<?xml version="1.0"?>
<Articles JournalTitle="Current Journal of Neurology">
  <Article>
    <Journal>
      <PublisherName>Tehran University of Medical Sciences</PublisherName>
      <JournalTitle>Current Journal of Neurology</JournalTitle>
      <Issn>2717-011X</Issn>
      <Volume>11</Volume>
      <Issue>1</Issue>
      <PubDate PubStatus="epublish">
        <Year>2012</Year>
        <Month>03</Month>
        <Day>15</Day>
      </PubDate>
    </Journal>
    <title locale="en_US">Amyotrophic lateral sclerosis with laboratory abnormalities of uncertain significance: A brief review.</title>
    <FirstPage>25</FirstPage>
    <LastPage>27</LastPage>
    <AuthorList>
      <Author>
        <FirstName>Majid</FirstName>
        <LastName>Ghasemi</LastName>
        <affiliation locale="en_US">Department of Neurology, Isfahan Neuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran.</affiliation>
      </Author>
      <Author>
        <FirstName>Farzad</FirstName>
        <LastName>Fatehi</LastName>
        <affiliation locale="en_US">Department of Neurology, Shariati Hospital, Iranian Center of Neurological Research, Tehran University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Bahador</FirstName>
        <LastName>Asadi</LastName>
        <affiliation locale="en_US">AJA University of Medical Sciences, Tehran, Iran</affiliation>
      </Author>
      <Author>
        <FirstName>Fariborz</FirstName>
        <LastName>Khorvash</LastName>
        <affiliation locale="en_US">Department of Neurology, Isfahan Neuroscience Research Center, Isfahan University of Medical Sciences, Isfahan, Iran</affiliation>
      </Author>
    </AuthorList>
    <History>
      <PubDate PubStatus="received">
        <Year>2015</Year>
        <Month>10</Month>
        <Day>17</Day>
      </PubDate>
    </History>
    <abstract locale="en_US">Amyotrophic lateral sclerosis (ALS), the most common form of motor neuron disease, is a progressive and devastating disease involving both lower and upper motor neurons, typically following a relentless progression towards death. Therefore, all efforts must be made by the clinician to exclude alternative and more treatable entities. ALS with laboratory abnormalities of uncertain significance is a subgroup of ALS that occurs in association with laboratory defined abnormalities that are of uncertain significance to the pathogenesis of ALS. The clinical utility of these abnormalities and what they ultimately mean in patients with ALS is discussed here, along with a review of the literature.</abstract>
    <web_url>https://ijnl.tums.ac.ir/index.php/ijnl/article/view/836</web_url>
    <pdf_url>https://ijnl.tums.ac.ir/index.php/ijnl/article/download/836/101</pdf_url>
  </Article>
</Articles>
