Transcranial magnetic stimulation (TMS) is a powerful tool to probe in vivo brain circuits, as it
allows to assess several cortical properties such as excitability, plasticity and connectivity in …

Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is the most common and best known monogenic small …

Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leucoencephalopathy (CADASIL) is the most common heritable cause of stroke and …

Neuronal intranuclear inclusion disease (NIID), caused by an expansion of GGC repeats in
the 5′-untranslated region of NOTCH2NLC, is an important but underdiagnosed cause of …

Ischaemic stroke is a heterogeneous multifactorial disorder. Epidemiological data provide
substantial evidence for a genetic component to the disease, but the extent of predisposition …

Background: Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is an inherited autosomal dominant condition …

With the availability of improved brain imaging techniques, the high prevalence and clinical
importance of cerebral small vessel disease have been increasingly recognised in recent …

Background and Purpose—A number of single gene disorders can cause cerebral small
vessel disease. Mutations in the COL4A1 gene encoding the type IV collagen alpha 1 chain …

Although the diagnosis of multiple sclerosis relies on the demonstration of disease
dissemination in space and time, the exclusion of other neurological disorders is also …

Cerebral autosomal dominant arteriopathy with subcortical infarcts and
leukoencephalopathy (CADASIL) is the most common monogenic disorder of the cerebral …