A family with atypical CADASIL
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,Neurology
Link
http://www.springerlink.com/index/pdf/10.1007/s00415-011-6023-z
Reference6 articles.
1. Chabriat H, Joutel A, Dichgans M, Tournier-Lasserve E, Bousser M-G (2009) CADASIL. Lancet Neurol 8:643–653
2. Choi JC (2010) Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease. J Clin Neurol 6:1–9
3. Herve D, Chabriat H (2010) CADASIL. J Ger Psych Neurol 23:269–276
4. Joutel A (2011) Pathogenesis of CADASIL: transgenic and knock-out mice to probe function and dysfunction of the mutated gene, Notch3, in the cerebrovasculature. Bioessays 33:73–80
5. Cumurciuc R, Massin P, Paques M, Krisovic V, Gadric A, Bousser MG, Chabriat H (2004) Retinal abnormalities in CADASIL: a retrospective study of 18 patients. J Neurol Neurosurg Psychiatry 75:1058–1060
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