Atypical Clinical Cases of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)-Reference-Cited by-同舟云学术

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Atypical Clinical Cases of Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL)

Published:2018-12 Issue:8 Volume:44 Page:860-863
ISSN:0362-1197
Container-title:Human Physiology
language:en
Short-container-title:Hum Physiol

Author:

Moroz A. A.,Abramycheva N. Yu.,Ivanova E. O.,Konovalov R. N.,Timerbaeva S. L.,Illarioshkin S. N.

Publisher

Pleiades Publishing Ltd

Subject

Physiology (medical),Physiology

Link

http://link.springer.com/content/pdf/10.1134/S0362119718080078.pdf

Reference26 articles.

1. Joutel, A., Corpechot, C., Ducros, A., et al., Notch3 mutations in CADASIL, a hereditary adult-onset condition causing stroke and dementia, Nature, 1996, vol. 383, pp. 707–710. PMID 8878478. doi 10.1038/ 383707a0

2. Tournier-Lasserve, E., Iba-Zizen, M.-T., Romero, N., et al., Autosomal dominant syndrome with stroke like episodes and leukoencephalopathy, Stroke, 1991, vol. 22, pp. 1297–1302. PMID 1926242. doi 10.1161/ 01.STR.22.10.1297

3. Choi, J., Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy: a genetic cause of cerebral small vessel disease, J. Clin. Neurol., 2010, vol. 6, pp. 1–9. PMID 20386637. doi 10.3988/jcn.2010.6.1.1

4. Dong, Y., Hassan, A., Zhang, Z., et al., Yield of screening for CADASIL mutations in lacunar stroke and leukoaraiosis, Stroke, 2003, vol. 34, pp. 203–205. PMID 12511775. doi 10.1161/01.STR.0000048162. 16852.88

5. Abramycheva, N., Stepanova, M., Kalashnikova, L., et al., New mutations in the Notch3 gene in patients with cerebral autosomal dominant arteriopathy with subcortical infarcts and leucoencephalopathy (CADASIL), J. Neurol. Sci., 2015, vol. 349, pp. 196–201. PMID 25623805. http://dx.doi.org/10.1016/j.jns.2015.01.018

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