Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhage

CHIH-HAO CHENChu, Yung-TsaiYung-TsaiChuYA-FANG CHENKo, Tzu-YuTzu-YuKoYU-WEN CHENGMING-JEN LEEPEI-LUNG CHENSUNG-CHUN TANGJIANN-SHING JENG2022-11-082022-11-082022-111351-5101https://scholars.lib.ntu.edu.tw/handle/123456789/624500The NOTCH3 mutation is a common cause of hereditary cerebral small vessel disease (CSVD) and may be a cause of spontaneous intracerebral haemorrhage (ICH). The aim was to investigate the clinical/imaging features for identifying the NOTCH3-mutation-related ICH.enNOTCH3; CADASIL; MRI; cerebral microbleed; intracerebral haemorrhage[SDGs]SDG3Comparison of clinical and neuroimaging features between NOTCH3 mutations and nongenetic spontaneous intracerebral haemorrhagejournal article10.1111/ene.15485357819122-s2.0-85135020021WOS:000826359100001https://scholars.lib.ntu.edu.tw/handle/123456789/617809