Corso Residenziale Siena 2011
HOME- Familial British dementia with amyloid angiopathy
- Cerebral autosomal recessive arteriopathy with subcortical infarcts and Leukoencephalopathy (CARASIL): from discovery to gene identification
- Association of HTRA1 mutations and familial ischemic cerebral small-vessel disease
- Genetics of cavernous angiomas
- Central nervous system vasculitis
- Chagas disease and stroke
- Central nervous system vasculitis
- Role of COL4A1 in Small-Vessel disease and hemorrhagic stroke
- COL4A1 mutations as a monogenic cause of cerebral small vessel disease
- Course of cerebral amyloid angiopathy related inlfammation
- Mortality from hereditary cerebral haemorrhage with amyloidosis. Duthc type. The impact of sex, parental transmission and year of birth
- Comparison of clinical, familial, and MRI features of CADASIL and NOTCH3-negative patients
- Primary angiitis of the Central Nervous System
- Paediatric stroke: genetic insights into disease mechanisms and treatment targets
- C-terminal truncations in human 3'-5' DNA exonuclease TREX1 cause autosomal dominant retinal vasculopathy with cerebral leukodystrophy