{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2024,6,7]],"date-time":"2024-06-07T00:33:42Z","timestamp":1717720422259},"reference-count":12,"publisher":"Springer Science and Business Media LLC","content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,6,6]]},"DOI":"10.7759\/cureus.61804","type":"journal-article","created":{"date-parts":[[2024,6,6]],"date-time":"2024-06-06T13:55:30Z","timestamp":1717682130000},"source":"Crossref","is-referenced-by-count":0,"title":["An Unusual Presentation of Moyamoya Disease in a Pediatric Patient"],"prefix":"10.7759","author":[{"given":"Ola","family":"Shahrour","sequence":"first","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Abdulqader","family":"Al Zubaidi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]},{"given":"Salwa","family":"Al Kaabi","sequence":"additional","affiliation":[],"role":[{"role":"author","vocabulary":"crossref"}]}],"member":"297","reference":[{"key":"ref1","doi-asserted-by":"publisher","DOI":"10.1177\/159101990300900105","article-title":"Moyamoya disease is a progressive occlusive arteriopathy of the primitive internal carotid artery","volume":"9","author":"Komiyama M","year":"2003","unstructured":"Komiyama M. Moyamoya disease is a progressive occlusive arteriopathy of the primitive internal carotid artery. Interv Neuroradiol. 2003, 9:39-45. 10.1177\/159101990300900105","journal-title":"Interv Neuroradiol"},{"key":"ref2","doi-asserted-by":"publisher","DOI":"10.1001\/archneur.1969.00480090076012","article-title":"Cerebrovascular \"moyamoya\" disease. Disease showing abnormal net-like vessels in base of brain","volume":"20","author":"Suzuki J","year":"1969","unstructured":"Suzuki J, Takaku A. Cerebrovascular \"moyamoya\" disease. Disease showing abnormal net-like vessels in base of brain. Arch Neurol. 1969, 20:288-99. 10.1001\/archneur.1969.00480090076012","journal-title":"Arch Neurol"},{"key":"ref3","doi-asserted-by":"publisher","DOI":"10.1055\/s-2005-868160","article-title":"Surgical management of moyamoya syndrome","volume":"15","author":"Smith ER","year":"2005","unstructured":"Smith ER, Scott RM. Surgical management of moyamoya syndrome. Skull Base. 2005, 15:15-26. 10.1055\/s-2005-868160","journal-title":"Skull Base"},{"key":"ref4","doi-asserted-by":"publisher","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 S","year":"2008","unstructured":"Kuriyama S, Kusaka Y, Fujimura M, et al.. Prevalence and clinicoepidemiological features of moyamoya disease in Japan: findings from a nationwide epidemiological survey. Stroke. 2008, 39:42-7. 10.1161\/STROKEAHA.107.490714","journal-title":"Stroke"},{"key":"ref5","doi-asserted-by":"publisher","DOI":"10.1002\/ana.21981","article-title":"Pediatric moyamoya disease: an analysis of 410 consecutive cases","volume":"68","author":"Kim SK","year":"2010","unstructured":"Kim SK, Cho BK, Phi JH, et al.. Pediatric moyamoya disease: an analysis of 410 consecutive cases. Ann Neurol. 2010, 68:92-101. 10.1002\/ana.21981","journal-title":"Ann Neurol"},{"key":"ref6","doi-asserted-by":"publisher","DOI":"10.2147\/TACG.S252736","article-title":"Genetic and proteomic contributions to the pathophysiology of moyamoya angiopathy and related vascular diseases","volume":"14","author":"Dorschel KB","year":"2021","unstructured":"Dorschel KB, Wanebo JE. Genetic and proteomic contributions to the pathophysiology of moyamoya angiopathy and related vascular diseases. Appl Clin Genet. 