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	<id>https://teaching.ncl.ac.uk/bms/wiki//api.php?action=feedcontributions&amp;feedformat=atom&amp;user=100474439</id>
	<title>The School of Biomedical Sciences Wiki - User contributions [en]</title>
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	<updated>2026-04-17T16:25:51Z</updated>
	<subtitle>User contributions</subtitle>
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	<entry>
		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Insomnia&amp;diff=2377</id>
		<title>Insomnia</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Insomnia&amp;diff=2377"/>
		<updated>2011-01-09T15:23:54Z</updated>

		<summary type="html">&lt;p&gt;100474439: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Insomia is having a difficulty&amp;amp;nbsp;with falling or staying asleep. It is more common in women &amp;lt;ref&amp;gt;NHS - http://www.nhs.uk/conditions/insomnia/Pages/Introduction.aspx (Last reviewed: 11/09/2009)&amp;lt;/ref&amp;gt;.Insomnia can occur if a patient is worried or [http://en.wikipedia.org/wiki/Stress_%28biology%29 stressed], it can lead to daytime tiredness which can cause poor performances at work.&amp;amp;nbsp;A self help measure for trying to avoid Insomnia is to not take naps during the day &amp;lt;ref&amp;gt;http://www.bbc.co.uk/health/physical_health/conditions/insomnia1.shtml&amp;lt;/ref&amp;gt;&amp;lt;ref&amp;gt;http://hcd2.bupa.co.uk/fact_sheets/html/insomnia.html#3&amp;lt;/ref&amp;gt;. &amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
=== Fatal Familial Insomnia  ===&lt;br /&gt;
&lt;br /&gt;
Fatal Familial Insomnia (FFI) is an extremely rare and devastating condition. As suggested by it&#039;s name, FFI is a hereditary disease caused by a mutation in the protein [[Prions|prion]] gene&amp;amp;nbsp;&amp;lt;ref name=&amp;quot;A deadly prion disease: fatal familial insomnia.&amp;quot;&amp;gt;http://www.ncbi.nlm.nih.gov/pubmed/14713095&amp;lt;/ref&amp;gt; and although the onset of the disease is generally around middle age; once symptoms appear death usually occurs within one year.&amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
Symptoms include&amp;amp;nbsp;&amp;lt;ref name=&amp;quot;Early age of onset in fatal familial insomnia. Two novel cases and review of the literature.&amp;quot;&amp;gt;http://www.ncbi.nlm.nih.gov/pubmed/15311348&amp;lt;/ref&amp;gt;: &lt;br /&gt;
&lt;br /&gt;
*Progressive Insomnia &lt;br /&gt;
*Dysautonomia &lt;br /&gt;
*Cognitive Decline &lt;br /&gt;
*Loss&amp;amp;nbsp;of Motor Skills&lt;br /&gt;
&lt;br /&gt;
=== References:  ===&lt;br /&gt;
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&amp;lt;references /&amp;gt;&lt;br /&gt;
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&amp;lt;br&amp;gt;&lt;/div&gt;</summary>
		<author><name>100474439</name></author>
	</entry>
	<entry>
		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Prions&amp;diff=2374</id>
		<title>Prions</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Prions&amp;diff=2374"/>
		<updated>2011-01-09T15:18:12Z</updated>

