{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,6]],"date-time":"2026-10-06T14:01:35Z","timestamp":1791295295617,"version":"4.1.0"},"reference-count":24,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2017,3,1]],"date-time":"2017-03-01T00:00:00Z","timestamp":1488326400000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/www.elsevier.com\/tdm\/userlicense\/1.0\/"}],"content-domain":{"domain":["clinicalkey.jp","clinicalkey.com","worldneurosurgery.org","clinicalkey.es","clinicalkey.com.au","clinicalkey.fr","elsevier.com","sciencedirect.com"],"crossmark-restriction":true},"short-container-title":["World Neurosurgery"],"published-print":{"date-parts":[[2017,3]]},"DOI":"10.1016\/j.wneu.2016.12.119","type":"journal-article","created":{"date-parts":[[2017,1,5]],"date-time":"2017-01-05T20:49:22Z","timestamp":1483649362000},"page":"701-708.e1","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":22,"special_numbering":"C","title":["The Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease and a Review of the Pertinent Literature"],"prefix":"10.1016","volume":"99","author":[{"given":"Qian","family":"Zhang","sequence":"first","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yaping","family":"Liu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Lebao","family":"Yu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Ran","family":"Duan","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yonggang","family":"Ma","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Peicong","family":"Ge","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dong","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yan","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Rong","family":"Wang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Shuo","family":"Wang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yuanli","family":"Zhao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Yong","family":"Cao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xingju","family":"Liu","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xiaofeng","family":"Deng","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Jizong","family":"Zhao","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Xue","family":"Zhang","sequence":"additional","affiliation":[],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"78","reference":[{"key":"10.1016\/j.wneu.2016.12.119_bib1","doi-asserted-by":"crossref","first-page":"245","DOI":"10.2176\/nmc.52.245","article-title":"Guidelines for diagnosis and treatment of moyamoya disease (spontaneous occlusion of the circle of Willis)","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 Disease","year":"2012","journal-title":"Neurol Med Chir"},{"key":"10.1016\/j.wneu.2016.12.119_bib2","doi-asserted-by":"crossref","first-page":"1226","DOI":"10.1056\/NEJMra0804622","article-title":"Moyamoya disease and moyamoya syndrome","volume":"360","author":"Scott","year":"2009","journal-title":"N\u00a0Engl J Med"},{"key":"10.1016\/j.wneu.2016.12.119_bib3","doi-asserted-by":"crossref","first-page":"935","DOI":"10.1007\/s00701-014-2013-0","article-title":"Nationwide survey on quasi-moyamoya disease in Japan","volume":"156","author":"Hayashi","year":"2014","journal-title":"Acta Neurochir"},{"key":"10.1016\/j.wneu.2016.12.119_bib4","doi-asserted-by":"crossref","first-page":"930","DOI":"10.1016\/j.clineuro.2012.09.020","article-title":"An epidemiological survey of moyamoya disease, unilateral moyamoya disease and quasi-moyamoya disease in Japan","volume":"115","author":"Hayashi","year":"2013","journal-title":"Clin Neurol Neurosurg"},{"key":"10.1016\/j.wneu.2016.12.119_bib5","doi-asserted-by":"crossref","first-page":"1344","DOI":"10.1016\/j.jstrokecerebrovasdis.2013.11.008","article-title":"Coexisting diseases