Chiara Casella

The paper uses MRI and histological analyses to show axonal and myelin changes in a Huntington's Disease mouse model, identifying FR as a potential MRI biomarker for WM microstructure changes.

This paper validates a motion correction technique, DISORDER, for pediatric brain morphometry, showing improved reliability for motion-degraded scans compared to conventional MPRAGE.

This study identifies depth-dependent cortical microstructure alterations in children with focal epilepsy using quantitative MRI, suggesting potential pre-symptomatic changes detectable regardless of radiological abnormalities.

The paper characterizes subiculum-BNST connectivity in humans and macaques using tracers and diffusion MRI, finding heritability and associations with BMI, age, and sex but not stress or alcohol use.

This study uses ultra-strong gradient MRI to show that myelin changes, not axon density, are linked to premanifest Huntington's disease, with mutation size correlating with myelin levels.

This study uses multi-compartment MRI signal analysis to quantify myelin breakdown in premanifest Huntington's disease, finding reduced myelin water fraction and age-related executive function decline.

This study examines if drumming training induces myelin remodelling in Huntington's disease patients using diffusion MRI and qMT imaging, finding increased MPF in specific white matter regions post-training.