{"title":"杜氏肌营养不良的综合治疗方案","authors":"Sanjana Kareti, A. Kapadia, S. Dravida","doi":"10.15406/jsrt.2016.01.00030","DOIUrl":null,"url":null,"abstract":"Duchenne muscular dystrophy (DMD), a genetic neuromuscular disorder, has a pernicious influence on skeletal and cardiac muscle tissue and results in a significant decline in the life span of those affected. The destruction is mainly attributed to perpetuating inflammation and fibrosis. This review explores the potential of a comprehensive therapeutic approach with an objective to minimize ongoing damage and reconstitute normal tissue.","PeriodicalId":91560,"journal":{"name":"Journal of stem cell research & therapeutics","volume":"45 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2016-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Integrated treatment regime for duchenne muscular dystrophy\",\"authors\":\"Sanjana Kareti, A. Kapadia, S. Dravida\",\"doi\":\"10.15406/jsrt.2016.01.00030\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Duchenne muscular dystrophy (DMD), a genetic neuromuscular disorder, has a pernicious influence on skeletal and cardiac muscle tissue and results in a significant decline in the life span of those affected. The destruction is mainly attributed to perpetuating inflammation and fibrosis. This review explores the potential of a comprehensive therapeutic approach with an objective to minimize ongoing damage and reconstitute normal tissue.\",\"PeriodicalId\":91560,\"journal\":{\"name\":\"Journal of stem cell research & therapeutics\",\"volume\":\"45 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2016-09-27\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of stem cell research & therapeutics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15406/jsrt.2016.01.00030\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of stem cell research & therapeutics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15406/jsrt.2016.01.00030","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Integrated treatment regime for duchenne muscular dystrophy
Duchenne muscular dystrophy (DMD), a genetic neuromuscular disorder, has a pernicious influence on skeletal and cardiac muscle tissue and results in a significant decline in the life span of those affected. The destruction is mainly attributed to perpetuating inflammation and fibrosis. This review explores the potential of a comprehensive therapeutic approach with an objective to minimize ongoing damage and reconstitute normal tissue.
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