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They focus on developing innovative therapies, including vesicular monoamine transporter 2 (VMAT2) inhibitors and alternative formulations, to improve patient outcomes and address unmet medical needs
Murine models utilising therapeutics of non-mouse origin appear to be poorly representative of irAEs in humans
The tip and hidden part of the iceberg: proteinogenic and non-proteinogenic aliphatic amino acids
Long-term Efficacy and Safety of Rifampin in the Treatment of a Patient Carrying a CYP24A1 Loss-of-Function Variant
