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<article article-type="research-article" dtd-version="1.3" 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" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">nnp</journal-id><journal-title-group><journal-title xml:lang="en">Neurology, Neuropsychiatry, Psychosomatics</journal-title><trans-title-group xml:lang="ru"><trans-title>Неврология, нейропсихиатрия, психосоматика</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2074-2711</issn><issn pub-type="epub">2310-1342</issn><publisher><publisher-name>"IMA-Press", LLC</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.14412/2074-2711-2018-1-90-95</article-id><article-id custom-type="elpub" pub-id-type="custom">nnp-838</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>REVIEWS</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>ОБЗОРЫ</subject></subj-group></article-categories><title-group><article-title>Cranial dystonia</article-title><trans-title-group xml:lang="ru"><trans-title>Краниальная дистония</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Толмачева</surname><given-names>В. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Tolmacheva</surname><given-names>V. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кафедра нервных болезней и нейрохирургии,</p><p>119021, Москва, ул. Россолимо, 11</p></bio><bio xml:lang="en"><p>Department of Nervous System Diseases and Neurosurgery, </p><p>111, Rossolimo St., Moscow 119021</p></bio><email xlink:type="simple">vtolmacheva@yandex.ru</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГАОУ ВО «Первый Московский государственный медицинский университет им. И.М. Сеченова (Сеченовский университет)» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>I.M. Sechenov First Moscow State Medical University (Sechenov University), Ministry of Health of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2018</year></pub-date><pub-date pub-type="epub"><day>02</day><month>04</month><year>2018</year></pub-date><volume>10</volume><issue>1</issue><fpage>90</fpage><lpage>95</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Tolmacheva V.A., 2018</copyright-statement><copyright-year>2018</copyright-year><copyright-holder xml:lang="ru">Толмачева В.А.</copyright-holder><copyright-holder xml:lang="en">Tolmacheva V.A.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://nnp.ima-press.net/nnp/article/view/838">https://nnp.ima-press.net/nnp/article/view/838</self-uri><abstract><p>Cranial dystonia is a common disease of the extrapyramidal nervous system. The clinical manifestations of dystonia are extremely variable; many of its forms are often undiagnosed. Dystonia is a sensorimotor disorder of the nervous system. Damage affects not only one structure, but also a network of the nodes interacting with each other in the somatosensory cortex and associative sensory and motor fields, which play a role in the integration of various sensory modalities coming from both outside the body and from the receptors within it. Botulinum toxin preparations show the highest efficacy in treating cranial dystonia. If their administration cannot achieve a positive result, oral drugs and surgical treatments should be used.</p></abstract><trans-abstract xml:lang="ru"><p>Краниальная дистония – распространенное заболевание экстрапирамидной нервной системы. Клинические проявления дистонии крайне вариабельны, многие ее формы часто не диагностируются. Дистония представляет собой сенсомоторное нарушение нервной системы. Повреждение затрагивает не одну структуру, а сеть взаимодействующих друг с другом узлов, расположенных в соматосенсорной коре и ассоциативных сенсорных и моторных полях, которые играют роль в интеграции различных сенсорных модальностей, поступающих как извне, так и от рецепторов внутри организма. При краниальной дистонии максимальной эффективностью отличаются препараты ботулотоксина. Если при их применении не удается достигнуть положительного результата, используют пероральные лекарственные средства и хирургические методы лечения.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>краниальная дистония</kwd><kwd>эпидемиология</kwd><kwd>патогенез</kwd><kwd>клинические проявления</kwd><kwd>лечение</kwd></kwd-group><kwd-group xml:lang="en"><kwd>cranial dystonia</kwd><kwd>epidemiology</kwd><kwd>pathogenesis</kwd><kwd>clinical manifestations</kwd><kwd>treatment</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Williams L, McGovern E, Kimmich O, et al. Epidemiological, clinical and genetic aspects of adult onset isolated focal dystonia in Ireland. Eur J Neurol. 2017 Jan;24(1):73-81. doi: 10.1111/ene.13133. Epub 2016 Sep 19.</mixed-citation><mixed-citation xml:lang="en">Williams L, McGovern E, Kimmich O, et al. Epidemiological, clinical and genetic aspects of adult onset isolated focal dystonia in Ireland. Eur J Neurol. 2017 Jan;24(1):73-81. doi: 10.1111/ene.13133. Epub 2016 Sep 19.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Defazio G, Abbruzzese G, Livrea P, Berardelli A. Epidimiology of primary dystonia. Lancet Neurol. 2004 Nov;3(11):673-8.</mixed-citation><mixed-citation xml:lang="en">Defazio G, Abbruzzese G, Livrea P, Berardelli A. Epidimiology of primary dystonia. Lancet Neurol. 2004 Nov;3(11):673-8.