{"title":"全胼胝体切开术治疗难治性lenox - gastaut综合征后改善21三体患者的发育质量:1例报告","authors":"Manami Mizumoto, Toshihiro Jogamoto, Takahiro Motoki, Satoshi Suehiro, T. Kunieda, Mariko Eguchi","doi":"10.3805/eands.14.71","DOIUrl":null,"url":null,"abstract":"","PeriodicalId":39430,"journal":{"name":"Epilepsy and Seizure","volume":"116 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Improved developmental quality in a patient with trisomy 21 following treatment for refractory Lennox-Gastaut syndrome by total corpus callosotomy: a case report\",\"authors\":\"Manami Mizumoto, Toshihiro Jogamoto, Takahiro Motoki, Satoshi Suehiro, T. Kunieda, Mariko Eguchi\",\"doi\":\"10.3805/eands.14.71\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"\",\"PeriodicalId\":39430,\"journal\":{\"name\":\"Epilepsy and Seizure\",\"volume\":\"116 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Epilepsy and Seizure\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3805/eands.14.71\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Epilepsy and Seizure","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3805/eands.14.71","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Improved developmental quality in a patient with trisomy 21 following treatment for refractory Lennox-Gastaut syndrome by total corpus callosotomy: a case report