Kamer Tandoğan, Ayça Özkul, M. Çabalar, Ö. Kılıçkesmez, Ugur Demir, Tevfik Güzelbey, Mehmet Cingöz
{"title":"基底动脉狭窄置入烟雾病病例","authors":"Kamer Tandoğan, Ayça Özkul, M. Çabalar, Ö. Kılıçkesmez, Ugur Demir, Tevfik Güzelbey, Mehmet Cingöz","doi":"10.4274/csmedj.galenos.2023.2022-2-2","DOIUrl":null,"url":null,"abstract":"Moyamoya disease is a chronic, progressive hereditary disease characterized by narrowing of the vascular lumen because of hypertrophy of smooth muscles in the walls of the arteries that form the circle of Willis. Cerebral vessels may be encountered in bleeding and occlusion clinics. Although it is seen as predominant in Asian races, cases have been reported worldwide. Although its etiopathogenesis is not clear, genetics, some infectious agents","PeriodicalId":366898,"journal":{"name":"Cam and Sakura Medical Journal","volume":"40 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-08-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Moyamoya Case with Stenting for Basilar Stenosis\",\"authors\":\"Kamer Tandoğan, Ayça Özkul, M. Çabalar, Ö. Kılıçkesmez, Ugur Demir, Tevfik Güzelbey, Mehmet Cingöz\",\"doi\":\"10.4274/csmedj.galenos.2023.2022-2-2\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Moyamoya disease is a chronic, progressive hereditary disease characterized by narrowing of the vascular lumen because of hypertrophy of smooth muscles in the walls of the arteries that form the circle of Willis. Cerebral vessels may be encountered in bleeding and occlusion clinics. Although it is seen as predominant in Asian races, cases have been reported worldwide. Although its etiopathogenesis is not clear, genetics, some infectious agents\",\"PeriodicalId\":366898,\"journal\":{\"name\":\"Cam and Sakura Medical Journal\",\"volume\":\"40 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2023-08-03\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Cam and Sakura Medical Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.4274/csmedj.galenos.2023.2022-2-2\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Cam and Sakura Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4274/csmedj.galenos.2023.2022-2-2","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Moyamoya disease is a chronic, progressive hereditary disease characterized by narrowing of the vascular lumen because of hypertrophy of smooth muscles in the walls of the arteries that form the circle of Willis. Cerebral vessels may be encountered in bleeding and occlusion clinics. Although it is seen as predominant in Asian races, cases have been reported worldwide. Although its etiopathogenesis is not clear, genetics, some infectious agents
求助内容：
应助结果提醒方式：
京公网安备 11010802042870号
