<?xml version="1.0" encoding="ISO-8859-1"?><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">
<front>
<journal-meta>
<journal-id>2393-6797</journal-id>
<journal-title><![CDATA[Revista Uruguaya de Medicina Interna ]]></journal-title>
<abbrev-journal-title><![CDATA[Rev. Urug. Med. Int.]]></abbrev-journal-title>
<issn>2393-6797</issn>
<publisher>
<publisher-name><![CDATA[Sociedad de Medicina Interna del Uruguay]]></publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id>S2393-67972017000200043</article-id>
<title-group>
<article-title xml:lang="es"><![CDATA[Estudio de las ataxias esporádicas de comienzo en el adulto en el Hospital de Clínicas de Montevideo - Uruguay]]></article-title>
<article-title xml:lang="en"><![CDATA[Study of sporadic ataxias of adult onset in Hospital de Clínicas de Montevideo - Uruguay]]></article-title>
<article-title xml:lang="pt"><![CDATA[Estudo de ataxias esporádicas de aparecimento de adultos no Hospital de Clínicas de Montevidéu - Uruguai]]></article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Urban]]></surname>
<given-names><![CDATA[Luis]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Higgie]]></surname>
<given-names><![CDATA[Juan]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Rozada]]></surname>
<given-names><![CDATA[Raúl]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Hackembruch]]></surname>
<given-names><![CDATA[H. Jochen]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
<contrib contrib-type="author">
<name>
<surname><![CDATA[Gaye]]></surname>
<given-names><![CDATA[Andrés]]></given-names>
</name>
<xref ref-type="aff" rid="Aff"/>
</contrib>
</contrib-group>
<aff id="Af1">
<institution><![CDATA[,Universidad de la República Hospital de Clínicas. Instituto de Neurología.]]></institution>
<addr-line><![CDATA[Montevideo ]]></addr-line>
<country>Uruguay</country>
</aff>
<pub-date pub-type="pub">
<day>00</day>
<month>08</month>
<year>2017</year>
</pub-date>
<pub-date pub-type="epub">
<day>00</day>
<month>08</month>
<year>2017</year>
</pub-date>
<volume>2</volume>
<numero>2</numero>
<fpage>43</fpage>
<lpage>51</lpage>
<copyright-statement/>
<copyright-year/>
<self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_arttext&amp;pid=S2393-67972017000200043&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_abstract&amp;pid=S2393-67972017000200043&amp;lng=en&amp;nrm=iso"></self-uri><self-uri xlink:href="http://www.scielo.edu.uy/scielo.php?script=sci_pdf&amp;pid=S2393-67972017000200043&amp;lng=en&amp;nrm=iso"></self-uri><abstract abstract-type="short" xml:lang="es"><p><![CDATA[Resumen:  Introducción:  El diagnóstico etiológico de las ataxias esporádicas de comienzo en el adulto (AECA) es un desafío clínico pues sus causas posibles son múltiples. No existen en el país estudios a este respecto.  Objetivo: Describir las características clínicas, imagenológicas y etiológicas de los pacientes con AECA.  Métodos:  Estudio prospectivo observacional de los pacientes con AECA que consultaron en el Hospital de Clínicas de Montevideo desde abril de 2010 a marzo de 2014. Se realizó una evaluación clínico-paraclínica protocolizada para llegar al diagnóstico etiológico.  Resultados:  Se incluyeron 36 pacientes. En 20 de ellos se logró demostrar una etiología definida, siendo las más frecuentes la degeneración cerebelosa alcohólica y la paraneoplásica. La mayoría de los casos en quienes se instauró un tratamiento de dicha etiología lograron un cese de la progresión o mejoría de los síntomas.  Discusión y Conclusiones: El estudio protocolizado de los pacientes con AECA logra el diagnóstico etiológico en más de 50% de los casos. Aún así un 44% de los pacientes quedan sin etiología demostrada, principalmente por la incapacidad de acceder a estudios genéticos. Los factores que más se asocian a encontrar una etiología adquirida demostrada fueron: rápida progresión, síndrome vermiano puro y franca asimetría del cuadro.]]></p></abstract>
