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pro vyhledávání: '"Lushi Liang"'
Autor:
Yuyi Chen, Dongling Yang, Xuelin Huang, Juntan Feng, Qingqing Zhao, Huixian Huang, Lushi Liang, Xinxin Zhang, Yiyan Ruan
Publikováno v:
Frontiers in Neurology, Vol 15 (2024)
BackgroundSpinal muscular atrophy (SMA) is a genetic progressive neuromuscular disease. Nusinersen is the first disease modifying drug approved to treat patients with SMA. Our study aimed to evaluate the efficacy of nusinersen treatment on motor func
Externí odkaz:
https://doaj.org/article/16b2efad4a1b4a9d9b78ac25be0b1340
