{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,23]],"date-time":"2026-10-23T13:27:40Z","timestamp":1792762060385,"version":"4.5.0"},"reference-count":25,"publisher":"Springer Science and Business Media LLC","issue":"9","license":[{"start":{"date-parts":[[2023,6,1]],"date-time":"2023-06-01T00:00:00Z","timestamp":1685577600000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"},{"start":{"date-parts":[[2023,6,1]],"date-time":"2023-06-01T00:00:00Z","timestamp":1685577600000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/www.springernature.com\/gp\/researchers\/text-and-data-mining"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["J Neurol"],"published-print":{"date-parts":[[2023,9]]},"DOI":"10.1007\/s00415-023-11793-0","type":"journal-article","created":{"date-parts":[[2023,6,1]],"date-time":"2023-06-01T09:02:29Z","timestamp":1685610149000},"page":"4415-4422","update-policy":"https:\/\/doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":11,"title":["Progression of initially unilateral Moyamoya angiopathy in Caucasian Europeans"],"prefix":"10.1007","volume":"270","author":[{"given":"Daniel","family":"Strunk","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rolf R.","family":"Diehl","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Roland","family":"Veltkamp","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Sven G.","family":"Meuth","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-5667-3621","authenticated-orcid":false,"given":"Markus","family":"Kraemer","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"297","published-online":{"date-parts":[[2023,6,1]]},"reference":[{"key":"11793_CR1","doi-asserted-by":"publisher","first-page":"245","DOI":"10.2176\/nmc.52.245","volume":"52","author":"Research Committee on the Pathology and Treatment of Spontaneous Occlusion of the Circle of Willis, Health Labour Sciences Research Grant for Research on Measures for Infractable Diseases","year":"2012","unstructured":"Research Committee on the Pathology and Treatment of Spontaneous Occlusion of the Circle of Willis, Health Labour Sciences Research Grant for Research on Measures for Infractable Diseases (2012) Guidelines for diagnosis and treatment of moyamoya disease (spontaneous occlusion of the circle of Willis). Neurol Med Chir (Tokyo) 52:245\u2013266. https:\/\/doi.org\/10.2176\/nmc.52.245","journal-title":"Neurol Med Chir (Tokyo)"},{"key":"11793_CR2","doi-asserted-by":"publisher","first-page":"1226","DOI":"10.1056\/NEJMra0804622","volume":"360","author":"RM Scott","year":"2009","unstructured":"Scott RM, Smith ER (2009) Moyamoya disease and moyamoya syndrome. N Engl J Med 360:1226\u20131237. https:\/\/doi.org\/10.1056\/NEJMra0804622","journal-title":"N Engl J Med"},{"key":"11793_CR3","doi-asserted-by":"publisher","first-page":"2590","DOI":"10.1161\/STROKEAHA.118.021556","volume":"49","author":"HJ Fullerton","year":"2018","unstructured":"Fullerton HJ, Stence N, Hills NK et al (2018) Focal cerebral arteriopathy of childhood. Stroke 49:2590\u20132596. https:\/\/doi.org\/10.1161\/STROKEAHA.118.021556","journal-title":"Stroke"},{"key":"11793_CR4","doi-asserted-by":"publisher","first-page":"2375","DOI":"10.1161\/STROKEAHA.117.016818","volume":"48","author":"M Steinlin","year":"2017","unstructured":"Steinlin M, Bigi S, Stojanovski B et al (2017) Focal cerebral arteriopathy: Do steroids improve outcome? Stroke 48:2375\u20132382. https:\/\/doi.org\/10.1161\/STROKEAHA.117.016818","journal-title":"Stroke"},{"key":"11793_CR5","doi-asserted-by":"publisher","first-page":"307","DOI":"10.2176\/jns-nmc.2022-0072","volume":"62","author":"S