of moyamoya vasculopathy","volume":"23","author":"Wei","year":"2014","journal-title":"J\u00a0Stroke Cerebrovasc Dis"},{"key":"10.1016\/j.wneu.2016.12.119_bib6","doi-asserted-by":"crossref","first-page":"803","DOI":"10.1212\/WNL.0b013e318249f71f","article-title":"Homozygous c.14576G>A variant of RNF213 predicts early-onset and severe form of moyamoya disease","volume":"78","author":"Miyatake","year":"2012","journal-title":"Neurology"},{"key":"10.1016\/j.wneu.2016.12.119_bib7","doi-asserted-by":"crossref","first-page":"e22542","DOI":"10.1371\/journal.pone.0022542","article-title":"Identification of RNF213 as a susceptibility gene for moyamoya disease and its possible role in vascular development","volume":"6","author":"Liu","year":"2011","journal-title":"PLoS One"},{"key":"10.1016\/j.wneu.2016.12.119_bib8","first-page":"1","article-title":"RNF213 as the major susceptibility gene for Chinese patients with moyamoya disease and its clinical relevance","author":"Zhang","year":"2016","journal-title":"J Neurosurg"},{"key":"10.1016\/j.wneu.2016.12.119_bib9","doi-asserted-by":"crossref","first-page":"3371","DOI":"10.1161\/STROKEAHA.112.663864","article-title":"Identification of a genetic variant common to moyamoya disease and intracranial major artery stenosis\/occlusion","volume":"43","author":"Miyawaki","year":"2012","journal-title":"Stroke"},{"key":"10.1016\/j.wneu.2016.12.119_bib10","doi-asserted-by":"crossref","first-page":"2894","DOI":"10.1161\/STROKEAHA.113.002477","article-title":"Genetic variant RNF213 c.14576G>A in various phenotypes of intracranial major artery stenosis\/occlusion","volume":"44","author":"Miyawaki","year":"2013","journal-title":"Stroke"},{"key":"10.1016\/j.wneu.2016.12.119_bib11","doi-asserted-by":"crossref","first-page":"e0156607","DOI":"10.1371\/journal.pone.0156607","article-title":"A\u00a0Polymorphism in RNF213 Is a Susceptibility Gene for Intracranial Atherosclerosis","volume":"11","author":"Bang","year":"2016","journal-title":"PLoS One"},{"key":"10.1016\/j.wneu.2016.12.119_bib12","doi-asserted-by":"crossref","first-page":"e0130663","DOI":"10.1371\/journal.pone.0130663","article-title":"Adult Moyamoya Disease: A Burden of Intracranial Stenosis in East Asians?","volume":"10","author":"Bang","year":"2015","journal-title":"PLoS One"},{"key":"10.1016\/j.wneu.2016.12.119_bib13","doi-asserted-by":"crossref","first-page":"1075","DOI":"10.1016\/j.jstrokecerebrovasdis.2015.01.005","article-title":"Genetic Analysis of RNF213 c.14576G>A Variant in Nonatherosclerotic Quasi-Moyamoya Disease","volume":"24","author":"Miyawaki","year":"2015","journal-title":"J\u00a0Stroke Cerebrovasc Dis"},{"key":"10.1016\/j.wneu.2016.12.119_bib14","doi-asserted-by":"crossref","first-page":"2632","DOI":"10.1016\/j.jstrokecerebrovasdis.2016.07.004","article-title":"Significant association of the RNF213 p.R4810K polymorphism with quasi-moyamoya disease","volume":"25","author":"Morimoto","year":"2016","journal-title":"J\u00a0Stroke Cerebrovasc Dis"},{"key":"10.1016\/j.wneu.2016.12.119_bib15","doi-asserted-by":"crossref","first-page":"373","DOI":"10.1016\/j.jstrokecerebrovasdis.2010.10.001","article-title":"Mechanism of moyamoya vessels secondary to intracranial atherosclerotic disease: angiographic findings in patients with middle cerebral artery occlusion","volume":"21","author":"Tanaka","year":"2012","journal-title":"J\u00a0Stroke Cerebrovasc Dis"},{"key":"10.1016\/j.wneu.2016.12.119_bib16","doi-asserted-by":"crossref","first-page":"530","DOI":"10.1016\/j.wneu.2015.12.093","article-title":"Clinical and Angiographic Features of Patients with Moyamoya Disease and the p.R4810K Heterozygous Variant","volume":"90","author":"Zhang","year":"2016","journal-title":"World