		<summary type="html">&lt;p&gt;100474439: &lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Not all infectious diseases are transmitted by bacteria or [[Virus|viruses]].&amp;amp;nbsp;Some neurological diseases, such as [[Creutzfeldt-Jaakob disease (CJD)|Creutzfeldt-Jaakob disease (CJD)]]&amp;amp;nbsp;or mad cow disease are in fact caused by agents called &#039;&#039;&#039;Prions, &#039;&#039;&#039;which are of similar size to viruses but are made up of only [[Protein|protein]] &amp;lt;ref name=&amp;quot;null&amp;quot;&amp;gt;J. M. Berg et. al (2007) p 53, Biochemistry, Sixth edition, New York, W.H. Freeman and Company&amp;lt;/ref&amp;gt;&amp;amp;nbsp; &lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Prions &#039;&#039;&#039;have these characteristics: &lt;br /&gt;
&lt;br /&gt;
1.) &amp;quot;The transmissible agent consists of aggregated forms of a specific protein&amp;quot; &amp;lt;ref&amp;gt;J. M. Berg et. al (2007) p 53, Biochemistry, Sixth edition, New York, W.H. Freeman and Company&amp;lt;/ref&amp;gt; &lt;br /&gt;
&lt;br /&gt;
2.) These protein aggregates cannot be degraded by the agents that degrade most other proteins &amp;lt;ref&amp;gt;J. M. Berg et. al (2007) p 53, Biochemistry, Sixth edition, New York, W.H. Freeman and Company&amp;lt;/ref&amp;gt; &lt;br /&gt;
&lt;br /&gt;
3.) &amp;quot;The protein is largely or completely derived from a cellular protein called PrP, that is normally present in the brain&amp;quot; &amp;lt;ref&amp;gt;J. M. Berg et. al (2007) p 53, Biochemistry, Sixth edition, New York, W.H. Freeman and Company&amp;lt;/ref&amp;gt; &lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
So an aggregated form of a protein (that is already present in the brain) is the infectious agent in prion diseases &amp;lt;ref name=&amp;quot;null&amp;quot;&amp;gt;J. M. Berg et. al (2007) p 54, Biochemistry, Sixth edition, New York, W.H. Freeman and Company&amp;lt;/ref&amp;gt; &lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&amp;lt;br&amp;gt;&lt;br /&gt;
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== References  ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;references /&amp;gt;&lt;/div&gt;</summary>
		<author><name>100474439</name></author>
	</entry>
	<entry>
		<id>https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Prions&amp;diff=2373</id>
		<title>Prions</title>
		<link rel="alternate" type="text/html" href="https://teaching.ncl.ac.uk/bms/wiki//index.php?title=Prions&amp;diff=2373"/>
		<updated>2011-01-09T15:17:07Z</updated>

		<summary type="html">&lt;p&gt;100474439: Created page with &amp;#039;Not all infectious diseases are transmitted by bacteria or viruses.&amp;amp;nbsp;Some neurological diseases, such as [[Creutzfeldt-Jaakob disease (CJD) |Creutzfeldt-Jaakob dise…&amp;#039;&lt;/p&gt;
&lt;hr /&gt;
&lt;div&gt;Not all infectious diseases are transmitted by bacteria or [[virus|viruses]].&amp;amp;nbsp;Some neurological diseases, such as [[Creutzfeldt-Jaakob disease (CJD) |Creutzfeldt-Jaakob disease (CJD) ]]or mad cow disease are in fact caused by agents called &#039;&#039;&#039;Prions, &#039;&#039;&#039;which are of similar size to viruses but are made up of only [[Protein|protein]] &amp;lt;ref name=&amp;quot;null&amp;quot;&amp;gt;J. M. Berg et. al (2007) p 53, Biochemistry, Sixth edition, New York, W.H. Freeman and Company&amp;lt;/ref&amp;gt;&amp;amp;nbsp;&lt;br /&gt;
&lt;br /&gt;
&#039;&#039;&#039;Prions &#039;&#039;&#039;have these characteristics:&lt;br /&gt;
&lt;br /&gt;
1.) &amp;quot;The transmissible agent consists of aggregated forms of a specific protein&amp;quot; &amp;lt;ref&amp;gt;J. M. Berg et. al (2007) p 53, Biochemistry, Sixth edition, New York, W.H. Freeman and Company&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
2.) These protein aggregates cannot be degraded by the agents that degrade most other proteins &amp;lt;ref&amp;gt;J. M. Berg et. al (2007) p 53, Biochemistry, Sixth edition, New York, W.H. Freeman and Company&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
3.) &amp;quot;The protein is largely or completely derived from a cellular protein called PrP, that is normally present in the brain&amp;quot; &amp;lt;ref&amp;gt;J. M. Berg et. al (2007) p 53, Biochemistry, Sixth edition, New York, W.H. Freeman and Company&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
So an aggregated form of a protein (that is already present in the brain) is the infectious agent in prion diseases &amp;lt;ref name=&amp;quot;null&amp;quot;&amp;gt;J. M. Berg et. al (2007) p 54, Biochemistry, Sixth edition, New York, W.H. Freeman and Company&amp;lt;/ref&amp;gt;&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
&lt;br /&gt;
== References ==&lt;br /&gt;
&lt;br /&gt;
&amp;lt;references /&amp;gt;&lt;/div&gt;</summary>
		<author><name>100474439</name></author>
	</entry>
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