{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,8,13]],"date-time":"2026-08-13T20:43:55Z","timestamp":1786653835202,"version":"build-2736575974"},"reference-count":12,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"3","license":[{"start":{"date-parts":[[2026,5,1]],"date-time":"2026-05-01T00:00:00Z","timestamp":1777593600000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2026,5]]},"abstract":"<jats:title>\n                    A\n                    <jats:sc>BSTRACT<\/jats:sc>\n                  <\/jats:title>\n                  <jats:p>Moyamoya syndrome (MMS) is a rare association of Moyamoya disease with underlying other disease, which mainly includes sickle cell disease and neurofibromatosis type 1 (NF1). We hereby report a case of MMS with an underlying ganglioneuroma, which has not been reported yet, and thus extend the spectrum of MMS.<\/jats:p>","DOI":"10.4103\/jiaps.jiaps_387_25","type":"journal-article","created":{"date-parts":[[2026,5,5]],"date-time":"2026-05-05T20:00:37Z","timestamp":1778011237000},"page":"501-504","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["Extending the Spectrum of Moyamoya Syndrome"],"prefix":"10.4103","volume":"31","author":[{"given":"Prince","family":"Raj","sequence":"first","affiliation":[{"name":"Department of Pediatric Surgery, AIIMS, Raipur, Chhattisgarh, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"T Narasimha","family":"Murty","sequence":"additional","affiliation":[{"name":"Department of Pediatric Surgery, AIIMS, Raipur, Chhattisgarh, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Nitin 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