2021, 14:145-71. 10.2147\/TACG.S252736","journal-title":"Appl Clin Genet"},{"key":"ref7","doi-asserted-by":"publisher","DOI":"10.12659\/AJCR.889170","article-title":"Pediatric moyamoya disease","volume":"14","author":"Nagiub M","year":"2013","unstructured":"Nagiub M, Allarakhia I. Pediatric moyamoya disease. Am J Case Rep. 2013, 14:134-8. 10.12659\/AJCR.889170","journal-title":"Am J Case Rep"},{"key":"ref8","doi-asserted-by":"publisher","DOI":"10.1590\/0100-3984.2021.0010","article-title":"Moyamoya disease and syndrome: a review","volume":"55","author":"Demartini Z Jr","year":"2022","unstructured":"Demartini Z Jr, Teixeira BC, Koppe GL, Gatto LA, Roman A, Munhoz RP. Moyamoya disease and syndrome: a review. Radiol Bras. 2022, 55:31-7. 10.1590\/0100-3984.2021.0010","journal-title":"Radiol Bras"},{"key":"ref9","doi-asserted-by":"publisher","DOI":"10.1371\/journal.pone.0048179","article-title":"Molecular analysis of RNF213 gene for moyamoya disease in the Chinese Han population","volume":"7","author":"Wu Z","year":"2012","unstructured":"Wu Z, Jiang H, Zhang L, et al.. Molecular analysis of RNF213 gene for moyamoya disease in the Chinese Han population. PLoS One. 2012, 7:e48179. 10.1371\/journal.pone.0048179","journal-title":"PLoS One"},{"key":"ref10","doi-asserted-by":"publisher","DOI":"10.2147\/TACG.S42772","article-title":"Moyamoya disease and syndromes: from genetics to clinical management","volume":"8","author":"Guey S","year":"2015","unstructured":"Guey S, Tournier-Lasserve E, Herv\u00e9 D, Kossorotoff M. Moyamoya disease and syndromes: from genetics to clinical management. Appl Clin Genet. 2015, 8:49-68. 10.2147\/TACG.S42772","journal-title":"Appl Clin Genet"},{"key":"ref11","doi-asserted-by":"publisher","DOI":"10.1111\/j.1600-0404.1999.tb01050.x","article-title":"Migraine with aura-like headache associated with moyamoya disease","volume":"100","author":"Park-Matsumoto YC","year":"2009","unstructured":"Park-Matsumoto YC, Tazawa T, Shimizu J. Migraine with aura-like headache associated with moyamoya disease. Acta Neurol Scand. 2009, 100:119-21. 10.1111\/j.1600-0404.1999.tb01050.x","journal-title":"Acta Neurol Scand"},{"key":"ref12","doi-asserted-by":"publisher","DOI":"10.1155\/2011\/329738","article-title":"Moya moya disease in a child: a case report","volume":"2011","author":"Goyal JP","year":"2011","unstructured":"Goyal JP, Rao SS, Trivedi S. Moya moya disease in a child: a case report. Case Rep Neurol Med. 2011, 2011:329738. 10.1155\/2011\/329738","journal-title":"Case Rep Neurol Med"}],"container-title":["Cureus"],"original-title":[],"language":"en","link":[{"URL":"https:\/\/www.cureus.com\/articles\/241613-an-unusual-presentation-of-moyamoya-disease-in-a-pediatric-patient","content-type":"unspecified","content-version":"vor","intended-application":"similarity-checking"}],"deposited":{"date-parts":[[2024,6,6]],"date-time":"2024-06-06T13:55:35Z","timestamp":1717682135000},"score":1,"resource":{"primary":{"URL":"https:\/\/www.cureus.com\/articles\/241613-an-unusual-presentation-of-moyamoya-disease-in-a-pediatric-patient"}},"subtitle":[],"short-title":[],"issued":{"date-parts":[[2024,6,6]]},"references-count":12,"URL":"https:\/\/doi.org\/10.7759\/cureus.61804","relation":{},"ISSN":["2168-8184"],"issn-type":[{"value":"2168-8184","type":"print"}],"subject":[],"published":{"date-parts":[[2024,6,6]]}}}