Changing clinical patterns and increasing prevalence in CADASIL

Author:

Moreton F. C.1,Razvi S. S. M.2,Davidson R.3,Muir K. W.1

Affiliation:

1. Institute of Neuroscience and Psychology; University of Glasgow; Southern General Hospital; Glasgow UK

2. Department of Neurology; Institute of Neurological Sciences; Southern General Hospital; Glasgow UK

3. West of Scotland Genetic Services; Southern General Hospital; Glasgow UK

Publisher

Wiley

Subject

Clinical Neurology,Neurology,General Medicine

Reference32 articles.

1. Encephalopathie sous-corticale progressive (Binswanger) a evolution rapide chez deux soeurs;Van Bogaert;Med Hellen,1955

2. Chronic familial vascular encephalopathy;Stevens;Lancet,1977

3. Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease;Sourander;Acta Neuropathol,1977

4. Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12;Tournier-Lasserve;Nat Genet,1993

5. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia;Joutel;Nature,1996

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