<abstract abstract-type="short" xml:lang="en"><p><![CDATA[Abstract:  Introduction:  Etiological diagnosis of Sporadic Ataxia of Adult Onset (SAAO) is a clinical challenge because its possible causes are multiple. There are no studies of SAAO in our country.  Objective:  To describe the clinical, imaging and etiological characteristics of patients with SAAO.  Methods:  Prospective observational study of patients with SAAO who consulted at Hospital de Clínicas de Montevideo from April 2010 to March 2014. A protocolized clinical-paraclinical evaluation was performed to reach the etiological diagnosis. Results: Thirty-six patients were included. In 20 of them an acquired definite etiology was demonstrated. The most frequent were alcoholic and paraneoplastic cerebellar degeneration . The majority of cases in which a treatment of this etiology was instituted resulted in a cessation of the progression or improvement of symptoms. Discussion and Conclusions: The protocolized study of patients with SAAO achieves the etiological diagnosis in more than 50% of the cases. Still, 44% of patients remained without proven etiology, mainly due to the inability to access genetic studies. The factors that are most associated with finding a proven acquired etiology were: rapid progression, pure vermis syndrome and frank asymmetry of symptoms.]]></p></abstract>
<abstract abstract-type="short" xml:lang="pt"><p><![CDATA[Resumo:  Introdução: O diagnóstico etiológico da ataxia esporádica do início do adulto (AECA) é um desafio clínico porque suas possíveis causas são múltiplas. Não há estudos neste país.  Objetivo:  Descrever as características clínicas, imagiológicas e etiológicas de pacientes com AECA.  Métodos:  estudo prospectivo observacional de pacientes com AECA que consultou no Hospital de Clínicas de Montevidéu de abril de 2010 a março de 2014. Foi realizada uma avaliação clínico-paraclínica para alcançar o diagnóstico etiológico.  Resultados:  Foram incluídos trinta e seis pacientes. Em 20 deles, foi possível demonstrar uma etiologia definida, sendo a mais frequente a degeneração cerebelar alcoólica e a degeneração paraneoplásica. A maioria dos casos em que o tratamento desta etiologia foi instituído resultou na cessação da progressão ou melhora dos sintomas.  Discussão e Conclusões:  O estudo protocolizado de pacientes com AECA atinge o diagnóstico etiológico em mais de 50% dos casos. Ainda assim, 44% dos pacientes estão sem etiologia comprovada, principalmente devido à incapacidade de acessar estudos genéticos. Os fatores mais associados com a obtenção de uma etiologia comprovada foram: progressão rápida, síndrome do vermimus puro e assimetria franca da condição.]]></p></abstract>
<kwd-group>
<kwd lng="es"><![CDATA[Ataxia]]></kwd>
<kwd lng="es"><![CDATA[Ataxia Esporádica de Comienzo en el Adulto]]></kwd>
<kwd lng="es"><![CDATA[Degeneración Cerebelosa]]></kwd>
<kwd lng="en"><![CDATA[Ataxia]]></kwd>
<kwd lng="en"><![CDATA[Sporadic Ataxia of Adult Onset]]></kwd>
<kwd lng="en"><![CDATA[Cerebellar Degeneration.]]></kwd>
<kwd lng="pt"><![CDATA[Ataxia]]></kwd>
<kwd lng="pt"><![CDATA[Ataxia Esporádica de Início do Adulto]]></kwd>
<kwd lng="pt"><![CDATA[Degeneração Cerebelar.]]></kwd>
</kwd-group>
</article-meta>
</front><back>
<ref-list>
<ref id="B1">
<label>1</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Klockgether]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Sporadic ataxia with adult onset: classification and diagnostic criteria]]></article-title>
<source><![CDATA[Lancet Neurol.]]></source>
<year>2010</year>
<volume>9</volume>
<page-range>94-104</page-range></nlm-citation>
</ref>
<ref id="B2">
<label>2</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Manto]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Marmolino]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Cerebellar ataxias]]></article-title>
