivanova N., Peycheva V., Kamenarova K. et al. Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome. Seizure 2018;54:41–4. DOI: 10.1016/j.seizure.2017.11.014</mixed-citation><mixed-citation xml:lang="ru">Ivanova N., Peycheva V., Kamenarova K. et al. Three novel SLC2A1 mutations in Bulgarian patients with different forms of genetic generalized epilepsy reflecting the clinical and genetic diversity of GLUT1-deficiency syndrome. Seizure 2018;54:41–4. DOI: 10.1016/j.seizure.2017.11.014</mixed-citation></citation-alternatives></ref><ref id="B67"><label>67.</label><citation-alternatives><mixed-citation xml:lang="en">Jain P. Absence seizures in children: usual and the unusual. Indian J Pediatr 2020;87(12):1047–56. DOI: 10.1007/s12098-020-03423-8</mixed-citation><mixed-citation xml:lang="ru">Jain P. Absence seizures in children: usual and the unusual. Indian J Pediatr 2020;87(12):1047–56. DOI: 10.1007/s12098-020-03423-8</mixed-citation></citation-alternatives></ref><ref id="B68"><label>68.</label><citation-alternatives><mixed-citation xml:lang="en">Jasper H.H., Droogleever-Fortuyn J. Experimental studies on the functional anatomy of petit mal epilepsy. Assoc Res Nerv Ment Dis 1947;26:272–98.</mixed-citation><mixed-citation xml:lang="ru">Jasper H.H., Droogleever-Fortuyn J. Experimental studies on the functional anatomy of petit mal epilepsy. Assoc Res Nerv Ment Dis 1947;26:272–98.</mixed-citation></citation-alternatives></ref><ref id="B69"><label>69.</label><mixed-citation>Kang J.Q., Macdonald R.L. Molecular pathogenic basis for GABRG2 mutations associated with a spectrum of epilepsy syndromes, from generalized absence epilepsy to Dravet syndrome. JAMA Neurol 2016;73(8):1009–16. DOI: 10.1001/jamaneurol.2016.0449</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Kessler S.K., McGinnis E. A practical guide to treatment of childhood absence epilepsy. Paediatr Drugs 2019;21(1):15–24. DOI: 10.1007/s40272-019-00325-x</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Kossoff E.H., Zupec-Kania B.A., Auvin S. et al. Charlie Foundation; Matthew’s Friends; Practice Committee of the Child Neurology Society. Optimal clinical management of children receiving dietary therapies for epilepsy: updated recommendations of the International Ketogenic Diet Study Group. Epilepsia Open 2018;3(2):175–92. DOI: 10.1002/epi4.12225</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Koutroumanidis M. The role of EEG in the diagnosis and classification of epilepsy syndromes. John Libbey Eurotext, 2017. P. 200.</mixed-citation></ref><ref id="B73"><label>73.</label><citation-alternatives><mixed-citation xml:lang="en">Koutroumanidis M., Arzimanoglou A., Caraballo R. et al. The role of EEG in the diagnosis and classification of the epilepsy syndromes: a tool for clinical practice by the ILAE Neurophysiology Task Force (Part 1). Epileptic Disord 2017;19(3):233–98. DOI: 10.1684/epd.2017.0935</mixed-citation><mixed-citation xml:lang="ru">Koutroumanidis M., Arzimanoglou A., Caraballo R. et al. The role of EEG in the diagnosis and classification of the epilepsy syndromes: a tool for clinical practice by the ILAE Neurophysiology Task Force (Part 1). Epileptic Disord 2017;19(3):233–98. DOI: 10.1684/epd.2017.0935</mixed-citation></citation-alternatives></ref><ref id="B74"><label>74.</label><mixed-citation>Koutroumanidis M., Aggelakis K., Panayiotopoulos C.P. Idiopathic epilepsy with generalized tonic-clonic seizures only versus idiopathic epilepsy with phantom absences and generalized tonic-clonic seizures: one or two syndromes? Epilepsia 2008;49:2050–62. DOI: 10.1111/j.1528-1167.2008.01702.x</mixed-citation></ref><ref id="B75"><label>75.</label><citation-alternatives><mixed-citation xml:lang="en">Larsen J., Johannesen K.M., Ek J. et al. The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome. Epilepsia 2015;56(12):e203–8. DOI: 10.1111/epi.13222</mixed-citation><mixed-citation xml:lang="ru">Larsen J., Johannesen K.M., Ek J. et al. The role of SLC2A1 mutations in myoclonic astatic epilepsy and absence epilepsy, and the estimated frequency of GLUT1 deficiency syndrome. Epilepsia 2015;56(12):e203–8. DOI: 10.1111/epi.13222</mixed-citation></citation-alternatives></ref><ref id="B76"><label>76.</label><mixed-citation>Liu Y., Bao X., Wang D. et al. Allelic variations of GLUT1 deficiency syndrome: the Chinese experience. Pediatr Neurol</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>;47(1):30–4. DOI: 10.1016/j.pediatrneurol.2012.04.010</mixed-citation></ref><ref id="B78"><label>78.