<?xml version="1.0" encoding="UTF-8"?><rss xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:content="http://purl.org/rss/1.0/modules/content/" xmlns:atom="http://www.w3.org/2005/Atom" version="2.0"><channel><title><![CDATA[RSS Feed]]></title><description><![CDATA[RSS Feed]]></description><link>http://direct.ecency.com</link><image><url>http://direct.ecency.com/logo512.png</url><title>RSS Feed</title><link>http://direct.ecency.com</link></image><generator>RSS for Node</generator><lastBuildDate>Sun, 19 Apr 2026 18:24:42 GMT</lastBuildDate><atom:link href="http://direct.ecency.com/created/ardalanshojakiuru/rss.xml" rel="self" type="application/rss+xml"/><item><title><![CDATA[Ardalan–Shoja–Kiuru syndrome]]></title><description><![CDATA[Ardalan–Shoja–Kiuru syndrome is a clinical syndrome featuring hereditary gelsolin [1] amyloidosis and retinitis pigmentosa.[2] This syndrome was first recognized by two Iranian physicians, Mohammad Ardalan]]></description><link>http://direct.ecency.com/ardalanshojakiuru/@karthikmbbs2/ardalan-shoja-kiuru-syndrome-919d10168e637</link><guid isPermaLink="true">http://direct.ecency.com/ardalanshojakiuru/@karthikmbbs2/ardalan-shoja-kiuru-syndrome-919d10168e637</guid><category><![CDATA[ardalanshojakiuru]]></category><dc:creator><![CDATA[karthikmbbs2]]></dc:creator><pubDate>Mon, 04 Jun 2018 17:53:36 GMT</pubDate></item></channel></rss>