{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,4,18]],"date-time":"2024-04-18T11:14:51Z","timestamp":1713438891123},"reference-count":18,"publisher":"Springer Science and Business Media LLC","issue":"5","license":[{"start":{"date-parts":[[2024,1,5]],"date-time":"2024-01-05T00:00:00Z","timestamp":1704412800000},"content-version":"tdm","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0"},{"start":{"date-parts":[[2024,1,5]],"date-time":"2024-01-05T00:00:00Z","timestamp":1704412800000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/creativecommons.org\/licenses\/by\/4.0"}],"content-domain":{"domain":["link.springer.com"],"crossmark-restriction":false},"short-container-title":["Childs Nerv Syst"],"published-print":{"date-parts":[[2024,5]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:p>The term Moyamoya , or \u201cpuff of smoke\u201d in Japanese , was first used in 1969 by Suzuki and Takaku to describe the\u00a0classical appearance of collateral blood vessels in response to progressive vascular stenosis of distal internal\u00a0carotid artery (ICA). Such condition may result in various clinical presentations ranging from strokes to\u00a0developmental delays. In order to cease the progression of such stenotic vasculopathy, several means of\u00a0revascularization have been developed over the years. In this paper we present a case of a two-year-old girl with\u00a0history of myelomeningocele repair and ventriculoperitoneal shunt insertion followed by manifestation of Moyamoya\u00a0syndrome later in childhood as an evidence of revascularization through a burr hole. To our knowledge, this paper\u00a0is the first of its kind to report such findings in one patient. Moreover, this paper provides a historical perspective on\u00a0the development of different types of revascularization techniques.<\/jats:p>","DOI":"10.1007\/s00381-023-06263-x","type":"journal-article","created":{"date-parts":[[2024,1,5]],"date-time":"2024-01-05T12:02:12Z","timestamp":1704456132000},"page":"1613-1616","update-policy":"http:\/\/dx.doi.org\/10.1007\/springer_crossmark_policy","source":"Crossref","is-referenced-by-count":0,"title":["Evidence of pial synagiosis through ventriculoperitoneal shunt entry site in a patient who manifested Moyamoya syndrome later in childhood: A case report and historical perspective"],"prefix":"10.1007","volume":"40","author":[{"given":"Awn","family":"AlEssa","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Alaa","family":"AlSahli","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Tariq","family":"AlJared","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","published-online":{"date-parts":[[2024,1,5]]},"reference":[{"issue":"12","key":"6263_CR1","doi-asserted-by":"publisher","first-page":"1226","DOI":"10.1056\/NEJMra0804622","volume":"360","author":"R Scott","year":"2009","unstructured":"Scott R, Smith E (2009) Moyamoya disease and Moyamoya syndrome. 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