<source><![CDATA[Curr Opin Neurol]]></source>
<year>2009</year>
<volume>22</volume>
<page-range>419-29</page-range></nlm-citation>
</ref>
<ref id="B3">
<label>3</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Barsottini]]></surname>
<given-names><![CDATA[OG]]></given-names>
</name>
<name>
<surname><![CDATA[Albuquerque]]></surname>
<given-names><![CDATA[MV]]></given-names>
</name>
<name>
<surname><![CDATA[Braga-Neto]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Pedroso]]></surname>
<given-names><![CDATA[JL]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Adult onset sporadic ataxias: a diagnostic challenge]]></article-title>
<source><![CDATA[Arq Neuropsiquiatr]]></source>
<year>2014</year>
<volume>72</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>232-40</page-range></nlm-citation>
</ref>
<ref id="B4">
<label>4</label><nlm-citation citation-type="book">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Klockgether]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Ataxias]]></article-title>
<person-group person-group-type="editor">
<name>
<surname><![CDATA[Goetz]]></surname>
<given-names><![CDATA[CG]]></given-names>
</name>
</person-group>
<source><![CDATA[Textbook of clinical neurology, vol 1]]></source>
<year>2007</year>
<page-range>741-57</page-range><publisher-loc><![CDATA[Toronto ]]></publisher-loc>
<publisher-name><![CDATA[Saunder]]></publisher-name>
</nlm-citation>
</ref>
<ref id="B5">
<label>5</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[de Bot]]></surname>
<given-names><![CDATA[ST]]></given-names>
</name>
<name>
<surname><![CDATA[Willemsen]]></surname>
<given-names><![CDATA[MA]]></given-names>
</name>
<name>
<surname><![CDATA[Vermeer]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Kremer]]></surname>
<given-names><![CDATA[HP]]></given-names>
</name>
<name>
<surname><![CDATA[van de Warrenburg]]></surname>
<given-names><![CDATA[BP]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Reviewing the genetic causes of spastic-ataxias]]></article-title>
<source><![CDATA[Neurology]]></source>
<year>2012</year>
<volume>79</volume>
<page-range>1507-14</page-range></nlm-citation>
</ref>
<ref id="B6">
<label>6</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Espinós-Armero]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[González-Cabo]]></surname>
<given-names><![CDATA[P]]></given-names>
</name>
<name>
<surname><![CDATA[Palau-Martínez]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Autosomal recessive cerebellar ataxias. Their classification, genetic features and pathophysiology]]></article-title>
<source><![CDATA[Rev Neurol]]></source>
<year>2005</year>
<volume>41</volume>
<numero>7</numero>
<issue>7</issue>
<page-range>409-22</page-range></nlm-citation>
</ref>
<ref id="B7">
<label>7</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Soto Lavastida]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Lara Fernández]]></surname>
<given-names><![CDATA[G]]></given-names>
</name>
<name>
<surname><![CDATA[Michel Esteban]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
<name>
<surname><![CDATA[Llibre Guerra]]></surname>
<given-names><![CDATA[JC]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Presentación de un caso clínico de atrofia multisistémica y actualización de criterios diagnósticos:A clinical case presentation]]></article-title>
<source><![CDATA[Rev cub med.]]></source>
<year>2011</year>
<volume>50</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>322-32</page-range></nlm-citation>
</ref>
<ref id="B8">
<label>8</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Graus]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Delattre]]></surname>
<given-names><![CDATA[JY]]></given-names>
</name>
<name>
<surname><![CDATA[Antoine]]></surname>
<given-names><![CDATA[JC]]></given-names>
</name>
<name>
