Assessing Regional Gray and White Matter Changes to Understand the CNS Related Symptoms of Myotonic Distrophy Type-1

Keywords

abnormalities account acquisitions adding aims already analyses anterior assess assessing assessment association associations atrophy battery bilaterally brain carriers central cerebellum clinical cluster cognitive confirmed confirms conflicting considered controls correction correlation correlations covariate cranial deficits design diagnosed diffusion direct disorders dominant dominated driven dual dysfunctions dystrophy efficacy entered equilibrium examination executive expansion explore exploring extension extensive fast features finally flair foundation framework frequent frontal functions gene general genetic genetically genetics gray healthy hospital impairment includes intra inverse investigated involvement kernel laboratory laura likely linear lobule loss maps matched matrix measures mechanisms might model modified morphological muscle muscular mutation neurological neurology participants particular patients performance picture pons post posterior potential presence processed produced protocol psychiatric ranging rating recruited regional regression related respectively revealed sample scale score scores served sixteen slices statistical statistics strict subjects suffering survived symptoms tissue torso trait transform transmitted triplets turbo type understand underwent unit volume volumes volumetric white widespread