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Asgeirsson H, Jakobsson F, Hjaltason H, et al. Prevalence study of primary dystonia in Iceland. Mov Disord. 2006 Mar;21(3):293-8.</mixed-citation><mixed-citation xml:lang="en">Asgeirsson H, Jakobsson F, Hjaltason H, et al. Prevalence study of primary dystonia in Iceland. Mov Disord. 2006 Mar;21(3):293-8.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Nutt JG, Muenter MD, Aronson A, et al. Epidemiology of focal and generalized dystonia in Rochester, Minnesota. Mov Disord. 1988; 3(3):188-94.</mixed-citation><mixed-citation xml:lang="en">Nutt JG, Muenter MD, Aronson A, et al. Epidemiology of focal and generalized dystonia in Rochester, Minnesota. Mov Disord. 1988; 3(3):188-94.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Fukuda H, Kusumi M, Nakashima K. Epidemiology of primary focal dystonias in the western area of Tottori Prefecture in Japan: comparison with prevalence evaluated in 1993. Mov Disord. 2006 Sep;21(9):1503-6.</mixed-citation><mixed-citation xml:lang="en">Fukuda H, Kusumi M, Nakashima K. Epidemiology of primary focal dystonias in the western area of Tottori Prefecture in Japan: comparison with prevalence evaluated in 1993. Mov Disord. 2006 Sep;21(9):1503-6.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Mü ller J, Kiechl S, Wenning GK, et al. The prevalence of primary dystonia in the general community. Neurology. 2002 Sep 24;59(6):941-3.</mixed-citation><mixed-citation xml:lang="en">Mü ller J, Kiechl S, Wenning GK, et al. The prevalence of primary dystonia in the general community. Neurology. 2002 Sep 24;59(6):941-3.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Molloy A, Williams L, Kimmich O, et al. Sun exposure is an environmental factor for the development of blepharospasm. J Neurol Neurosurg Psychiatry. 2016 Apr;87(4):420-4. doi: 10.1136/jnnp-2014-310266. Epub 2015 Apr 22.</mixed-citation><mixed-citation xml:lang="en">Molloy A, Williams L, Kimmich O, et al. Sun exposure is an environmental factor for the development of blepharospasm. J Neurol Neurosurg Psychiatry. 2016 Apr;87(4):420-4. doi: 10.1136/jnnp-2014-310266. Epub 2015 Apr 22.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Petrucci S, Valente EM. Genetic issues in the diagnosis of dystonias. Front Neurol. 2013 Apr 10; 4:34. doi: 10.3389/fneur.2013.00034. eCollection 2013.</mixed-citation><mixed-citation xml:lang="en">Petrucci S, Valente EM. Genetic issues in the diagnosis of dystonias. Front Neurol. 2013 Apr 10; 4:34. doi: 10.3389/fneur.2013.00034. eCollection 2013.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Papantonio AM, Beghi E, Fogli D, et al. Prevalence of primary focal or segmental dystonia in adults in the district of Foggia, southern Italy: a service-based study. Neuroepidemiology. 2009;33(2):117-23. doi: 10.1159/000226124. Epub 2009 Jun 26.</mixed-citation><mixed-citation xml:lang="en">Papantonio AM, Beghi E, Fogli D, et al. Prevalence of primary focal or segmental dystonia in adults in the district of Foggia, southern Italy: a service-based study. Neuroepidemiology. 2009;33(2):117-23. doi: 10.1159/000226124. Epub 2009 Jun 26.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Defazio G, Gigante AF, Abbruzzese G, et al. Tremor in primary adult-onset dystonia: prevalence and associated clinical features. J Neurol Neurosurg Psychiatry. 2013 Apr; 84(4):404-8. doi: 10.1136/jnnp-2012-303782. Epub 2012 Nov 10.</mixed-citation><mixed-citation xml:lang="en">Defazio G, Gigante AF, Abbruzzese G, et al. Tremor in primary adult-onset dystonia: prevalence and associated clinical features. J Neurol Neurosurg Psychiatry. 2013 Apr; 84(4):404-8. doi: 10.1136/jnnp-2012-303782. Epub 2012 Nov 10.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Sugawara M, Watanabe S, Toyoshima I. Prevalence of dystonia in Akita Prefecture in Northern Japan. Mov Disord. 2006 Jul;21(7): 1047-9.</mixed-citation><mixed-citation xml:lang="en">Sugawara M, Watanabe S, Toyoshima I. Prevalence of dystonia in Akita Prefecture in Northern Japan. Mov Disord. 2006 Jul;21(7): 1047-9.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Groen JL, Kallen MC, van de Warrenburg BP, et al. Phenotypes and genetic architecture of focal primary torsion dystonia. J Neurol Neurosurg Psychiatry. 2012 Oct;83(10):1006-11. doi: 10.1136/jnnp-2012-302729. Epub 2012 Jul 8.</mixed-citation><mixed-citation xml:lang="en">Groen JL, Kallen MC, van de Warrenburg BP, et al. Phenotypes and genetic architecture of focal primary torsion dystonia. J Neurol Neurosurg Psychiatry. 2012 Oct;83(10):1006-11. doi: 10.1136/jnnp-2012-302729. Epub 2012 Jul 8.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Butler AG, Duffey PO, Hawthorne MR, Barnes MP. An epidemiologic survey of dystonia within the entire population of northeast England over the past nine years. Adv Neurol. 2004;94:95-9.</mixed-citation><mixed-citation xml:lang="en">Butler AG, Duffey PO, Hawthorne MR, Barnes MP. An epidemiologic survey of dystonia within the entire population of northeast England over the past nine years. Adv Neurol. 2004;94:95-9.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Soland VL, Bhatia KP, Marsden CD. Sex prevalence of focal dystonias. J Neurol Neurosurg Psychiatry. 1996 Feb;60(2):204-5.