</label><citation-alternatives><mixed-citation xml:lang="en">Matricardi S., Verrotti A., Chiarelli F. et al. Current advances in childhood absence epilepsy. Pediatr Neurol 2014;50(3):205–12. DOI: 10.1016/j.pediatrneurol.2013.10.009</mixed-citation><mixed-citation xml:lang="ru">Matricardi S., Verrotti A., Chiarelli F. et al. Current advances in childhood absence epilepsy. Pediatr Neurol 2014;50(3):205–12. DOI: 10.1016/j.pediatrneurol.2013.10.009</mixed-citation></citation-alternatives></ref><ref id="B79"><label>79.</label><citation-alternatives><mixed-citation xml:lang="en">Mattozzi S., Cerminara C., Sotgiu M.A. et al. Occurrence of hyperventilation-induced high amplitude rhythmic slowing with altered awareness after successful treatment of typical absence seizures and a network hypothesis. Clin Neurophysiol Pract 2021;6:185–8. DOI: 10.1016/j.cnp.2021.03.009</mixed-citation><mixed-citation xml:lang="ru">Mattozzi S., Cerminara C., Sotgiu M.A. et al. Occurrence of hyperventilation-induced high amplitude rhythmic slowing with altered awareness after successful treatment of typical absence seizures and a network hypothesis. Clin Neurophysiol Pract 2021;6:185–8. DOI: 10.1016/j.cnp.2021.03.009</mixed-citation></citation-alternatives></ref><ref id="B80"><label>80.</label><citation-alternatives><mixed-citation xml:lang="en">Medina M., Genton P., Bureau M. et al. Absence epilepsies. In: Epileptic syndromes in infancy, childhood and adolescence. Eds.: M. Bureau, P. Genton, C. Dravet et al. 6th ed. Paris: John Libbey Eurotext Ltd., 2019. Pp. 285–320.</mixed-citation><mixed-citation xml:lang="ru">Medina M., Genton P., Bureau M. et al. Absence epilepsies. In: Epileptic syndromes in infancy, childhood and adolescence. Eds.: M. Bureau, P. Genton, C. Dravet et al. 6th ed. Paris: John Libbey Eurotext Ltd., 2019. Pp. 285–320.</mixed-citation></citation-alternatives></ref><ref id="B81"><label>81.</label><mixed-citation>Mignot K., von St lpnagel C., Nava C. et al. Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy [published correction appears in J Med Genet 2016;53(10):720]. J Med Genet 2016;53(8):511–22. DOI: 10.1136/jmedgenet-2015-103451</mixed-citation></ref><ref id="B82"><label>82.</label><citation-alternatives><mixed-citation xml:lang="en">Moavero R., Pisani L.R., Pisani F., Curatolo P. Safety and tolerability profile of new antiepileptic drug treatment in children with epilepsy. Expert Opin Drug Saf 2018;17(10):1015–28. DOI: 10.1080/14740338.2018.1518427</mixed-citation><mixed-citation xml:lang="ru">Moavero R., Pisani L.R., Pisani F., Curatolo P. Safety and tolerability profile of new antiepileptic drug treatment in children with epilepsy. Expert Opin Drug Saf 2018;17(10):1015–28. DOI: 10.1080/14740338.2018.1518427</mixed-citation></citation-alternatives></ref><ref id="B83"><label>83.</label><citation-alternatives><mixed-citation xml:lang="en">Mori T., Sakamoto M., Tayama T. et al. A case of epilepsy with myoclonic atonic seizures caused by SLC6A1 gene mutation due to balanced chromosomal translocation. Brain Dev 2023;45(7):395–400. DOI: 10.1016/j.braindev.2023.03.001 83.	Mostacci B., Ranzato F., Giuliano L. et al. Alternatives to valproate in girls and women of childbearing potential with idiopathic generalized epilepsies: state of the art and guidance for the clinician proposed by the Epilepsy and Gender Commission of the Italian League Against Epilepsy (LICE). Seizure 2021;85:26–38. DOI: 10.1016/j.seizure.2020.12.005</mixed-citation><mixed-citation xml:lang="ru">Mori T., Sakamoto M., Tayama T. et al. A case of epilepsy with myoclonic atonic seizures caused by SLC6A1 gene mutation due to balanced chromosomal translocation. Brain Dev 2023;45(7):395–400. DOI: 10.1016/j.braindev.2023.03.001</mixed-citation></citation-alternatives></ref><ref id="B84"><label>84.</label><citation-alternatives><mixed-citation xml:lang="en">Mukhin K.Yu., Medvedev M.I., Petrukhin A.S. Epilepsy with myoclonic-astatic seizures: diagnostic criterion and treatment. Brain Dev 1998;20(6):481.</mixed-citation><mixed-citation xml:lang="ru">Mostacci B., Ranzato F., Giuliano L. et al. Alternatives to valproate in girls and women of childbearing potential with idiopathic generalized epilepsies: state of the art and guidance for the clinician proposed by the Epilepsy and Gender Commission of the Italian League Against Epilepsy (LICE). Seizure 2021;85:26–38. DOI: 10.1016/j.seizure.2020.12.005</mixed-citation></citation-alternatives></ref><ref id="B85"><label>85.