Hemizentralarterienverschluss bei Moyamoya-Syndrom
Author:
Publisher
Springer Science and Business Media LLC
Subject
Ophthalmology
Link
http://link.springer.com/content/pdf/10.1007/s00347-006-1401-0.pdf
Reference10 articles.
1. Calderelli M, Di Rocco C, Gaglini P (2001) Surgical treatment of moyamoya disease in pediatric age. J Neurosurg Sci 45: 83–91
2. Chace R, Hedges TH (1984) Retinal artery occlusion due to moyamoya disease. J Clin Neuro-Ophthalmol 4: 31–34
3. Ikeda H, Sasaki T, Yoshimoto T et al. (1999) Mapping of a familial moyamoya disease gene to chromosome 3p24.2-p26. Am J Hum Genet 64: 533–537
4. Krishnan C, Roy A, Traboulsi E (2000) Morning glory disk anomaly, choroidal coloboma, and congenital constirictive malformations of the internal carotid arteries (moyamoya disease). Ophthalmic Genet 21: 21–24
5. Lie JT (1990) Illustrated histopathologic classification criteria for selected vasculitissyndromes. Arthritis Rheum 33: 1074–1087
Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Central retinal artery occlusion occurring 30 years after successful revascularization surgery for moyamoya disease: case report;Acta Neurochirurgica;2020-07-23
2. Central retinal artery occlusion as initial presentation of Moyamoya disease in a middle-aged woman;American Journal of Ophthalmology Case Reports;2020-06
3. CRAO in Moyamoya Disease;JOURNAL of CLINICAL AND DIAGNOSTIC RESEARCH;2013
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