</mixed-citation><mixed-citation xml:lang="en">Soland VL, Bhatia KP, Marsden CD. Sex prevalence of focal dystonias. J Neurol Neurosurg Psychiatry. 1996 Feb;60(2):204-5.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Duffey PO, Butler AG, Hawthorne MR, Barnes MP. The epidemiology of the primary dystonias in the north of England. Adv Neurol. 1998;78:121-5.</mixed-citation><mixed-citation xml:lang="en">Duffey PO, Butler AG, Hawthorne MR, Barnes MP. The epidemiology of the primary dystonias in the north of England. Adv Neurol. 1998;78:121-5.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Tolosa ES, Klawans HL. Meige’s disease. A clinical form of facial convulsion bilateral and medial. Arch Neurol. 1979 Oct;36(10):635-7.</mixed-citation><mixed-citation xml:lang="en">Tolosa ES, Klawans HL. Meige’s disease. A clinical form of facial convulsion bilateral and medial. Arch Neurol. 1979 Oct;36(10):635-7.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Jankovic J, Orman J. Blepharospasm: demographic and clinical survey of 250 patients. Ann Ophthalmol. 1984 Apr;16(4):371-6.</mixed-citation><mixed-citation xml:lang="en">Jankovic J, Orman J. Blepharospasm: demographic and clinical survey of 250 patients. Ann Ophthalmol. 1984 Apr;16(4):371-6.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">LeDoux MS. Meige’s syndrome: what’s in a name? Parkinsonism Relat Disord. 2009 Aug;15(7): 483-9. doi: 10.1016/j.parkreldis.2009.04.006. Epub 2009 May 19.</mixed-citation><mixed-citation xml:lang="en">LeDoux MS. Meige’s syndrome: what’s in a name? Parkinsonism Relat Disord. 2009 Aug;15(7): 483-9. doi: 10.1016/j.parkreldis.2009.04.006. Epub 2009 May 19.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">O’Riordan S, Raymond D, Lynch T, et al. Age of onset as a factor in determining the phenotype of primary torsion dystonia. Neurology. 2004 Oct 26;63(8):1423-6.</mixed-citation><mixed-citation xml:lang="en">O’Riordan S, Raymond D, Lynch T, et al. Age of onset as a factor in determining the phenotype of primary torsion dystonia. Neurology. 2004 Oct 26;63(8):1423-6.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Tolosa ES. Clinical features of Meige's disease (idiopathic orofacial dystonia): a report of 17 cases. Arch Neurol. 1981 Mar;38(3):147-51.</mixed-citation><mixed-citation xml:lang="en">Tolosa ES. Clinical features of Meige's disease (idiopathic orofacial dystonia): a report of 17 cases. Arch Neurol. 1981 Mar;38(3):147-51.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Marsden CD. Blepharospasm-oromandibular dystonia syndrome (Brueghel's syndrome). A variant of adult-onset torsion dystonia. J Neurol Neurosurg Psychiatry. 1976 Dec;39(12):1204-9.</mixed-citation><mixed-citation xml:lang="en">Marsden CD. Blepharospasm-oromandibular dystonia syndrome (Brueghel's syndrome). A variant of adult-onset torsion dystonia. J Neurol Neurosurg Psychiatry. 1976 Dec;39(12):1204-9.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Allam N, Frank JE, Pereira C, Tomaz C. Sustainet attention in cranial dystonia patients treated with botulinum toxin. Acta Neurol Scand. 2007 Sep;116(3):196-200.</mixed-citation><mixed-citation xml:lang="en">Allam N, Frank JE, Pereira C, Tomaz C. Sustainet attention in cranial dystonia patients treated with botulinum toxin. Acta Neurol Scand. 2007 Sep;116(3):196-200.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Fabbrini G, Pantano P, Totaro P, et al. Diffusion tensor imaging in patients with primary cervical dystonia and in patients with blepharospasm. Eur J Neurol. 2008 Feb;15(2): 185-9. doi: 10.1111/j.1468-1331.2007.02034.x.</mixed-citation><mixed-citation xml:lang="en">Fabbrini G, Pantano P, Totaro P, et al. Diffusion tensor imaging in patients with primary cervical dystonia and in patients with blepharospasm. Eur J Neurol. 2008 Feb;15(2): 185-9. doi: 10.1111/j.1468-1331.2007.02034.x.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Hallett M. Blepharospasm: recent advances. Neurology. 2002 Nov 12;59(9):1306-12.</mixed-citation><mixed-citation xml:lang="en">Hallett M. Blepharospasm: recent advances. Neurology. 2002 Nov 12;59(9):1306-12.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Tolosa E, Marti MJ. Blepharospasm-oromandibular dystonia syndrome (Meige's syndrome): clinical aspects. Adv Neurol. 1988; 49:73-84.</mixed-citation><mixed-citation xml:lang="en">Tolosa E, Marti MJ. Blepharospasm-oromandibular dystonia syndrome (Meige's syndrome): clinical aspects. Adv Neurol. 1988; 49:73-84.</mixed-citation></citation-alternatives></ref><ref id="cit26"><label>26</label><citation-alternatives><mixed-citation xml:lang="ru">Peckham EL, Lopez G, Shamim EA, et al. Clinical features of patients with blepharospasm: a report of 240 patients. Eur J Neurol. 2011 Mar;18(3):382-6. doi: 10.1111/j.1468-1331.2010.03161.x.</mixed-citation><mixed-citation xml:lang="en">Peckham EL, Lopez G, Shamim EA, et al. Clinical features of patients with blepharospasm: a report of 240 patients. Eur J Neurol. 2011 Mar;18(3):382-6. doi: 10.1111/j.1468-1331.2010.03161.x.</mixed-citation></citation-alternatives></ref><ref id="cit27"><label>27</label><citation-alternatives><mixed-citation xml:lang="ru">Abbruzzese G, Berardelli A, Girlanda P, et al. Long-term assessment of the risk of spread in primary late-onset focal dystonia. J Neurol Neurosurg Psychiatry. 