</label><citation-alternatives><mixed-citation xml:lang="en">Myers K.A. Genetic epilepsy syndromes. Continuum (Minneap Minn) 2022;28(2):339–62. DOI: 10.1212/CON.0000000000001077</mixed-citation><mixed-citation xml:lang="ru">Mukhin K.Yu., Medvedev M.I., Petrukhin A.S. Epilepsy with myoclonic-astatic seizures: diagnostic criterion and treatment. Brain Dev 1998;20(6):481.</mixed-citation></citation-alternatives></ref><ref id="B86"><label>86.</label><citation-alternatives><mixed-citation xml:lang="en">Epilepsies in children, young people and adults. National Institute for Health and Care Excellence guideline. 2022. Available at: https://www.nice.org.uk/guidance/ng217/.</mixed-citation><mixed-citation xml:lang="ru">Myers K.A. Genetic epilepsy syndromes. Continuum (Minneap Minn) 2022;28(2):339–62. DOI: 10.1212/CON.0000000000001077</mixed-citation></citation-alternatives></ref><ref id="B87"><label>87.</label><citation-alternatives><mixed-citation xml:lang="en">Nickels K., Kossoff E.H., Eschbach K., Joshi C. Epilepsy with myoclonic-atonic seizures (Doose syndrome): clarification of diagnosis and treatment options through a large retrospective multicenter cohort. Epilepsia 2021;62(1):120–7. DOI: 10.1111/epi.16752</mixed-citation><mixed-citation xml:lang="ru">Epilepsies in children, young people and adults. National Institute for Health and Care Excellence guideline. 2022. Available at: https://www.nice.org.uk/guidance/ng217/.</mixed-citation></citation-alternatives></ref><ref id="B88"><label>88.</label><citation-alternatives><mixed-citation xml:lang="en">Panayiotopoulos C.P. Idiopathic generalized epilepsies. Springer, 2012. Pp. 41–44.</mixed-citation><mixed-citation xml:lang="ru">Nickels K., Kossoff E.H., Eschbach K., Joshi C. Epilepsy with myoclonic-atonic seizures (Doose syndrome): clarification of diagnosis and treatment options through a large retrospective multicenter cohort. Epilepsia 2021;62(1):120–7. DOI: 10.1111/epi.16752</mixed-citation></citation-alternatives></ref><ref id="B89"><label>89.</label><citation-alternatives><mixed-citation xml:lang="en">Panayiotopoulos C.P. A clinical guide to epileptic syndromes and their treatment. 2nd edn. Springer, 2010. Pp. 45–49; 325–335.</mixed-citation><mixed-citation xml:lang="ru">Panayiotopoulos C.P. Idiopathic generalized epilepsies. Springer, 2012. Pp. 41–44.</mixed-citation></citation-alternatives></ref><ref id="B90"><label>90.</label><citation-alternatives><mixed-citation xml:lang="en">Panayiotopoulos C.P. Syndromes of idiopathic generalized epilepsies not recognized by the International League against epilepsy. Epilepsia 2005;46(Suppl 9):57–66. DOI: 10.1111/j.1528-1167.2005.00314.x</mixed-citation><mixed-citation xml:lang="ru">Panayiotopoulos C.P. A clinical guide to epileptic syndromes and their treatment. 2nd edn. Springer, 2010. Pp. 45–49; 325–335.</mixed-citation></citation-alternatives></ref><ref id="B91"><label>91.</label><citation-alternatives><mixed-citation xml:lang="en">Panayiotopoulos C.P., Ferrie C.D., Koutroumanidis M. et al. Idiopathic generalised epilepsy with phantom absences and absence status in a child. Epileptic Disord 2001;3(2):63–6.</mixed-citation><mixed-citation xml:lang="ru">Panayiotopoulos C.P. Syndromes of idiopathic generalized epilepsies not recognized by the International League against epilepsy. Epilepsia 2005;46(Suppl 9):57–66. DOI: 10.1111/j.1528-1167.2005.00314.x</mixed-citation></citation-alternatives></ref><ref id="B92"><label>92.</label><citation-alternatives><mixed-citation xml:lang="en">Panayiotopoulos C.P., Koutroumanidis M., Giannakodimos S., Agathonikou A. Idiopathic generalised epilepsy in adults manifested by phantom absences, generalised tonic-clonic seizures, and frequent absence status. J Neurol Neurosurg Psychiatry 1997;63:622–7. DOI: 10.1136/jnnp.63.5.622</mixed-citation><mixed-citation xml:lang="ru">Panayiotopoulos C.P., Ferrie C.D., Koutroumanidis M. et al. Idiopathic generalised epilepsy with phantom absences and absence status in a child. Epileptic Disord 2001;3(2):63–6.</mixed-citation></citation-alternatives></ref><ref id="B93"><label>93.</label><citation-alternatives><mixed-citation xml:lang="en">Panayiotopoulos С.P. Principles of therapy in the epilepsies. In: Clinical guide to epileptic syndromes and their treatment. Springer, 2007. Pp. 155–184.</mixed-citation><mixed-citation xml:lang="ru">Panayiotopoulos C.P., Koutroumanidis M., Giannakodimos S., Agathonikou A. Idiopathic generalised epilepsy in adults manifested by phantom absences, generalised tonic-clonic seizures, and frequent absence status. J Neurol Neurosurg Psychiatry 1997;63:622–7. DOI: 10.1136/jnnp.63.5.622</mixed-citation></citation-alternatives></ref><ref id="B94"><label>94.