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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">46</article-id><article-id pub-id-type="doi">10.17650/2073-8803-2015-1-40-46</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>REVIEW OF FOREIGN LITERATURE</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ОБЗОР ЗАРУБЕЖНОЙ ЛИТЕРАТУРЫ</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">EPILEPSY SURGERY IN PATIENTS WITH TUBEROUS SCLEROSIS</article-title><trans-title-group xml:lang="ru"><trans-title>Хирургическое лечение эпилепсии у пациентов с туберозным склерозом</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name><surname>Holthausen</surname><given-names>Hans</given-names></name><address><country country="RU">Russian Federation</country></address><email>jholthausen@schoen-kliniken.de</email><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Pieper</surname><given-names>Tom</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Eitel</surname><given-names>Hans</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib><contrib contrib-type="author"><name><surname>Kudernatsch</surname><given-names>Manfred</given-names></name><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff4"/><xref ref-type="aff" rid="aff2"/><xref ref-type="aff" rid="aff3"/></contrib></contrib-group><aff id="aff1"><institution>Neuropediatric Clinic and Clinic for Neurorehabiltation, Epilepsy Center for Children and Adolescents</institution></aff><aff id="aff2"><institution>Schoen-Klinik Vogtareuth</institution></aff><aff id="aff3"><institution>20 Krankenhausstrasse, D-83569, Vogtareuth, Deutschland</institution></aff><aff id="aff4"><institution>Neurosurgery Clinic and Clinic for Epilepsy Surgery</institution></aff><pub-date date-type="pub" iso-8601-date="2015-01-15" publication-format="electronic"><day>15</day><month>01</month><year>2015</year></pub-date><volume>10</volume><issue>1</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>40</fpage><lpage>46</lpage><history><date date-type="received" iso-8601-date="2015-04-19"><day>19</day><month>04</month><year>2015</year></date><date date-type="accepted" iso-8601-date="2015-04-19"><day>19</day><month>04</month><year>2015</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2015, ABV-Press</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2015, АБВ-пресс</copyright-statement><copyright-year>2015</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/46">https://rjdn.abvpress.ru/jour/article/view/46</self-uri><abstract xml:lang="en"><p>With a few exceptions patients with tuberous sclerosis (TS) suffering from drug-resistant epilepsies have potentially epileptogenic lesionswithin both hemispheres. Until one decade ago in general such a constellation was an xclusion criteria for considerations with respect to epilepsy surgery. However experience has shown that it is not so rare to find patients in whom over the ears seizures are generated from just one single focus and that these patients can be good candidates for epilepsy surgery. Almost revolutionary was the further evelopment: multi-step procedures in patients with bilateral epileptogenic lesions – with promising results in terms of postoperative seizure outcome. Also, with increasing experience, it becomes more and more possible to differentiate already non-invasively which lesions could be epileptogenic and which are rather not the source of the seizures. The most important achievement of epilepsy surgery in TS however is that in selected cases early surgical intervention is able to prevent severe mental retardations, which are often the main burden for families who have members with this peculiar disease.</p></abstract><trans-abstract xml:lang="ru"><p/></trans-abstract><kwd-group xml:lang="en"><kwd>tuberous sclerosis</kwd><kwd>epilepsy</kwd><kwd>mental retardation</kwd><kwd>epilepsy surgery</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>туберозный склероз</kwd><kwd>эпилепсия</kwd><kwd>умственная отсталость</kwd><kwd>хирургическое лечение эпилепсии</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Abolan M.S., Wong-Kisiel L., Rank M. et al. SISCOM in children with tuberous sclerosiscomplexrelated epilepsy. 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