2008 Apr;79(4):392-6. Epub 2007 Jul 17.</mixed-citation><mixed-citation xml:lang="en">Abbruzzese G, Berardelli A, Girlanda P, et al. Long-term assessment of the risk of spread in primary late-onset focal dystonia. J Neurol Neurosurg Psychiatry. 2008 Apr;79(4):392-6. Epub 2007 Jul 17.</mixed-citation></citation-alternatives></ref><ref id="cit28"><label>28</label><citation-alternatives><mixed-citation xml:lang="ru">Weiss EM, Hershey T, Karimi M, et al. Relative risk of spread of symptoms among the focal onset primary dystonias. Mov Disord. 2006 Aug;21(8):1175-81.</mixed-citation><mixed-citation xml:lang="en">Weiss EM, Hershey T, Karimi M, et al. Relative risk of spread of symptoms among the focal onset primary dystonias. Mov Disord. 2006 Aug;21(8):1175-81.</mixed-citation></citation-alternatives></ref><ref id="cit29"><label>29</label><citation-alternatives><mixed-citation xml:lang="ru">Defazio G, Berardelli A, Abbruzzese G, et al. Risk factors for spread of primary adult onset blepharospasm: a multicentre investigation of the Italian movement disorders study group. J Neurol Neurosurg Psychiatry. 1999 Nov;67(5):613-9.</mixed-citation><mixed-citation xml:lang="en">Defazio G, Berardelli A, Abbruzzese G, et al. Risk factors for spread of primary adult onset blepharospasm: a multicentre investigation of the Italian movement disorders study group. J Neurol Neurosurg Psychiatry. 1999 Nov;67(5):613-9.</mixed-citation></citation-alternatives></ref><ref id="cit30"><label>30</label><citation-alternatives><mixed-citation xml:lang="ru">Martino D, Berardelli A, Abbruzzese G, et al. Age at onset and symptom spread in primary adult-onset blepharospasm and cervical dystonia. Mov Disord. 2012 Sep 15;27(11):1447-50. doi: 10.1002/mds.25088. Epub 2012 Aug 13.</mixed-citation><mixed-citation xml:lang="en">Martino D, Berardelli A, Abbruzzese G, et al. Age at onset and symptom spread in primary adult-onset blepharospasm and cervical dystonia. Mov Disord. 2012 Sep 15;27(11):1447-50. doi: 10.1002/mds.25088. Epub 2012 Aug 13.</mixed-citation></citation-alternatives></ref><ref id="cit31"><label>31</label><citation-alternatives><mixed-citation xml:lang="ru">Svetel M, Pekmezovic T, Tomic A, et al. The spread of primary late-onset focal dystonia in a long-term follow up study, Clin. Neurol. Neurosurg. 132 (May 2015) 41–43.</mixed-citation><mixed-citation xml:lang="en">Svetel M, Pekmezovic T, Tomic A, et al. The spread of primary late-onset focal dystonia in a long-term follow up study, Clin. Neurol. Neurosurg. 132 (May 2015) 41–43.</mixed-citation></citation-alternatives></ref><ref id="cit32"><label>32</label><citation-alternatives><mixed-citation xml:lang="ru">Svetel M., Pekmezovic T., Jovic J., Ivanovic N., Dragasevic N., Maric J., Kostic V.S., Spread of primary dystonia in relation to initially affected region, J. Neurol. 254 (7) (Jul 2007) 879–883.</mixed-citation><mixed-citation xml:lang="en">Svetel M., Pekmezovic T., Jovic J., Ivanovic N., Dragasevic N., Maric J., Kostic V.S., Spread of primary dystonia in relation to initially affected region, J. Neurol. 254 (7) (Jul 2007) 879–883.</mixed-citation></citation-alternatives></ref><ref id="cit33"><label>33</label><citation-alternatives><mixed-citation xml:lang="ru">DeVeaugh-Geiss J., Clinical changes in tardive dyskinesia during long term follow up, in: Wolf M.E., Mosina A.D. (Eds.), Tardive Dyskinesia: Biological Mechanisms and Clinical Aspects, American Psychiatric Press, Washington, DC 1988, pp. 89–105.</mixed-citation><mixed-citation xml:lang="en">DeVeaugh-Geiss J., Clinical changes in tardive dyskinesia during long term follow up, in: Wolf M.E., Mosina A.D. (Eds.), Tardive Dyskinesia: Biological Mechanisms and Clinical Aspects, American Psychiatric Press, Washington, DC 1988, pp. 89–105.</mixed-citation></citation-alternatives></ref><ref id="cit34"><label>34</label><citation-alternatives><mixed-citation xml:lang="ru">Kimura T., Deshimaru M., Inukai K., Matsunaga T., Hisano T., Watanabe K., Miyakawa T., Schizophrenic mother and daughter with Meige's syndrome, Rinsho Scishin Igaku (Clin. Psychiatry Med.) 21 (1992) 1213–1220.</mixed-citation><mixed-citation xml:lang="en">Kimura T., Deshimaru M., Inukai K., Matsunaga T., Hisano T., Watanabe K., Miyakawa T., Schizophrenic mother and daughter with Meige's syndrome, Rinsho Scishin Igaku (Clin. Psychiatry Med.) 21 (1992) 1213–1220.</mixed-citation></citation-alternatives></ref><ref id="cit35"><label>35</label><citation-alternatives><mixed-citation xml:lang="ru">Jankovic J., Drug-induced and other orofacial-cervical dyskinesias, Ann. Intern. Med. 94 (1981) 788–793.</mixed-citation><mixed-citation xml:lang="en">Jankovic J., Drug-induced and other orofacial-cervical dyskinesias, Ann. Intern. Med. 94 (1981) 788–793.</mixed-citation></citation-alternatives></ref><ref id="cit36"><label>36</label><citation-alternatives><mixed-citation xml:lang="ru">Mauriello J.A., Carbonaro P., Dhillon S., Leone T., Franklin M., Drug-associated facialdyskinesias—a study of 238 patients, J. Neuroophthalmol. 18 (2) (1998 Jun) 153–157</mixed-citation><mixed-citation xml:lang="en">Mauriello J.A., Carbonaro P., Dhillon S., Leone T., Franklin M., Drug-associated facialdyskinesias—a study of 238 patients, J. Neuroophthalmol. 