<?xml version="1.0" encoding="UTF-8"?>
<rss version="2.0"
	xmlns:content="http://purl.org/rss/1.0/modules/content/"
	xmlns:atom="http://www.w3.org/2005/Atom"
	xmlns:sy="http://purl.org/rss/1.0/modules/syndication/"
	xmlns:slash="http://purl.org/rss/1.0/modules/slash/"
	>

<channel>
	<title>Recash test site | Hildebrandt Pike | Activity</title>
	<link>https://recash.wpsoul.net/members/zipperplough5/activity/</link>
	<atom:link href="https://recash.wpsoul.net/members/zipperplough5/activity/feed/" rel="self" type="application/rss+xml" />
	<description>Activity feed for Hildebrandt Pike.</description>
	<lastBuildDate>Tue, 19 May 2026 03:00:09 +0000</lastBuildDate>
	<generator>https://buddypress.org/?v=</generator>
	<language>en-US</language>
	<ttl>30</ttl>
	<sy:updatePeriod>hourly</sy:updatePeriod>
	<sy:updateFrequency>2</sy:updateFrequency>
	
						<item>
				<guid isPermaLink="false">d987e1355fa7268f7ba04084a427fa32</guid>
				<title>Hildebrandt Pike posted an update: NLSDM is a rare metabolic myopathy caused by mutations in the [&#133;]</title>
				<link>https://recash.wpsoul.net/activity/p/52817/</link>
				<pubDate>Wed, 11 Dec 2024 17:10:13 +0000</pubDate>

									<content:encoded><![CDATA[<p>NLSDM is a rare metabolic myopathy caused by mutations in the patatin-like phosphatase domain protein 2 (PAPLA2) genes. In the present study, we describe the clinical and genetic findings in our Chinese patient with NLSDM. Sequence analysis of PNPLA2 gene was performed. Gene analysis for PNPLA2 revealed an identical homozygous mutation c.757+1G&gt;T&hellip;<span class="activity-read-more" id="activity-read-more-52817"><a href="https://recash.wpsoul.net/activity/p/52817/" rel="nofollow ugc">[Read more]</a></span></p>
]]></content:encoded>
				
									<slash:comments>0</slash:comments>
				
							</item>
					<item>
				<guid isPermaLink="false">8920ed932973d2f50e22af220d4ba153</guid>
				<title>Hildebrandt Pike became a registered member</title>
				<link>https://recash.wpsoul.net/activity/p/52685/</link>
				<pubDate>Wed, 11 Dec 2024 16:52:01 +0000</pubDate>

				
									<slash:comments>0</slash:comments>
				
							</item>
		
	</channel>
</rss>