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SUMMARY:Cystic Fibrosis: Precision Treatment of a Rare Monogenic Disease
DESCRIPTION:Wednesday\, October 4 | 3 – 5 p.m. ET | Online \nJoin the UNC Program for Precision Medicine in Healthcare (PPMH) for Cystic Fibrosis: Precision Treatment of a Rare Monogenic Disease\, a free virtual mini-symposium. At this interactive event\, participants will engage in discussion with leading precision nutrition researchers at UNC. \nPresentation: Developing small-molecule therapies to rescue rare CFTR variants\nSpeaker:\nRhianna Lee\, PhD\nPostdoctoral associate\, Duke University\, Cell Biology Department \nPresentation: Personalized medicine\, the fight against antibiotic resistance\, and precision dosing\nSpeaker:\nGauri Rao\, PharmD\nAssociate Professor\, USC Mann School of Pharmacy and Pharmaceutical Sciences\, University of Southern California\nAdjunct Associate Professor\, UNC Eshelman School of Pharmacy\, UNC Chapel Hill \nPresentation: From Data to Dosing: Streamlining CF Modulator Choices\nSpeaker:\nMichael Adams\, MD\nClinical Instructor\, Division of Genetics & Metabolism\, Department of Pediatrics\, UNC School of Medicine \nLearn more and register on the PPMH website.
URL:https://gmkb.org/event/cystic-fibrosis-precision-treatment-of-a-rare-monogenic-disease/
LOCATION:Virtual
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