Genotypic and phenotypic spectrum of CADASIL in Japan: the experience at a referral center in Kumamoto University from 1997 to 2014-Reference-Cited by-同舟云学术

Genotypic and phenotypic spectrum of CADASIL in Japan: the experience at a referral center in Kumamoto University from 1997 to 2014

Published:2015-05-16 Issue:8 Volume:262 Page:1828-1836
ISSN:0340-5354
Container-title:Journal of Neurology
language:en
Short-container-title:J Neurol

Author:

Ueda Akihiko,Ueda Mitsuharu,Nagatoshi Akihito,Hirano Teruyuki,Ito Takaaki,Arai Nobutaka,Uyama Eiichiro,Mori Kota,Nakamura Masaaki,Shinriki Satoru,Ikeda Katsuyoshi,Ando Yukio

Funder

Grants-in-Aid for Science Research from the Ministry of Education, Culture, Sports, Science and Technology of Japan

Publisher

Springer Science and Business Media LLC

Subject

Clinical Neurology,Neurology

Link

http://link.springer.com/content/pdf/10.1007/s00415-015-7782-8.pdf

Reference33 articles.

1. Chabriat H, Joutel A, Dichgans M et al (2009) CADASIL. Lancet Neurol 8:643–653

2. Joutel A, Corpechot C, Ducros A et al (1996) Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia. Nature 383:707–710

3. Joutel A, Andreux F, Gaulis S et al (2000) The ectodomain of the Notch3 receptor accumulates within the cerebrovasculature of CADASIL patients. J Clin Invest 105:597–605

4. Tikka S, Baumann M, Siitonen M et al (2014) CADASIL and CARASIL. Brain Pathol 24:525–544

5. Pescini F, Nannucci S, Bertaccini B et al (2012) The cerebral autosomal-dominant arteriopathy with subcortical infarcts and leukoencephalopathy (CADASIL) scale: a screening tool to select patients for NOTCH3 gene analysis. Stroke 43:2871–2876

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