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	<title>Niemann-Pick Children&#039;s Fund, Inc &#187; Zevesca</title>
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		<title>New therapies &#8211; Niemann-Pick type C disease</title>
		<link>http://www.npcfund.org/2009/11/new-therapies-niemann-pick-type-c-disease/</link>
		<comments>http://www.npcfund.org/2009/11/new-therapies-niemann-pick-type-c-disease/#comments</comments>
		<pubDate>Sat, 21 Nov 2009 16:13:37 +0000</pubDate>
		<dc:creator>Michael G Stults</dc:creator>
				<category><![CDATA[Blog]]></category>
		<category><![CDATA[News]]></category>
		<category><![CDATA[Therapies]]></category>
		<category><![CDATA[What is NPC]]></category>
		<category><![CDATA[Jackie Imrie]]></category>
		<category><![CDATA[James E Wraith]]></category>
		<category><![CDATA[Manchester]]></category>
		<category><![CDATA[Miglustat]]></category>
		<category><![CDATA[Niemann-Pick Type C Disease]]></category>
		<category><![CDATA[NP-C]]></category>
		<category><![CDATA[NPC]]></category>
		<category><![CDATA[Research]]></category>
		<category><![CDATA[Royal Manchester Children’s Hospital]]></category>
		<category><![CDATA[UK]]></category>
		<category><![CDATA[Willink Biochemical Genetics Unit]]></category>
		<category><![CDATA[Zevesca]]></category>

		<guid isPermaLink="false">http://www.npcfund.org/?p=180</guid>
		<description><![CDATA[Abstract: Niemann-Pick disease type C (NP-C) is an autosomal recessive disorder characterized by progressive neurological deterioration leading to premature death. ]]></description>
			<content:encoded><![CDATA[<p><strong>New therapies in the management of Niemann-Pick type C disease: clinical utility of miglustat</strong></p>
<p><span style="color: #000000;"><a title="New therapies in the management of Niemann-Pick type C disease: clinical utility of miglustat" href="http://www.dovepress.com/new-therapies-in-the-management-of-niemann-pick-type-c-disease-clinica-peer-reviewed-article-TCRM" target="_blank">Authors: James E Wraith, Jackie Imrie<br />
Published Date November 2009 </a></span></p>
<p><em><span style="color: #000000;">James E Wraith, Jackie Imrie</span></em></p>
<p><em><span style="color: #000000;">Willink Biochemical Genetics Unit, Royal Manchester Children’s Hospital, Manchester, UK</span></em></p>
<p><span style="color: #000000;">Abstract: Niemann-Pick disease type C (NP-C) is an autosomal recessive disorder characterized by progressive neurological deterioration leading to premature death. The disease is caused by mutations in one of two genes, NPC1 or NPC2, leading to impaired intracellular lipid transport and build-up of lipids in various tissues, particularly the brain.</span></p>
<p><span style="color: #000000;"><strong><a title="New therapies in the management of Niemann-Pick type C disease: clinical utility of miglustat" href="http://www.dovepress.com/new-therapies-in-the-management-of-niemann-pick-type-c-disease-clinica-peer-reviewed-article-TCRM" target="_blank">Read the full abstract here.</a></strong></span></p>
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<p><span style="color: #000000;"><em>*This post does not reflect the views and opinions of Niemann-Pick Children’s Fund, Inc. This article is for informational purposes only. The sole credit of this article belongs to the author/website listed above.</em></span></p>


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