Kuroda","year":"2022","unstructured":"Kuroda S, Fujimura M, Takahashi J et al (2022) Diagnostic criteria for Moyamoya disease\u20142021 revised version. Neurol Med Chir (Tokyo) 62:307\u2013312. https:\/\/doi.org\/10.2176\/jns-nmc.2022-0072","journal-title":"Neurol Med Chir (Tokyo)"},{"key":"11793_CR6","doi-asserted-by":"publisher","first-page":"474","DOI":"10.1016\/j.wneu.2016.09.018","volume":"96","author":"Q Zhang","year":"2016","unstructured":"Zhang Q, Wang R, Liu Y et al (2016) Clinical features and long-term outcomes of unilateral Moyamoya disease. World Neurosurg 96:474\u2013482. https:\/\/doi.org\/10.1016\/j.wneu.2016.09.018","journal-title":"World Neurosurg"},{"key":"11793_CR7","doi-asserted-by":"publisher","first-page":"2973","DOI":"10.1161\/STROKEAHA.111.622522","volume":"42","author":"JY Yeon","year":"2011","unstructured":"Yeon JY, Shin HJ, Kong D-S et al (2011) The prediction of contralateral progression in children and adolescents with unilateral Moyamoya disease. Stroke 42:2973\u20132976. https:\/\/doi.org\/10.1161\/STROKEAHA.111.622522","journal-title":"Stroke"},{"key":"11793_CR8","doi-asserted-by":"publisher","first-page":"765","DOI":"10.3109\/02688697.2015.1096902","volume":"29","author":"P Hever","year":"2015","unstructured":"Hever P, Alamri A, Tolias C (2015) Moyamoya angiopathy\u2014Is there a Western phenotype? Br J Neurosurg 29:765\u2013771. https:\/\/doi.org\/10.3109\/02688697.2015.1096902","journal-title":"Br J Neurosurg"},{"key":"11793_CR9","doi-asserted-by":"publisher","first-page":"605","DOI":"10.1007\/s12041-013-0304-5","volume":"92","author":"W Liu","year":"2013","unstructured":"Liu W, Senevirathna STMLD, Hitomi T et al (2013) Genomewide association study identifies no major founder variant in Caucasian moyamoya disease. J Genet 92:605\u2013609. https:\/\/doi.org\/10.1007\/s12041-013-0304-5","journal-title":"J Genet"},{"key":"11793_CR10","doi-asserted-by":"publisher","DOI":"10.1177\/23969873221144089","author":"A Bersano","year":"2023","unstructured":"Bersano A, Khan N, Fuentes B et al (2023) European Stroke Organisation (ESO) Guidelines on Moyamoya angiopathy: endorsed by Vascular European Reference Network (VASCERN). Eur Stroke J. https:\/\/doi.org\/10.1177\/23969873221144089","journal-title":"Eur Stroke J"},{"key":"11793_CR11","doi-asserted-by":"publisher","first-page":"1262","DOI":"10.1093\/neuros\/nyaa284","volume":"87","author":"EW Church","year":"2020","unstructured":"Church EW, Bell-Stephens TE, Bigder MG et al (2020) Clinical course of unilateral Moyamoya disease. Neurosurgery 87:1262. https:\/\/doi.org\/10.1093\/neuros\/nyaa284","journal-title":"Neurosurgery"},{"key":"11793_CR12","doi-asserted-by":"publisher","first-page":"103","DOI":"10.1007\/s00701-013-1921-8","volume":"156","author":"SC Lee","year":"2014","unstructured":"Lee SC, Jeon JS, Kim JE et al (2014) Contralateral progression and its risk factor in surgically treated unilateral adult moyamoya disease with a review of pertinent literature. Acta Neurochir (Wien) 156:103\u2013111. https:\/\/doi.org\/10.1007\/s00701-013-1921-8","journal-title":"Acta Neurochir (Wien)"},{"key":"11793_CR13","doi-asserted-by":"publisher","first-page":"284","DOI":"10.1024\/0301-1526\/a000364","volume":"43","author":"N Veselinovic","year":"2014","unstructured":"Veselinovic N, Zidverc-Trajkovic J, Semnic R et al (2014) Moyamoya, unilateral to bilateral in one year. Vasa 43:284\u2013286. https:\/\/doi.org\/10.1024\/0301-1526\/a000364","journal-title":"Vasa"},{"key":"11793_CR14","doi-asserted-by":"crossref","unstructured":"Kim TW, Seo BR, Kim JH, Kim YO Rapid Progression of Unilateral Moyamoya