Community Research Partners presents Tennessee Sickle Cell Disease Network
Matt Schorr
August 29, 2016
NASHVILLE, Tenn. The Tennessee Sickle Cell Disease Network seeks to engage sickle cell disease community stakeholders in Patient Centered Outcomes Research as an essential mechanism for advancing care and meaningful research for this rare disease population. Initial engagement phases and findings of a statewide research and engagement program will be discussed.
Dr. Murry appointed to NIH Psychosocial Development, Risk and Prevention Study Section, Center for Scientific Review
Matt Schorr
June 27, 2016