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& Akbulut, B

doi: 10.1002/jcp.26052

Clichici et al., 2016)

Fourth, the lack of prospective symptom assessment with the same questionnaires in OAB and IC/BPS patients

By comparing our in vitro predictive data to clinical liver toxicity monitoring in patients undergoing ribociclib treatment, we found that patient #2078 experienced grade 3 liver toxicity approximately 4 months after starting therapy, while patients #2080 and #2081 exhibited no hepatotoxic effects