<?xml version="1.0" encoding="utf-8"?>
<!DOCTYPE article PUBLIC "-//NLM//DTD JATS (Z39.96) Journal Publishing DTD v1.0 20120330//EN" "JATS-journalpublishing1.dtd">
<article article-type="research-article" dtd-version="1.0" xml:lang="en" 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 journal-id-type="publisher-id">kjcn</journal-id>
<journal-title-group>
<journal-title>Korean Journal of Community Nutrition</journal-title>
<abbrev-journal-title>Korean J Community Nutr</abbrev-journal-title>
</journal-title-group>
<issn pub-type="ppub">1226-0983</issn>
<issn pub-type="epub">2287-1624</issn>
<publisher>
<publisher-name>Journal of the Korean Society of Community Nutrition</publisher-name>
</publisher>
</journal-meta>
<article-meta>
<article-id pub-id-type="doi">10.14253/KJCN.2015.17.1.38</article-id>
<article-id pub-id-type="publisher-id">kjcn-17-38</article-id>
<article-categories>
<subj-group subj-group-type="heading">
<subject>Original Article</subject>
</subj-group>
</article-categories>
<title-group>
<article-title>The Abnormalities in Neuro-Imaging and Somatosensory Evoked Potentials in Hirayama Disease</article-title>
</title-group>
<contrib-group>
<contrib contrib-type="author">
<name name-style="western" xml:lang="en">
<surname>Park</surname><given-names>Jin-Sung</given-names></name>
<xref ref-type="corresp" rid="c1-kjcn-17-38"/>
<xref ref-type="aff" rid="aff1-kjcn-17-38"><sup>1</sup></xref>
</contrib>
<contrib contrib-type="author">
<name name-style="western" xml:lang="en">
<surname>Lee</surname><given-names>Sang-Hoon</given-names></name>
<xref ref-type="corresp" rid="c1-kjcn-17-38"/>
<xref ref-type="aff" rid="aff2-kjcn-17-38"><sup>2</sup></xref>
</contrib>
<aff id="aff1-kjcn-17-38" xml:lang="en"><label>1</label>Department of Neurology, Kyungpook National University School of Medicine, Daegu, <country>Korea</country></aff>
<aff id="aff2-kjcn-17-38" xml:lang="en"><label>2</label>Department of Radiology, Kyungpook National University Medical Center, Daegu, <country>Korea</country></aff>
</contrib-group>
<author-notes>
<corresp id="c1-kjcn-17-38">Address for correspondence; Jin-Sung Park Department of Neurology, Kyungpook National University Hospital, 680 Gukchaebosang-ro, Jung-gu, Daegu 700-842, Korea Tel: +82-53-200-2753 Fax: +82-53-200-2168 E-mail: <email>jinforeva@gmail.com</email></corresp>
</author-notes>
<pub-date pub-type="ppub"><month>12</month><year>2015</year></pub-date>
<pub-date pub-type="epub"><day>18</day><month>12</month><year>2015</year></pub-date>
<volume>17</volume><issue>1</issue>
<fpage>38</fpage><lpage>40</lpage>
<history>
<date date-type="received"><day>12</day><month>11</month><year>2014</year></date>
<date date-type="rev-recd"><day>06</day><month>02</month><year>2015</year></date>
<date date-type="accepted"><day>26</day><month>02</month><year>2015</year></date>
</history>
<permissions>
<copyright-statement>Copyright &#x00A9; 2015 Journal of the Korean Society of Community Nutrition</copyright-statement>
<copyright-year>2015</copyright-year>
<license><license-p>This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (<ext-link ext-link-type="uri" xlink:href="http://creativecommons.org/licenses/by-nc/3.0/">http://creativecommons.org/licenses/by-nc/3.0/</ext-link>) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.</license-p></license>
</permissions>
<kwd-group xml:lang="en">
<kwd>Hirayama disease</kwd>
<kwd>Magnetic resonance imaging</kwd>
<kwd>Evoked potentials</kwd>
</kwd-group>
</article-meta>
</front>
<back>
<ref-list xml:lang="en">
<title>REFERENCES</title>
<ref id="b1"><element-citation publication-type="journal"><label>1.</label><person-group person-group-type="author"><name><surname>Tashiro</surname> <given-names>K</given-names></name> <name><surname>Kikuchi</surname> <given-names>S</given-names></name> <name><surname>Itoyama</surname> <given-names>Y</given-names></name> <name><surname>Tokumaru</surname> <given-names>Y</given-names></name> <name><surname>Sobue</surname> <given-names>G</given-names></name> <name><surname>Akiguchi</surname> <given-names>I</given-names></name> <etal/></person-group> <article-title>Nationwide survey of juvenile muscular atrophy of distal upper extremity (Hirayama disease) in Japan</article-title> <source>Amyotroph Lateral Scler</source> <year>2006</year><volume>7</volume> <fpage>38</fpage><lpage>45</lpage></element-citation></ref>