</label><citation-alternatives><mixed-citation xml:lang="en">Pearl P.L. Epilepsy syndromes in childhood. Continuum (Minneap Minn) 2018;24(1, Child Neurology):186–209. DOI: 10.1212/CON.0000000000000568</mixed-citation><mixed-citation xml:lang="ru">Panayiotopoulos С.P. Principles of therapy in the epilepsies. In: Clinical guide to epileptic syndromes and their treatment. Springer, 2007. Pp. 155–184.</mixed-citation></citation-alternatives></ref><ref id="B95"><label>95.</label><citation-alternatives><mixed-citation xml:lang="en">Pellock J., Montouris G.D., Ramsay R.E. New developments in the treatment of epilepsy. CNS Spectrums 2000;5(S2):1–8. DOI: 10.1017/S1092852900023579</mixed-citation><mixed-citation xml:lang="ru">Pearl P.L. Epilepsy syndromes in childhood. Continuum (Minneap Minn) 2018;24(1, Child Neurology):186–209. DOI: 10.1212/CON.0000000000000568</mixed-citation></citation-alternatives></ref><ref id="B96"><label>96.</label><citation-alternatives><mixed-citation xml:lang="en">Peltola M.E., Leitinger M., Halford J.J. et al. Routine and sleep EEG: minimum recording standards of the International Federation of Clinical Neurophysiology and the International League Against Epilepsy. Epilepsia 2023;64(3):602–18. DOI: 10.1111/epi.17448</mixed-citation><mixed-citation xml:lang="ru">Pellock J., Montouris G.D., Ramsay R.E. New developments in the treatment of epilepsy. CNS Spectrums 2000;5(S2):1–8. DOI: 10.1017/S1092852900023579</mixed-citation></citation-alternatives></ref><ref id="B97"><label>97.</label><citation-alternatives><mixed-citation xml:lang="en">Porwal M.H., Razzak A.N., Kumar V. et al. An analysis of suicidal and self-injurious behavior reports with antiseizure medications in the FDA adverse event database. Epilepsy Res 2024;203:107382. DOI: 10.1016/j.eplepsyres.2024.107382</mixed-citation><mixed-citation xml:lang="ru">Peltola M.E., Leitinger M., Halford J.J. et al. Routine and sleep EEG: minimum recording standards of the International Federation of Clinical Neurophysiology and the International League Against Epilepsy. Epilepsia 2023;64(3):602–18. DOI: 10.1111/epi.17448</mixed-citation></citation-alternatives></ref><ref id="B98"><label>98.</label><citation-alternatives><mixed-citation xml:lang="en">Posner E.B., Mohamed K., Marson A.G. A systematic review of treatment of typical absence seizures in children and adolescents with ethosuximide, sodium valproate or lamotrigine. Seizure 2005;14(2):117–22. DOI: 10.1016/j.seizure.2004.12.003</mixed-citation><mixed-citation xml:lang="ru">Porwal M.H., Razzak A.N., Kumar V. et al. An analysis of suicidal and self-injurious behavior reports with antiseizure medications in the FDA adverse event database. Epilepsy Res 2024;203:107382. DOI: 10.1016/j.eplepsyres.2024.107382</mixed-citation></citation-alternatives></ref><ref id="B99"><label>99.</label><citation-alternatives><mixed-citation xml:lang="en">Ramm-Pettersen A., Nakken K.O., Haavardsholm K.C., Selmer K.K. GLUT1-deficiency syndrome: report of a four-generation Norwegian family with a mild phenotype. Epilepsy Behav 2017;70(Pt A):1–4. DOI: 10.1016/j.yebeh.2017.02.016</mixed-citation><mixed-citation xml:lang="ru">Posner E.B., Mohamed K., Marson A.G. A systematic review of treatment of typical absence seizures in children and adolescents with ethosuximide, sodium valproate or lamotrigine. Seizure 2005;14(2):117–22. DOI: 10.1016/j.seizure.2004.12.003</mixed-citation></citation-alternatives></ref><ref id="B100"><label>100.</label><citation-alternatives><mixed-citation xml:lang="en">Reed L., Ciliberto M., Fong S.L. et al. Efficacy of felbamate in a cohort of patients with epilepsy with myoclonic atonic seizures (EMAtS). Epilepsy Res 2024;201:107314. DOI: 10.1016/j.eplepsyres.2024.107314</mixed-citation><mixed-citation xml:lang="ru">Ramm-Pettersen A., Nakken K.O., Haavardsholm K.C., Selmer K.K. GLUT1-deficiency syndrome: report of a four-generation Norwegian family with a mild phenotype. Epilepsy Behav 2017;70(Pt A):1–4. DOI: 10.1016/j.yebeh.2017.02.016</mixed-citation></citation-alternatives></ref><ref id="B101"><label>101.</label><citation-alternatives><mixed-citation xml:lang="en">Rinaldi V.E., Di Cara G., Mencaroni E., Verrotti A. Therapeutic options for childhood absence epilepsy. Pediatr Rep 2021;13(4):658–67. DOI: 10.3390/pediatric13040078</mixed-citation><mixed-citation xml:lang="ru">Reed L., Ciliberto M., Fong S.L. et al. Efficacy of felbamate in a cohort of patients with epilepsy with myoclonic atonic seizures (EMAtS). Epilepsy Res 2024;201:107314. DOI: 10.1016/j.eplepsyres.2024.107314</mixed-citation></citation-alternatives></ref><ref id="B102"><label>102.