<surname><![CDATA[Dalmau]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Giometto]]></surname>
<given-names><![CDATA[B]]></given-names>
</name>
<name>
<surname><![CDATA[Grisold]]></surname>
<given-names><![CDATA[W]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Recommended diagnostic criteria for paraneoplastic neurological syndromes]]></article-title>
<source><![CDATA[J Neurol Neurosurg Psychiatry]]></source>
<year>2004</year>
<volume>75</volume>
<numero>8</numero>
<issue>8</issue>
<page-range>1135-40</page-range></nlm-citation>
</ref>
<ref id="B9">
<label>9</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Chamorro]]></surname>
<given-names><![CDATA[FA]]></given-names>
</name>
<name>
<surname><![CDATA[Marcos]]></surname>
<given-names><![CDATA[MM]]></given-names>
</name>
<name>
<surname><![CDATA[Laso]]></surname>
<given-names><![CDATA[GF]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Wernicke encephalopathy in alcoholic patients]]></article-title>
<source><![CDATA[Rev clín esp.]]></source>
<year>2011</year>
</nlm-citation>
</ref>
<ref id="B10">
<label>10</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Caine]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
<name>
<surname><![CDATA[Halliday]]></surname>
<given-names><![CDATA[GM]]></given-names>
</name>
<name>
<surname><![CDATA[Kril]]></surname>
<given-names><![CDATA[JJ]]></given-names>
</name>
<name>
<surname><![CDATA[Harper]]></surname>
<given-names><![CDATA[CG]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Operational criteria for the classification of chronic alcoholics: identification of Wernicke&#8217;s encephalopathy]]></article-title>
<source><![CDATA[J Neurol Neurosurg Psychiatry]]></source>
<year>1997</year>
<volume>62</volume>
<numero>1</numero>
<issue>1</issue>
<page-range>51-60</page-range></nlm-citation>
</ref>
<ref id="B11">
<label>11</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Stabler]]></surname>
<given-names><![CDATA[SP]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Deficiencia de vitamina B12]]></article-title>
<source><![CDATA[N Engl J Med]]></source>
<year>2013</year>
<volume>368</volume>
<page-range>149-60</page-range></nlm-citation>
</ref>
<ref id="B12">
<label>12</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Bernal-Cano]]></surname>
<given-names><![CDATA[F]]></given-names>
</name>
<name>
<surname><![CDATA[Suárez]]></surname>
<given-names><![CDATA[J]]></given-names>
</name>
<name>
<surname><![CDATA[Meek]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Leucoencefalopatía multifocal progresiva en el contexto de un síndrome de reconstitución inmunológica inflamatoria]]></article-title>
<source><![CDATA[Acta neurol. colomb]]></source>
<year>2009</year>
<volume>25</volume>
<page-range>257-61</page-range></nlm-citation>
</ref>
<ref id="B13">
<label>13</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Lasso]]></surname>
<given-names><![CDATA[BM]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Diagnóstico y tratamiento de infecciones oportunistas en el paciente adulto con infección por VIH/SIDA]]></article-title>
<source><![CDATA[Rev chil infectol.]]></source>
<year>2011</year>
<volume>28</volume>
<numero>5</numero>
<issue>5</issue>
<page-range>440-60</page-range></nlm-citation>
</ref>
<ref id="B14">
<label>14</label><nlm-citation citation-type="">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Hadjivassiliou]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Sanders]]></surname>
<given-names><![CDATA[DS]]></given-names>
</name>
<name>
<surname><![CDATA[Grünewald]]></surname>
<given-names><![CDATA[RA]]></given-names>
</name>
<name>
<surname><![CDATA[Woodroofe]]></surname>
<given-names><![CDATA[N]]></given-names>
</name>
<name>
<surname><![CDATA[Boscolo]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Aeschlimann]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
</person-group>
<source><![CDATA[Lancet Neurol.]]></source>
