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Baseline information and MRI data were extracted from a computerized database. For the collection of adverse events, all patients were contacted once by phone in 2019. Patients voluntarily provided information on whether they experienced symptomatic cerebral hemorrhage or recurrent cerebral infarction after discharge. The identification of adverse events was based on disease certificates provided by patients or their relatives.
Copyright and License information: The Author(s) ©2020
Creative Commons Non Commercial CC BY-NC: This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
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