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Funding This study was supported in part by a Grant-in-Aid for Scientific Research from the Japan Society for the Promotion of Science (18H03171) and the Japan Agency for Medical Research and Development under Grant Number JP18ek0210111
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PubMed Wijeysundera, D
pat Js sutinkate, kad js duomenys bt tvarkomi tiesiogins rinkodaros tikslu
For most participants, symptoms resolved or became manageable within the first two to three weeks at each dose level
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