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. 2012 Mar 27;78(13):1025-7.
doi: 10.1212/WNL.0b013e31824d586c. Epub 2012 Mar 14.

The minimum prevalence of CADASIL in northeast England

S K Narayan  1 , G Gorman, R N Kalaria, G A Ford, P F Chinnery
Affiliations

The minimum prevalence of CADASIL in northeast England

S K Narayan et al. Neurology. .
No abstract available

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Figures

Figure 1
Figure 1. Pedigree charts of affected families
See this image and copyright information in PMC

References

    1. Adib-Samii P, Brice G, Martin RJ, Markus HS. Clinical spectrum of CADASIL and the effect of cardiovascular risk factors on phenotype: study in 200 consecutively recruited individuals. Stroke 2010; 41: 630– 634 - PubMed
    1. Opherk C, Peters N, Herzog J, Luedtke R, Dichgans M. Long-term prognosis and causes of death in CADASIL: a retrospective study in 411 patients. Brain 2004; 127: 2533– 2539 - PubMed
    1. Kalimo H, Ruchoux MM, Viitanen M, Kalaria RN. CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia. Brain Pathol 2002; 12: 371– 84 - PMC - PubMed
    1. Razvi SS, Davidson R, Bone I, Muir KW. The prevalence of cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL) in the west of Scotland. J Neurol Neurosurg Psychiatry 2005; 76: 739– 741 - PMC - PubMed
    1. Markus HS, Martin RJ, Simpson MA, et al. Diagnostic strategies in CADASIL. Neurology 2002; 59: 1134– 1138 - PubMed

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