4 research outputs found
Histogram metrics of DTI-derived indices in control subjects and SCA2 patients.
<p>Median (interquartile range) data are reported. MD/AD/RD median and peak location are expressed in ×10<sup>−3</sup> mm<sup>2</sup>/s, while FA/MO median and peak location are unitless.</p
Processing pipeline for T<sub>1</sub>-weighted and diffusion-weighted images of a single subject.
<p>Processing pipeline for T<sub>1</sub>-weighted and diffusion-weighted images of a single subject.</p
Demographic, genetic and clinical data in 10 SCA2 patients.
<p>F, female; IACRS, Inherited Ataxia Clinical Rating Scale; M, male; SD, standard deviation.</p
Results of the baseline between group (SCA2 vs. controls) TBM analysis.
<p>Voxel-wise corrected p-value maps (threshold-free cluster enhancement, TFCE), testing the null hypothesis of zero differences in <b>|J|</b><sub>baseline</sub> between SCA2 patients and healthy controls. Highlighted clusters indicate significantly (p<0.05) more pronounced mean atrophy in SCA2 patients when compared to healthy controls (i.e. <b>|J|</b><sub>baseline</sub> in SCA2 patients significantly lower than <b>|J|</b><sub>baseline</sub> in healthy controls). All maps are overlayed on population-specific T1 template. These maps show significant symmetric atrophic changes in SCA2 patients (with respect to controls) in the brainstem, middle cerebellar peduncels, and cerebellar WM and adjacent cortical GM. No significant differences are observed in the supratentorial compartment.</p