A rare case of pediatric moyamoya disease with reversible white matter lesions in a 3-year-old Chinese girl
Author:
Publisher
Springer Science and Business Media LLC
Subject
Clinical Neurology,General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://link.springer.com/content/pdf/10.1007/s00381-019-04391-x.pdf
Reference28 articles.
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2. Piao J, Wu W, Yang Z (2015) Research progress of moyamoya disease in children. Int J Med Sci 12:566–575
3. Fujimura M, Tominaga T (2015) Diagnosis of moyamoya disease: international standard and regional differences. Neurol Med Chir (Tokyo) 55:189–193
4. Liao X, Deng J, Dai W, Zhang T, Yan J (2017) Rare variants of RNF213 and moyamoya/non-moyamoya intracranial artery stenosis/occlusion disease risk: a meta-analysis and systematic review. Environ Health Prev Med 22:75
5. Morimoto T, Enmi JI, Hattori Y, Iguchi S, Saito S, Harada KH, Okuda H, Mineharu Y, Takagi Y, Youssefian S, Iida H, Miyamoto S, Ihara M, Kobayashi H, Koizumi A (2018) Dysregulation of RNF213 promotes cerebral hypoperfusion. Sci Rep 8:3607
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3. Development and External Validation of Nomogram for Cerebral Infarction in Moyamoya Diseases;Translational Stroke Research;2023-01-19
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