</label><citation-alternatives><mixed-citation xml:lang="en">Sadleir L.G., Scheffer I.E., Smith S. et al. EEG features of absence seizures in idiopathic generalized epilepsy: impact of syndrome, age, and state. Epilepsia 2009;50(6):1572–8. DOI: 10.1111/j.1528-1167.2008.02001.x</mixed-citation><mixed-citation xml:lang="ru">Rinaldi V.E., Di Cara G., Mencaroni E., Verrotti A. Therapeutic options for childhood absence epilepsy. Pediatr Rep 2021;13(4):658–67. DOI: 10.3390/pediatric13040078</mixed-citation></citation-alternatives></ref><ref id="B103"><label>103.</label><citation-alternatives><mixed-citation xml:lang="en">Sadleir L.G., Farrell K., Smith S. et al. Electroclinical features of absence seizures in childhood absence epilepsy. Neurology 2006;67(3):413–8. DOI: 10.1212/01.wnl.0000228257.60184.82</mixed-citation><mixed-citation xml:lang="ru">Sadleir L.G., Scheffer I.E., Smith S. et al. EEG features of absence seizures in idiopathic generalized epilepsy: impact of syndrome, age, and state. Epilepsia 2009;50(6):1572–8. DOI: 10.1111/j.1528-1167.2008.02001.x</mixed-citation></citation-alternatives></ref><ref id="B104"><label>104.</label><citation-alternatives><mixed-citation xml:lang="en">Scheffer I.E., Berkovic S., Capovilla G. et al. ILAE classification of the epilepsies: position paper of the ILAE Commission for Classification and Terminology. Epilepsia 2017;58(4):512–21. DOI: 10.1111/epi.13709</mixed-citation><mixed-citation xml:lang="ru">Sadleir L.G., Farrell K., Smith S. et al. Electroclinical features of absence seizures in childhood absence epilepsy. Neurology 2006;67(3):413–8. DOI: 10.1212/01.wnl.0000228257.60184.82</mixed-citation></citation-alternatives></ref><ref id="B105"><label>105.</label><citation-alternatives><mixed-citation xml:lang="en">Seneviratne U., Cook M.J., D’Souza W.J. Electroencephalography in the diagnosis of genetic generalized epilepsy syndromes. Front Neurol 2017;8:499. DOI: 10.3389/fneur.2017.00499</mixed-citation><mixed-citation xml:lang="ru">Scheffer I.E., Berkovic S., Capovilla G. et al. ILAE classification of the epilepsies: position paper of the ILAE Commission for Classification and Terminology. Epilepsia 2017;58(4):512–21. DOI: 10.1111/epi.13709</mixed-citation></citation-alternatives></ref><ref id="B106"><label>106.</label><citation-alternatives><mixed-citation xml:lang="en">Smith D., Baker G., Davies G. et al. Outcomes of add-on treatment with lamotrigine in partial epilepsy. Epilepsia 1993;34(2):312–22. DOI: 10.1111/j.1528-1157.1993.tb02417.x</mixed-citation><mixed-citation xml:lang="ru">Seneviratne U., Cook M.J., D’Souza W.J. Electroencephalography in the diagnosis of genetic generalized epilepsy syndromes. Front Neurol 2017;8:499. DOI: 10.3389/fneur.2017.00499</mixed-citation></citation-alternatives></ref><ref id="B107"><label>107.</label><citation-alternatives><mixed-citation xml:lang="en">Smith K.M., Wirrell E.C., Andrade D.M. et al. Management of epilepsy with eyelid myoclonia: results of an international expert consensus panel. Epilepsia 2023;64(9):2342–50. DOI: 10.1111/epi.17682</mixed-citation><mixed-citation xml:lang="ru">Smith D., Baker G., Davies G. et al. Outcomes of add-on treatment with lamotrigine in partial epilepsy. Epilepsia 1993;34(2):312–22. DOI: 10.1111/j.1528-1157.1993.tb02417.x</mixed-citation></citation-alternatives></ref><ref id="B108"><label>108.</label><citation-alternatives><mixed-citation xml:lang="en">Smith K.M., Wirrell E.C., Andrade D.M. et al. Clinical presentation and evaluation of epilepsy with eyelid myoclonia: results of an international expert consensus panel. Epilepsia 2023;64(9):2330–41. DOI: 10.1111/epi.17683</mixed-citation><mixed-citation xml:lang="ru">Smith K.M., Wirrell E.C., Andrade D.M. et al. Management of epilepsy with eyelid myoclonia: results of an international expert consensus panel. Epilepsia 2023;64(9):2342–50. DOI: 10.1111/epi.17682</mixed-citation></citation-alternatives></ref><ref id="B109"><label>109.</label><citation-alternatives><mixed-citation xml:lang="en">Smith K.M., Wirrell E.C., Andrade D.M. et al. A comprehensive narrative review of epilepsy with eyelid myoclonia. Epilepsy Res 2023;193:107147. DOI: 10.1016/j.eplepsyres.2023.107147</mixed-citation><mixed-citation xml:lang="ru">Smith K.M., Wirrell E.C., Andrade D.M. et al. Clinical presentation and evaluation of epilepsy with eyelid myoclonia: results of an international expert consensus panel. Epilepsia 2023;64(9):2330–41. DOI: 10.1111/epi.17683</mixed-citation></citation-alternatives></ref><ref id="B110"><label>110.