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Article

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

European journal of neurology - 1 Nov 2022

Chen Chih-Hao, Chu Yung-Tsai, Chen Ya-Fang, Ko Tzu-Yu, Cheng Yu-Wen, Lee Ming-Jen, Chen Pei-Lung, Tang Sung-Chun, Jeng Jiann-Shing

Abstract excerpt

BACKGROUND AND PURPOSE: The 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. METHODS: The study was based on a cohort of 749 CSVD patients in Taiwan who received next-generation sequencing of CSVD genes...

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Identifiers

PMID: 35781912
DOI: 10.1111/ene.15485

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

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