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

On October 9–11, 2003, the third meeting of the White Matter Study Group of the International
Society for Magnetic Resonance in Medicine was held in Venice, Italy. This article is the …

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 …

Two cases of metastases from carcinoma to intracranial meningioma are presented. In the
first case the presence of the malignant tumor was unsuspected at the time of intracranial …

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 …

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 …

✓ The clinical and neuroradiological findings and the surgical results in a series of 18
patients with meningiomas of the lateral ventricles, operated on over a 23-year period, are …

Ethylmalonic encephalopathy is caused by mutations in ETHE1, a mitochondrial matrix sulfur
dioxygenase, leading to failure to detoxify sulfide, a product of intestinal anaerobes and, in …