</label><citation-alternatives><mixed-citation xml:lang="en">Specchio N., Wirrell E.C., Scheffer I.E. et al. International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: position statement by the ILAE Task Force on Nosology and Definitions. Epilepsia 2022;63(6):1398–442. DOI: 10.1111/epi.17241</mixed-citation><mixed-citation xml:lang="ru">Smith K.M., Wirrell E.C., Andrade D.M. et al. A comprehensive narrative review of epilepsy with eyelid myoclonia. Epilepsy Res 2023;193:107147. DOI: 10.1016/j.eplepsyres.2023.107147</mixed-citation></citation-alternatives></ref><ref id="B111"><label>111.</label><citation-alternatives><mixed-citation xml:lang="en">St Louis E.K., Gidal B.E., Henry T.R. et al. Conversions between monotherapies in epilepsy: expert consensus. Epilepsy Behav 2007;11(2):222–34. DOI: 10.1016/j.yebeh.2007.04.007</mixed-citation><mixed-citation xml:lang="ru">Specchio N., Wirrell E.C., Scheffer I.E. et al. International League Against Epilepsy classification and definition of epilepsy syndromes with onset in childhood: position statement by the ILAE Task Force on Nosology and Definitions. Epilepsia 2022;63(6):1398–442. DOI: 10.1111/epi.17241</mixed-citation></citation-alternatives></ref><ref id="B112"><label>112.</label><citation-alternatives><mixed-citation xml:lang="en">Stafstrom C.E. Dietary approaches to epilepsy treatment: old and new options on the menu. Epilepsy Curr 2004;4(6):215–22. DOI: 10.1111/j.1535-7597.2004. 46001.x</mixed-citation><mixed-citation xml:lang="ru">St Louis E.K., Gidal B.E., Henry T.R. et al. Conversions between monotherapies in epilepsy: expert consensus. Epilepsy Behav 2007;11(2):222–34. DOI: 10.1016/j.yebeh.2007.04.007</mixed-citation></citation-alternatives></ref><ref id="B113"><label>113.</label><citation-alternatives><mixed-citation xml:lang="en">Strzelczyk A., Schubert-Bast S. Psychobehavioural and cognitive adverse events of anti-seizure medications for the treatment of developmental and epileptic encephalopathies. CNS Drugs 2022;36(10):1079–111.</mixed-citation><mixed-citation xml:lang="ru">Stafstrom C.E. Dietary approaches to epilepsy treatment: old and new options on the menu. Epilepsy Curr 2004;4(6):215–22. DOI: 10.1111/j.1535-7597.2004. 46001.x</mixed-citation></citation-alternatives></ref><ref id="B114"><label>114.</label><citation-alternatives><mixed-citation xml:lang="en">Tassinari C.A., Lyagoubi S., Santos V. et al. Study on spike and wave discharges in man. II. Clinical and electroencephalographic aspects of myoclonic absences. Rev Neurol (Paris) 1969;121(3):379–83. (In French).</mixed-citation><mixed-citation xml:lang="ru">Strzelczyk A., Schubert-Bast S. Psychobehavioural and cognitive adverse events of anti-seizure medications for the treatment of developmental and epileptic encephalopathies. CNS Drugs 2022;36(10):1079–111.</mixed-citation></citation-alternatives></ref><ref id="B115"><label>115.</label><citation-alternatives><mixed-citation xml:lang="en">Tissot S.A. Trait de l’ pilepsie. Faisant le tome troisi me du Trait des nerfs &amp; de leurs maladies. Paris: Didot Le Jeune, 1770. (In French).</mixed-citation><mixed-citation xml:lang="ru">Tassinari C.A., Lyagoubi S., Santos V. et al. Study on spike and wave discharges in man. II. Clinical and electroencephalographic aspects of myoclonic absences. Rev Neurol (Paris) 1969;121(3):379–83. (In French).</mixed-citation></citation-alternatives></ref><ref id="B116"><label>116.</label><citation-alternatives><mixed-citation xml:lang="en">Tomson T., Battino D., Bromley R. et al. Management of epilepsy in pregnancy: a report from the International League Against Epilepsy Task Force on Women and Pregnancy. Epileptic Disord 2019;21(6):497–517. DOI: 10.1684/epd.2019.1105</mixed-citation><mixed-citation xml:lang="ru">Tissot S.A. Trait de l’ pilepsie. Faisant le tome troisi me du Trait des nerfs &amp; de leurs maladies. Paris: Didot Le Jeune, 1770. (In French).</mixed-citation></citation-alternatives></ref><ref id="B117"><label>117.</label><citation-alternatives><mixed-citation xml:lang="en">Topiramate side effects (Topamax) guide. Most common to severe side effects of topiramate. Side effects topiramate prescription can cause. Topiramate side effects 25 mg to the highest dosage.Topiramate side effect treatment. Ed. by Y. Francese. 