A large number of cerebral microbleeds in CADASIL patients presenting with recurrent seizures: a case report
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),General Medicine
Link
http://link.springer.com/content/pdf/10.1186/s12883-019-1342-2.pdf
Reference13 articles.
1. Joutel A, Corpechot C, Ducros A, Vahedi K, Chabriat H, Mouton P, et al. Notch3 mutations in CADASIL: a hereditary adult-onset condition causing stroke and dementia. Nature. 1996;383:707–10.
2. Dichgans M, Mayer M, Uttner I, Brüning R, Müller-Höcker J, Rungger G, et al. The phenotypic spectrum of CADASIL: clinical findings in 102 cases. Ann Neurol. 1998;44:731–9.
3. Bersano A, Bedini G, Markus HS, Vitali P, Tibaldi EC, Taroni F, et al. The role of clinical and neuroimaging features in the diagnosis of CADASIL. J Neurol. 2018;265:2934–43.
4. Nannucci S, Rinnoci V, Pracucci G, MacKinnon AD, Pescini F, Adib-Samii P, et al. Location, number and factors associated with cerebral microbleeds in an Italian-British cohort of CADASIL patients. PLoS ONE. 2018;13(1):e0190878 https://doi.org/10.1371/journal.pone.0190878 .
5. O’Sullivan M, Jarosz JM, Martin RJ, Deasy N, Powell JF, Markus HS. MRI hyperintensities of the temporal lobe and external capsule in patients with CADASIL. Neurology. 2001;56:628–34.
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