Neurosurg"},{"key":"10.1016\/j.wneu.2016.12.119_bib17","doi-asserted-by":"crossref","first-page":"717","DOI":"10.3171\/2015.10.PEDS15537","article-title":"Association between moyamoya syndrome and the RNF213 c.14576G>A variant in patients with neurofibromatosis Type 1","volume":"17","author":"Phi","year":"2016","journal-title":"J\u00a0Neurosurg Pediatr"},{"key":"10.1016\/j.wneu.2016.12.119_bib18","doi-asserted-by":"crossref","first-page":"822","DOI":"10.1016\/j.braindev.2014.12.006","article-title":"Early onset of moyamoya syndrome in a Down syndrome patient with the genetic variant RNF213 p.R4810K","volume":"37","author":"Chong","year":"2015","journal-title":"Brain Dev"},{"key":"10.1016\/j.wneu.2016.12.119_bib19","doi-asserted-by":"crossref","first-page":"299","DOI":"10.2176\/nmc.52.299","article-title":"Distribution of moyamoya disease susceptibility polymorphism p.R4810K in RNF213 in East and Southeast Asian populations","volume":"52","author":"Liu","year":"2012","journal-title":"Neurol Med Chir"},{"key":"10.1016\/j.wneu.2016.12.119_bib20","doi-asserted-by":"crossref","first-page":"173","DOI":"10.1161\/STROKEAHA.109.562264","article-title":"Association of thyroid autoantibodies with moyamoya-type cerebrovascular disease: a prospective study","volume":"41","author":"Kim","year":"2010","journal-title":"Stroke"},{"key":"10.1016\/j.wneu.2016.12.119_bib21","doi-asserted-by":"crossref","first-page":"13191","DOI":"10.1038\/srep13191","article-title":"Moyamoya disease susceptibility gene RNF213 links inflammatory and angiogenic signals in endothelial cells","volume":"5","author":"Ohkubo","year":"2015","journal-title":"Sci Rep"},{"key":"10.1016\/j.wneu.2016.12.119_bib22","doi-asserted-by":"crossref","first-page":"3200","DOI":"10.1161\/STROKEAHA.114.006244","article-title":"RNF213 rare variants in an ethnically diverse population with Moyamoya disease","volume":"45","author":"Cecchi","year":"2014","journal-title":"Stroke"},{"key":"10.1016\/j.wneu.2016.12.119_bib23","doi-asserted-by":"crossref","first-page":"e49222","DOI":"10.1371\/journal.pone.0049222","article-title":"Loss of NF1 expression in human endothelial cells promotes autonomous proliferation and altered vascular morphogenesis","volume":"7","author":"Bajaj","year":"2012","journal-title":"PLoS One"},{"key":"10.1016\/j.wneu.2016.12.119_bib24","doi-asserted-by":"crossref","first-page":"155","DOI":"10.1159\/000352065","article-title":"Rapid progression of unilateral moyamoya disease in a patient with a family history and an RNF213 risk variant","volume":"36","author":"Mineharu","year":"2013","journal-title":"Cerebrovasc Dis"}],"container-title":["World Neurosurgery"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1878875016314346?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1878875016314346?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,9,5]],"date-time":"2018-09-05T08:53:53Z","timestamp":1536137633000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1878875016314346"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,3]]},"references-count":24,"alternative-id":["S1878875016314346"],"URL":"https:\/\/doi.org\/10.1016\/j.wneu.2016.12.119","relation":{},"ISSN":["1878-8750"],"issn-type":[{"value":"1878-8750","type":"print"}],"subject":[],"published":{"date-parts":[[2017,3]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"The Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease and a Review of the Pertinent Literature","name":"articletitle","label":"Article Title"},{"value":"World Neurosurgery","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.wneu.2016.12.119","name":"articlelink","label":"CrossRef DOI link to publisher maintained version"},{"value":"article","name":"content_type","label":"Content Type"},{"value":"\u00a9 2017 Elsevier Inc. All rights reserved.","name":"copyright","label":"Copyright"}]}}