2023. Available at: https://welevelupnj.com/treatment/topiramate-sideeffects/.</mixed-citation><mixed-citation xml:lang="ru">Tomson T., Battino D., Bromley R. et al. Management of epilepsy in pregnancy: a report from the International League Against Epilepsy Task Force on Women and Pregnancy. Epileptic Disord 2019;21(6):497–517. DOI: 10.1684/epd.2019.1105</mixed-citation></citation-alternatives></ref><ref id="B118"><label>118.</label><citation-alternatives><mixed-citation xml:lang="en">Trevathan E., Kerls S.P., Hammer A.E. et al. Lamotrigine adjunctive therapy among children and adolescents with primary generalized tonic-clonic seizures. Pediatrics 2006;118(2):e371–8. DOI: 10.1542/peds.2006-0148</mixed-citation><mixed-citation xml:lang="ru">Topiramate side effects (Topamax) guide. Most common to severe side effects of topiramate. Side effects topiramate prescription can cause. Topiramate side effects 25 mg to the highest dosage.Topiramate side effect treatment. Ed. by Y. Francese. 2023. Available at: https://welevelupnj.com/treatment/topiramate-sideeffects/.</mixed-citation></citation-alternatives></ref><ref id="B119"><label>119.</label><citation-alternatives><mixed-citation xml:lang="en">Typical absence seizure. Clinical overview. Available at: https://www.epilepsydiagnosis.org/seizure/absence-typicaloverview.html.</mixed-citation><mixed-citation xml:lang="ru">Trevathan E., Kerls S.P., Hammer A.E. et al. Lamotrigine adjunctive therapy among children and adolescents with primary generalized tonic-clonic seizures. Pediatrics 2006;118(2):e371–8. DOI: 10.1542/peds.2006-0148</mixed-citation></citation-alternatives></ref><ref id="B120"><label>120.</label><citation-alternatives><mixed-citation xml:lang="en">Typical Absenсe Seizures. International League Against Epilepsy. Available at: https://www.epilepsydiagnosis.org/seizure/absencetypicalrelatedsyndromes.html.</mixed-citation><mixed-citation xml:lang="ru">Typical absence seizure. Clinical overview. Available at: https://www.epilepsydiagnosis.org/seizure/absence-typicaloverview.html.</mixed-citation></citation-alternatives></ref><ref id="B121"><label>121.</label><citation-alternatives><mixed-citation xml:lang="en">Typical absence seizure. Related syndromes. Available at: https://www.epilepsydiagnosis.org/seizure/absencetypicalrelatedsyndromes.html.</mixed-citation><mixed-citation xml:lang="ru">Typical Absenсe Seizures. International League Against Epilepsy. Available at: https://www.epilepsydiagnosis.org/seizure/absencetypicalrelatedsyndromes.html.</mixed-citation></citation-alternatives></ref><ref id="B122"><label>122.</label><citation-alternatives><mixed-citation xml:lang="en">Unterberger I., Trinka E., Kaplan P.W. et al. Generalized nonmotor (absence) seizures – what do absence, generalized, and nonmotor mean? Epilepsia 2018;59(3):523–9. DOI: 10.1111/epi.13996</mixed-citation><mixed-citation xml:lang="ru">Typical absence seizure. Related syndromes. Available at: https://www.epilepsydiagnosis.org/seizure/absencetypicalrelatedsyndromes.html.</mixed-citation></citation-alternatives></ref><ref id="B123"><label>123.</label><citation-alternatives><mixed-citation xml:lang="en">Beniczky S., Trinka E., Abdulla F. Updated classification of epileptic seizures: position paper of the International League Against Epilepsy. Available at: https://www.ilae.org/files/dmfile/updated-sz-classification2.pdf.</mixed-citation><mixed-citation xml:lang="ru">Unterberger I., Trinka E., Kaplan P.W. et al. Generalized nonmotor (absence) seizures – what do absence, generalized, and nonmotor mean? Epilepsia 2018;59(3):523–9. DOI: 10.1111/epi.13996</mixed-citation></citation-alternatives></ref><ref id="B124"><label>124.</label><citation-alternatives><mixed-citation xml:lang="en">Valproate use in men: as a precaution, men and their partners should use effective contraception. 2024. Available at: https://www.gov.uk/drug-safety-update/valproate-use-in-men-as-a-precaution-menand-their-partners-should-use-effectivecontraception.</mixed-citation><mixed-citation xml:lang="ru">Beniczky S., Trinka E., Abdulla F. Updated classification of epileptic seizures: position paper of the International League Against Epilepsy. Available at: https://www.ilae.org/files/dmfile/updated-sz-classification2.pdf.</mixed-citation></citation-alternatives></ref><ref id="B125"><label>125.