Recognizing CADASIL: a Secondary Cause of Migraine with Aura
Author:
Publisher
Springer Science and Business Media LLC
Subject
Anesthesiology and Pain Medicine,Clinical Neurology,General Medicine
Link
http://link.springer.com/content/pdf/10.1007/s11916-017-0621-0.pdf
Reference29 articles.
1. • Chabriat H, Joutel A, Dichgans M, Tournier-Lasserve E, Bousser M. CADASIL. Lancet Neurol. 2009;8:643–53. Comprehensive review article from 2009 discussing pathophysiology, symptoms, diagnosis, treatment and progression.
2. Joutel A, Corpechot C, Ducros A, et al. Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature. 1996;383:707–10.
3. • Tikka S, Baumann M, Siitonen M, et al. CADASIL and CARASIL. Brain Pathol. 2014;24:525–44. Recent article on the genetics and pathology of CADASIL and CARASIL.
4. Kalimo H, Ruchoux M, Viitanen M, Kalaria R. CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia. Brain Pathol. 2002;12:371–84.
5. Joutel A, Andreux F, Gaulis S, Domenga V, Cecillon M, Battail N, et al. The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients. J Clin Investig. 2000;105:597–605.
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