White matter bundle segmentation using diffusion MRI fiber tractography has become the
method of choice to identify white matter fiber pathways in vivo in human brains. However, like …

Purpose Cerebellar ataxias are a large and heterogeneous group of disorders. The evaluation
of brain parenchyma via MRI plays a central role in the diagnostic assessment of these …

Cognitive impairment is a frequent and meaningful symptom in multiple sclerosis (MS),
caused by the accrual of brain structural damage only partially counteracted by effective …

Fabry disease (FD) is a rare X-linked disorder characterised by abnormal progressive lysosomal
deposition of globotriaosylceramide in a large variety of cell types. The central nervous …

Importance Multiple sclerosis (MS) misdiagnosis remains an important issue in clinical
practice. Objective To quantify the performance of cortical lesions (CLs) and central vein sign (…

Background and purpose Heterozygous mutations in the STUB1 gene have recently been
associated with an autosomal dominant form of spinocerebellar ataxia (SCA) associated with …

BACKGROUND AND PURPOSE: Modifications of magnetic susceptibility have been
consistently demonstrated in the subcortical gray matter of MS patients, but some uncertainties …

Background & Aims In the context of the Italian severe acute respiratory syndrome
coronavirus 2 vaccination program, liver transplant (LT) recipients were prioritized for vaccine …

Objective To investigate global and lobular cerebellar volumetries in patients with progressive
multiple sclerosis (MS), testing the contribution of cerebellar lobular atrophy to both motor …

Objective Friedreich ataxia (FRDA) is an inherited neurological disease defined by progressive
movement incoordination. We undertook a comprehensive characterization of the spatial …