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	<title>Cure CMD &#187; News from Other Sources</title>
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	<description>Cure CMD provides Congenital Muscular Dystrophy resources, information, and support to families, doctors, and researchers.</description>
	<lastBuildDate>Thu, 17 May 2012 18:35:53 +0000</lastBuildDate>
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		<title>Neuralstem Seeks to Expand Stem Cell Trial</title>
		<link>http://alsn.mda.org/news/neuralstem-seeks-expand-stem-cell-trial</link>
		<comments>http://alsn.mda.org/news/neuralstem-seeks-expand-stem-cell-trial#comments</comments>
		<pubDate>Thu, 17 May 2012 18:35:53 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News from Other Sources]]></category>

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		<description><![CDATA[Neuralstem is seeking permission to evaluate efficacy in its phase 1 safety trial, as well as to increase the dosage and number of trial participants]]></description>
			<content:encoded><![CDATA[Neuralstem is seeking permission to evaluate efficacy in its phase 1 safety trial, as well as to increase the dosage and number of trial participants]]></content:encoded>
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		<title>SMA Research Briefs: New Gene ID&#8217;d; Disease Modifier Explored</title>
		<link>http://quest.mda.org/news/sma-research-briefs-new-gene-id-disease-modifier-explored</link>
		<comments>http://quest.mda.org/news/sma-research-briefs-new-gene-id-disease-modifier-explored#comments</comments>
		<pubDate>Tue, 15 May 2012 22:25:49 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News from Other Sources]]></category>

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		<description><![CDATA[Mutations in the DYNC1H1 gene cause a rare form of spinal muscular atrophy; plastin 3 contributes to movement problems in SMN-related SMA]]></description>
			<content:encoded><![CDATA[Mutations in the DYNC1H1 gene cause a rare form of spinal muscular atrophy; plastin 3 contributes to movement problems in SMN-related SMA]]></content:encoded>
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		<title>MMD1: &#8216;Invasive&#8217; Approach to Cardiac Management Improved Survival</title>
		<link>http://quest.mda.org/news/mmd1-invasive-approach-cardiac-improved-survival</link>
		<comments>http://quest.mda.org/news/mmd1-invasive-approach-cardiac-improved-survival#comments</comments>
		<pubDate>Tue, 15 May 2012 02:22:37 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News from Other Sources]]></category>

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		<description><![CDATA[Adults with MMD1 and minor cardiac conduction defects benefit from invasive testing and possible pacemaker insertion.]]></description>
			<content:encoded><![CDATA[Adults with MMD1 and minor cardiac conduction defects benefit from invasive testing and possible pacemaker insertion.]]></content:encoded>
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		<title>Decision Making About PGD Is Complex, Study Finds</title>
		<link>http://quest.mda.org/news/decision-making-about-pgd-complex</link>
		<comments>http://quest.mda.org/news/decision-making-about-pgd-complex#comments</comments>
		<pubDate>Mon, 14 May 2012 18:21:26 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News from Other Sources]]></category>

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		<description><![CDATA[A study of 22 couples considering preimplantation genetic diagnosis (PGD) has revealed a four-phase decision-making process]]></description>
			<content:encoded><![CDATA[A study of 22 couples considering preimplantation genetic diagnosis (PGD) has revealed a four-phase decision-making process]]></content:encoded>
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		<title>2012 AAN Meeting: Limb-Girdle MD, Distal MD Briefs</title>
		<link>http://quest.mda.org/news/2012-aan-meeting-lgmd-distal-md-briefs</link>
		<comments>http://quest.mda.org/news/2012-aan-meeting-lgmd-distal-md-briefs#comments</comments>
		<pubDate>Wed, 09 May 2012 22:01:26 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News from Other Sources]]></category>

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		<description><![CDATA[Findings about ANO5 mutations, DNAJB6 mutations and dysferlin gene transfer were presented]]></description>
			<content:encoded><![CDATA[Findings about ANO5 mutations, DNAJB6 mutations and dysferlin gene transfer were presented]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<title>Press Release: MDA-Supported Scientists Identify New &#8216;Switch&#8217; That Could Lead to Treatment for FSH Muscular Dystrophy</title>
		<link>http://www.mda.org/research/120507-MDA-Supported-Scientists-FSH.html</link>
		<comments>http://www.mda.org/research/120507-MDA-Supported-Scientists-FSH.html#comments</comments>
		<pubDate>Tue, 08 May 2012 21:58:26 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News from Other Sources]]></category>