18 (2) (1998 Jun) 153–157</mixed-citation></citation-alternatives></ref><ref id="cit37"><label>37</label><citation-alternatives><mixed-citation xml:lang="ru">Jankovic J., Patel S.C., Blepharospasm associated with brainstem lesions, Neurology 33 (1983) 1237–1240.</mixed-citation><mixed-citation xml:lang="en">Jankovic J., Patel S.C., Blepharospasm associated with brainstem lesions, Neurology 33 (1983) 1237–1240.</mixed-citation></citation-alternatives></ref><ref id="cit38"><label>38</label><citation-alternatives><mixed-citation xml:lang="ru">Keane JR., Young JA. Blepharospasm with bilateral basal ganglia infarction, Arch. Neurol. 42 (12) (Dec 1, 1985) 1206–1208.</mixed-citation><mixed-citation xml:lang="en">Keane JR., Young JA. Blepharospasm with bilateral basal ganglia infarction, Arch. Neurol. 42 (12) (Dec 1, 1985) 1206–1208.</mixed-citation></citation-alternatives></ref><ref id="cit39"><label>39</label><citation-alternatives><mixed-citation xml:lang="ru">Sandyk R, Gillman MA. Blepharospasm associated with communicating hydrocephalus, Neurology 34 (1984) 1522–1523.</mixed-citation><mixed-citation xml:lang="en">Sandyk R, Gillman MA. Blepharospasm associated with communicating hydrocephalus, Neurology 34 (1984) 1522–1523.</mixed-citation></citation-alternatives></ref><ref id="cit40"><label>40</label><citation-alternatives><mixed-citation xml:lang="ru">Lang AE, Sharpe JA. Blepharospasm associated with palatal myoclonus and communicating hydrocephalus, Neurology 34 (11) (Nov 1, 1984) 1522.</mixed-citation><mixed-citation xml:lang="en">Lang AE, Sharpe JA. Blepharospasm associated with palatal myoclonus and communicating hydrocephalus, Neurology 34 (11) (Nov 1, 1984) 1522.</mixed-citation></citation-alternatives></ref><ref id="cit41"><label>41</label><citation-alternatives><mixed-citation xml:lang="ru">Jankovic J. Blepharospasm with basal ganglia lesions, Arch. Neurol. 43 (9) (Sep 1,1986) 866–868.</mixed-citation><mixed-citation xml:lang="en">Jankovic J. Blepharospasm with basal ganglia lesions, Arch. Neurol. 43 (9) (Sep 1,1986) 866–868.</mixed-citation></citation-alternatives></ref><ref id="cit42"><label>42</label><citation-alternatives><mixed-citation xml:lang="ru">O'Rourke K, O'Riordan S, Gallagher J, Hutchinson M. Paroxysmal torticollis and blepharospasm following bilateral cerebellar infarction. J Neurol. 2006 Dec;253(12):1644-5.</mixed-citation><mixed-citation xml:lang="en">O'Rourke K, O'Riordan S, Gallagher J, Hutchinson M. Paroxysmal torticollis and blepharospasm following bilateral cerebellar infarction. J Neurol. 2006 Dec;253(12):1644-5.</mixed-citation></citation-alternatives></ref><ref id="cit43"><label>43</label><citation-alternatives><mixed-citation xml:lang="ru">Jankovic J, Ford J. Blepharospasm and orofacial-cervical dystonia clinical and pharmacological findings in 100 patients. Ann Neurol. 1983 Apr;13(4):402-11.</mixed-citation><mixed-citation xml:lang="en">Jankovic J, Ford J. Blepharospasm and orofacial-cervical dystonia clinical and pharmacological findings in 100 patients. Ann Neurol. 1983 Apr;13(4):402-11.</mixed-citation></citation-alternatives></ref><ref id="cit44"><label>44</label><citation-alternatives><mixed-citation xml:lang="ru">Machado A, Chien HF, Deguti MM, et al. Neurological manifestations in Wilson's disease: report of 119 cases. Mov Disord. 2006 Dec;21(12):2192-6.</mixed-citation><mixed-citation xml:lang="en">Machado A, Chien HF, Deguti MM, et al. Neurological manifestations in Wilson's disease: report of 119 cases. Mov Disord. 2006 Dec;21(12):2192-6.</mixed-citation></citation-alternatives></ref><ref id="cit45"><label>45</label><citation-alternatives><mixed-citation xml:lang="ru">Lou JS, Jankovic J. Essential tremor: clinical correlates in 350 patients. Neurology. 1991 Feb;41(2 ( Pt 1)):234-8.</mixed-citation><mixed-citation xml:lang="en">Lou JS, Jankovic J. Essential tremor: clinical correlates in 350 patients. Neurology. 1991 Feb;41(2 ( Pt 1)):234-8.</mixed-citation></citation-alternatives></ref><ref id="cit46"><label>46</label><citation-alternatives><mixed-citation xml:lang="ru">Hedera P, Phibbs FT, Fang JY, et al. Clustering of dystonia in some pedigrees with autosomal dominant essential tremor suggests the existence of a distinct subtype of essential tremor. BMC Neurol. 2010 Jul 29;10:66. doi: 10.1186/1471-2377-10-66.</mixed-citation><mixed-citation xml:lang="en">Hedera P, Phibbs FT, Fang JY, et al. Clustering of dystonia in some pedigrees with autosomal dominant essential tremor suggests the existence of a distinct subtype of essential tremor. BMC Neurol. 2010 Jul 29;10:66. doi: 10.1186/1471-2377-10-66.</mixed-citation></citation-alternatives></ref><ref id="cit47"><label>47</label><citation-alternatives><mixed-citation xml:lang="ru">Martinelli P, Gabellini AS, Gulli MR Lugaresi E. Different clinical features of essential tremor: a 200-patient study. Acta Neurol Scand. 1987 Feb;75(2):106-11.</mixed-citation><mixed-citation xml:lang="en">Martinelli P, Gabellini AS, Gulli MR Lugaresi E. Different clinical features of essential tremor: a 200-patient study. Acta Neurol Scand. 1987 Feb;75(2):106-11.