Novel Development in Treatment for Hemorrhagic Moyamoya Disease
Author:
Affiliation:
1. JAM Trial Group
Publisher
The Japanese Congress of Neurological Surgeons
Subject
Neurology (clinical),Surgery
Link
https://www.jstage.jst.go.jp/article/jcns/28/3/28_149/_pdf
Reference27 articles.
1. 1) Akashi T, Takahashi S, Mugikura S, Sato S, Murata T, Umetsu A, Takase K : Ischemic White Matter Lesions Associated With Medullary Arteries : Classification of MRI Findings Based on the Anatomic Arterial Distributions. AJR Am J Roentgenol 209 : W160-W168, 2017.
2. 2) Baltsavias G, Khan N, Filipce V, Valavanis A : Selective and superselective angiography of pediatric moyamoya disease angioarchitecture in the posterior circulation. Interv Neuroradiol 20 : 403-412, 2014.
3. 3) Baltsavias G, Valavanis A, Filipce V, Khan N : Selective and superselective angiography of pediatric moyamoya disease angioarchitecture : the anterior circulation. Interv Neuroradiol 20 : 391-402, 2014.
4. 4) Cho WS, Chung YS, Kim JE, Jeon JP, Son YJ, Bang JS, Kang HS, Sohn CH, Oh CW : The natural clinical course of hemodynamically stable adult moyamoya disease. J Neurosurg 122 : 82-89, 2015.
5. 5) Fujimura M, Funaki T, Houkin K, Takahashi JC, Kuroda S, Tomata Y, Tominaga T, Miyamoto S ; Japan Adult Moyamoya Trial Investigators : Intrinsic development of choroidal and thalamic collaterals in hemorrhagic-onset moyamoya disease : case-control study of the Japan Adult Moyamoya Trial. J Neurosurg 4 : 1-7, 2018. [epub ahead of print]
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