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		<description><![CDATA[The Muscular Dystrophy Association announced today that an MDA-supported research team in Italy and Japan has identified a promising new target at which to aim experimental therapies to treat facioscapulohumeral muscular dystrophy (FSHD).]]></description>
			<content:encoded><![CDATA[The Muscular Dystrophy Association announced today that an MDA-supported research team in Italy and Japan has identified a promising new target at which to aim experimental therapies to treat facioscapulohumeral muscular dystrophy (FSHD).]]></content:encoded>
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		<title>&#8216;Turning Off the Switch&#8217; May Provide New FSHD Strategy</title>
		<link>http://quest.mda.org/news/turning-switch-may-provide-new-fshd-strategy</link>
		<comments>http://quest.mda.org/news/turning-switch-may-provide-new-fshd-strategy#comments</comments>
		<pubDate>Mon, 07 May 2012 17:47:45 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News from Other Sources]]></category>

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		<description><![CDATA[Researchers have identified a molecular switch that appears to lead to harmful gene activation in facioscapulohumeral MD.]]></description>
			<content:encoded><![CDATA[Researchers have identified a molecular switch that appears to lead to harmful gene activation in facioscapulohumeral MD.]]></content:encoded>
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		<title>Research Briefs: New Tools for CMT</title>
		<link>http://quest.mda.org/news/research-briefs-new-tools-cmt</link>
		<comments>http://quest.mda.org/news/research-briefs-new-tools-cmt#comments</comments>
		<pubDate>Fri, 04 May 2012 17:36:29 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News from Other Sources]]></category>

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		<description><![CDATA[Recent developments in Charcot-Marie-Tooth disease include CMT2E research mice, CMT1A stem cells, progress toward CMT1A gene therapy and a new pediatric disability scale.]]></description>
			<content:encoded><![CDATA[Recent developments in Charcot-Marie-Tooth disease include CMT2E research mice, CMT1A stem cells, progress toward CMT1A gene therapy and a new pediatric disability scale.]]></content:encoded>
			<wfw:commentRss>http://curecmd.org/archives/5409/feed</wfw:commentRss>
		<slash:comments>0</slash:comments>
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		<item>
		<title>2012 AAN Meeting: Myasthenia Gravis Briefs</title>
		<link>http://quest.mda.org/news/2012-aan-meeting-myasthenia-gravis-briefs</link>
		<comments>http://quest.mda.org/news/2012-aan-meeting-myasthenia-gravis-briefs#comments</comments>
		<pubDate>Thu, 03 May 2012 21:21:15 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News from Other Sources]]></category>

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		<description><![CDATA[Encouraging findings about eculizumab and GM-CSF were presented]]></description>
			<content:encoded><![CDATA[Encouraging findings about eculizumab and GM-CSF were presented]]></content:encoded>
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		<slash:comments>0</slash:comments>
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		<item>
		<title>MDA Funds Development of Gentler Glucocorticoid for DMD</title>
		<link>http://quest.mda.org/news/mda-funds-gentler-glucocorticoid-dmd</link>
		<comments>http://quest.mda.org/news/mda-funds-gentler-glucocorticoid-dmd#comments</comments>
		<pubDate>Thu, 03 May 2012 21:21:14 +0000</pubDate>
		<dc:creator>admin</dc:creator>
				<category><![CDATA[News from Other Sources]]></category>

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		<description><![CDATA[MDA has awarded $1.5 million to ReveraGen BioPharma to develop a drug with the benefits of prednisone, but without the side effects, for Duchenne MD.]]></description>
			<content:encoded><![CDATA[MDA has awarded $1.5 million to ReveraGen BioPharma to develop a drug with the benefits of prednisone, but without the side effects, for Duchenne MD.]]></content:encoded>
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