Disease. J Korean Neurosurg Soc 49:65\u201367","DOI":"10.3340\/jkns.2011.49.1.65"},{"key":"11793_CR15","doi-asserted-by":"publisher","first-page":"e388","DOI":"10.1212\/WNL.0000000000007819","volume":"93","author":"D Herv\u00e9","year":"2019","unstructured":"Herv\u00e9 D, Ibos-Aug\u00e9 N, Calvi\u00e8re L et al (2019) Predictors of clinical or cerebral lesion progression in adult moyamoya angiopathy. Neurology 93:e388\u2013e397. https:\/\/doi.org\/10.1212\/WNL.0000000000007819","journal-title":"Neurology"},{"key":"11793_CR16","doi-asserted-by":"publisher","first-page":"574","DOI":"10.1007\/s00415-018-9154-7","volume":"266","author":"M Savolainen","year":"2019","unstructured":"Savolainen M, Mustanoja S, Pekkola J et al (2019) Moyamoya angiopathy: long-term follow-up study in a Finnish population. J Neurol 266:574\u2013581. https:\/\/doi.org\/10.1007\/s00415-018-9154-7","journal-title":"J Neurol"},{"key":"11793_CR17","doi-asserted-by":"publisher","first-page":"E17","DOI":"10.3171\/FOC\/2008\/24\/2\/E17","volume":"24","author":"ER Smith","year":"2008","unstructured":"Smith ER, Scott RM (2008) Progression of disease in unilateral moyamoya syndrome. Neurosurg Focus 24:E17. https:\/\/doi.org\/10.3171\/FOC\/2008\/24\/2\/E17","journal-title":"Neurosurg Focus"},{"key":"11793_CR18","doi-asserted-by":"publisher","first-page":"109","DOI":"10.1159\/000093238","volume":"22","author":"ME Kelly","year":"2006","unstructured":"Kelly ME, Bell-Stephens TE, Marks MP et al (2006) Progression of unilateral Moyamoya disease: a clinical series. Cerebrovasc Dis 22:109\u2013115. https:\/\/doi.org\/10.1159\/000093238","journal-title":"Cerebrovasc Dis"},{"key":"11793_CR19","doi-asserted-by":"publisher","first-page":"1837","DOI":"10.1007\/s00701-022-05153-6","volume":"164","author":"X Tian","year":"2022","unstructured":"Tian X, Hu M, Zhang J (2022) The contralateral progression in a cohort of Chinese adult patients with unilateral moyamoya disease after revascularization: a single-center long-term retrospective study. Acta Neurochir (Wien) 164:1837\u20131844. https:\/\/doi.org\/10.1007\/s00701-022-05153-6","journal-title":"Acta Neurochir (Wien)"},{"key":"11793_CR20","doi-asserted-by":"publisher","first-page":"1005","DOI":"10.3171\/2021.3.JNS203913","volume":"136","author":"Y Mineharu","year":"2021","unstructured":"Mineharu Y, Takagi Y, Koizumi A et al (2021) Genetic and nongenetic factors for contralateral progression of unilateral moyamoya disease: the first report from the SUPRA Japan Study Group. J Neurosurg 136:1005\u20131014. https:\/\/doi.org\/10.3171\/2021.3.JNS203913","journal-title":"J Neurosurg"},{"key":"11793_CR21","doi-asserted-by":"publisher","DOI":"10.1161\/JAHA.122.025676","volume":"11","author":"T Ok","year":"2022","unstructured":"Ok T, Jung YH, Kim J et al (2022) RNF213 R4810K variant in suspected unilateral Moyamoya disease predicts contralateral progression. J Am Heart Assoc 11:e025676. https:\/\/doi.org\/10.1161\/JAHA.122.025676","journal-title":"J Am Heart Assoc"},{"key":"11793_CR22","doi-asserted-by":"publisher","first-page":"155","DOI":"10.1159\/000352065","volume":"36","author":"Y Mineharu","year":"2013","unstructured":"Mineharu Y, Takagi Y, Takahashi JC et al (2013) Rapid progression of unilateral Moyamoya disease in a patient with a family history and an RNF213 risk variant. Cerebrovasc Dis 36:155\u2013157. https:\/\/doi.org\/10.1159\/000352065","journal-title":"Cerebrovasc Dis"},{"key":"11793_CR23","doi-asserted-by":"publisher","first-page":"25","DOI":"10.1007\/s12975-021-00940-2","volume":"13","author":"R Mertens","year":"2022","unstructured":"Mertens R, Graupera