</mixed-citation></citation-alternatives></ref><ref id="cit48"><label>48</label><citation-alternatives><mixed-citation xml:lang="ru">Koller WC, Busenbark K, Miner K. The relationship of essential tremor to other movement disorders: report on 678 patients. Essential Tremor Study Group. Ann Neurol. 1994 Jun;35(6):717-23.</mixed-citation><mixed-citation xml:lang="en">Koller WC, Busenbark K, Miner K. The relationship of essential tremor to other movement disorders: report on 678 patients. Essential Tremor Study Group. Ann Neurol. 1994 Jun;35(6):717-23.</mixed-citation></citation-alternatives></ref><ref id="cit49"><label>49</label><citation-alternatives><mixed-citation xml:lang="ru">Boesch SM, Wenning GK, Ransmayr G, Poewe W. Dystonia in multiple system atrophy. J Neurol Neurosurg Psychiatry. 2002 Mar;72(3): 300-3.</mixed-citation><mixed-citation xml:lang="en">Boesch SM, Wenning GK, Ransmayr G, Poewe W. Dystonia in multiple system atrophy. J Neurol Neurosurg Psychiatry. 2002 Mar;72(3): 300-3.</mixed-citation></citation-alternatives></ref><ref id="cit50"><label>50</label><citation-alternatives><mixed-citation xml:lang="ru">Louis ED, Hernandez N, Alcalay RN, et al. Prevalence and features of unreported dystonia in a family study of «pure» essential tremor. Parkinsonism Relat Disord. 2013 Mar;19(3): 359-62. doi: 10.1016/j.parkreldis.2012.09.015. Epub 2012 Oct 23.</mixed-citation><mixed-citation xml:lang="en">Louis ED, Hernandez N, Alcalay RN, et al. Prevalence and features of unreported dystonia in a family study of «pure» essential tremor. Parkinsonism Relat Disord. 2013 Mar;19(3): 359-62. doi: 10.1016/j.parkreldis.2012.09.015. Epub 2012 Oct 23.</mixed-citation></citation-alternatives></ref><ref id="cit51"><label>51</label><citation-alternatives><mixed-citation xml:lang="ru">Rana AQ, Kabir A, Dogu O, et al. Prevalence of blepharospasm and apraxia of eyelid opening in patients with parkinsonism, cervical dystonia and essential tremor. Eur Neurol. 2012;68(5):318-21. doi: 10.1159/ 000341621. Epub 2012 Oct 11.</mixed-citation><mixed-citation xml:lang="en">Rana AQ, Kabir A, Dogu O, et al. Prevalence of blepharospasm and apraxia of eyelid opening in patients with parkinsonism, cervical dystonia and essential tremor. Eur Neurol. 2012;68(5):318-21. doi: 10.1159/ 000341621. Epub 2012 Oct 11.</mixed-citation></citation-alternatives></ref><ref id="cit52"><label>52</label><citation-alternatives><mixed-citation xml:lang="ru">Barclay CL, Lang AE. Dystonia in progressive supranuclear palsy. J Neurol Neurosurg Psychiatry. 1997 Apr;62(4):352-6.</mixed-citation><mixed-citation xml:lang="en">Barclay CL, Lang AE. Dystonia in progressive supranuclear palsy. J Neurol Neurosurg Psychiatry. 1997 Apr;62(4):352-6.</mixed-citation></citation-alternatives></ref><ref id="cit53"><label>53</label><citation-alternatives><mixed-citation xml:lang="ru">Yoon WT, Chung EJ, Lee SH, et al. Clinical analysis of blepharospasm and apraxia of eyelid opening in patients with parkinsonism. J Clin Neurol. 2005 Oct;1(2):159-65. doi: 10.3988/jcn. 2005.1.2.159. Epub 2005 Oct 20.</mixed-citation><mixed-citation xml:lang="en">Yoon WT, Chung EJ, Lee SH, et al. Clinical analysis of blepharospasm and apraxia of eyelid opening in patients with parkinsonism. J Clin Neurol. 2005 Oct;1(2):159-65. doi: 10.3988/jcn. 2005.1.2.159. Epub 2005 Oct 20.</mixed-citation></citation-alternatives></ref><ref id="cit54"><label>54</label><citation-alternatives><mixed-citation xml:lang="ru">Godeiro-Junior C, Felicio AC, Barsottini OG, et al. Clinical features of dystonia in atypical parkinsonism. Arq Neuropsiquiatr. 2008 Dec;66(4):800-4.</mixed-citation><mixed-citation xml:lang="en">Godeiro-Junior C, Felicio AC, Barsottini OG, et al. Clinical features of dystonia in atypical parkinsonism. Arq Neuropsiquiatr. 2008 Dec;66(4):800-4.</mixed-citation></citation-alternatives></ref><ref id="cit55"><label>55</label><citation-alternatives><mixed-citation xml:lang="ru">Tallon-Barranco A, Vazquez A, Javier Jimenez-Jimenez F, et al. Clinical features of essential tremor seen in neurology practice: a study of 357 patients. Parkinsonism Relat Disord. 1997 Dec;3(4):187-90.</mixed-citation><mixed-citation xml:lang="en">Tallon-Barranco A, Vazquez A, Javier Jimenez-Jimenez F, et al. Clinical features of essential tremor seen in neurology practice: a study of 357 patients. Parkinsonism Relat Disord. 1997 Dec;3(4):187-90.</mixed-citation></citation-alternatives></ref><ref id="cit56"><label>56</label><citation-alternatives><mixed-citation xml:lang="ru">Jankovic J, Beach J, Pandolfo M, Patel PI. Familial essential tremor in 4 kindreds. Prospects for genetic mapping. Arch Neurol. 1997 Mar;54(3):289-94.</mixed-citation><mixed-citation xml:lang="en">Jankovic J, Beach J, Pandolfo M, Patel PI. Familial essential tremor in 4 kindreds. Prospects for genetic mapping. Arch Neurol. 1997 Mar;54(3):289-94.</mixed-citation></citation-alternatives></ref><ref id="cit57"><label>57</label><citation-alternatives><mixed-citation xml:lang="ru">Mark MH, Sage JI, Dickson DW. Meige's syndrome in the spectrum of Lewy body disease. Neurology. 1994 Aug;44(8):1432-6.</mixed-citation><mixed-citation xml:lang="en">Mark MH, Sage JI, Dickson DW. Meige's syndrome in the spectrum of Lewy body disease. Neurology. 1994 Aug;44(8):1432-6.