<ref id="b2"><element-citation publication-type="journal"><label>2.</label><person-group person-group-type="author"><name><surname>Zhou</surname> <given-names>B</given-names></name> <name><surname>Chen</surname> <given-names>L</given-names></name> <name><surname>Fan</surname> <given-names>D</given-names></name> <name><surname>Zhou</surname> <given-names>D</given-names></name></person-group> <article-title>Clinical features of Hirayama disease in mainland China</article-title> <source>Amyotroph Lateral Scler</source> <year>2010</year><volume>11</volume> <fpage>133</fpage><lpage>139</lpage></element-citation></ref>
<ref id="b3"><element-citation publication-type="journal"><label>3.</label><person-group person-group-type="author"><name><surname>Sonwalkar</surname> <given-names>HA</given-names></name> <name><surname>Shah</surname> <given-names>RS</given-names></name> <name><surname>Khan</surname> <given-names>FK</given-names></name> <name><surname>Gupta</surname> <given-names>AK</given-names></name> <name><surname>Bodhey</surname> <given-names>NK</given-names></name> <name><surname>Vottath</surname> <given-names>S</given-names></name> <etal/></person-group> <article-title>Imaging features in Hirayama disease</article-title> <source>Neurol India</source> <year>2008</year><volume>56</volume> <fpage>22</fpage><lpage>26</lpage></element-citation></ref>
<ref id="b4"><element-citation publication-type="journal"><label>4.</label><person-group person-group-type="author"><name><surname>Hassan</surname> <given-names>KM</given-names></name> <name><surname>Sahni</surname> <given-names>H</given-names></name> <name><surname>Jha</surname> <given-names>A</given-names></name></person-group> <article-title>Clinical and radiological profile of hirayama disease: a flexion myelopathy due to tight cervical dural canal amenable to collar therapy</article-title> <source>Ann Indian Acad Neurol</source> <year>2012</year><volume>15</volume> <fpage>106</fpage><lpage>112</lpage></element-citation></ref>
<ref id="b5"><element-citation publication-type="journal"><label>5.</label><person-group person-group-type="author"><name><surname>Yin</surname> <given-names>B</given-names></name> <name><surname>Liu</surname> <given-names>L</given-names></name> <name><surname>Geng</surname> <given-names>DY</given-names></name></person-group> <article-title>Features of Hirayama disease on fully flexed position cervical MRI</article-title> <source>J Int Med Res</source> <year>2011</year><volume>39</volume> <fpage>222</fpage><lpage>228</lpage></element-citation></ref>
<ref id="b6"><element-citation publication-type="journal"><label>6.</label><person-group person-group-type="author"><name><surname>Finsterer</surname> <given-names>J</given-names></name> <name><surname>Loscher</surname> <given-names>W</given-names></name> <name><surname>Wanschitz</surname> <given-names>J</given-names></name> <name><surname>Baumann</surname> <given-names>M</given-names></name> <name><surname>Quasthoff</surname> <given-names>S</given-names></name> <name><surname>Grisold</surname> <given-names>W</given-names></name></person-group> <article-title>Hirayama disease in Austria</article-title> <source>Joint Bone Spine</source> <year>2013</year><volume>80</volume> <fpage>503</fpage><lpage>507</lpage></element-citation></ref>
<ref id="b7"><element-citation publication-type="journal"><label>7.</label><person-group person-group-type="author"><name><surname>Wang</surname> <given-names>XN</given-names></name> <name><surname>Cui</surname> <given-names>LY</given-names></name> <name><surname>Liu</surname> <given-names>MS</given-names></name> <name><surname>Guan</surname> <given-names>YZ</given-names></name> <name><surname>Li</surname> <given-names>BH</given-names></name> <name><surname>DU</surname> <given-names>H</given-names></name></person-group> <article-title>A Clinical neurophysiology study of Hirayama disease</article-title> <source>Chin Med J (Engl)</source> <year>2012</year><volume>125</volume> <fpage>1115</fpage><lpage>1120</lpage></element-citation></ref>
</ref-list>
<sec sec-type="display-objects">
<title>Figures</title>
<fig id="f1-kjcn-17-38" position="float">
<label>Fig. 1.</label>
<caption xml:lang="en"><p>Cervical magnetic resonance imaging (MRI) and right median somatosensory evoked potentials (SEP) of the patient. The T2 weighted MRI with neck in neutral position was unremarkable while T2 weighted MRI with neck in flexion shows anterior displacement of the posterior dural sac (A, B). The reversible inter-peak latency between N13 and N19 on supine (5.5 ms) (C) and flexed (7.45 ms) (D) somatosensory evoked potentials (SEP) in the symptomatic side also support the diagnosis of Hirayama disease. (Normal SEP interpeak latency &#x003C; 6.59 ms).</p></caption>
<graphic xlink:href="kjcn-17-38f1.tif"/>
</fig>
</sec>
</back>
</article>