Moyamoya Disease: A Rare Vascular Disease of the CNS
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Publisher
IntechOpen
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http://www.intechopen.com/download/pdf/68650
Reference53 articles.
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3. Fukui M. Guidelines for the diagnosis and treatment of spontaneous occlusion of the circle of Willis (‘moyamoya’ disease). Clinical Neurology and Neurosurgery. 1997;99(Suppl 2):S238-S240
4. Miyawaki S, Imai H, Takayanagi S, et al. Identification of a genetic variant common to moyamoya disease and intracranial major artery stenosis/occlusion. Stroke. 2012;43:3371.9
5. Miyatake S, Miyake N, Touho H, et al. Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease. Neurology. 2012;78:803
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1. Moyamoya Disease in a Child With Fanconi Anemia: An Anomaly or a Complication;Cureus;2024-02-19
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