{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,1,9]],"date-time":"2026-01-09T01:05:11Z","timestamp":1767920711719,"version":"3.49.0"},"reference-count":19,"publisher":"Elsevier BV","license":[{"start":{"date-parts":[[2017,9,1]],"date-time":"2017-09-01T00:00:00Z","timestamp":1504224000000},"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":[[2017,9]]},"DOI":"10.1016\/j.wneu.2017.06.036","type":"journal-article","created":{"date-parts":[[2017,6,12]],"date-time":"2017-06-12T20:17:16Z","timestamp":1497298636000},"page":"1035.e1-1035.e4","update-policy":"https:\/\/doi.org\/10.1016\/elsevier_cm_policy","source":"Crossref","is-referenced-by-count":6,"special_numbering":"C","title":["Case of Familial Moyamoya Disease Presenting 10 Years After Initial Negative Magnetic Resonance Screening in Childhood"],"prefix":"10.1016","volume":"105","author":[{"given":"Jiro","family":"Aoyama","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"ORCID":"https:\/\/orcid.org\/0000-0001-8819-4855","authenticated-orcid":false,"given":"Tadashi","family":"Nariai","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Maki","family":"Mukawa","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Motoki","family":"Inaji","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Yoji","family":"Tanaka","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Taketoshi","family":"Maehara","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"78","reference":[{"key":"10.1016\/j.wneu.2017.06.036_bib1","doi-asserted-by":"crossref","first-page":"288","DOI":"10.1001\/archneur.1969.00480090076012","article-title":"Cerebrovascular \u201cmoyamoya\u201d disease showing abnormal net-like vessels in base of brain","volume":"20","author":"Suzuki","year":"1969","journal-title":"Arch Neurol"},{"key":"10.1016\/j.wneu.2017.06.036_bib2","doi-asserted-by":"crossref","first-page":"34","DOI":"10.1038\/jhg.2010.132","article-title":"A\u00a0genome-wide association study identifies RNF213 as the first moyamoya disease gene","volume":"56","author":"Kamada","year":"2011","journal-title":"J\u00a0Hum Genet"},{"key":"10.1016\/j.wneu.2017.06.036_bib3","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.2017.06.036_bib4","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.2017.06.036_bib5","doi-asserted-by":"crossref","first-page":"e2","DOI":"10.3171\/foc.1998.5.5.5","article-title":"Role of basic fibroblast growth factor in the pathogenesis of moyamoya disease","volume":"5","author":"Houkin","year":"1998","journal-title":"Neurosurg Focus"},{"key":"10.1016\/j.wneu.2017.06.036_bib6","doi-asserted-by":"crossref","first-page":"476","DOI":"10.1016\/j.surneu.2008.10.009","article-title":"Increased expression of serum Matrix Metalloproteinase-9 in patients with moyamoya disease","volume":"72","author":"Fujimura","year":"2009","journal-title":"Surg Neurol"},{"key":"10.1016\/j.wneu.2017.06.036_bib7","doi-asserted-by":"crossref","first-page":"313","DOI":"10.1016\/S0090-3019(81)80017-1","article-title":"A\u00a0new surgical treatment of moyamoya disease in children: a preliminary report","volume":"15","author":"Matsushima","year":"1981","journal-title":"Surg Neurol"},{"key":"10.1016\/j.wneu.2017.06.036_bib8","doi-asserted-by":"crossref","first-page":"696","DOI":"10.3174\/ajnr.A5068","article-title":"Noninvasive evaluation of CBF and perfusion delay of moyamoya disease using arterial spin-labeling MRI with multiple postlabeling delays: comparison with 15O-Gas PET and DSC-MRI","volume":"38","author":"Hara","year":"2017","journal-title":"Am J Neuroradiol"},{"key":"10.1016\/j.wneu.2017.06.036_bib9","doi-asserted-by":"crossref","first-page":"302","DOI":"10.1227\/NEU.0000000000000266","article-title":"Practical clinical use of dynamic susceptibility contrast magnetic resonance imaging for the surgical treatment of moyamoya disease","volume":"74","author":"Ishii","year":"2014","journal-title":"Neurosurgery"},{"key":"10.1016\/j.wneu.2017.06.036_bib10","doi-asserted-by":"crossref","first-page":"1014","DOI":"10.1161\/01.STR.25.5.1014","article-title":"Surgically induced angiogenesis to compensate for hemodynamic cerebral ischemia","volume":"25","author":"Nariai","year":"1994","journal-title":"Stroke"},{"key":"10.1016\/j.wneu.2017.06.036_bib11","doi-asserted-by":"crossref","first-page":"353","DOI":"10.3171\/2011.12.PEDS1172","article-title":"Spontaneous