Comparison of models for stroke-free survival prediction in patients with CADASIL

Abstract Cerebral autosomal dominant arteriopathy with subcortical infarcts and leukoencephalopathy, which is caused by mutations of the NOTCH3 gene, has a large heterogeneous progression, presenting with declines of various clinical scores and occurrences of various clinical event. To help assess d...

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Bibliographic Details
Main Authors: Henri Chhoa, Hugues Chabriat, Sylvie Chevret, Lucie Biard
Format: Article
Language:English
Published: Nature Portfolio 2023-12-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-023-49552-w