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Keywords

Notch3 Gene Smooth Muscle Fibre Subcortical Infarct Notch3 Mutation Cerebral Autosomal Dominant Arteriopathy 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

References

  1. Baudrimont M, Chabriat H, Vahedi K, and Bousser M (1998) Diagnostic value of skin biopsies in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL). Neuropathol Appl Neurobiol 24: 148Google Scholar
  2. Hassan A, and Markus HS (2000) Genetics and ischaemic stroke Brain 123: 1784Google Scholar
  3. Joutel A, Andreux F, Gaulis S, Domenga V, Cecillon M, Battail, N, Piga N, Chapon F, Godfrain C, and Tournier-Lasserve E (2000) The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients. J Clin Invest 105: 597PubMedGoogle Scholar
  4. Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, Alamowitch S, Domenga V, Cecillion M, Marechal E, et al (1996) Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 383: 707Google Scholar
  5. Kalaria RN (2001) Advances in molecular genetics and pathology of cerebrovascular disorders. Trends Neurosci 24: 392CrossRefPubMedGoogle Scholar
  6. Kalimo H, Viitanen M, Amberla K, Juvonen V, Marttila R, Poyhonen M, Rinne JO, Savontaus M, Tuisku S, and Winblad B (1999) CADASIL: hereditary disease of arteries causing brain infarcts and dementia. Neuropathol Appl Neurobiol 25: 257CrossRefPubMedGoogle Scholar
  7. Ruchoux M, and Maurage E (1997) Review on CADASIL. J Neuropathol Exp Neurol 56: 947PubMedGoogle Scholar
  8. Ruchoux MM, Guerouaou D, Vandenhaute B, Pruvo JP, Vermersch P, and Leys D (1995) Systemic vascular smooth muscle cell impairment in cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy. Acta Neuropathol (Berlin) 89: 500PubMedGoogle Scholar
  9. Sourander P, and Walinder J (1977) Hereditary multi-infarct dementia. Morphological and clinical studies of a new disease. Acta Neuropathol (Berlin) 39: 247CrossRefPubMedGoogle Scholar
  10. Tournier-Lasserve E, Joutel A, Melki J, Weissenbach J, Lathrop GM, Chabriat H, Mas JL, Cabanis EA, Baudrimont M, Maciazek J, and et al (1993) Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy maps to chromosome 19q12. Nat Genet 3: 256CrossRefPubMedGoogle Scholar

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© Springer-Verlag/Wien 2005

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