M, Gerhardt H et al (2022) The genetic basis of Moyamoya disease. Transl Stroke Res 13:25\u201345. https:\/\/doi.org\/10.1007\/s12975-021-00940-2","journal-title":"Transl Stroke Res"},{"key":"11793_CR24","doi-asserted-by":"publisher","first-page":"130","DOI":"10.1016\/j.ejpn.2021.10.007","volume":"35","author":"A Hackenberg","year":"2021","unstructured":"Hackenberg A, Battilana B, Hebeisen M et al (2021) Preoperative clinical symptomatology and stroke burden in pediatric moyamoya angiopathy: defining associated risk variables. Eur J Paediatr Neurol EJPN Off J Eur Paediatr Neurol Soc 35:130\u2013136. https:\/\/doi.org\/10.1016\/j.ejpn.2021.10.007","journal-title":"Eur J Paediatr Neurol EJPN Off J Eur Paediatr Neurol Soc"},{"key":"11793_CR25","doi-asserted-by":"publisher","first-page":"789","DOI":"10.1161\/STROKEAHA.118.023972","volume":"50","author":"L Grangeon","year":"2019","unstructured":"Grangeon L, Guey S, Schwitalla JC et al (2019) Clinical and molecular features of 5 European multigenerational families with Moyamoya angiopathy. Stroke 50:789\u2013796. https:\/\/doi.org\/10.1161\/STROKEAHA.118.023972","journal-title":"Stroke"}],"container-title":["Journal of Neurology"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s00415-023-11793-0.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/article\/10.1007\/s00415-023-11793-0\/fulltext.html","content-type":"text\/html","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/link.springer.com\/content\/pdf\/10.1007\/s00415-023-11793-0.pdf","content-type":"application\/pdf","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2023,8,11]],"date-time":"2023-08-11T12:07:16Z","timestamp":1691755636000},"score":1,"resource":{"primary":{"URL":"https:\/\/link.springer.com\/10.1007\/s00415-023-11793-0"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2023,6,1]]},"references-count":25,"journal-issue":{"issue":"9","published-print":{"date-parts":[[2023,9]]}},"alternative-id":["11793"],"URL":"https:\/\/doi.org\/10.1007\/s00415-023-11793-0","relation":{},"ISSN":["0340-5354","1432-1459"],"issn-type":[{"value":"0340-5354","type":"print"},{"value":"1432-1459","type":"electronic"}],"subject":[],"published":{"date-parts":[[2023,6,1]]},"assertion":[{"value":"5 April 2023","order":1,"name":"received","label":"Received","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"20 May 2023","order":2,"name":"revised","label":"Revised","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"20 May 2023","order":3,"name":"accepted","label":"Accepted","group":{"name":"ArticleHistory","label":"Article History"}},{"value":"1 June 2023","order":4,"name":"first_online","label":"First Online","group":{"name":"ArticleHistory","label":"Article History"}},{"order":1,"name":"Ethics","group":{"name":"EthicsHeading","label":"Declarations"}},{"value":"The authors declare no competing interests.","order":2,"name":"Ethics","group":{"name":"EthicsHeading","label":"Conflicts of interest"}},{"value":"This study was performed in accordance with the ethical standards of the institutional and\/or national research committee and with the 1964 Helsinki Declaration.","order":3,"name":"Ethics","group":{"name":"EthicsHeading","label":"Ethical approval"}},{"value":"This work is based on retrospective data collection, obtained from the routine monitoring of patients\u2019 treatments and their clinical evaluation in the hospital setting. As such, and according to national regulations, it does not require specific approval from the ethics committee.","order":4,"name":"Ethics","group":{"name":"EthicsHeading","label":"Research ethic and patient consent"}}]}}