<year>2010</year>
<volume>9</volume>
<numero>3</numero>
<issue>3</issue>
<page-range>318-30</page-range></nlm-citation>
</ref>
<ref id="B15">
<label>15</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Ojea Ortega]]></surname>
<given-names><![CDATA[T]]></given-names>
</name>
<name>
<surname><![CDATA[González Alvarez de Sotomayor]]></surname>
<given-names><![CDATA[MM]]></given-names>
</name>
<name>
<surname><![CDATA[Fernández Sánchez]]></surname>
<given-names><![CDATA[V]]></given-names>
</name>
<name>
<surname><![CDATA[Fernández Fernández]]></surname>
<given-names><![CDATA[O]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Demencias degenerativas de perfil atípico y tiroiditis de Hashimoto]]></article-title>
<source><![CDATA[Alzheimer. Real Invest Demenc]]></source>
<year>2010</year>
<volume>45</volume>
<page-range>4-15</page-range></nlm-citation>
</ref>
<ref id="B16">
<label>16</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Galdeano Mondragón]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Oliván Roldán]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Barbadillo Izquierdo]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Clínica psiquiátrica en la encefalopatía de Hashimoto]]></article-title>
<source><![CDATA[Arch Psiquiatr.]]></source>
<year>2010</year>
<volume>73</volume>
<page-range>7</page-range></nlm-citation>
</ref>
<ref id="B17">
<label>17</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Zerr]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
<name>
<surname><![CDATA[Kallenberg]]></surname>
<given-names><![CDATA[K]]></given-names>
</name>
<name>
<surname><![CDATA[Summers]]></surname>
<given-names><![CDATA[DM]]></given-names>
</name>
<name>
<surname><![CDATA[Romero]]></surname>
<given-names><![CDATA[C]]></given-names>
</name>
<name>
<surname><![CDATA[Taratuto]]></surname>
<given-names><![CDATA[A]]></given-names>
</name>
<name>
<surname><![CDATA[Heinemann]]></surname>
<given-names><![CDATA[U]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease]]></article-title>
<source><![CDATA[Brain]]></source>
<year>2009</year>
<volume>132</volume>
<numero>10</numero>
<issue>10</issue>
<page-range>2659-68</page-range></nlm-citation>
</ref>
<ref id="B18">
<label>18</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Santos]]></surname>
<given-names><![CDATA[S]]></given-names>
</name>
<name>
<surname><![CDATA[Pascual-Millán]]></surname>
<given-names><![CDATA[LF]]></given-names>
</name>
<name>
<surname><![CDATA[Escalza-Codina]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
<name>
<surname><![CDATA[Navas Vinagre]]></surname>
<given-names><![CDATA[I]]></given-names>
</name>
<name>
<surname><![CDATA[López del Val]]></surname>
<given-names><![CDATA[L]]></given-names>
</name>
<name>
<surname><![CDATA[Mostacero-Migeul]]></surname>
<given-names><![CDATA[E]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Progressive myoclonic cerebellar ataxia as a manifestation of Creutzfeldt-Jakob disease]]></article-title>
<source><![CDATA[Rev Neurol]]></source>
<year>2003</year>
<volume>37</volume>
<page-range>535-8</page-range></nlm-citation>
</ref>
<ref id="B19">
<label>19</label><nlm-citation citation-type="journal">
<person-group person-group-type="author">
<name>
<surname><![CDATA[Mocellin]]></surname>
<given-names><![CDATA[R]]></given-names>
</name>
<name>
<surname><![CDATA[Walterfang]]></surname>
<given-names><![CDATA[M]]></given-names>
</name>
<name>
<surname><![CDATA[Velakoulis]]></surname>
<given-names><![CDATA[D]]></given-names>
</name>
</person-group>
<article-title xml:lang=""><![CDATA[Hashimoto&#8217;s encephalopathy: epidemiology, pathogenesis and management]]></article-title>
<source><![CDATA[CNS Drugs]]></source>
<year>2007</year>
<volume>21</volume>
<numero>10</numero>
<issue>10</issue>
<page-range>799-811</page-range></nlm-citation>
</ref>
</ref-list>
</back>
</article>
