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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| Autori principali: | , , , |
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| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Nature Portfolio
2023-12-01
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| Serie: | Scientific Reports |
| Accesso online: | https://doi.org/10.1038/s41598-023-49552-w |
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