Long-term mortality in patients with moyamoya angiopathy according to stroke presentation type in South Korea
Author:
Publisher
Springer Science and Business Media LLC
Subject
Neurology (clinical),Surgery
Link
https://link.springer.com/content/pdf/10.1007/s00701-021-04959-0.pdf
Reference19 articles.
1. Ahn IM, Park DH, Hann HJ, Kim KH, Kim HJ, Ahn HS (2014) Incidence, prevalence, and survival of moyamoya disease in Korea: a nationwide, population-based study. Stroke 45:1090–1095. https://doi.org/10.1161/STROKEAHA.113.004273
2. Ahn SH, Lee J, Kim YJ, Kwon SU, Lee D, Jung SC, Kang DW, Kim JS (2015) Isolated MCA disease in patients without significant atherosclerotic risk factors: a high-resolution magnetic resonance imaging study. Stroke 46:697–703. https://doi.org/10.1161/STROKEAHA.114.008181
3. Baba T, Houkin K, Kuroda S (2008) Novel epidemiological features of moyamoya disease. J Neurol Neurosurg Psychiatry 79:900–904. https://doi.org/10.1136/jnnp.2007.130666
4. Cheng JH, Ye Q, Ye ZS, Li ZQ, Xu AD (2016) Five-year experience of 101 adult patients with moyamoya disease at a single institution in Eastern China. J Clin Neurosci 32:30–34. https://doi.org/10.1016/j.jocn.2015.12.042
5. Ge P, Zhang Q, Ye X, Liu X, Deng X, Li H, Wang R, Zhang Y, Zhang D, Cao Y, Wang S, Zhao J (2017) Clinical features of hemorrhagic moyamoya disease in China. World Neurosurg 106:224–230. https://doi.org/10.1016/j.wneu.2017.06.145
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