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KCNT1基因突变 新生儿恶性癫痫
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KCNT1基因突变 新生儿恶性癫痫
卡维地洛抑制KCNT1基因突变引起的新生儿恶性癫痫，为治疗难治性癫痫提供新希望
https://www.ebiotrade.com/newsf/2024-11/20241102063949052.htm
http://www.pubmedplus.cn/P/SearchQuickResult?wd=f7b0402d-e82d-4e7e-9cbb-88f3cbc409f3
| 01. | Humans | 48 篇 | 85.714% |
| 02. | Infant, Newborn | 44 篇 | 78.571% |
| 03. | Infant | 34 篇 | 60.714% |
| 04. | Female | 33 篇 | 58.929% |
| 05. | Tuberous Sclerosis | 27 篇 | 48.214% |
| 06. | Child, Preschool | 26 篇 | 46.429% |
| 07. | Epilepsy | 26 篇 | 46.429% |
| 08. | Male | 26 篇 | 46.429% |
| 09. | Child | 22 篇 | 39.286% |
| 10. | Mutation | 21 篇 | 37.500% |
https://blog.sciencenet.cn/blog-280034-1458149.html
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