</mixed-citation></citation-alternatives></ref><ref id="cit58"><label>58</label><citation-alternatives><mixed-citation xml:lang="ru">Micheli F, Scorticati M, Folgar S, Gatto E. Development of Parkinson’s Disease in Patients With Blepharospasm. Mov Disord. 2004 Sep; 19(9):1069-1072.</mixed-citation><mixed-citation xml:lang="en">Micheli F, Scorticati M, Folgar S, Gatto E. Development of Parkinson’s Disease in Patients With Blepharospasm. Mov Disord. 2004 Sep; 19(9):1069-1072.</mixed-citation></citation-alternatives></ref><ref id="cit59"><label>59</label><citation-alternatives><mixed-citation xml:lang="ru">Soonawala N, Bhatia KP, Yeung JH, et al. Idiopathic blepharospasm does not lead to a parkinsonian syndrome: results of a questionnaire-based follow-up study. J Neurol. 1999 Apr;246(4):283-6.</mixed-citation><mixed-citation xml:lang="en">Soonawala N, Bhatia KP, Yeung JH, et al. Idiopathic blepharospasm does not lead to a parkinsonian syndrome: results of a questionnaire-based follow-up study. J Neurol. 1999 Apr;246(4):283-6.</mixed-citation></citation-alternatives></ref><ref id="cit60"><label>60</label><citation-alternatives><mixed-citation xml:lang="ru">Jankovic J. Medical treatment of dystonia. Mov Disord. 2013 Jun 15;28(7):1001-12. doi: 10.1002/mds.25552.</mixed-citation><mixed-citation xml:lang="en">Jankovic J. Medical treatment of dystonia. Mov Disord. 2013 Jun 15;28(7):1001-12. doi: 10.1002/mds.25552.</mixed-citation></citation-alternatives></ref><ref id="cit61"><label>61</label><citation-alternatives><mixed-citation xml:lang="ru">Jankovic J, Hallett M, editors. Therapy With Botulinum Toxin. New York: Marcel Dekker; 1994. 608 p.</mixed-citation><mixed-citation xml:lang="en">Jankovic J, Hallett M, editors. Therapy With Botulinum Toxin. New York: Marcel Dekker; 1994. 608 p.</mixed-citation></citation-alternatives></ref><ref id="cit62"><label>62</label><citation-alternatives><mixed-citation xml:lang="ru">Brin MF, Hallett M, Jankovic J. Scientific and Therapeutic Aspects of Botulinum Toxin. Philadelphia: Lippincott Williams &amp; Wilkins; 2002. 507 p.</mixed-citation><mixed-citation xml:lang="en">Brin MF, Hallett M, Jankovic J. Scientific and Therapeutic Aspects of Botulinum Toxin. Philadelphia: Lippincott Williams &amp; Wilkins; 2002. 507 p.</mixed-citation></citation-alternatives></ref><ref id="cit63"><label>63</label><citation-alternatives><mixed-citation xml:lang="ru">Jankovic J, Albanese A, Atassi MZ, et al. Botulinum Toxin. Therapeutic Clinical Practice and Science. Philadelphia: Saunders (Elsevier); 2009. 492 p.</mixed-citation><mixed-citation xml:lang="en">Jankovic J, Albanese A, Atassi MZ, et al. Botulinum Toxin. Therapeutic Clinical Practice and Science. Philadelphia: Saunders (Elsevier); 2009. 492 p.</mixed-citation></citation-alternatives></ref><ref id="cit64"><label>64</label><citation-alternatives><mixed-citation xml:lang="ru">Simpson DM, Blitzer A, Brashear A, et al. Assessment: Botulinum neurotoxin in the treatment of autonomic disorders and pain (an evidence-based review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology. 2008 May 6;70(19):1699-706. doi: 10.1212/01.wnl.0000311389.26145.95.</mixed-citation><mixed-citation xml:lang="en">Simpson DM, Blitzer A, Brashear A, et al. Assessment: Botulinum neurotoxin in the treatment of autonomic disorders and pain (an evidence-based review): Report of the Therapeutics and Technology Assessment Subcommittee of the American Academy of Neurology. Neurology. 2008 May 6;70(19):1699-706. doi: 10.1212/01.wnl.0000311389.26145.95.</mixed-citation></citation-alternatives></ref><ref id="cit65"><label>65</label><citation-alternatives><mixed-citation xml:lang="ru">Mehlan J, Brosig H, Schmitt O, et al. Intrastriatal injection of botulinum neurotoxinA is not cytotoxic in rat brain – a histological and stereological analysis. Brain Res. 2016 Jan 1;1630:18-24. doi: 10.1016/j.brainres.2015. 10.056. Epub 2015 Nov 10.</mixed-citation><mixed-citation xml:lang="en">Mehlan J, Brosig H, Schmitt O, et al. Intrastriatal injection of botulinum neurotoxinA is not cytotoxic in rat brain – a histological and stereological analysis. Brain Res. 2016 Jan 1;1630:18-24. doi: 10.1016/j.brainres.2015. 10.056. Epub 2015 Nov 10.</mixed-citation></citation-alternatives></ref><ref id="cit66"><label>66</label><citation-alternatives><mixed-citation xml:lang="ru">Restani L, Antonucci F, Gianfranceschi L, et al. Evidence for anterograde transport and transcytosis of botulinum neurotoxin A (BoNT/A). J Neurosci. 2011 Nov 2;31(44): 15650-9. doi: 10.1523/JNEUROSCI.2618-11.2011.</mixed-citation><mixed-citation xml:lang="en">Restani L, Antonucci F, Gianfranceschi L, et al. Evidence for anterograde transport and transcytosis of botulinum neurotoxin A (BoNT/A). J Neurosci. 2011 Nov 2;31(44): 15650-9. doi: 10.1523/JNEUROSCI.2618-11.2011.</mixed-citation></citation-alternatives></ref><ref id="cit67"><label>67</label><citation-alternatives><mixed-citation xml:lang="ru">Mazzocchio R, Caleo M. More than at the neuromuscular synapse: actions of botulinum neurotoxin A in the central nervous system. Neuroscientist. 2015 Feb;21(1):44-61. doi: 10.1177/1073858414524633. Epub 2014 Feb 26.</mixed-citation><mixed-citation xml:lang="en">Mazzocchio R, Caleo M. More than at the neuromuscular synapse: actions of botulinum neurotoxin A in the central nervous system. Neuroscientist. 