Latest papers

[Was Nietzsche's genius a consequence of mental disease].

Genetic assessment and management of dementia.

Homozygosity for a NOTCH3 mutation in a 65-year-old CADASIL patient with mild symptoms: a family report.

Psychiatric disturbances in CADASIL: a brief review.

CSF levels of beta-amyloid 1-42, tau and phosphorylated tau protein in CADASIL.

Increased QT variability in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy.

Structural and metabolic brain abnormalities in preclinical cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.

Right-to-left shunt in CADASIL patients: a comorbidity factor?

John Ruskin's relapsing encephalopathy.

Cysteine-sparing notch3 mutations: cadasil or cadasil variants?

Notch3: from subtle structural differences to functional diversity.

Acute vestibular syndrome in a patient with cerebral autosomal dominant leukoencephalopathy with subcortical infarcts and leukoencephalopathy (CADASIL).

Sporadic vascular dementia as clinical presentation of a new missense mutation within exon 7 of NOTCH3 gene.

Measurement of meaningful treatment effects in CADASIL.

Migraine and ischemic stroke: a debated question.

Nephroangiosclerosis in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: is NOTCH3 mutation the common culprit?

Retinal arterial abnormalities correlate with brain white matter lesions in cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy.

Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy in Arabs.

The genetic architecture of intracerebral hemorrhage.

Right-to-left shunt in CADASIL patients: prevalence and correlation with clinical and MRI findings.