To review the literature on primary dystonia and dystonia plus and to provide evidence‐based
recommendations. Primary dystonia and dystonia plus are chronic and often disabling …

Alexander disease (AD) in its typical form is an infantile lethal leucodystrophy, characterized
pathologically by Rosenthal fibre accumulation. Following the identification of glial fibrillary …

The tau gene has been found to be the locus of dementia with rigidity linked to chromosome
17. Exonic and intronic mutations have been described in a number of families. Here we …

Magnetic resonance imaging (MRI) is not usually considered helpful for establishing the
diagnosis of Parkinson's disease, but it is much more important to support the clinical diagnosis …

Purpose: To determine the values of iron accumulation in the basal ganglia of healthy
volunteers of different ages with R2* and raw signal intensity measurements from T1-weighted …

Clinical diagnosis of olivopontocerebellar atrophy (OPCA) must be confirmed by radiologic
demonstration of atrophy in an appropriate distribution. OPCA may be associated with …

Reliable data on large cohorts of patients with glioblastoma are needed because such
studies differ importantly from trials that have a strong bias toward the recruitment of younger …

Objective Cerebral amyloid angiopathy–related inflammation (CAA‐ri) is characterized by
vasogenic edema and multiple cortical/subcortical microbleeds, sharing several aspects with …

Objectives: The study was focused on leukoencephalopathies of unknown cause in order to
define a novel, homogeneous phenotype suggestive of a common genetic defect, based on …

Rasmussen's encephalitis (RE) is a rare, progressive, chronic encephalitis characterised by
drug-resistant epilepsy, progressive hemiparesis and mental impairment. It typically involves …