<?xml version="1.0" encoding="utf-8" standalone="yes"?><rss version="2.0" xmlns:atom="http://www.w3.org/2005/Atom"><channel><title>Heterogeneity | Robel Gebre</title><link>https://iborz.org/tags/heterogeneity/</link><atom:link href="https://iborz.org/tags/heterogeneity/index.xml" rel="self" type="application/rss+xml"/><description>Heterogeneity</description><generator>HugoBlox Kit (https://hugoblox.com)</generator><language>en-us</language><lastBuildDate>Sun, 01 Jun 2025 00:00:00 +0000</lastBuildDate><image><url>https://iborz.org/media/logo.svg</url><title>Heterogeneity</title><link>https://iborz.org/tags/heterogeneity/</link></image><item><title>HET</title><link>https://iborz.org/projects/het/</link><pubDate>Sun, 01 Jun 2025 00:00:00 +0000</pubDate><guid>https://iborz.org/projects/het/</guid><description>&lt;p&gt;Measuring how differently neurodegeneration expresses across patients and across the brain.&lt;/p&gt;
&lt;p&gt;Multiple system atrophy (MSA) is a fatal, rapidly progressive, and debilitating movement disorder. It has two main subtypes, cerebellar (MSA-C) and parkinsonian (MSA-P). The imaging features of MSA-C are well established and localize to the cerebellum, whereas those of MSA-P overlap with Parkinson&amp;rsquo;s disease (PD) in the early stages. Using regional volume and diffusion MRI measures across the brain, we show that each subtype carries a unique, non-overlapping signature, distinct from the other subtype and from PD.&lt;/p&gt;</description></item></channel></rss>