</label><citation-alternatives><mixed-citation xml:lang="en">Van der Louw E., Trimmel-Schwahofer P., Devlin A. et al. Human milk and breastfeeding during ketogenic diet therapy in infants with epilepsy: clinical practice guideline. Dev Med Child Neurol 2024;66(10):1276–88. DOI: 10.1111/dmcn.15928</mixed-citation><mixed-citation xml:lang="ru">Valproate use in men: as a precaution, men and their partners should use effective contraception. 2024. Available at: https://www.gov.uk/drug-safety-update/valproate-use-in-men-as-a-precaution-menand-their-partners-should-use-effectivecontraception.</mixed-citation></citation-alternatives></ref><ref id="B126"><label>126.</label><citation-alternatives><mixed-citation xml:lang="en">Varesio C., Provenzi L., Donetti Dontin S. et al. Pathways to quality of life in adolescents with genetic generalized epilepsy: the role of seizure features and affective symptoms. Epilepsy Behav 2020;109:107115. DOI: 10.1016/j.yebeh.2020.107115</mixed-citation><mixed-citation xml:lang="ru">Van der Louw E., Trimmel-Schwahofer P., Devlin A. et al. Human milk and breastfeeding during ketogenic diet therapy in infants with epilepsy: clinical practice guideline. Dev Med Child Neurol 2024;66(10):1276–88. DOI: 10.1111/dmcn.15928</mixed-citation></citation-alternatives></ref><ref id="B127"><label>127.</label><citation-alternatives><mixed-citation xml:lang="en">Videira G., Raimundo R., Chor o R. Epilepsy with myoclonic absences: a case series. Seizure 2023;106:162–3. DOI: 10.1016/j.seizure.2023.02.017</mixed-citation><mixed-citation xml:lang="ru">Varesio C., Provenzi L., Donetti Dontin S. et al. Pathways to quality of life in adolescents with genetic generalized epilepsy: the role of seizure features and affective symptoms. Epilepsy Behav 2020;109:107115. DOI: 10.1016/j.yebeh.2020.107115</mixed-citation></citation-alternatives></ref><ref id="B128"><label>128.</label><citation-alternatives><mixed-citation xml:lang="en">Vining E.P., Freeman J.M., Ballaban-Gil K. et al. A multicenter study of the efficacy of the ketogenic diet. Arch Neurol 1998;55(11):1433–7. DOI: 10.1001/archneur.55.11.1433</mixed-citation><mixed-citation xml:lang="ru">Videira G., Raimundo R., Chor o R. Epilepsy with myoclonic absences: a case series. Seizure 2023;106:162–3. DOI: 10.1016/j.seizure.2023.02.017</mixed-citation></citation-alternatives></ref><ref id="B129"><label>129.</label><citation-alternatives><mixed-citation xml:lang="en">Williams D. A study of thalamic and cortical rhythms in petit mal. Brain 1953;76(1):50–69. DOI: 10.1093/brain/76.1.50</mixed-citation><mixed-citation xml:lang="ru">Vining E.P., Freeman J.M., Ballaban-Gil K. et al. A multicenter study of the efficacy of the ketogenic diet. Arch Neurol 1998;55(11):1433–7. DOI: 10.1001/archneur.55.11.1433</mixed-citation></citation-alternatives></ref><ref id="B130"><label>130.</label><citation-alternatives><mixed-citation xml:lang="en">Wirrell E.С., Nabbout R., Scheffer I. et al. Methodology for classification and definition of epilepsy syndromes: report of the ILAE Task Force on Nosology and Definitions. Epilepsia 2022;63(6):1333–48. DOI: 10.1111/epi.17237</mixed-citation><mixed-citation xml:lang="ru">Williams D. A study of thalamic and cortical rhythms in petit mal. Brain 1953;76(1):50–69. DOI: 10.1093/brain/76.1.50</mixed-citation></citation-alternatives></ref><ref id="B131"><label>131.</label><citation-alternatives><mixed-citation xml:lang="en">Wirrell E., Sirven J.I., Fisher R. Juvenile myoclonic epilepsy. 2019. Available at: https://www.epilepsy.com/what-is-epilepsy/syndromes/juvenile-myoclonic-epilepsy.</mixed-citation><mixed-citation xml:lang="ru">Wirrell E.С., Nabbout R., Scheffer I. et al. Methodology for classification and definition of epilepsy syndromes: report of the ILAE Task Force on Nosology and Definitions. Epilepsia 2022;63(6):1333–48. DOI: 10.1111/epi.17237</mixed-citation></citation-alternatives></ref><ref id="B132"><label>132.</label><citation-alternatives><mixed-citation xml:lang="en">Xiong Z.G., Chu X.P., MacDonald J.F. Effect of lamotrigine on the Ca2+-sensing cation current in cultured hippocampal neurons. J Neurophysiol 2001;86:2520–6. DOI: 10.1152/jn.2001.86.5.2520</mixed-citation><mixed-citation xml:lang="ru">Wirrell E., Sirven J.I., Fisher R. Juvenile myoclonic epilepsy. 2019. Available at: https://www.epilepsy.com/what-is-epilepsy/syndromes/juvenile-myoclonic-epilepsy.</mixed-citation></citation-alternatives></ref><ref id="B133"><label>133.</label><mixed-citation>Xiong Z.G., Chu X.P., MacDonald J.F. Effect of lamotrigine on the Ca2+-sensing cation current in cultured hippocampal neurons. J Neurophysiol 2001;86:2520–6. DOI: 10.1152/jn.2001.86.5.2520</mixed-citation></ref></ref-list></back></article>
