医学
临床试验
髓鞘少突胶质细胞糖蛋白
多发性硬化
免疫疗法
免疫学
重症监护医学
生物信息学
临床神经学
靶向治疗
疾病
梅德林
神经科学
免疫系统
临床研究设计
转化研究
肿瘤科
少突胶质细胞
芬戈莫德
个性化医疗
神经保护
人口
作者
Edgar Carnero Contentti,Vinícius Boldrini,Adriana Casallas‐Vanegas,Sanja Gluščević,Emine Rabia Koç,Sara Samadzadeh,Meral Seferoğlu,Natalia Szejko,Michael Levy
标识
DOI:10.1080/14728214.2025.2565189
摘要
Targeted immunotherapies have the potential to transform MOGAD management. In the next five years, one or more of these agents may achieve regulatory approval, particularly if biomarker-driven strategies and trial designs are refined. Addressing unmet needs in pediatric populations and low-resource settings will be essential to ensure equitable, personalized treatment.
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