2015 Feb;21(1):44-61. doi: 10.1177/1073858414524633. Epub 2014 Feb 26.</mixed-citation></citation-alternatives></ref><ref id="cit68"><label>68</label><citation-alternatives><mixed-citation xml:lang="ru">Cai BB, Francis J, Brin MF, Broide RS. Botulinum neirotoxin type A-cleaved SNAP25 is confined to primary motor neurons and localized on the plasma membrane following intramuscular toxin injection. Neuroscience. 2017 Jun 3;352:155-169. doi: 10.1016/j.neuroscience.2017.03.049. Epub 2017 Apr 5.</mixed-citation><mixed-citation xml:lang="en">Cai BB, Francis J, Brin MF, Broide RS. Botulinum neirotoxin type A-cleaved SNAP25 is confined to primary motor neurons and localized on the plasma membrane following intramuscular toxin injection. Neuroscience. 2017 Jun 3;352:155-169. doi: 10.1016/j.neuroscience.2017.03.049. Epub 2017 Apr 5.</mixed-citation></citation-alternatives></ref><ref id="cit69"><label>69</label><citation-alternatives><mixed-citation xml:lang="ru">Muta D, Goto S, Nishikawa S, et al. Bilateral pallidal stimulation for idiopathic segmental axial dystonia advanced from Meige syndrome refractory to bilateral thalamotomy. Mov Disord. 2001 Jul;16(4):774-7.</mixed-citation><mixed-citation xml:lang="en">Muta D, Goto S, Nishikawa S, et al. Bilateral pallidal stimulation for idiopathic segmental axial dystonia advanced from Meige syndrome refractory to bilateral thalamotomy. Mov Disord. 2001 Jul;16(4):774-7.</mixed-citation></citation-alternatives></ref><ref id="cit70"><label>70</label><citation-alternatives><mixed-citation xml:lang="ru">Capelle HH, Weigel R, Krauss JK. Bilateral pallidalstimulation for blepharospasm-oromandibular dystonia (Meige syndrome). Neurology. 2003 Jun 24;60(12):2017-8.</mixed-citation><mixed-citation xml:lang="en">Capelle HH, Weigel R, Krauss JK. Bilateral pallidalstimulation for blepharospasm-oromandibular dystonia (Meige syndrome). Neurology. 2003 Jun 24;60(12):2017-8.</mixed-citation></citation-alternatives></ref><ref id="cit71"><label>71</label><citation-alternatives><mixed-citation xml:lang="ru">Speelman JD, Contarino MF, Schuurman PR, et al. Deep brain stimulation for dystonia: patient selection and outcomes. Eur J Neurol. 2010 Jul;17 Suppl 1:102-6. doi: 10.1111/j.1468-1331.2010.03060.x.</mixed-citation><mixed-citation xml:lang="en">Speelman JD, Contarino MF, Schuurman PR, et al. Deep brain stimulation for dystonia: patient selection and outcomes. Eur J Neurol. 2010 Jul;17 Suppl 1:102-6. doi: 10.1111/j.1468-1331.2010.03060.x.</mixed-citation></citation-alternatives></ref><ref id="cit72"><label>72</label><citation-alternatives><mixed-citation xml:lang="ru">Andrews C, Aviles-Olmos I, Hariz M, Foltynie T. Which patients with dystonia benefit from deep brain stimulation? A metaregression of individual patient outcomes. J Neurol Neurosurg Psychiatry. 2010 Dec;81(12):1383-9. doi: 10.1136/jnnp.2010.207993. Epub 2010 Sep 14.</mixed-citation><mixed-citation xml:lang="en">Andrews C, Aviles-Olmos I, Hariz M, Foltynie T. Which patients with dystonia benefit from deep brain stimulation? A metaregression of individual patient outcomes. J Neurol Neurosurg Psychiatry. 2010 Dec;81(12):1383-9. doi: 10.1136/jnnp.2010.207993. Epub 2010 Sep 14.</mixed-citation></citation-alternatives></ref><ref id="cit73"><label>73</label><citation-alternatives><mixed-citation xml:lang="ru">Markun LC, Starr PA, Air EL, et al. Shorter disease duration correlates with improved longterm deep brain stimulation outcomes in youngonset DYT1 dystonia. Neurosurgery. 2012 Aug; 71(2):325-30. doi: 10.1227/NEU.0b013e 318258e21b.</mixed-citation><mixed-citation xml:lang="en">Markun LC, Starr PA, Air EL, et al. Shorter disease duration correlates with improved longterm deep brain stimulation outcomes in youngonset DYT1 dystonia. Neurosurgery. 2012 Aug; 71(2):325-30. doi: 10.1227/NEU.0b013e 318258e21b.</mixed-citation></citation-alternatives></ref><ref id="cit74"><label>74</label><citation-alternatives><mixed-citation xml:lang="ru">Isaias IU, Volkmann J, Kupsch A, et al. Factors predicting protracted improvement after pallidal DBS for primary dystonia: the role of age and disease duration. J Neurol. 2011 Aug; 258(8):1469-76. doi: 10.1007/s00415-011-5961-9. Epub 2011 Mar 2.</mixed-citation><mixed-citation xml:lang="en">Isaias IU, Volkmann J, Kupsch A, et al. Factors predicting protracted improvement after pallidal DBS for primary dystonia: the role of age and disease duration. J Neurol. 2011 Aug; 258(8):1469-76. doi: 10.1007/s00415-011-5961-9. Epub 2011 Mar 2.</mixed-citation></citation-alternatives></ref><ref id="cit75"><label>75</label><citation-alternatives><mixed-citation xml:lang="ru">Tagliati M, Krack P, Volkmann J, et al. Long-Term management of DBS in dystonia: response to stimulation, adverse events, battery changes, and special considerations. Mov Disord. 2011 Jun;26 Suppl 1:S54-62. doi: 10.1002/mds. 23535.</mixed-citation><mixed-citation xml:lang="en">Tagliati M, Krack P, Volkmann J, et al. Long-Term management of DBS in dystonia: response to stimulation, adverse events, battery changes, and special considerations. Mov Disord. 2011 Jun;26 Suppl 1:S54-62. doi: 10.1002/mds. 23535.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
