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Journal of Neurology
Literature
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Chabriat H, Joutel A, Dichgans M, Tournier-Lasserve E, Bousser M-G (2009) CADASIL. Lancet Neurol 8:643–653PubMedCrossRef
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Choi JC (2010) Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease. J Clin Neurol 6:1–9PubMedCrossRef
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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 33:73–80PubMedCrossRef
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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 75:1058–1060PubMedCrossRef
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Rufa A, Pretregiani A, Fressotti P, De Stefano N, Cevenini G, Dotti MT, Federico A (2011) Retinal nerve fiber layer thinning in CADASIL: an optical coherence tomography and MRI study. Cerebrovasc Dis 31:72–77CrossRef
Metadata
Title
A family with atypical CADASIL
Authors
Christian Vedeler
Laurence Bindoff
Publication date
01-10-2011
Publisher
Springer-Verlag
Published in
Journal of Neurology / Issue 10/2011
Print ISSN: 0340-5354
Electronic ISSN: 1432-1459
DOI
https://doi.org/10.1007/s00415-011-6023-z

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