occlusion of the circle of Willis in children: pediatric moyamoya summary with proposed evidence-based practice guidelines. A review","volume":"9","author":"Smith","year":"2012","journal-title":"J\u00a0Neurosurg Pediatr"},{"key":"10.1016\/j.wneu.2017.06.036_bib12","doi-asserted-by":"crossref","first-page":"123","DOI":"10.1016\/j.clineuro.2008.09.022","article-title":"Efficacy of the revascularization surgery for adult-onset moyamoya disease with the progression of cerebrovascular lesions","volume":"111","author":"Narisawa","year":"2009","journal-title":"Clin Neurol Neurosurg"},{"key":"10.1016\/j.wneu.2017.06.036_bib13","doi-asserted-by":"crossref","first-page":"42","DOI":"10.1161\/STROKEAHA.107.490714","article-title":"Prevalence and clinicoepidemiological features of moyamoya disease in Japan: findings from a nationwide epidemiological survey","volume":"39","author":"Kuriyama","year":"2008","journal-title":"Stroke"},{"key":"10.1016\/j.wneu.2017.06.036_bib14","doi-asserted-by":"crossref","first-page":"S162","DOI":"10.1016\/S0303-8467(97)00054-1","article-title":"Familial occurrence of moyamoya disease","volume":"99","author":"Yamauchi","year":"1997","journal-title":"Clin Neurol Neurosurg"},{"key":"10.1016\/j.wneu.2017.06.036_bib15","doi-asserted-by":"crossref","first-page":"1056","DOI":"10.1016\/S1474-4422(08)70240-0","article-title":"Moyamoya disease: current concepts and future perspectives","volume":"7","author":"Kuroda","year":"2008","journal-title":"Lancet Neurol"},{"key":"10.1016\/j.wneu.2017.06.036_bib16","doi-asserted-by":"crossref","first-page":"175","DOI":"10.3171\/2013.4.PEDS12420","article-title":"Clinical features of familial juvenile cases of moyamoya disease: analysis of patients treated in a single institute over a 28-year period","volume":"12","author":"Mukawa","year":"2013","journal-title":"J Neurosurg Pediatr"},{"key":"10.1016\/j.wneu.2017.06.036_bib17","doi-asserted-by":"crossref","first-page":"405","DOI":"10.1179\/016164103101201571","article-title":"Temporal profile of angiographical stages of moyamoya disease: when does moyamoya disease progress?","volume":"4","author":"Ishii","year":"2003","journal-title":"Neurol Res"},{"key":"10.1016\/j.wneu.2017.06.036_bib18","doi-asserted-by":"crossref","first-page":"e8","DOI":"10.1016\/j.jstrokecerebrovasdis.2016.09.035","article-title":"De novo development of moyamoya disease in an adult female with a genetic variant of the RNF-213 gene: case report","volume":"26","author":"Tashiro","year":"2017","journal-title":"J\u00a0Stroke Cerebrovasc Dis"},{"key":"10.1016\/j.wneu.2017.06.036_bib19","doi-asserted-by":"crossref","first-page":"e001862","DOI":"10.1161\/JAHA.115.001862","article-title":"Systematic validation of RNF213 coding variants in Japanese patients with moyamoya disease","volume":"4","author":"Moteki","year":"2015","journal-title":"J\u00a0Am Heart Assoc"}],"container-title":["World Neurosurgery"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1878875017309282?httpAccept=text\/xml","content-type":"text\/xml","content-version":"vor","intended-application":"text-mining"},{"URL":"https:\/\/api.elsevier.com\/content\/article\/PII:S1878875017309282?httpAccept=text\/plain","content-type":"text\/plain","content-version":"vor","intended-application":"text-mining"}],"deposited":{"date-parts":[[2018,8,31]],"date-time":"2018-08-31T19:01:13Z","timestamp":1535742073000},"score":1,"resource":{"primary":{"URL":"https:\/\/linkinghub.elsevier.com\/retrieve\/pii\/S1878875017309282"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2017,9]]},"references-count":19,"alternative-id":["S1878875017309282"],"URL":"https:\/\/doi.org\/10.1016\/j.wneu.2017.06.036","relation":{},"ISSN":["1878-8750"],"issn-type":[{"value":"1878-8750","type":"print"}],"subject":[],"published":{"date-parts":[[2017,9]]},"assertion":[{"value":"Elsevier","name":"publisher","label":"This article is maintained by"},{"value":"Case of Familial Moyamoya Disease Presenting 10 Years After Initial Negative Magnetic Resonance Screening in Childhood","name":"articletitle","label":"Article Title"},{"value":"World Neurosurgery","name":"journaltitle","label":"Journal Title"},{"value":"https:\/\/doi.org\/10.1016\/j.wneu.2017.06.036","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"}]}}