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occlusion of the circle of Willis, <i>in<\/i>: <i>The Research Committee on Spontaneous Occlusion of the Circle of Willis (Moyamoya Disease) of the Ministry of Health and Welfare Japan Annual Report 1992<\/i>. 1992"},{"key":"51","doi-asserted-by":"crossref","unstructured":"51) Rafat N, Beck G, Pena-Tapia PG, Schmiedek P, Vajkoczy P: Increased levels of circulating endothelial progenitor cells in patients with Moyamoya disease. <i>Stroke<\/i> 40: 432-438, 2009","DOI":"10.1161\/STROKEAHA.108.529420"},{"key":"52","doi-asserted-by":"crossref","unstructured":"52) Roder C, Nayak NR, Khan N, Tatagiba M, Inoue I, Krischek B: Genetics of Moyamoya disease. <i>J Hum Genet<\/i> 55: 711-716, 2010","DOI":"10.1038\/jhg.2010.103"},{"key":"53","doi-asserted-by":"crossref","unstructured":"53) Roder C, Peters V, Kasuya H, Nishizawa T, Takehara Y, Berg D, Schulte C, Khan N, Tatagiba M, Krischek B: Polymorphisms in TGFB1 and PDGFRB are associated with Moyamoya disease in European patients. <i>Acta Neurochir (Wien)<\/i> 152: 2153-2160, 2010","DOI":"10.1007\/s00701-010-0711-9"},{"key":"54","doi-asserted-by":"crossref","unstructured":"54) Sakurai K, Horiuchi Y, Ikeda H, Ikezaki K, Yoshimoto T, Fukui M, Arinami T: A novel susceptibility locus for moyamoya disease on chromosome 8q23. <i>J Hum Genet<\/i> 49: 278-281, 2004","DOI":"10.1007\/s10038-004-0143-6"},{"key":"55","doi-asserted-by":"crossref","unstructured":"55) Sata M, Saiura A, Kunisato A, Tojo A, Okada S, Tokuhisa T, Hirai H, Makuuchi M, Hirata Y, Nagai R: Hematopoietic stem cells differentiate into vascular cells that participate in the pathogenesis of atherosclerosis. <i>Nat Med<\/i> 8: 403-409, 2002","DOI":"10.1038\/nm0402-403"},{"key":"56","doi-asserted-by":"crossref","unstructured":"56) Schoning M, Klein R, Krageloh-Mann I, Falck M, Bien S, Berg PA, Michaelis R: Antiphospholipid antibodies in cerebrovascular ischemia and stroke in childhood. <i>Neuropediatrics<\/i> 25: 8-14, 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Collateral routes to forebrain via ethmoid sinus and superior nasal meatus. <i>Angiology<\/i> 22: 223-236, 1971","DOI":"10.1177\/000331977102200408"},{"key":"63","doi-asserted-by":"crossref","unstructured":"63) Suzuki J, Takaku A: Cerebrovascular &ldquo;moyamoya&rdquo; disease. Disease showing abnormal net-like vessels in base of brain. <i>Arch Neurol<\/i> 20: 288-299, 1969","DOI":"10.1001\/archneur.1969.00480090076012"},{"key":"64","doi-asserted-by":"crossref","unstructured":"64) Suzuki S, Mitsuyama T, Horiba A, Fukushima S, Hashimoto N, Kawamata T: Moyamoya disease complicated by Graves&rsquo; disease and type 2 diabetes mellitus: report of two cases. <i>Clin Neurol Neurosurg<\/i> 113: 325-329, 2011","DOI":"10.1016\/j.clineuro.2010.11.022"},{"key":"65","doi-asserted-by":"crossref","unstructured":"65) Takagi Y, Kikuta K, Nozaki K, Fujimoto M, Hayashi J, Imamura H, Hashimoto N: Expression of hypoxia-inducing factor-1 alpha and endoglin in intimal hyperplasia of the middle cerebral artery of patients with Moyamoya disease. <i>Neurosurgery<\/i> 60: 338-345, 2007","DOI":"10.1227\/01.NEU.0000249275.87310.FF"},{"key":"66","unstructured":"66) Takasugi H, Maemoto T, Kitazawa K, Honda A: [A case of Down syndrome with moyamoya syndrome presenting extensive multiple 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